HUGO Gene Nomenclature Committee
Names
More detailed information about this field from each metasource.
HUGO Gene Nomenclature Committee
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
HGNC
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: Biontology / Bioportal
version: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
HUGO Gene Nomenclature
metasource: Biontology / Bioportal
version: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
Human gene nomenclature database (HGNC)
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
hgnc
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
Names
More detailed information about this field from each metasource.
HUGO Gene Nomenclature Committee
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
HGNC
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: Biontology / Bioportal
version: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
HUGO Gene Nomenclature
metasource: Biontology / Bioportalversion: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
Human gene nomenclature database (HGNC)
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
hgnc
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
Other names: HGNC, HUGO Gene Nomenclature, Human gene nomenclature database (HGNC), hgnc
Names
More detailed information about this field from each metasource.
HUGO Gene Nomenclature Committee
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
HGNC
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: Biontology / Bioportal
version: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
HUGO Gene Nomenclature
metasource: Biontology / Bioportalversion: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
Human gene nomenclature database (HGNC)
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
hgnc
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
HGNC is responsible for approving unique symbols and names for human loci, including protein coding genes, ncRNA genes and pseudogenes, to allow unambiguous scientific communication.
Description
More detailed information about this field from each metasource.
HGNC is responsible for approving unique symbols and names for human loci, including protein coding genes, ncRNA genes and pseudogenes, to allow unambiguous scientific communication.
metasource: BiŌkeanós-Medsourcingversion: 0.0.1:2022-11-04T13:34:25.975929
The HUGO Gene Nomenclature Committee (HGNC) is responsible for approving unique symbols, names and IDs for human loci, including protein coding genes, ncRNA genes and pseudogenes, to allow unambiguous scientific communication. The HGNC database is the resource for approved human gene nomenclature and is accessed via the website genenames.org. The website displays a page for every named gene and includes curated nomenclature information (including approved, previous and alias gene names and symbols). The website also displays manually curated gene group pages, the HCOP orthology tool and multi-symbol checker, and links to many other resources.
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
Human Genome Organisation (HUGO) Gene Nomenclature Committee at the European Bioinformatics Institute approves a gene name and symbol (short-form abbreviation) for each known human gene. All approved symbols are stored in the HGNC database.
metasource: Biontology / Bioportalversion: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
The HUGO Gene Nomenclature Committee (HGNC) assigned unique gene symbols and names to over 35,000 human loci, of which around 19,000 are protein coding. This curated online repository of HGNC-approved gene nomenclature and associated resources includes links to genomic, proteomic and phenotypic information, as well as dedicated gene family pages.
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
Database of unique and meaningful names for all human genes.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
Webpage:
https://www.genenames.orgWebpage
More detailed information about this field from each metasource.
https://www.genenames.org
metasource: BiŌkeanós-Medsourcingversion: 0.0.1:2022-11-04T13:34:25.975929
https://www.genenames.org/
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
http://www.genenames.org/
metasource: Biontology / Bioportalversion: July2010 extracted_at: 2022-11-04T11:10:15.597147, http://bioportal.bioontology.org/ontologies/HGNC
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
Licence:
Name: HGNC - specific / no license / permissive / free for allLicence name
More detailed information about this field from each metasource.
HGNC - specific / no license / permissive / free for all
metasource: BiŌkeanós-Medsourcingversion: 0.0.1:2022-11-04T13:34:25.975929
Open Data Commons (ODC) Public Domain Dedication and Licence (PDDL) 1.0
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
other
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
Licence URL
More detailed information about this field from each metasource.
https://www.genenames.org/about/
metasource: BiŌkeanós-Medsourcingversion: 0.0.1:2022-11-04T13:34:25.975929
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
http://opendatacommons.org/licenses/pddl/1.0/
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
Publications:
(9)
Publications
More detailed information about this field from each metasource.
Genenames.org: the HGNC resources in 2015
PMID: 25361968
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
The HUGO Gene Nomenclature Committee (HGNC)
PMID: 11810281
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
Genenames.org: the HGNC and VGNC resources in 2017
PMID: 27799471
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
Genenames.org: the HGNC and VGNC resources in 2019
PMID: 30304474
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
Genenames.org: the HGNC resources in 2013
PMID: 23161694
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
genenames.org: the HGNC resources in 2011
PMID: 20929869
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
The HGNC Database in 2008: a resource for the human genome
PMID: 17984084
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
The HUGO Gene Nomenclature Database, 2006 updates
PMID: 16381876
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
Genew: the Human Gene Nomenclature Database, 2004 updates
PMID: 14681406
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
Publications
More detailed information about this field from each metasource.
Genenames.org: the HGNC resources in 2015
PMID: 25361968
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
The HUGO Gene Nomenclature Committee (HGNC)
PMID: 11810281
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
Genenames.org: the HGNC and VGNC resources in 2017
PMID: 27799471
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
Genenames.org: the HGNC and VGNC resources in 2019
PMID: 30304474
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
Genenames.org: the HGNC resources in 2013
PMID: 23161694
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
genenames.org: the HGNC resources in 2011
PMID: 20929869
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
The HGNC Database in 2008: a resource for the human genome
PMID: 17984084
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
The HUGO Gene Nomenclature Database, 2006 updates
PMID: 16381876
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
Genew: the Human Gene Nomenclature Database, 2004 updates
PMID: 14681406
metasource: BiŌkeanós-Medsourcing
version: 0.0.1:2022-11-04T13:34:25.975929
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Genenames.org: the HGNC resources in 2015
PubMed citations: 287.
287 articles citing: Genenames.org: the HGNC resources in 2015
dbEssLnc: A manually curated database of human and mouse essential lncRNA genes. PMID:35685362
Precision medicine journey through omics approach. PMID:35673436
Lymph node colonization induces tumor-immune tolerance to promote distant metastasis. PMID:35525247
The Role of Zinc Finger Proteins in Various Oral Conditions. PMID:35463825
The State of Data in Healthcare: Path Towards Standardization. PMID:35415409
Syndromic male subfertility: A network view of genome-phenome associations. PMID:35218153
Zinc Finger Proteins in Neuro-Related Diseases Progression. PMID:34867169
Cyclosporin A: A Repurposable Drug in the Treatment of COVID-19? PMID:34552938
Feasibility of using probabilistic methods to analyse microRNA quantitative data in forensically relevant body fluids: a proof-of-principle study. PMID:34477924
Metabolomics and Network Pharmacology-Based Investigation into the Mechanisms Underlying the Therapeutic Effect of a New Chinese Traditional Medicine (Cui Nai Ling) on Bromocriptine-Induced Hypogalactia. PMID:34221092
A Systems-Based Key Innovation-Driven Approach Infers Co-option of Jaw Developmental Programs During Cancer Progression. PMID:34150777
PharmVar GeneFocus: CYP2C9. PMID:34109627
Towards FAIR protocols and workflows: the OpenPREDICT use case. PMID:33816932
Functional Prediction of Long Noncoding RNAs in Cutaneous Melanoma Using a Systems Biology Approach. PMID:33613027
Designed leucine-rich repeat proteins bind two muramyl dipeptide ligands. PMID:33512005
An empirical meta-analysis of the life sciences linked open data on the web. PMID:33479214
TGFBR3L-An Uncharacterised Pituitary Specific Membrane Protein Detected in the Gonadotroph Cells in Non-Neoplastic and Tumour Tissue. PMID:33396509
Neural Networks Recapitulation by Cancer Cells Promotes Disease Progression: A Novel Role of p73 Isoforms in Cancer-Neuronal Crosstalk. PMID:33339112
A comprehensive library of human transcription factors for cell fate engineering. PMID:33257861
Pharmacogenomics for Primary Care: An Overview. PMID:33198260
Identification of Latent Oncogenes with a Network Embedding Method and Random Forest. PMID:33029511
Systematics for types and effects of RNA variations. PMID:32951567
Signatures of co-deregulated genes and their transcriptional regulators in colorectal cancer. PMID:32737302
PharmVar GeneFocus: CYP2C19. PMID:32602114
A pan-cancer analysis of the frequency of DNA alterations across cell cycle activity levels. PMID:32581248
IRESbase: A Comprehensive Database of Experimentally Validated Internal Ribosome Entry Sites. PMID:32512182
A meta-analysis of gene expression data highlights synaptic dysfunction in the hippocampus of brains with Alzheimer's disease. PMID:32433480
Gene Ontology Curation of Neuroinflammation Biology Improves the Interpretation of Alzheimer's Disease Gene Expression Data. PMID:32417785
DRUGPATH: The Drug Gene Pathway Meta-Database. PMID:32365960
PRIORI-T: A tool for rare disease gene prioritization using MEDLINE. PMID:32315351
FHIR Genomics: enabling standardization for precision medicine use cases. PMID:32194985
Zinc Finger Proteins in the Human Fungal Pathogen Cryptococcus neoformans. PMID:32085473
Evidences for Expression and Location of ANGPTL8 in Human Adipose Tissue. PMID:32069954
Variation benchmark datasets: update, criteria, quality and applications. PMID:32016318
A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease. PMID:31767637
A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS. PMID:31724694
Identification of DHODH as a therapeutic target in small cell lung cancer. PMID:31694929
Uncovering extensive post-translation regulation during human cell cycle progression by integrative multi-'omics analysis. PMID:31664894
Genome wide survey, evolution and expression analysis of PHD finger genes reveal their diverse roles during the development and abiotic stress responses in Brassica rapa L. PMID:31651238
Olfactory receptor gene abundance in invasive breast carcinoma. PMID:31551495
AVADA: toward automated pathogenic variant evidence retrieval directly from the full-text literature. PMID:31467448
Comprehensive Cell Surface Antigen Analysis Identifies Transferrin Receptor Protein-1 (CD71) as a Negative Selection Marker for Human Neuronal Cells. PMID:31381839
Survival analysis and functional annotation of long non-coding RNAs in lung adenocarcinoma. PMID:31211495
CAM: an alignment-free method to recover phylogenies using codon aversion motifs. PMID:31198636
Fido-SNP: the first webserver for scoring the impact of single nucleotide variants in the dog genome. PMID:31114899
QBiC-Pred: quantitative predictions of transcription factor binding changes due to sequence variants. PMID:31114870
Multi-omic Profiling Reveals Dynamics of the Phased Progression of Pluripotency. PMID:31078527
CANCROX: a cross-species cancer therapy database. PMID:31032838
A signature of circulating inflammatory proteins and development of end-stage renal disease in diabetes. PMID:31011203
HumCFS: a database of fragile sites in human chromosomes. PMID:30999860
Gene expression shifts in yellow-bellied marmots prior to natal dispersal. PMID:30971856
Analysis of the role of the Hippo pathway in cancer. PMID:30961610
Context-sensitive network analysis identifies food metabolites associated with Alzheimer's disease: an exploratory study. PMID:30704467
Matching tRNA modifications in humans to their known and predicted enzymes. PMID:30698754
Human Testis Phosphoproteome Reveals Kinases as Potential Targets in Spermatogenesis and Testicular Cancer. PMID:30683686
Modeling cell line-specific recruitment of signaling proteins to the insulin-like growth factor 1 receptor. PMID:30653502
A unified solution for different scenarios of predicting drug-target interactions via triple matrix factorization. PMID:30598094
Systematics for types and effects of DNA variations. PMID:30591019
A Curated Resource for Phosphosite-specific Signature Analysis. PMID:30563849
LCE: an open web portal to explore gene expression and clinical associations in lung cancer. PMID:30532070
Improving the Gene Ontology Resource to Facilitate More Informative Analysis and Interpretation of Alzheimer's Disease Data. PMID:30501127
Plasma proteome correlates of lipid and lipoprotein: biomarkers of metabolic diversity and inflammation in children of rural Nepal. PMID:30473544
Variant information systems for precision oncology. PMID:30463544
BioGraph: a web application and a graph database for querying and analyzing bioinformatics resources. PMID:30458802
Lnc2Cancer v2.0: updated database of experimentally supported long non-coding RNAs in human cancers. PMID:30407549
Characterization of Squamous Cell Lung Cancers from Appalachian Kentucky. PMID:30377206
Arena-Idb: a platform to build human non-coding RNA interaction networks. PMID:30367585
Identification of two principal amyloid-driving segments in variable domains of Ig light chains in systemic light-chain amyloidosis. PMID:30355736
Transcriptome evidence reveals enhanced autophagy-lysosomal function in centenarians. PMID:30352807
Analysis of impact metrics for the Protein Data Bank. PMID:30325351
SMART Cancer Navigator: A Framework for Implementing ASCO Workshop Recommendations to Enable Precision Cancer Medicine. PMID:30238071
Copy Number Alterations in Tumor Genomes Deleting Antineoplastic Drug Targets Partially Compensated by Complementary Amplifications. PMID:30194077
ESCC ATLAS: A population wide compendium of biomarkers for Esophageal Squamous Cell Carcinoma. PMID:30143675
Proteomics for blood biomarker exploration of severe mental illness: pitfalls of the past and potential for the future. PMID:30115926
JustOrthologs: a fast, accurate and user-friendly ortholog identification algorithm. PMID:30084941
Cyclophilins and cyclophilin inhibitors in nidovirus replication. PMID:30014857
Netpredictor: R and Shiny package to perform drug-target network analysis and prediction of missing links. PMID:30012095
Clinical and Genomic Characterization of Treatment-Emergent Small-Cell Neuroendocrine Prostate Cancer: A Multi-institutional Prospective Study. PMID:29985747
Phenotype-driven gene prioritization for rare diseases using graph convolution on heterogeneous networks. PMID:29980210
Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners. PMID:29971594
Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. PMID:29942513
Neuronal integrity and complement control synaptic material clearance by microglia after CNS injury. PMID:29941548
Integrated multi-omics data analysis identifying novel drug sensitivity-associated molecular targets of hepatocellular carcinoma cells. PMID:29930714
A cytokine protein-protein interaction network for identifying key molecules in rheumatoid arthritis. PMID:29928007
Clinical response of the novel activating ALK-I1171T mutation in neuroblastoma to the ALK inhibitor ceritinib. PMID:29907598
CATCH-KB: Establishing a Pharmacogenomics Variant Repository for Chemotherapy-Induced Cardiotoxicity. PMID:29888066
Negative selection in tumor genome evolution acts on essential cellular functions and the immunopeptidome. PMID:29855388
The Cellosaurus, a Cell-Line Knowledge Resource. PMID:29805321
Carbonyl reduction of NNK by recombinant human lung enzymes: identification of HSD17β12 as the reductase important in (R)-NNAL formation in human lung. PMID:29788210
Systematic interrogation of diverse Omic data reveals interpretable, robust, and generalizable transcriptomic features of clinically successful therapeutic targets. PMID:29782487
Mammalian EAK-7 activates alternative mTOR signaling to regulate cell proliferation and migration. PMID:29750193
Structural Insights into N6-methyladenosine (m6A) Modification in the Transcriptome. PMID:29709557
NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database. PMID:29688368
Community-driven roadmap for integrated disease maps. PMID:29688273
Viral Induced Oxidative and Inflammatory Response in Alzheimer's Disease Pathogenesis with Identification of Potential Drug Candidates: A Systematic Review using Systems Biology Approach. PMID:29676229
Bipartite graphs in systems biology and medicine: a survey of methods and applications. PMID:29648623
Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa. PMID:29642851
Deep Learning for Drug Design: an Artificial Intelligence Paradigm for Drug Discovery in the Big Data Era. PMID:29603063
Teleost Fish-Specific Preferential Retention of Pigmentation Gene-Containing Families After Whole Genome Duplications in Vertebrates. PMID:29599177
SMILE: a novel procedure for subcellular module identification with localisation expansion. PMID:29533218
From gene networks to drugs: systems pharmacology approaches for AUD. PMID:29497781
Integrated Theory- and Data-driven Feature Selection in Gene Expression Data Analysis. PMID:29422764
Long non-coding RNA GAS5 and ZFAS1 are prognostic markers involved in translation targeted by miR-940 in prostate cancer. PMID:29416676
Peptide Level Turnover Measurements Enable the Study of Proteoform Dynamics. PMID:29414762
XRCC3 Thr241Met and TYMS variable number tandem repeat polymorphisms are associated with time-to-metastasis in colorectal cancer. PMID:29394274
Genetic sex determination assays in 53 mammalian species: Literature analysis and guidelines for reporting standardization. PMID:29375774
Genome-wide protein phylogenies for four African cichlid species. PMID:29368592
DataMed - an open source discovery index for finding biomedical datasets. PMID:29346583
Genomic repeats, misassembly and reannotation: a case study with long-read resequencing of Porphyromonas gingivalis reference strains. PMID:29338683
Multiple Inhibitory Factors Act in the Late Phase of HIV-1 Replication: a Systematic Review of the Literature. PMID:29321222
Linking FOXO3, NCOA3, and TCF7L2 to Ras pathway phenotypes through a genome-wide forward genetic screen in human colorectal cancer cells. PMID:29301589
A systematic atlas of chaperome deregulation topologies across the human cancer landscape. PMID:29293508
Characterization of host proteins interacting with the lymphocytic choriomeningitis virus L protein. PMID:29261807
Membrane Transporters for Bilirubin and Its Conjugates: A Systematic Review. PMID:29259555
Genomic regression analysis of coordinated expression. PMID:29259170
Co-expression Patterns between ATN1 and ATXN2 Coincide with Brain Regions Affected in Huntington's Disease. PMID:29249939
The European Bioinformatics Institute in 2017: data coordination and integration. PMID:29186510
PlanNET: homology-based predicted interactome for multiple planarian transcriptomes. PMID:29186384
The OncoPPi Portal: an integrative resource to explore and prioritize protein-protein interactions for cancer target discovery. PMID:29186335
Zinc-finger proteins in health and disease. PMID:29152378
Comprehensive investigation of cytokine- and immune-related gene variants in HBV-associated hepatocellular carcinoma patients. PMID:29138264
The DNA methyltransferase family: a versatile toolkit for epigenetic regulation. PMID:29033456
Epigenome alterations in aortic valve stenosis and its related left ventricular hypertrophy. PMID:29026447
Differential Expression Profile of lncRNAs from Primary Human Hepatocytes Following DEET and Fipronil Exposure. PMID:28991164
MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis. PMID:28986402
The pharmacogenomics of severe traumatic brain injury. PMID:28975867
Gene Expression Signatures and Immunohistochemical Subtypes Add Prognostic Value to Each Other in Breast Cancer Cohorts. PMID:28972043
HUMA: A platform for the analysis of genetic variation in humans. PMID:28967693
Drug enrichment and discovery from schizophrenia genome-wide association results: an analysis and visualisation approach. PMID:28963561
High rate of adaptation of mammalian proteins that interact with Plasmodium and related parasites. PMID:28957326
Human hepatic gene expression signature of non-alcoholic fatty liver disease progression, a meta-analysis. PMID:28955037
Combinatorial ensemble miRNA target prediction of co-regulation networks with non-prediction data. PMID:28911111
Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. PMID:28874452
FANTOM5 CAGE profiles of human and mouse reprocessed for GRCh38 and GRCm38 genome assemblies. PMID:28850105
Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse. PMID:28838066
Current progress in innovative engineered antibodies. PMID:28822103
Cancerouspdomains: comprehensive analysis of cancer type-specific recurrent somatic mutations in proteins and domains. PMID:28814324
Settling the score: variant prioritization and Mendelian disease. PMID:28804138
MINERVA-a platform for visualization and curation of molecular interaction networks. PMID:28725475
Benchmarking selected computational gene network growing tools in context of virus-host interactions. PMID:28724991
CancerGD: A Resource for Identifying and Interpreting Genetic Dependencies in Cancer. PMID:28711281
Expression and regulation of drug transporters in vertebrate neutrophils. PMID:28694436
Epistasis in genomic and survival data of cancer patients. PMID:28678836
Pattern recognition for predictive, preventive, and personalized medicine in cancer. PMID:28620443
Improving biocuration of microRNAs in diseases: a case study in idiopathic pulmonary fibrosis. PMID:28605770
Prostaglandin E2 glyceryl ester is an endogenous agonist of the nucleotide receptor P2Y6. PMID:28539604
Recent advances in predicting gene-disease associations. PMID:28529714
Skeletal muscle metabolism during prolonged exercise in Pompe disease. PMID:28490439
Identification of a novel RASD1 somatic mutation in a USP8-mutated corticotroph adenoma. PMID:28487882
PhD-SNPg: a webserver and lightweight tool for scoring single nucleotide variants. PMID:28482034
Mining Exosomal Genes for Pancreatic Cancer Targets. PMID:28446531
Epigenomics of human CD8 T cell differentiation and aging. PMID:28439570
Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder. PMID:28419775
Transcriptome analysis reveals differentially expressed lncRNAs between oral squamous cell carcinoma and healthy oral mucosa. PMID:28415559
Rewiring of the inferred protein interactome during blood development studied with the tool PPICompare. PMID:28376810
Network-based characterization and prediction of human DNA repair genes and pathways. PMID:28368026
Ensembl core software resources: storage and programmatic access for DNA sequence and genome annotation. PMID:28365736
Comparison of tissue/disease specific integrated networks using directed graphlet signatures. PMID:28361704
ExCAPE-DB: an integrated large scale dataset facilitating Big Data analysis in chemogenomics. PMID:28316655
Development of Bioinformatics Infrastructure for Genomics Research. PMID:28302555
Systematic protein-protein interaction mapping for clinically relevant human GPCRs. PMID:28298427
An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils. PMID:28293191
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease. PMID:28267784
Potential Role of ANGPTL4 in the Cross Talk between Metabolism and Cancer through PPAR Signaling Pathway. PMID:28182091
Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites. PMID:28158543
Identifying the missing proteins in human proteome by biological language model. PMID:28155671
The Plasma Proteome Is Associated with Anthropometric Status of Undernourished Nepalese School-Aged Children. PMID:28148680
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78). PMID:28137957
A Systematic Framework for Drug Repositioning from Integrated Omics and Drug Phenotype Profiles Using Pathway-Drug Network. PMID:28127549
Hydrogel scaffolds promote neural gene expression and structural reorganization in human astrocyte cultures. PMID:28097054
RAIN: RNA-protein Association and Interaction Networks. PMID:28077569
Evolution of protein N-glycosylation process in Golgi apparatus which shapes diversity of protein N-glycan structures in plants, animals and fungi. PMID:28074929
KinMap: a web-based tool for interactive navigation through human kinome data. PMID:28056780
The 24th annual Nucleic Acids Research database issue: a look back and upcoming changes. PMID:28053160
TCGA2BED: extracting, extending, integrating, and querying The Cancer Genome Atlas. PMID:28049410
Convergent evidence for the molecular basis of musical traits. PMID:28004803
A bedr way of genomic interval processing. PMID:27999613
Characterization of meningeal type 2 innate lymphocytes and their response to CNS injury. PMID:27994070
Functional and Genomic Features of Human Genes Mutated in Neuropsychiatric Disorders. PMID:27990183
Leigh map: A novel computational diagnostic resource for mitochondrial disease. PMID:27977873
Exploring FlyBase Data Using QuickSearch. PMID:27930807
FlyRNAi.org-the database of the Drosophila RNAi screening center and transgenic RNAi project: 2017 update. PMID:27924039
AAgAtlas 1.0: a human autoantigen database. PMID:27924021
Mouse Genome Database (MGD)-2017: community knowledge resource for the laboratory mouse. PMID:27899570
dbDEMC 2.0: updated database of differentially expressed miRNAs in human cancers. PMID:27899556
ANOS1: a unified nomenclature for Kallmann syndrome 1 gene (KAL1) and anosmin-1. PMID:27899353
Size distribution of function-based human gene sets and the split-merge model. PMID:27853602
Measuring the Kinetic and Mechanical Properties of Non-processive Myosins Using Optical Tweezers. PMID:27844441
Improving Gene-Set Enrichment Analysis of RNA-Seq Data with Small Replicates. PMID:27829002
Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unravelling the full complexity of multi-factorial multidrug resistance. PMID:27824156
Genenames.org: the HGNC and VGNC resources in 2017. PMID:27799471
Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODE. PMID:27793185
The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations. PMID:27789569
Integrating cancer genomic data into electronic health records. PMID:27784327
The state of play in higher eukaryote gene annotation. PMID:27773922
Activity-Dependent Changes in Gene Expression in Schizophrenia Human-Induced Pluripotent Stem Cell Neurons. PMID:27732689
Using FlyBase, a Database of Drosophila Genes and Genomes. PMID:27730573
Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis. PMID:27701660
Gene expression elucidates functional impact of polygenic risk for schizophrenia. PMID:27668389
Potential synergistic action of 19 schizophrenia risk genes in the thalamus. PMID:27645107
Local microRNA delivery targets Palladin and prevents metastatic breast cancer. PMID:27641360
FBW7 suppression leads to SOX9 stabilization and increased malignancy in medulloblastoma. PMID:27625374
Comparative analysis of housekeeping and tissue-specific driver nodes in human protein interaction networks. PMID:27612563
ExonImpact: Prioritizing Pathogenic Alternative Splicing Events. PMID:27604408
Training and evaluation corpora for the extraction of causal relationships encoded in biological expression language (BEL). PMID:27554092
Integrating genomic information with protein sequence and 3D atomic level structure at the RCSB protein data bank. PMID:27551105
Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases. PMID:27544590
Mouse models of Down syndrome: gene content and consequences. PMID:27538963
Membranome: a database for proteome-wide analysis of single-pass membrane proteins. PMID:27510400
Data and programs in support of network analysis of genes and their association with diseases. PMID:27508260
DTMiner: identification of potential disease targets through biomedical literature mining. PMID:27506226
Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution. PMID:27493218
Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. PMID:27490719
Combined genetic and epigenetic interferences with interferon signaling expose prostate cancer cells to viral infection. PMID:27366948
A Perspective on the Role of Myosins as Mechanosensors. PMID:27332116
Jumping across biomedical contexts using compressive data fusion. PMID:27307649
Bioinformatic Studies to Predict MicroRNAs with the Potential of Uncoupling RECK Expression from Epithelial-Mesenchymal Transition in Cancer Cells. PMID:27226706
Deep Learning Applications for Predicting Pharmacological Properties of Drugs and Drug Repurposing Using Transcriptomic Data. PMID:27200455
Pan-cancer analyses of the nuclear receptor superfamily. PMID:27200367
An Integrated Data Driven Approach to Drug Repositioning Using Gene-Disease Associations. PMID:27196054
Viruses are a dominant driver of protein adaptation in mammals. PMID:27187613
BELTracker: evidence sentence retrieval for BEL statements. PMID:27173525
Building a glaucoma interaction network using a text mining approach. PMID:27152122
The ANGPTL3-4-8 model, a molecular mechanism for triglyceride trafficking. PMID:27053679
Long non-coding RNA Databases in Cardiovascular Research. PMID:27049585
SMART precision cancer medicine: a FHIR-based app to provide genomic information at the point of care. PMID:27018265
CUSTOM-SEQ: a prototype for oncology rapid learning in a comprehensive EHR environment. PMID:27008846
Müller glia reactivity follows retinal injury despite the absence of the glial fibrillary acidic protein gene in Xenopus. PMID:26996101
Wikidata as a semantic framework for the Gene Wiki initiative. PMID:26989148
shRNA target prediction informed by comprehensive enquiry (SPICE): a supporting system for high-throughput screening of shRNA library. PMID:26941783
FlyBase portals to human disease research using Drosophila models. PMID:26935103
Genomics of Rapid Incipient Speciation in Sympatric Threespine Stickleback. PMID:26925837
Human Variome Project Quality Assessment Criteria for Variation Databases. PMID:26919176
Distinct Activities of Myf5 and MyoD Indicate Separate Roles in Skeletal Muscle Lineage Specification and Differentiation. PMID:26906734
Featured Article: Genotation: Actionable knowledge for the scientific reader. PMID:26900164
The UniProtKB guide to the human proteome. PMID:26896845
LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer. PMID:26860319
A review of the new HGNC gene family resource. PMID:26842383
BISQUE: locus- and variant-specific conversion of genomic, transcriptomic and proteomic database identifiers. PMID:26803163
A network analysis of cofactor-protein interactions for analyzing associations between human nutrition and diseases. PMID:26777674
The clinical trial landscape in oncology and connectivity of somatic mutational profiles to targeted therapies. PMID:26772741
The Molecular Signatures Database (MSigDB) hallmark gene set collection. PMID:26771021
The aminoacyl-tRNA synthetases of Drosophila melanogaster. PMID:26761199
Understanding transport by the major facilitator superfamily (MFS): structures pave the way. PMID:26758938
A common molecular signature in ASD gene expression: following Root 66 to autism. PMID:26731442
Challenges in the development of therapeutics for narcolepsy. PMID:26721620
Computational selection of antibody-drug conjugate targets for breast cancer. PMID:26700623
Bioinformatics Mining and Modeling Methods for the Identification of Disease Mechanisms in Neurodegenerative Disorders. PMID:26690135
Systems Proteomics View of the Endogenous Human Claudin Protein Family. PMID:26680015
Plasma Proteome Biomarkers of Inflammation in School Aged Children in Nepal. PMID:26636573
Mouse genome database 2016. PMID:26578600
pubmed.mineR: an R package with text-mining algorithms to analyse PubMed abstracts. PMID:26564970
Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation. PMID:26553804
WITHDRAWN--a resource for withdrawn and discontinued drugs. PMID:26553801
DASHR: database of small human noncoding RNAs. PMID:26553799
KLIFS: a structural kinase-ligand interaction database. PMID:26496949
Prognostic Utility of Molecular Factors by Age at Diagnosis of Colorectal Cancer. PMID:26490308
DIDA: A curated and annotated digenic diseases database. PMID:26481352
Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting. PMID:26479518
Definition of a consensus integrin adhesome and its dynamics during adhesion complex assembly and disassembly. PMID:26479319
FlyBase: establishing a Gene Group resource for Drosophila melanogaster. PMID:26467478
The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. PMID:26464438
miRSponge: a manually curated database for experimentally supported miRNA sponges and ceRNAs. PMID:26424084
Comprehensive comparative homeobox gene annotation in human and mouse. PMID:26412852
PathwaysWeb: a gene pathways API with directional interactions, expanded gene ontology, and versioning. PMID:26400039
Constitutive Activity among Orphan Class-A G Protein Coupled Receptors. PMID:26384023
Quantitative Genetics of Food Intake in Drosophila melanogaster. PMID:26375667
Devising a Consensus Framework for Validation of Novel Human Coding Loci. PMID:26367542
Gene expression meta-analysis reveals immune response convergence on the IFNγ-STAT1-IRF1 axis and adaptive immune resistance mechanisms in lymphoma. PMID:26362649
Data integration in biological research: an overview. PMID:26336651
Histoimmunogenetics Markup Language 1.0: Reporting next generation sequencing-based HLA and KIR genotyping. PMID:26319908
The Mitochondrial Genomes of Aquila fasciata and Buteo lagopus (Aves, Accipitriformes): Sequence, Structure and Phylogenetic Analyses. PMID:26295156
Transcriptional maturation of the mouse auditory forebrain. PMID:26271746
Identification of Region-Specific Myocardial Gene Expression Patterns in a Chronic Swine Model of Repaired Tetralogy of Fallot. PMID:26252659
Orthology for comparative genomics in the mouse genome database. PMID:26223881
SHIELD: an integrative gene expression database for inner ear research. PMID:26209310
RefSeq curation and annotation of antizyme and antizyme inhibitor genes in vertebrates. PMID:26170238
Xenbase: Core features, data acquisition, and data processing. PMID:26150211
Biological determinants of bladder cancer gene expression subtypes. PMID:26051783
GLASS: a comprehensive database for experimentally validated GPCR-ligand associations. PMID:25971743
Determining minimum set of driver nodes in protein-protein interaction networks. PMID:25947063
A property-based analysis of human transcription factors. PMID:25890365
The emerging landscape of small nucleolar RNAs in cell biology. PMID:25879954
Biological databases for human research. PMID:25712261
The Chlamydomonas cell cycle. PMID:25690512
The landscape of long noncoding RNAs in the human transcriptome. PMID:25599403
Next-generation sequencing in clinical oncology: next steps towards clinical validation. PMID:25412366 -
The HUGO Gene Nomenclature Committee (HGNC)
PubMed citations: 180.
180 articles citing: The HUGO Gene Nomenclature Committee (HGNC)
Network Proximity-Based Drug Repurposing Strategy for Early and Late Stages of Primary Biliary Cholangitis. PMID:35884999
Integrative mRNA and Long Noncoding RNA Analysis Reveals the Regulatory Network of Floral Bud Induction in Longan (Dimocarpus longan Lour.). PMID:35774802
PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine. PMID:35743744
BETA: a comprehensive benchmark for computational drug-target prediction. PMID:35649342
Strategies for Successful Over-Expression of Human Membrane Transport Systems Using Bacterial Hosts: Future Perspectives. PMID:35409183
Comment on Li et al. BDP1 Variants I1264M and V1347M Significantly Associated with Clinical Outcomes of Pediatric Neuroblastoma Patients Imply a New Prognostic Biomarker: A 121-Patient Cancer Genome Study. Diagnostics 2021, 11, 2364. PMID:35328161
Machine Learning-Based Analysis of Glioma Grades Reveals Co-Enrichment. PMID:35205761
Zebrafish information network, the knowledgebase for Danio rerio research. PMID:35166825
Pairs of Mutually Compensatory Frameshifting Mutations Contribute to Protein Evolution. PMID:35137193
An Uninvited Seat at the Dinner Table: How Apicomplexan Parasites Scavenge Nutrients from the Host. PMID:34946193
New data and collaborations at the Saccharomyces Genome Database: updated reference genome, alleles, and the Alliance of Genome Resources. PMID:34897464
Unifying heterogeneous expression data to predict targets for CAR-T cell therapy. PMID:34858726
The phenotypic characteristics of patients with athelia and tooth agenesis. PMID:34790789
Text mining-based word representations for biomedical data analysis and protein-protein interaction networks in machine learning tasks. PMID:34653224
Three decades of the Human Genome Organization. PMID:34581472
KinOrtho: a method for mapping human kinase orthologs across the tree of life and illuminating understudied kinases. PMID:34537014
Gotree/Goalign: toolkit and Go API to facilitate the development of phylogenetic workflows. PMID:34396097
Signature Panel of 11 Methylated mRNAs and 3 Methylated lncRNAs for Prediction of Recurrence-Free Survival in Prostate Cancer Patients. PMID:34285549
Identification of a Seven-lncRNA-mRNA Signature for Recurrence and Prognostic Prediction in Relapsed Acute Lymphoblastic Leukemia Based on WGCNA and LASSO Analyses. PMID:34211824
Integrated network analysis identifying potential novel drug candidates and targets for Parkinson's disease. PMID:34162989
History of the methodology of disease gene identification. PMID:34159713
DGLinker: flexible knowledge-graph prediction of disease-gene associations. PMID:34125897
Swarm: A federated cloud framework for large-scale variant analysis. PMID:33979321
Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia. PMID:33958802
A genome-wide atlas of co-essential modules assigns function to uncharacterized genes. PMID:33859415
A Review of Cancer Genetics and Genomics Studies in Africa. PMID:33659210
Algorithmic Annotation of Functional Roles for Components of 3,044 Human Molecular Pathways. PMID:33633781
Degree Adjusted Large-Scale Network Analysis Reveals Novel Putative Metabolic Disease Genes. PMID:33546175
GeneWalk identifies relevant gene functions for a biological context using network representation learning. PMID:33526072
Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease. PMID:33288751
Chemocentric Informatics Analysis: Dexamethasone Versus Combination Therapy for COVID-19. PMID:33251412
Identification of Crucial lncRNAs, miRNAs, mRNAs, and Potential Therapeutic Compounds for Polycystic Ovary Syndrome by Bioinformatics Analysis. PMID:33224973
Prognosis prediction model based on competing endogenous RNAs for recurrence of colon adenocarcinoma. PMID:33028275
Integrated analysis identifies a long non-coding RNAs-messenger RNAs signature for prediction of prognosis in hepatitis B virus-hepatocellular carcinoma patients. PMID:33019382
Coexpression Network Analysis Identifies a Novel Nine-RNA Signature to Improve Prognostic Prediction for Prostate Cancer Patients. PMID:32953881
A guide to plasma membrane solute carrier proteins. PMID:32810346
Identification and Validation of an Energy Metabolism-Related lncRNA-mRNA Signature for Lower-Grade Glioma. PMID:32802843
EHR-Independent Predictive Decision Support Architecture Based on OMOP. PMID:32492716
Developing a Search Engine for Precision Medicine. PMID:32477680
Identification of a Novel Eight-lncRNA Prognostic Signature for HBV-HCC and Analysis of Their Functions Based on Coexpression and ceRNA Networks. PMID:32382578
GOLD standard dataset for Alzheimer genes. PMID:32337326
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer. PMID:32246132
Transfer learning with convolutional neural networks for cancer survival prediction using gene-expression data. PMID:32214348
Role of the XIST-miR-181a-COL4A1 axis in the development and progression of keratoconus. PMID:32165822
Recurrence-Associated Multi-RNA Signature to Predict Disease-Free Survival for Ovarian Cancer Patients. PMID:32149080
A 6 lncRNA-Based Risk Score System for Predicting the Recurrence of Colon Adenocarcinoma Patients. PMID:32117736
The Impact of Pathway Database Choice on Statistical Enrichment Analysis and Predictive Modeling. PMID:31824580
Identification of differentially expressed genes between the colon and ileum of patients with inflammatory bowel disease by gene co-expression analysis. PMID:31822145
A Bioinformatic Approach for the Identification of Molecular Determinants of Resistance/Sensitivity to Cancer Thermotherapy. PMID:31814876
KETOS: Clinical decision support and machine learning as a service - A training and deployment platform based on Docker, OMOP-CDM, and FHIR Web Services. PMID:31581246
Using MARRVEL v1.2 for Bioinformatics Analysis of Human Genes and Variant Pathogenicity. PMID:31524990
Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information. PMID:31475990
Phenome-wide Burden of Copy-Number Variation in the UK Biobank. PMID:31353025
Genome-wide identification and expression profiling of the C2H2-type zinc finger protein genes in the silkworm Bombyx mori. PMID:31316872
HNCDB: An Integrated Gene and Drug Database for Head and Neck Cancer. PMID:31139565
Geneshot: search engine for ranking genes from arbitrary text queries. PMID:31114885
PathMe: merging and exploring mechanistic pathway knowledge. PMID:31092193
Genes with High Network Connectivity Are Enriched for Disease Heritability. PMID:31051114
Integrated analysis of lncRNA-associated ceRNA network reveals potential biomarkers for the prognosis of hepatitis B virus-related hepatocellular carcinoma. PMID:30697079
Detecting protein complexes based on a combination of topological and biological properties in protein-protein interaction network. PMID:30647725
SMART Cancer Navigator: A Framework for Implementing ASCO Workshop Recommendations to Enable Precision Cancer Medicine. PMID:30238071
Disruption of microglia histone acetylation and protein pathways in mice exhibiting inflammation-associated depression-like symptoms. PMID:30005281
Mechanism-based Pharmacovigilance over the Life Sciences Linked Open Data Cloud. PMID:29854169
PhLeGrA: Graph Analytics in Pharmacology over the Web of Life Sciences Linked Open Data. PMID:29479581
Protein complex finding and ranking: An application to Alzheimer's disease. PMID:29358552
The Porphyromonas gingivalis/Host Interactome Shows Enrichment in GWASdb Genes Related to Alzheimer's Disease, Diabetes and Cardiovascular Diseases. PMID:29311898
Chromosome preference of disease genes and vectorization for the prediction of non-coding disease genes. PMID:29108274
Intracrine androgen biosynthesis, metabolism and action revisited. PMID:28865807
Bridging Plant and Human Radiation Response and DNA Repair through an In Silico Approach. PMID:28587301
Testing for differentially expressed genetic pathways with single-subject N-of-1 data in the presence of inter-gene correlation. PMID:28552011
RNA-Seq based genome-wide analysis reveals loss of inter-chromosomal regulation in breast cancer. PMID:28496157
ChimeRScope: a novel alignment-free algorithm for fusion transcript prediction using paired-end RNA-Seq data. PMID:28472320
Deep mining heterogeneous networks of biomedical linked data to predict novel drug-target associations. PMID:28430977
Integrated network analysis reveals potentially novel molecular mechanisms and therapeutic targets of refractory epilepsies. PMID:28388656
Cross disease analysis of co-functional microRNA pairs on a reconstructed network of disease-gene-microRNA tripartite. PMID:28340554
Predicting disease-related genes using integrated biomedical networks. PMID:28198675
eUnaG: a new ligand-inducible fluorescent reporter to detect drug transporter activity in live cells. PMID:28176814
Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis. PMID:27844330
Applicability of predictive toxicology methods for monoclonal antibody therapeutics: status Quo and scope. PMID:27766364
Computational methods for direct cell conversion. PMID:27736295
The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes. PMID:27503295
Analysis of aggregated cell-cell statistical distances within pathways unveils therapeutic-resistance mechanisms in circulating tumor cells. PMID:27307648
Evidence for embryonic stem-like signature and epithelial-mesenchymal transition features in the spheroid cells derived from lung adenocarcinoma. PMID:27048287
DenguePredict: An Integrated Drug Repositioning Approach towards Drug Discovery for Dengue. PMID:26958268
Prognostic role of microRNA-210 in various carcinomas: a meta-analysis. PMID:26629015
OCDB: a database collecting genes, miRNAs and drugs for obsessive-compulsive disorder. PMID:26228432
Curcumin Resource Database. PMID:26220923
A genome-wide systems analysis reveals strong link between colorectal cancer and trimethylamine N-oxide (TMAO), a gut microbial metabolite of dietary meat and fat. PMID:26100814
Dynamic changes of RNA-sequencing expression for precision medicine: N-of-1-pathways Mahalanobis distance within pathways of single subjects predicts breast cancer survival. PMID:26072495
PolySearch2: a significantly improved text-mining system for discovering associations between human diseases, genes, drugs, metabolites, toxins and more. PMID:25925572
The BioMart community portal: an innovative alternative to large, centralized data repositories. PMID:25897122
Gateways to the FANTOM5 promoter level mammalian expression atlas. PMID:25723102
BGMUT Database of Allelic Variants of Genes Encoding Human Blood Group Antigens. PMID:25538536
Using VisANT to Analyze Networks. PMID:25422679
Etiology of autism spectrum disorder: a genomics perspective. PMID:25212713
A short guide to long non-coding RNA gene nomenclature. PMID:24716852
lncRNome: a comprehensive knowledgebase of human long noncoding RNAs. PMID:23846593
PharmGKB: the Pharmacogenomics Knowledge Base. PMID:23824865
PiHelper: an open source framework for drug-target and antibody-target data. PMID:23766416
Methylation state of the EDA gene promoter in Chinese X-linked hypohidrotic ectodermal dysplasia carriers. PMID:23626789
MalaCards: an integrated compendium for diseases and their annotation. PMID:23584832
Molecular modeling and ligand docking for solute carrier (SLC) transporters. PMID:23578028
Clinical value of prognosis gene expression signatures in colorectal cancer: a systematic review. PMID:23145004
Knowledge building insights on biomarkers of arsenic toxicity to keratinocytes and melanocytes. PMID:23115478
SigCS base: an integrated genetic information resource for human cerebral stroke. PMID:22784567
An ovary transcriptome for all maturational stages of the striped bass (Morone saxatilis), a highly advanced perciform fish. PMID:22353237
BioMart Central Portal: an open database network for the biological community. PMID:21930507
BioMart: a data federation framework for large collaborative projects. PMID:21930506
Moara: a Java library for extracting and normalizing gene and protein mentions. PMID:20346105
Comparison of human solute carriers. PMID:20052679
OmicBrowse: a Flash-based high-performance graphics interface for genomic resources. PMID:19528066
[A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter]. PMID:19183916
CRONOS: the cross-reference navigation server. PMID:19010804
Age-dependent dichotomous effect of superoxide dismutase Ala16Val polymorphism on oxidized LDL levels. PMID:18305395
[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15]. PMID:18066515
TreeFam: 2008 Update. PMID:18056084
Investigation of the association between normal-tension glaucoma and single nucleotide polymorphisms in natriuretic peptide gene. PMID:17460430
SNP@Ethnos: a database of ethnically variant single-nucleotide polymorphisms. PMID:17135185
An algorithm for model construction and its applications to pharmacogenomic studies. PMID:16900297
Challenges and strategies of the Genetics Home Reference. PMID:16888669
Functional nsSNPs from carcinogenesis-related genes expressed in breast tissue: potential breast cancer risk alleles and their distribution across human populations. PMID:16595073
Polymorphisms of estrogen receptor beta gene are associated with hypospadias. PMID:16553027
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss. PMID:16459341
Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria. PMID:16385445
The Gene Set Builder: collation, curation, and distribution of sets of genes. PMID:16371163
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12. PMID:16158433
Using co-occurrence network structure to extract synonymous gene and protein names from MEDLINE abstracts. PMID:15847682
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1. PMID:15711797
HAGR: the Human Ageing Genomic Resources. PMID:15608256
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1. PMID:15538632
Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells. PMID:15338276
Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing. PMID:15338275
Lipoprotein lipase gene is in linkage with blood pressure phenotypes in Chinese pedigrees. PMID:15127290
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype. PMID:15118904
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions. PMID:15103551
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. PMID:15057556
Variants of CYP46A1 may interact with age and APOE to influence CSF Abeta42 levels in Alzheimer's disease. PMID:15034781
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. PMID:15014980
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene. PMID:15007729
Chasing genes in Alzheimer's and Parkinson's disease. PMID:14999561
New genomic region for Wegener's granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes. PMID:14968360
Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II. PMID:14758537
The Gene Ontology Annotation (GOA) Database: sharing knowledge in Uniprot with Gene Ontology. PMID:14681408
Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28. PMID:14673643
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. PMID:14669009
Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria. PMID:14614622
Genetic and clinical mosaicism in a patient with neurofibromatosis type 1. PMID:14605872
Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation. PMID:14598163
Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome. PMID:14579146
De novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent's disease. PMID:14569459
Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1. PMID:14520560
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians. PMID:14505035
Molecular variation at the apolipoprotein B gene locus in relation to lipids and cardiovascular disease: a systematic meta-analysis. PMID:12942366
Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China. PMID:12938036
Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin. PMID:12928864
Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods. PMID:12928863
Functional analysis of intra-allelic variation at NACP-Rep1 in the alpha-synuclein gene. PMID:12923682
Mutational analysis of the human FATE gene in 144 infertile men. PMID:12811541
Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France. PMID:12768409
Cis-acting variation in the expression of a high proportion of genes in human brain. PMID:12728311
Disruption of exon definition produces a dominant-negative growth hormone isoform that causes somatotroph death and IGHD II. PMID:12720086
SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activity. PMID:12709790
A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis. PMID:12709789
ProSplicer: a database of putative alternative splicing information derived from protein, mRNA and expressed sequence tag sequence data. PMID:12702210
Interphase FISH, the structure of reciprocal translocation chromosomes and physical mapping studies rule out the duplication of the NF1 gene at 17q11.2. A reply. PMID:12698359
Complex haplotypes of IRS2 gene are associated with severe obesity and reveal heterogeneity in the effect of Gly1057Asp mutation. PMID:12687350
GALA, a database for genomic sequence alignments and annotations. PMID:12671007
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. PMID:12658451
Modulating action of the new polymorphism L436F detected in the GLB1 gene of a type-II GM1 gangliosidosis patient. PMID:12644936
Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome. PMID:12616398
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse. PMID:12607115
Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics. PMID:12601471
Linkage analysis of prostate cancer susceptibility: confirmation of linkage at 8p22-23. PMID:12594535
Notch4, a non-HLA gene in the MHC is strongly associated with the most severe form of alopecia areata. PMID:12589427
Gene rearrangements in the glucocerebrosidase-metaxin region giving rise to disease-causing mutations and polymorphisms. Analysis of 25 Rec NciI alleles in Gaucher disease patients. PMID:12589426
An Alu-mediated rearrangement as cause of exon skipping in Hunter disease. PMID:12579417
Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin. PMID:12574939
Nucleotide and haplotypic diversity of the NOS2A promoter region and its relationship to cerebral malaria. PMID:12552317
SOURCE: a unified genomic resource of functional annotations, ontologies, and gene expression data. PMID:12519986
Human members of the eukaryotic protein kinase family. PMID:12225582 -
Genenames.org: the HGNC and VGNC resources in 2017
PubMed citations: 164.
164 articles citing: Genenames.org: the HGNC and VGNC resources in 2017
Mitochondrial Ribosome Dysfunction in Human Alveolar Type II Cells in Emphysema. PMID:35884802
DES-Amyloidoses "Amyloidoses through the looking-glass": A knowledgebase developed for exploring and linking information related to human amyloid-related diseases. PMID:35877764
Follistatin-like 1 and its paralogs in heart development and cardiovascular disease. PMID:35867287
OncoboxPD: human 51 672 molecular pathways database with tools for activity calculating and visualization. PMID:35615022
Impaired phosphate transport in SLC34A2 variants in patients with pulmonary alveolar microlithiasis. PMID:35443721
A single-cell regulatory map of postnatal lung alveologenesis in humans and mice. PMID:35434692
B4GALT5 high expression associated with poor prognosis of hepatocellular carcinoma. PMID:35410157
Gene Expression-Based Signature Can Predict Sorafenib Response in Kidney Cancer. PMID:35359606
Silencing of lncRNA CHRM3-AS2 Expression Exerts Anti-Tumour Effects Against Glioma via Targeting microRNA-370-5p/KLF4. PMID:35359381
Pulmonary surfactant protein B carried by HDL predicts incident CVD in patients with type 1 diabetes. PMID:35300983
The EurOPDX Data Portal: an open platform for patient-derived cancer xenograft data sharing and visualization. PMID:35193494
The Genome of the "Sea Vomit" Didemnum vexillum. PMID:34947908
Labour classified by cervical dilatation & fetal membrane rupture demonstrates differential impact on RNA-seq data for human myometrium tissues. PMID:34797869
SeekFusion - A Clinically Validated Fusion Transcript Detection Pipeline for PCR-Based Next-Generation Sequencing of RNA. PMID:34745213
Lung Microenvironments and Disease Progression in Fibrotic Hypersensitivity Pneumonitis. PMID:34724391
Interpretation of cancer mutations using a multiscale map of protein systems. PMID:34591613
Human cytomegalovirus expands a CD8+ T cell population with loss of BCL11B expression and gain of NK cell identity. PMID:34559552
A domain damage index to prioritizing the pathogenicity of missense variants. PMID:34350656
SISTEMA: A large and standardized collection of transcriptome data sets for human pluripotent stem cell research. PMID:34278269
Talin rod domain-containing protein 1 (TLNRD1) is a novel actin-bundling protein which promotes filopodia formation. PMID:34264272
DES-Tcell is a knowledgebase for exploring immunology-related literature. PMID:34253812
Niacin Increases Atherogenic Proteins in High-Density Lipoprotein of Statin-Treated Subjects. PMID:34134520
R2DT is a framework for predicting and visualising RNA secondary structure using templates. PMID:34108470
Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease. PMID:34012061
Identification of upregulated NF-κB inhibitor alpha and IRAK3 targeting lncRNA following intracranial aneurysm rupture-induced subarachnoid hemorrhage. PMID:33990177
Analysis of Zika virus capsid-Aedes aegypti mosquito interactome reveals pro-viral host factors critical for establishing infection. PMID:33986255
Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data. PMID:33972534
A resource to explore the discovery of rare diseases and their causative genes. PMID:33947870
Machine Learning Applicability for Classification of PAD/VCD Chemotherapy Response Using 53 Multiple Myeloma RNA Sequencing Profiles. PMID:33937058
Pathogenic missense protein variants affect different functional pathways and proteomic features than healthy population variants. PMID:33909605
Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG). PMID:33795824
DNA repair pathway activation features in follicular and papillary thyroid tumors, interrogated using 95 experimental RNA sequencing profiles. PMID:33748479
Global DNA hypermethylation pattern and unique gene expression signature in liver cancer from patients with Indigenous American ancestry. PMID:33747361
Extracellular signal-regulated kinase regulates microglial immune responses in Alzheimer's disease. PMID:33729626
A ligand-receptor interactome platform for discovery of pain mechanisms and therapeutic targets. PMID:33727337
HIR V2: a human interactome resource for the biological interpretation of differentially expressed genes via gene set linkage analysis. PMID:33677507
Single-cell transcriptomic profiling and characterization of endothelial progenitor cells: new approach for finding novel markers. PMID:33627177
Factorial study of the RNA-seq computational workflow identifies biases as technical gene signatures. PMID:33575596
HGNChelper: identification and correction of invalid gene symbols for human and mouse. PMID:33564398
Genetic history of Calabrian Greeks reveals ancient events and long term isolation in the Aspromonte area of Southern Italy. PMID:33542324
My personal mutanome: a computational genomic medicine platform for searching network perturbing alleles linking genotype to phenotype. PMID:33514395
Minimal genome-wide human CRISPR-Cas9 library. PMID:33478580
DIPPER, a spatiotemporal proteomics atlas of human intervertebral discs for exploring ageing and degeneration dynamics. PMID:33382035
The status of causality in biological databases: data resources and data retrieval possibilities to support logical modeling. PMID:33378765
Identification of inflammation‑associated circulating long non‑coding RNAs and genes in intracranial aneurysm rupture‑induced subarachnoid hemorrhage. PMID:33174039
Genenames.org: the HGNC and VGNC resources in 2021. PMID:33152070
Toward Preparing a Knowledge Base to Explore Potential Drugs and Biomedical Entities Related to COVID-19: Automated Computational Approach. PMID:33055059
Protein ontology on the semantic web for knowledge discovery. PMID:33046717
Pulmonary alveolar microlithiasis: no longer in the stone age. PMID:32964001
High expression of MKK3 is associated with worse clinical outcomes in African American breast cancer patients. PMID:32873298
A Human IgSF Cell-Surface Interactome Reveals a Complex Network of Protein-Protein Interactions. PMID:32822567
Glucose Availability Alters Gene and Protein Expression of Several Newly Classified and Putative Solute Carriers in Mice Cortex Cell Culture and D. melanogaster. PMID:32733888
A Pharmacological Interactome between COVID-19 Patient Samples and Human Sensory Neurons Reveals Potential Drivers of Neurogenic Pulmonary Dysfunction. PMID:32714114
Weighed Gene Coexpression Network Analysis Screens the Potential Long Noncoding RNAs and Genes Associated with Progression of Coronary Artery Disease. PMID:32695216
Single-cell RNA sequencing reveals cell type- and artery type-specific vascular remodelling in male spontaneously hypertensive rats. PMID:32589721
Differential methylation and expression of genes in the hypoxia-inducible factor 1 signaling pathway are associated with paclitaxel-induced peripheral neuropathy in breast cancer survivors and with preclinical models of chemotherapy-induced neuropathic pain. PMID:32586194
Microtubule Organization in Striated Muscle Cells. PMID:32503326
A pharmacological interactome between COVID-19 patient samples and human sensory neurons reveals potential drivers of neurogenic pulmonary dysfunction. PMID:32497778
Evaluating drug targets through human loss-of-function genetic variation. PMID:32461653
Exosomal Long Non-Coding RNAs in Lung Diseases. PMID:32438606
A risk score system based on DNA methylation levels and a nomogram survival model for lung squamous cell carcinoma. PMID:32377703
Nuclear-encoded mitochondrial ribosomal proteins are required to initiate gastrulation. PMID:32376682
Towards the routine use of in silico screenings for drug discovery using metabolic modelling. PMID:32369553
DES-ROD: Exploring Literature to Develop New Links between RNA Oxidation and Human Diseases. PMID:32308806
Active constituents and mechanisms of Respiratory Detox Shot, a traditional Chinese medicine prescription, for COVID-19 control and prevention: Network-molecular docking-LC-MSE analysis. PMID:32307268
A unified nomenclature for vertebrate olfactory receptors. PMID:32295537
Design and analysis of CRISPR-Cas experiments. PMID:32284587
Automated gene data integration with Databio. PMID:32238171
CRISPR/Cas9-Mediated Genome Editing Reveals Oosp Family Genes are Dispensable for Female Fertility in Mice. PMID:32231122
Evidence of constraint in the 3D genome for trans-splicing in human cells. PMID:32221814
Hepamine - A Liver Disease Microarray Database, Visualization Platform and Data-Mining Resource. PMID:32179762
Effects of High-Dose Ionizing Radiation in Human Gene Expression: A Meta-Analysis. PMID:32178397
OncoMX: A Knowledgebase for Exploring Cancer Biomarkers in the Context of Related Cancer and Healthy Data. PMID:32142370
Evolutionary Dynamics of the POTE Gene Family in Human and Nonhuman Primates. PMID:32085667
Oxidative Stress in Canine Histiocytic Sarcoma Cells Induced by an Infection with Canine Distemper Virus Led to a Dysregulation of HIF-1α Downstream Pathway Resulting in a Reduced Expression of VEGF-B in vitro. PMID:32054075
NANOG expression in human development and cancerogenesis. PMID:32041418
ABC transporters control ATP release through cholesterol-dependent volume-regulated anion channel activity. PMID:31988241
Mutation Enrichment and Transcriptomic Activation Signatures of 419 Molecular Pathways in Cancer. PMID:31979117
Identification of pathogenic variant enriched regions across genes and gene families. PMID:31871067
The Emerging Role of Gβ Subunits in Human Genetic Diseases. PMID:31817184
Lithium alters expression of RNAs in a type-specific manner in differentiated human neuroblastoma neuronal cultures, including specific genes involved in Alzheimer's disease. PMID:31797941
The integrative knowledge base for miRNA-mRNA expression in colorectal cancer. PMID:31792281
Screening potential prognostic biomarkers of long non-coding RNAs for predicting the risk of chronic kidney disease. PMID:31721901
The Year of the Rat: The Rat Genome Database at 20: a multi-species knowledgebase and analysis platform. PMID:31713623
New developments on the Encyclopedia of DNA Elements (ENCODE) data portal. PMID:31713622
Cisplatin-resistant triple-negative breast cancer subtypes: multiple mechanisms of resistance. PMID:31684899
Paralog buffering contributes to the variable essentiality of genes in cancer cell lines. PMID:31652272
Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells. PMID:31635416
snoDB: an interactive database of human snoRNA sequences, abundance and interactions. PMID:31598696
X-chromosome-linked miR548am-5p is a key regulator of sex disparity in the susceptibility to mitochondria-mediated apoptosis. PMID:31511496
Why digital medicine depends on interoperability. PMID:31453374
Transcriptome and Network Dissection of Microsatellite Stable and Highly Instable Colorectal Cancer. PMID:31450919
Global Text Mining and Development of Pharmacogenomic Knowledge Resource for Precision Medicine. PMID:31447668
Exploring the molecular basis of neuronal excitability in a vocal learner. PMID:31375088
A Web Tool for Ranking Candidate Drugs Against a Selected Disease Based on a Combination of Functional and Structural Criteria. PMID:31360332
Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis. PMID:31348891
Enzymatic Logic of Ubiquitin Chain Assembly. PMID:31333493
PhenPath: a tool for characterizing biological functions underlying different phenotypes. PMID:31307376
The Generation of a Comprehensive Spectral Library for the Analysis of the Guinea Pig Proteome by SWATH-MS. PMID:31301205
Landscape of innate immune system transcriptome and acute T cell-mediated rejection of human kidney allografts. PMID:31292297
GAIL: An interactive webserver for inference and dynamic visualization of gene-gene associations based on gene ontology guided mining of biomedical literature. PMID:31260503
FunSet: an open-source software and web server for performing and displaying Gene Ontology enrichment analysis. PMID:31248361
Non-Invasive Biomarkers for Celiac Disease. PMID:31234270
Re-curation and rational enrichment of knowledge graphs in Biological Expression Language. PMID:31225582
Literature-Based Enrichment Insights into Redox Control of Vascular Biology. PMID:31223421
Gene Information eXtension (GIX): effortless retrieval of gene product information on any website. PMID:31217594
CoCoScore: context-aware co-occurrence scoring for text mining applications using distant supervision. PMID:31199464
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse. PMID:31171447
MTR-Viewer: identifying regions within genes under purifying selection. PMID:31170280
Integrative Analysis of Somatic Mutations in Non-coding Regions Altering RNA Secondary Structures in Cancer Genomes. PMID:31160636
Tissue-specific genes as an underutilized resource in drug discovery. PMID:31076736
Exploration of prognosis-related microRNA and transcription factor co-regulatory networks across cancer types. PMID:31046554
Screening for mutations in selected miRNA genes in hypogonadotropic hypogonadism patients. PMID:30999277
Selective translational usage of TSS and core promoters revealed by translatome sequencing. PMID:30987607
A network of human functional gene interactions from knockout fitness screens in cancer cells. PMID:30979825
INKA, an integrative data analysis pipeline for phosphoproteomic inference of active kinases. PMID:30979792
EFCAB2 is a novel calcium-binding protein in mouse testis and sperm. PMID:30933994
Late-onset Leber's hereditary optic neuropathy: the role of environmental factors in hereditary diseases. PMID:30898963
Mutations in DNA repair genes are associated with increased neoantigen burden and a distinct immunophenotype in lung squamous cell carcinoma. PMID:30824826
Identification of biomarkers associated with the recurrence of osteosarcoma using ceRNA regulatory network analysis. PMID:30816442
Modulation of cell adhesion and migration through regulation of the immunoglobulin superfamily member ALCAM/CD166. PMID:30778704
deepDriver: Predicting Cancer Driver Genes Based on Somatic Mutations Using Deep Convolutional Neural Networks. PMID:30761181
LIVE: a manually curated encyclopedia of experimentally validated interactions of lncRNAs. PMID:30759219
NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans. PMID:30744685
Introducing WikiPathways as a Data-Source to Support Adverse Outcome Pathways for Regulatory Risk Assessment of Chemicals and Nanomaterials. PMID:30622555
SIX2 Mediates Late-Stage Metastasis via Direct Regulation of SOX2 and Induction of a Cancer Stem Cell Program. PMID:30606720
HIV Disease Progression: Overexpression of the Ectoenzyme CD38 as a Contributory Factor? PMID:30537007
PDX Finder: A portal for patient-derived tumor xenograft model discovery. PMID:30535239
RefSeq curation and annotation of stop codon recoding in vertebrates. PMID:30535227
Genetic variants of erythropoietin (EPO) and EPO receptor genes in familial erythrocytosis. PMID:30507031
Ontology-based validation and identification of regulatory phenotypes. PMID:30423068
PreMedKB: an integrated precision medicine knowledgebase for interpreting relationships between diseases, genes, variants and drugs. PMID:30407536
The protein interaction networks of mucolipins and two-pore channels. PMID:30395881
RNAcentral: a hub of information for non-coding RNA sequences. PMID:30395267
DrugThatGene: integrative analysis to streamline the identification of druggable genes, pathways and protein complexes from CRISPR screens. PMID:30395160
COSMIC: the Catalogue Of Somatic Mutations In Cancer. PMID:30371878
LNCipedia 5: towards a reference set of human long non-coding RNAs. PMID:30371849
PubChem 2019 update: improved access to chemical data. PMID:30371825
Re-thinking Alzheimer's disease therapeutic targets using gene-based tests. PMID:30314892
Multimodal network diffusion predicts future disease-gene-chemical associations. PMID:30304494
Genenames.org: the HGNC and VGNC resources in 2019. PMID:30304474
OrthoList 2: A New Comparative Genomic Analysis of Human and Caenorhabditis elegans Genes. PMID:30120140
Challenges of Connecting Chemistry to Pharmacology: Perspectives from Curating the IUPHAR/BPS Guide to PHARMACOLOGY. PMID:30087946
Loose ends: almost one in five human genes still have unresolved coding status. PMID:29982784
Non-classical monocytes as mediators of tissue destruction in arthritis. PMID:29959183
Sequence diversity of tubulin isotypes in regulation of the mitochondrial voltage-dependent anion channel. PMID:29777059
TelNet - a database for human and yeast genes involved in telomere maintenance. PMID:29776332
Using FlyBase to Find Functionally Related Drosophila Genes. PMID:29761468
Systematic identification of latent disease-gene associations from PubMed articles. PMID:29373609
ClinVar: improving access to variant interpretations and supporting evidence. PMID:29165669
The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY. PMID:29149325
ReMap 2018: an updated atlas of regulatory regions from an integrative analysis of DNA-binding ChIP-seq experiments. PMID:29126285
ActiveDriverDB: human disease mutations and genome variation in post-translational modification sites of proteins. PMID:29126202
Consensus coding sequence (CCDS) database: a standardized set of human and mouse protein-coding regions supported by expert curation. PMID:29126148
Interactive phenotyping of large-scale histology imaging data with HistomicsML. PMID:29109450
The OMA orthology database in 2018: retrieving evolutionary relationships among all domains of life through richer web and programmatic interfaces. PMID:29106550
Lnc2Meth: a manually curated database of regulatory relationships between long non-coding RNAs and DNA methylation associated with human disease. PMID:29069510
EVLncRNAs: a manually curated database for long non-coding RNAs validated by low-throughput experiments. PMID:28985416
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions. PMID:28967166
Gestational diabetes exacerbates maternal immune activation effects in the developing brain. PMID:28948973
eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes. PMID:28812536
Naming CRISPR alleles: endonuclease-mediated mutation nomenclature across species. PMID:28589392
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. PMID:28502612
BRIDG: a domain information model for translational and clinical protocol-driven research. PMID:28339791 -
Genenames.org: the HGNC and VGNC resources in 2019
PubMed citations: 159.
159 articles citing: Genenames.org: the HGNC and VGNC resources in 2019
PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care. PMID:35902925
The Aminoacyl-tRNA Synthetase and tRNA Expression Levels Are Deregulated in Cancer and Correlate Independently with Patient Survival. PMID:35877431
The Big Picture of Neurodegeneration: A Meta Study to Extract the Essential Evidence on Neurodegenerative Diseases in a Network-Based Approach. PMID:35832065
A scalable, open-source implementation of a large-scale mechanistic model for single cell proliferation and death signaling. PMID:35729113
High-intensity interval training remodels the proteome and acetylome of human skeletal muscle. PMID:35638262
Pan-cancer analyses reveal the genetic and pharmacogenomic landscape of transient receptor potential channels. PMID:35614079
Framework of Intrinsic Immune Landscape of Dormant Prostate Cancer. PMID:35563856
NIBAN1, Exploring its Roles in Cell Survival Under Stress Context. PMID:35517496
Extracting functional insights from loss-of-function screens using deep link prediction. PMID:35474966
Bioinformatic Challenges Detecting Genetic Variation in Precision Medicine Programs. PMID:35463004
Scaling up oligogenic diseases research with OLIDA: the Oligogenic Diseases Database. PMID:35411390
Providing Adverse Outcome Pathways from the AOP-Wiki in a Semantic Web Format to Increase Usability and Accessibility of the Content. PMID:35388368
The AOP-DB RDF: Applying FAIR Principles to the Semantic Integration of AOP Data Using the Research Description Framework. PMID:35295213
Computing microRNA-gene interaction networks in pan-cancer using miRDriver. PMID:35260634
Computational Resources for the Interpretation of Variations in Cancer. PMID:35230689
c-Met and EPHA7 Receptor Tyrosine Kinases Are Related to Prognosis in Clear Cell Renal Cell Carcinoma: Focusing on the Association with Myoferlin Expression. PMID:35205843
Single-cell RNA sequencing reveals time- and sex-specific responses of mouse spinal cord microglia to peripheral nerve injury and links ApoE to chronic pain. PMID:35149686
A platform for oncogenomic reporting and interpretation. PMID:35140225
In silico prediction of HIV-1-host molecular interactions and their directionality. PMID:35134057
Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease. PMID:35068457
Diffusion kernel-based predictive modeling of KRAS dependency in KRAS wild type cancer cell lines. PMID:35046405
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines. PMID:35039090
Meta-analysis of whole-genome gene expression datasets assessing the effects of IDH1 and IDH2 mutations in isogenic disease models. PMID:34997121
Long Non-Coding RNA- Associated Competing Endogenous RNA Axes in T-Cells in Multiple Sclerosis. PMID:34956196
Bioinformatics analysis of long non-coding RNA-associated competing endogenous RNA network in schizophrenia. PMID:34952924
Malaria protection due to sickle haemoglobin depends on parasite genotype. PMID:34883497
A Standardized Brain Molecular Atlas: A Resource for Systems Modeling and Simulation. PMID:34858137
Yersinia remodels epigenetic histone modifications in human macrophages. PMID:34793580
CyFi-MAP: an interactive pathway-based resource for cystic fibrosis. PMID:34782688
LncRNAWiki 2.0: a knowledgebase of human long non-coding RNAs with enhanced curation model and database system. PMID:34751395
Peripheral Blood-Based Gene Expression Studies in Schizophrenia: A Systematic Review. PMID:34721526
BrainBase: a curated knowledgebase for brain diseases. PMID:34718720
Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level. PMID:34674628
Steroid Receptors in Breast Cancer: Understanding of Molecular Function as a Basis for Effective Therapy Development. PMID:34638264
A metric for evaluating biological information in gene sets and its application to identify co-expressed gene clusters in PBMC. PMID:34613979
Biomolecule and Bioentity Interaction Databases in Systems Biology: A Comprehensive Review. PMID:34439912
Mining Natural Products with Anticancer Biological Activity through a Systems Biology Approach. PMID:34422220
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes. PMID:34419158
NetControl4BioMed: A web-based platform for controllability analysis of protein-protein interaction networks. PMID:34352070
Discovering and Summarizing Relationships Between Chemicals, Genes, Proteins, and Diseases in PubChem. PMID:34322655
CFTR Lifecycle Map-A Systems Medicine Model of CFTR Maturation to Predict Possible Active Compound Combinations. PMID:34299207
DysPIA: A Novel Dysregulated Pathway Identification Analysis Method. PMID:34290733
Matrisome, innervation and oxidative metabolism affected in older compared with younger males with similar physical activity. PMID:34219410
A Literature-Derived Knowledge Graph Augments the Interpretation of Single Cell RNA-seq Datasets. PMID:34200671
Criteria-based curation of a therapy-focused compendium to support treatment recommendations in precision oncology. PMID:34162978
Transcriptomic Signature Differences Between SARS-CoV-2 and Influenza Virus Infected Patients. PMID:34135895
Screening of Biological Target Molecules Related to Glucocorticoid-Induced Cataract (GIC) on the Basis of Constructing ceRNA Network. PMID:34076796
Methylation and Expression of FTO and PLAG1 Genes in Childhood Obesity: Insight into Anthropometric Parameters and Glucose-Lipid Metabolism. PMID:34063412
KEA3: improved kinase enrichment analysis via data integration. PMID:34019655
CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare disease patients. PMID:34019647
Host pharmacogenetic factors that may affect liver neoplasm incidence upon using direct-acting antivirals for treating hepatitis C infection. PMID:34013078
Signature RNAS and related regulatory roles in type 1 diabetes mellitus based on competing endogenous RNA regulatory network analysis. PMID:34006268
Comprehensive Analysis of Cyclin Family Gene Expression in Colon Cancer. PMID:33996604
Updates to HCOP: the HGNC comparison of orthology predictions tool. PMID:33959747
IBDDB: a manually curated and text-mining-enhanced database of genes involved in inflammatory bowel disease. PMID:33929018
On the Unfounded Enthusiasm for Soft Selective Sweeps III: The Supervised Machine Learning Algorithm That Isn't. PMID:33916341
Investigating Molecular Determinants of Cancer Cell Resistance to Ionizing Radiation Through an Integrative Bioinformatics Approach. PMID:33898418
Elucidating molecular mechanisms of acquired resistance to BRAF inhibitors in melanoma using a microfluidic device and deep sequencing. PMID:33840166
MODOMICS: An Operational Guide to the Use of the RNA Modification Pathways Database. PMID:33835459
Ten Years of Collaborative Progress in the Quest for Orthologs. PMID:33822172
Diversity of Receptor Expression in Central and Peripheral Mouse Neurons Estimated from Single Cell RNA Sequencing. PMID:33774127
Regulation of hippocampal excitatory synapses by the Zdhhc5 palmitoyl acyltransferase. PMID:33758079
Identification of disease treatment mechanisms through the multiscale interactome. PMID:33741907
FAM83A and FAM83A-AS1 both play oncogenic roles in lung adenocarcinoma. PMID:33732373
Temporal mechanisms of myogenic specification in human induced pluripotent stem cells. PMID:33731358
The immunohistochemical profile of basal cell nevus syndrome-associated and sporadic odontogenic keratocysts: a systematic review and meta-analysis. PMID:33730212
A ligand-receptor interactome platform for discovery of pain mechanisms and therapeutic targets. PMID:33727337
Deciphering the genetic alterations in matrix metallo-proteinase gene family and its putative association with head and neck squamous cell carcinoma. PMID:33681393
Persistent COUP-TFII expression underlies the myopathy and impaired muscle regeneration observed in resistance to thyroid hormone-alpha. PMID:33633251
BioDWH2: an automated graph-based data warehouse and mapping tool. PMID:33618440
Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing. PMID:33606250
Pharmacology of T2R Mediated Host-Microbe Interactions. PMID:33580389
Mucociliary Respiratory Epithelium Integrity in Molecular Defense and Susceptibility to Pulmonary Viral Infections. PMID:33572760
AlzGPS: a genome-wide positioning systems platform to catalyze multi-omics for Alzheimer's drug discovery. PMID:33441136
Opinion: Standardizing gene product nomenclature-a call to action. PMID:33408252
DIPPER, a spatiotemporal proteomics atlas of human intervertebral discs for exploring ageing and degeneration dynamics. PMID:33382035
Guanine Nucleotide-Binding Protein-Like 1 (GNL1) binds RNA G-quadruplex structures in genes associated with Parkinson's disease. PMID:33305682
Common Factors in Neurodegeneration: A Meta-Study Revealing Shared Patterns on a Multi-Omics Scale. PMID:33302607
Diversification of molecularly defined myenteric neuron classes revealed by single-cell RNA sequencing. PMID:33288908
In silico identification of Drosophila melanogaster genes encoding RNA polymerase subunits. PMID:33274328
Mining potentially actionable kinase gene fusions in cancer cell lines with the KuNG FU database. PMID:33257674
Chemocentric Informatics Analysis: Dexamethasone Versus Combination Therapy for COVID-19. PMID:33251412
Immune-related gene data-based molecular subtyping related to the prognosis of breast cancer patients. PMID:33245478
DNA methylation and body mass index from birth to adolescence: meta-analyses of epigenome-wide association studies. PMID:33239103
The UCSC Genome Browser database: 2021 update. PMID:33221922
Lnc2Cancer 3.0: an updated resource for experimentally supported lncRNA/circRNA cancer associations and web tools based on RNA-seq and scRNA-seq data. PMID:33219685
FlyBase: updates to the Drosophila melanogaster knowledge base. PMID:33219682
Insertions of codons encoding basic amino acids in H7 hemagglutinins of influenza A viruses occur by recombination with RNA at hotspots near snoRNA binding sites. PMID:33188057
Identification of biomarkers and pathways in hypertensive nephropathy based on the ceRNA regulatory network. PMID:33176720
OMA orthology in 2021: website overhaul, conserved isoforms, ancestral gene order and more. PMID:33174605
Genenames.org: the HGNC and VGNC resources in 2021. PMID:33152070
Blackout in the powerhouse: clinical phenotypes associated with defects in the assembly of OXPHOS complexes and the mitoribosome. PMID:33151299
KinaseMD: kinase mutations and drug response database. PMID:33137204
An in-silico method leads to recognition of hub genes and crucial pathways in survival of patients with breast cancer. PMID:33128008
RNAcentral 2021: secondary structure integration, improved sequence search and new member databases. PMID:33106848
TPR is required for the efficient nuclear export of mRNAs and lncRNAs from short and intron-poor genes. PMID:33091126
KLIFS: an overhaul after the first 5 years of supporting kinase research. PMID:33084889
tRFtarget: a database for transfer RNA-derived fragment targets. PMID:33035346
Comprehensive Analysis of Differential Immunocyte Infiltration and Potential ceRNA Networks Involved in the Development of Atrial Fibrillation. PMID:33015181
COVID-19 Patients Upregulate Toll-like Receptor 4-mediated Inflammatory Signaling That Mimics Bacterial Sepsis. PMID:32989935
Molecular subtyping of glioblastoma based on immune-related genes for prognosis. PMID:32968155
Determining the Molecular Background of Endometrial Receptivity in Adenomyosis. PMID:32933042
Leucocyte-Rich Platelet-Rich Plasma Enhances Fibroblast and Extracellular Matrix Activity: Implications in Wound Healing. PMID:32900003
A mega-analysis of expression quantitative trait loci in retinal tissue. PMID:32870927
Expression profiling of WD40 family genes including DDB1- and CUL4- associated factor (DCAF) genes in mice and human suggests important regulatory roles in testicular development and spermatogenesis. PMID:32867693
miRNA-based biomarkers, therapies, and resistance in Cancer. PMID:32792861
The methylation status of the chemerin promoter region located from - 252 to + 258 bp regulates constitutive but not acute-phase cytokine-inducible chemerin expression levels. PMID:32792625
Dissecting diagnostic heterogeneity in depression by integrating neuroimaging and genetics. PMID:32781460
Guidelines for human gene nomenclature. PMID:32747822
Overview of PAX gene family: analysis of human tissue-specific variant expression and involvement in human disease. PMID:32728807
Copy Number Loss of 17q22 Is Associated with Enzalutamide Resistance and Poor Prognosis in Metastatic Castration-Resistant Prostate Cancer. PMID:32727885
Chemically Induced Hypoxia Enhances miRNA Functions in Breast Cancer. PMID:32707933
Association study based on topological constraints of protein-protein interaction networks. PMID:32612246
Genome-wide investigation of gene-cancer associations for the prediction of novel therapeutic targets in oncology. PMID:32612205
Genetic relationship between Hashimoto`s thyroiditis and papillary thyroid carcinoma with coexisting Hashimoto`s thyroiditis. PMID:32603365
Host-Pathogen Responses to Pandemic Influenza H1N1pdm09 in a Human Respiratory Airway Model. PMID:32599823
Automated generation of gene summaries at the Alliance of Genome Resources. PMID:32559296
What's in a name? Issues to consider when naming Mendelian disorders. PMID:32555417
Using online tools at the Bovine Genome Database to manually annotate genes in the new reference genome. PMID:32537769
PINOT: an intuitive resource for integrating protein-protein interactions. PMID:32527260
Molecular signature of eutopic endometrium in endometriosis based on the multi-omics integrative synthesis. PMID:32474803
Progress, Challenges, and Surprises in Annotating the Human Genome. PMID:32421357
MyoMiner: explore gene co-expression in normal and pathological muscle. PMID:32393257
Testis-specific serine kinase protein family in male fertility and as targets for non-hormonal male contraception†. PMID:32337545
Ribosome heterogeneity in stem cells and development. PMID:32330234
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa. PMID:32326576
Setting the basis of best practices and standards for curation and annotation of logical models in biology-highlights of the [BC]2 2019 CoLoMoTo/SysMod Workshop. PMID:32313939
MaveQuest: a web resource for planning experimental tests of human variant effects. PMID:32251504
Formation of human long intergenic non-coding RNA genes, pseudogenes, and protein genes: Ancestral sequences are key players. PMID:32214344
PHARMIP: An insilico method to predict genetics that underpin adverse drug reactions. PMID:32123669
Comprehensive analysis of differential immunocyte infiltration and the potential ceRNA networks during epicardial adipose tissue development in congenital heart disease. PMID:32122382
A guide to naming human non-coding RNA genes. PMID:32090359
COA6 Facilitates Cytochrome c Oxidase Biogenesis as Thiol-reductase for Copper Metallochaperones in Mitochondria. PMID:32061935
Identification of Prognostic Dosage-Sensitive Genes in Colorectal Cancer Based on Multi-Omics. PMID:31998369
Incremental data integration for tracking genotype-disease associations. PMID:31986132
Biobtree: A tool to search, map and visualize bioinformatics identifiers and special keywords. PMID:31984130
Compartment and hub definitions tune metabolic networks for metabolomic interpretations. PMID:31972021
The DNA polymerases of Drosophila melanogaster. PMID:31933406
Comprehensive transcriptome analysis of cochlear spiral ganglion neurons at multiple ages. PMID:31913118
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework. PMID:31892348
A Structurally-Validated Multiple Sequence Alignment of 497 Human Protein Kinase Domains. PMID:31875044
Prognostic significance and molecular mechanisms of adenosine triphosphate-binding cassette subfamily C members in gastric cancer. PMID:31852133
The Melanin-Concentrating Hormone (MCH) System: A Tale of Two Peptides. PMID:31849590
A Bioinformatic Approach for the Identification of Molecular Determinants of Resistance/Sensitivity to Cancer Thermotherapy. PMID:31814876
Inhibition of the Dead Box RNA Helicase 3 Prevents HIV-1 Tat and Cocaine-Induced Neurotoxicity by Targeting Microglia Activation. PMID:31802418
DAISY: A Data Information System for accountability under the General Data Protection Regulation. PMID:31800037
A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease. PMID:31767637
RPGeNet v2.0: expanding the universe of retinal disease gene interactions network. PMID:31712826
EPD in 2020: enhanced data visualization and extension to ncRNA promoters. PMID:31680159
ReMap 2020: a database of regulatory regions from an integrative analysis of Human and Arabidopsis DNA-binding sequencing experiments. PMID:31665499
Pathway Commons 2019 Update: integration, analysis and exploration of pathway data. PMID:31647099
Fasciola hepatica Infection in Cattle: Analyzing Responses of Peripheral Blood Mononuclear Cells (PBMC) Using a Transcriptomics Approach. PMID:31555289
Reconstruction and Analysis of Gene Networks of Human Neurotransmitter Systems Reveal Genes with Contentious Manifestation for Anxiety, Depression, and Intellectual Disabilities. PMID:31514272
Mammalian Annotation Database for improved annotation and functional classification of Omics datasets from less well-annotated organisms. PMID:31353404
VarMap: a web tool for mapping genomic coordinates to protein sequence and structure and retrieving protein structural annotations. PMID:31192369
ChEA3: transcription factor enrichment analysis by orthogonal omics integration. PMID:31114921
Ten quick tips for biocuration. PMID:31048830
Mapping the transcriptional diversity of genetically and anatomically defined cell populations in the mouse brain. PMID:30977723
The European Bioinformatics Institute in 2018: tools, infrastructure and training. PMID:30445657 -
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134 articles citing: Genenames.org: the HGNC resources in 2013
Diseases 2.0: a weekly updated database of disease-gene associations from text mining and data integration. PMID:35348648
Gene Expression Profile Analyses of the Skin Response of Balb/c-Nu Mice Model Injected by Staphylococcus aureus. PMID:35210800
ACO2 clinicobiological dataset with extensive phenotype ontology annotation. PMID:34354088
Gene Expression Differences Between Young Adults Based on Trauma History and Post-traumatic Stress Disorder. PMID:33897478
Assessing the Role of Long Noncoding RNA in Nucleus Accumbens in Subjects With Alcohol Dependence. PMID:33067813
Role of ACE2 receptor and the landscape of treatment options from convalescent plasma therapy to the drug repurposing in COVID-19. PMID:33029696
Perturbations in Endocytotic and Apoptotic Pathways Are Associated With Chemotherapy-Induced Nausea. PMID:32815385
Network Properties of Cancer Prognostic Gene Signatures in the Human Protein Interactome. PMID:32111006
FusionScan: accurate prediction of fusion genes from RNA-Seq data. PMID:31610622
OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database. PMID:31500643
Signaling pathways and gene co-expression modules associated with cytoskeleton and axon morphology in breast cancer survivors with chronic paclitaxel-induced peripheral neuropathy. PMID:31486345
Perturbations in neuroinflammatory pathways are associated with paclitaxel-induced peripheral neuropathy in breast cancer survivors. PMID:31401418
Systems Approach to Identify Common Genes and Pathways Associated with Response to Selective Serotonin Reuptake Inhibitors and Major Depression Risk. PMID:31018568
Identification of pharmacodynamic biomarker hypotheses through literature analysis with IBM Watson. PMID:30958864
Repository of Enriched Structures of Proteins Involved in the Red Blood Cell Environment (RESPIRE). PMID:30794542
Expression of mitochondrial dysfunction-related genes and pathways in paclitaxel-induced peripheral neuropathy in breast cancer survivors. PMID:30426838
Sequence Variations in pxr (nr1i2) From Zebrafish (Danio rerio) Strains Affect Nuclear Receptor Function. PMID:30371853
Recent stimulant use and leukocyte gene expression in methamphetamine users with treated HIV infection. PMID:29679637
Mechanisms of action of Coxiella burnetii effectors inferred from host-pathogen protein interactions. PMID:29176882
Mutation-profile-based methods for understanding selection forces in cancer somatic mutations: a comparative analysis. PMID:28938601
C1orf64 is a novel androgen receptor target gene and coregulator that interacts with 14-3-3 protein in breast cancer. PMID:28915724
The elusive MAESTRO gene: Its human reproductive tissue-specific expression pattern. PMID:28406912
Protein-Protein Interactions: Gene Acronym Redundancies and Current Limitations Precluding Automated Data Integration. PMID:28250396
Protein Bioinformatics Databases and Resources. PMID:28150231
To Unveil the Molecular Mechanisms of Qi and Blood through Systems Biology-Based Investigation into Si-Jun-Zi-Tang and Si-Wu-Tang formulae. PMID:27677604
Deregulation of the protein phosphatase 2A, PP2A in cancer: complexity and therapeutic options. PMID:27444275
Network Analysis Identifies Proinflammatory Plasma Cell Polarization for Secretion of ISG15 in Human Autoimmunity. PMID:27357150
The Ensembl gene annotation system. PMID:27337980
How far from the SNP may the causative genes be? PMID:27269582
CoReCG: a comprehensive database of genes associated with colon-rectal cancer. PMID:27114494
BioSig3D: High Content Screening of Three-Dimensional Cell Culture Models. PMID:26978075
shRNA target prediction informed by comprehensive enquiry (SPICE): a supporting system for high-throughput screening of shRNA library. PMID:26941783
Complementary Post Transcriptional Regulatory Information is Detected by PUNCH-P and Ribosome Profiling. PMID:26898226
Mitochondrial cytochrome c oxidase deficiency. PMID:26846578
A review of the new HGNC gene family resource. PMID:26842383
TRANS PROF DB: A new resource for sharing translational profiles. PMID:26779411
Using host-pathogen protein interactions to identify and characterize Francisella tularensis virulence factors. PMID:26714771
A lipasin/Angptl8 monoclonal antibody lowers mouse serum triglycerides involving increased postprandial activity of the cardiac lipoprotein lipase. PMID:26687026
Enhancer Turnover Is Associated with a Divergent Transcriptional Response to Glucocorticoid in Mouse and Human Macrophages. PMID:26663721
Characterization of the biological processes shaping the genetic structure of the Italian population. PMID:26553317
Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection. PMID:26515609
miRNA Nomenclature: A View Incorporating Genetic Origins, Biosynthetic Pathways, and Sequence Variants. PMID:26453491
Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence. PMID:26381263
Enrichment Analysis Identifies Functional MicroRNA-Disease Associations in Humans. PMID:26296081
Distilling a Visual Network of Retinitis Pigmentosa Gene-Protein Interactions to Uncover New Disease Candidates. PMID:26267445
A draft network of ligand-receptor-mediated multicellular signalling in human. PMID:26198319
Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals. PMID:26193471
Finding directionality and gene-disease predictions in disease associations. PMID:26168918
The extracellular matrix: Tools and insights for the "omics" era. PMID:26163349
Heterogeneous Network Edge Prediction: A Data Integration Approach to Prioritize Disease-Associated Genes. PMID:26158728
Metrabase: a cheminformatics and bioinformatics database for small molecule transporter data analysis and (Q)SAR modeling. PMID:26106450
Network-based gene prediction for Plasmodium falciparum malaria towards genetics-based drug discovery. PMID:26099491
Multidimensional gene search with Genehopper. PMID:25990726
Clinical decision support for whole genome sequence information leveraging a service-oriented architecture: a prototype. PMID:25954430
Digital gene expression approach over multiple RNA-Seq data sets to detect neoblast transcriptional changes in Schmidtea mediterranea. PMID:25952370
Cis-regulatory somatic mutations and gene-expression alteration in B-cell lymphomas. PMID:25903198
GeneTIER: prioritization of candidate disease genes using tissue-specific gene expression profiles. PMID:25861967
The classic cadherins in synaptic specificity. PMID:25837840
Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes. PMID:25819010
Mining host-pathogen protein interactions to characterize Burkholderia mallei infectivity mechanisms. PMID:25738731
mRNA profiling reveals determinants of trastuzumab efficiency in HER2-positive breast cancer. PMID:25710561
Enabling the curation of your pharmacogenetic study. PMID:25670512
Computational deconvolution of genome wide expression data from Parkinson's and Huntington's disease brain tissues using population-specific expression analysis. PMID:25620908
DBC1/CCAR2 and CCAR1 Are Largely Disordered Proteins that Have Evolved from One Common Ancestor. PMID:25610865
Comprehensive reconstruction and visualization of non-coding regulatory networks in human. PMID:25540777
Systematic exploration of autonomous modules in noisy microRNA-target networks for testing the generality of the ceRNA hypothesis. PMID:25539629
Pathway analysis and transcriptomics improve protein identification by shotgun proteomics from samples comprising small number of cells--a benchmarking study. PMID:25521637
HGV&TB: a comprehensive online resource on human genes and genetic variants associated with tuberculosis. PMID:25502817
FLAGS, frequently mutated genes in public exomes. PMID:25466818
Genome-wide transcriptome analysis of human epidermal melanocytes. PMID:25451175
Coagulation factor VII is regulated by androgen receptor in breast cancer. PMID:25447311
Prediction of DNA binding motifs from 3D models of transcription factors; identifying TLX3 regulated genes. PMID:25428367
Proteomics-Based Identification of Differentially Abundant Proteins from Human Keratinocytes Exposed to Arsenic Trioxide. PMID:25419056
EHFPI: a database and analysis resource of essential host factors for pathogenic infection. PMID:25414353
A proposed clinical decision support architecture capable of supporting whole genome sequence information. PMID:25411644
Beyond protein expression, MOPED goes multi-omics. PMID:25404128
CMPD: cancer mutant proteome database. PMID:25398898
IMGT®, the international ImMunoGeneTics information system® 25 years on. PMID:25378316
Rare diseases in clinical endocrinology: a taxonomic classification system. PMID:25376364
Human cancer databases (review). PMID:25369839
Genenames.org: the HGNC resources in 2015. PMID:25361968
Ensembl 2015. PMID:25352552
The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease. PMID:25348401
Mouse Tumor Biology (MTB): a database of mouse models for human cancer. PMID:25332399
The human DEPhOsphorylation database DEPOD: a 2015 update. PMID:25332398
CLIP2 as radiation biomarker in papillary thyroid carcinoma. PMID:25284583
Integrative post-genome-wide association analysis of CDKN2A and TP53 SNPs and risk of esophageal adenocarcinoma. PMID:25280564
Joint genetic analysis of hippocampal size in mouse and human identifies a novel gene linked to neurodegenerative disease. PMID:25280473
Guidelines for the nomenclature of genetic elements in tunicate genomes. PMID:25220678
A systematic review and meta-analysis of somatic and germline DNA sequence biomarkers of esophageal cancer survival, therapy response and stage. PMID:25214541
A dual role of lipasin (betatrophin) in lipid metabolism and glucose homeostasis: consensus and controversy. PMID:25212743
Principal component analysis characterizes shared pathogenetics from genome-wide association studies. PMID:25211452
Identification of highly related references about gene-disease association. PMID:25155502
Integrating biological pathways and genomic profiles with ChiBE 2. PMID:25086704
SNP@lincTFBS: an integrated database of polymorphisms in human LincRNA transcription factor binding sites. PMID:25075616
IthaGenes: an interactive database for haemoglobin variations and epidemiology. PMID:25058394
Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomes. PMID:25033203
Nonlinear quantitative radiation sensitivity prediction model based on NCI-60 cancer cell lines. PMID:25032244
Large scale analysis of phenotype-pathway relationships based on GWAS results. PMID:25007247
Processing biological literature with customizable Web services supporting interoperable formats. PMID:25006225
Characterization of human gene locus CYYR1: a complex multi-transcript system. PMID:24981926
A controlled vocabulary for pathway entities and events. PMID:24951798
Biochemical and bioinformatic methods for elucidating the role of RNA-protein interactions in posttranscriptional regulation. PMID:24951655
SemFunSim: a new method for measuring disease similarity by integrating semantic and gene functional association. PMID:24932637
MOPED 2.5--an integrated multi-omics resource: multi-omics profiling expression database now includes transcriptomics data. PMID:24910945
Integrative transcriptome meta-analysis reveals widespread sex-biased gene expression at the human fetal-maternal interface. PMID:24867328
Structuring osteosarcoma knowledge: an osteosarcoma-gene association database based on literature mining and manual annotation. PMID:24865352
StemCellNet: an interactive platform for network-oriented investigations in stem cell biology. PMID:24852251
RAID: a comprehensive resource for human RNA-associated (RNA-RNA/RNA-protein) interaction. PMID:24803509
A short guide to long non-coding RNA gene nomenclature. PMID:24716852
GeneSense: a new approach for human gene annotation integrated with protein-protein interaction networks. PMID:24667292
A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE). PMID:24667251
Genomic convergence and network analysis approach to identify candidate genes in Alzheimer's disease. PMID:24628925
Cancer evolution is associated with pervasive positive selection on globally expressed genes. PMID:24603726
Competitive and cooperative interactions mediate RNA transfer from herpesvirus saimiri ORF57 to the mammalian export adaptor ALYREF. PMID:24550725
Quantitative phosphoproteomics unveils temporal dynamics of thrombin signaling in human endothelial cells. PMID:24501219
Functional understanding of the diverse exon-intron structures of human GPCR genes. PMID:24467758
RefPrimeCouch--a reference gene primer CouchApp. PMID:24368831
Systematic discovery and characterization of regulatory motifs in ENCODE TF binding experiments. PMID:24335146
Systematic genomic identification of colorectal cancer genes delineating advanced from early clinical stage and metastasis. PMID:24308539
PDBe: Protein Data Bank in Europe. PMID:24288376
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants. PMID:24285302
RefSeq: an update on mammalian reference sequences. PMID:24259432
The IUPHAR/BPS Guide to PHARMACOLOGY: an expert-driven knowledgebase of drug targets and their ligands. PMID:24234439
UniHI 7: an enhanced database for retrieval and interactive analysis of human molecular interaction networks. PMID:24214987
CpGislandEVO: a database and genome browser for comparative evolutionary genomics of CpG islands. PMID:24205506
hMOF acetylation of DBC1/CCAR2 prevents binding and inhibition of SirT1. PMID:24126058
Functional characterization of a full length pregnane X receptor, expression in vivo, and identification of PXR alleles, in zebrafish (Danio rerio). PMID:24121122
Potential biomarkers for the clinical prognosis of severe dengue. PMID:24037198
Towards precision medicine: advances in computational approaches for the analysis of human variants. PMID:23962656
dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations. PMID:23843252
DigSee: Disease gene search engine with evidence sentences (version cancer). PMID:23761452
PosMed: Ranking genes and bioresources based on Semantic Web Association Study. PMID:23761449
Vive la différence: naming structural variants in the human reference genome. PMID:23634723 -
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127 articles citing: genenames.org: the HGNC resources in 2011
Drugs and Epigenetic Molecular Functions. A Pharmacological Data Scientometric Analysis. PMID:34298869
Deconvoluting global cytokine signaling networks in natural killer cells. PMID:33859404
Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases. PMID:32500119
Transcriptional Basis of Mouse and Human Dendritic Cell Heterogeneity. PMID:31668803
SingleCellNet: A Computational Tool to Classify Single Cell RNA-Seq Data Across Platforms and Across Species. PMID:31377170
The integrated National NeuroAIDS Tissue Consortium database: a rich platform for neuroHIV research. PMID:30624650
A phenotype centric benchmark of variant prioritisation tools. PMID:29423277
Integrated Computational Analysis of Genes Associated with Human Hereditary Insensitivity to Pain. A Drug Repurposing Perspective. PMID:28848388
Long noncoding RNAs are dynamically regulated during β-cell mass expansion in mouse pregnancy and control β-cell proliferation in vitro. PMID:28796801
GEAR: A database of Genomic Elements Associated with drug Resistance. PMID:28294141
TRAP-seq Profiling and RNAi-Based Genetic Screens Identify Conserved Glial Genes Required for Adult Drosophila Behavior. PMID:28066175
A machine-learned computational functional genomics-based approach to drug classification. PMID:27695919
Comprehensive coverage of cardiovascular disease data in the disease portals at the Rat Genome Database. PMID:27287925
WDR5 high expression and its effect on tumorigenesis in leukemia. PMID:27192115
An inter-species protein-protein interaction network across vast evolutionary distance. PMID:27107014
Extracting genetic alteration information for personalized cancer therapy from ClinicalTrials.gov. PMID:27013523
The pig X and Y Chromosomes: structure, sequence, and evolution. PMID:26560630
Computational functional genomics based analysis of pain-relevant micro-RNAs. PMID:26385553
The National NeuroAIDS Tissue Consortium (NNTC) Database: an integrated database for HIV-related studies. PMID:26228431
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease. PMID:26193622
Phenolyzer: phenotype-based prioritization of candidate genes for human diseases. PMID:26192085
A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides? PMID:26168747
In-silico analysis of inflammatory bowel disease (IBD) GWAS loci to novel connections. PMID:25786114
Drug-target based cross-sectional analysis of olfactory drug effects. PMID:25666029
Sgo1 is a potential therapeutic target for hepatocellular carcinoma. PMID:25638162
Zebrafish Rab5 proteins and a role for Rab5ab in nodal signalling. PMID:25478908
What do all the (human) micro-RNAs do? PMID:25404408
Chimera: a Bioconductor package for secondary analysis of fusion products. PMID:25286921
Identification of a dinucleotide signature that discriminates coding from non-coding long RNAs. PMID:25250049
Functional implications of long non-coding RNAs in the pancreatic islets of Langerhans. PMID:25071836
Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain. PMID:24979789
CancerEST: a web-based tool for automatic meta-analysis of public EST data. PMID:24715218
Long non-coding RNA and alternative splicing modulations in Parkinson's leukocytes identified by RNA sequencing. PMID:24651478
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Differential evolutionary constraints in the evolution of chemoreceptors: a murine and human case study. PMID:24587745
Variation ontology: annotator guide. PMID:24533660
DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma. PMID:24481001
Evolutionary dynamics and tissue specificity of human long noncoding RNAs in six mammals. PMID:24429298
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Discovering disease-disease associations by fusing systems-level molecular data. PMID:24232732
Evaluating the pharmacological mechanism of Chinese medicine Si-Wu-Tang through multi-level data integration. PMID:24223693
Functional networking of human divergently paired genes (DPGs). PMID:24205343
The promise of whole-exome sequencing in medical genetics. PMID:24196381
Variation Ontology for annotation of variation effects and mechanisms. PMID:24162187
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Prioritizing disease candidate proteins in cardiomyopathy-specific protein-protein interaction networks based on "guilt by association" analysis. PMID:23940716
Clinical analysis of genome next-generation sequencing data using the Omicia platform. PMID:23895124
Support Vector Machine classifier for estrogen receptor positive and negative early-onset breast cancer. PMID:23894323
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Integrating pathways of Parkinson's disease in a molecular interaction map. PMID:23832570
A comparison of 100 human genes using an alu element-based instability model. PMID:23755193
Evaluation of the contribution of the ATP binding cassette transporter, P-glycoprotein, to in vivo cholesterol homeostasis. PMID:23750858
Identification of driver genes in hepatocellular carcinoma by exome sequencing. PMID:23728943
Dissection of protein interactomics highlights microRNA synergy. PMID:23691029
International Union of Basic and Clinical Pharmacology. LXXXVIII. G protein-coupled receptor list: recommendations for new pairings with cognate ligands. PMID:23686350
Structural and functional annotation of the porcine immunome. PMID:23676093
Hypoxic tumor kinase signaling mediated by STAT5A in development of castration-resistant prostate cancer. PMID:23675504
Reproducible probe-level analysis of the Affymetrix Exon 1.0 ST array with R/Bioconductor. PMID:23603090
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Transcriptome sequencing of tumor subpopulations reveals a spectrum of therapeutic options for squamous cell lung cancer. PMID:23527012
Where in the genome are we? A cautionary tale of database use in genomics research. PMID:23519237
Transcriptional regulation and its misregulation in disease. PMID:23498934
A library of TAL effector nucleases spanning the human genome. PMID:23417094
Defensin DEFB103 bidirectionally regulates chemokine and cytokine responses to a pro-inflammatory stimulus. PMID:23390582
Proline: the distribution, frequency, positioning, and common functional roles of proline and polyproline sequences in the human proteome. PMID:23372670
Knowledge Driven Variable Selection (KDVS) - a new approach to enrichment analysis of gene signatures obtained from high-throughput data. PMID:23302187
Identifying the status of genetic lesions in cancer clinical trial documents using machine learning. PMID:23282337
IntPath--an integrated pathway gene relationship database for model organisms and important pathogens. PMID:23282057
Gene family matters: expanding the HGNC resource. PMID:23245209
ChIP-on-chip analysis identifies IL-22 as direct target gene of ectopically expressed FOXP3 transcription factor in human T cells. PMID:23244505
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The BioGRID interaction database: 2013 update. PMID:23203989
Ensembl 2013. PMID:23203987
The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency. PMID:23193275
GenomeRNAi: a database for cell-based and in vivo RNAi phenotypes, 2013 update. PMID:23193271
Autworks: a cross-disease network biology application for Autism and related disorders. PMID:23190929
Interactogeneous: disease gene prioritization using heterogeneous networks and full topology scores. PMID:23185389
Genenames.org: the HGNC resources in 2013. PMID:23161694
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Analysis of the swine tracheobronchial lymph node transcriptomic response to infection with a Chinese highly pathogenic strain of porcine reproductive and respiratory syndrome virus. PMID:23110781
IUPHAR-DB: updated database content and new features. PMID:23087376
A hybrid distance measure for clustering expressed sequence tags originating from the same gene family. PMID:23071763
Comparative study of human and mouse postsynaptic proteomes finds high compositional conservation and abundance differences for key synaptic proteins. PMID:23071613
MK4MDD: a multi-level knowledge base and analysis platform for major depressive disorder. PMID:23071556
Dynamics of microRNAs in bull spermatozoa. PMID:22978562
Notch signaling is activated in human hepatocellular carcinoma and induces tumor formation in mice. PMID:22974708
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The genetics and neuropathology of neurodegenerative disorders: perspectives and implications for research and clinical practice. PMID:22875012
Cell-type specificity of ChIP-predicted transcription factor binding sites. PMID:22863112
Transcription factor zinc finger and BTB domain 1 is essential for lymphocyte development. PMID:22753936
The effects of oxidative stress on female reproduction: a review. PMID:22748101
Evolution of the eukaryotic dynactin complex, the activator of cytoplasmic dynein. PMID:22726940
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Advanced comparative cytogenetic analysis of X chromosomes in river buffalo, cattle, sheep, and human. PMID:22669522
Locus-specific mutation databases for neurodegenerative brain diseases. PMID:22581678
A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins. PMID:22547224
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Community gene annotation in practice. PMID:22434843
A comparative structural bioinformatics analysis of inherited mutations in β-D-Mannosidase across multiple species reveals a genotype-phenotype correlation. PMID:22369051
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Novel search method for the discovery of functional relationships. PMID:22180409
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Abundant pleiotropy in human complex diseases and traits. PMID:22077970
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Prioritizing cancer-related genes with aberrant methylation based on a weighted protein-protein interaction network. PMID:21985575
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Clarity and claims in variation/mutation databasing. PMID:21904316
Two functional S100A4 monomers are necessary for regulating nonmuscle myosin-IIA and HCT116 cell invasion. PMID:21721535
A revised nomenclature for transcribed human endogenous retroviral loci. PMID:21542922
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Coexpression reveals conserved gene programs that co-vary with cell type across kingdoms. PMID:35451481
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Deciphering the Interactions of SARS-CoV-2 Proteins with Human Ion Channels Using Machine-Learning-Based Methods. PMID:35215201
Tumor relevant protein functional interactions identified using bipartite graph analyses. PMID:34728699
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A pathway map of signaling events triggered upon SARS-CoV infection. PMID:34487344
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Identification of potential biomarkers for lung adenocarcinoma. PMID:33251353
IDDB: a comprehensive resource featuring genes, variants and characteristics associated with infertility. PMID:32941628
Systems Biology Approach Identifies Prognostic Signatures of Poor Overall Survival and Guides the Prioritization of Novel BET-CHK1 Combination Therapy for Osteosarcoma. PMID:32859084
HISTome2: a database of histone proteins, modifiers for multiple organisms and epidrugs. PMID:32746900
OmicsON - Integration of omics data with molecular networks and statistical procedures. PMID:32726348
Serum beta-secretase 1 (BACE1) activity as candidate biomarker for late-onset Alzheimer's disease. PMID:31745860
ABCD: Alzheimer's disease Biomarkers Comprehensive Database. PMID:31501752
T cell receptor signaling pathway and cytokine-cytokine receptor interaction affect the rehabilitation process after respiratory syncytial virus infection. PMID:31223533
Integration of genomic copy number variations and chemotherapy-response biomarkers in pediatric sarcoma. PMID:30704460
A 44-gene set constructed for predicting the prognosis of clear cell renal cell carcinoma. PMID:30272265
Automatic extraction of gene-disease associations from literature using joint ensemble learning. PMID:30048465
A Novel Statistical Method to Diagnose, Quantify and Correct Batch Effects in Genomic Studies. PMID:28883548
Association Study of Vitamin D Receptor (VDR) - Related Genetic Polymorphisms and their Haplotypes with Chronic Periodontitis in Colombian Population. PMID:28384983
Annotating the Function of the Human Genome with Gene Ontology and Disease Ontology. PMID:27635398
dbPEC: a comprehensive literature-based database for preeclampsia related genes and phenotypes. PMID:26946289
The Implicitome: A Resource for Rationalizing Gene-Disease Associations. PMID:26919047
Immunoglobulins: 25 years of immunoinformatics and IMGT-ONTOLOGY. PMID:25521638
Conserved syntenic clusters of protein coding genes are missing in birds. PMID:25518852
Transcriptome reconstruction and annotation of cynomolgus and African green monkey. PMID:25277458
Identification of a dinucleotide signature that discriminates coding from non-coding long RNAs. PMID:25250049
Pancreatic Cancer Database: an integrative resource for pancreatic cancer. PMID:24839966
Immunoglobulin and T Cell Receptor Genes: IMGT(®) and the Birth and Rise of Immunoinformatics. PMID:24600447
Generic information can retrieve known biological associations: implications for biomedical knowledge discovery. PMID:24260124
The human urine metabolome. PMID:24023812
Genomics analysis of potassium channel genes in songbirds reveals molecular specializations of brain circuits for the maintenance and production of learned vocalizations. PMID:23845108
Overcoming NS1-mediated immune antagonism involves both interferon-dependent and independent mechanisms. PMID:23772952
Molecular characteristics of malignant ovarian germ cell tumors and comparison with testicular counterparts: implications for pathogenesis. PMID:23575763
Host responses to melioidosis and tuberculosis are both dominated by interferon-mediated signaling. PMID:23383015
PRISM offers a comprehensive genomic approach to transcription factor function prediction. PMID:23382538
Using genome-wide expression profiling to define gene networks relevant to the study of complex traits: from RNA integrity to network topology. PMID:23195313
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Research resources: curating the new eagle-i discovery system. PMID:22434835
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Animal Toxins: How is Complexity Represented in Databases? PMID:22069583
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Identification of novel NPRAP/δ-catenin-interacting proteins and the direct association of NPRAP with dynamin 2. PMID:22022388
Serotonin, via HTR2 receptors, excites neurons in a cortical-like premotor nucleus necessary for song learning and production. PMID:21957243
Whole genome expression array profiling highlights differences in mucosal defense genes in Barrett's esophagus and esophageal adenocarcinoma. PMID:21829465
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The IDOL-UBE2D complex mediates sterol-dependent degradation of the LDL receptor. PMID:21685362
Mitotic spindle proteomics in Chinese hamster ovary cells. PMID:21647379
Metabolic changes in skin caused by Scd1 deficiency: a focus on retinol metabolism. PMID:21573029
Massive-scale RNA-Seq analysis of non ribosomal transcriptome in human trisomy 21. PMID:21533138
Radiation-induced micro-RNA expression changes in peripheral blood cells of radiotherapy patients. PMID:21420249
A comparison of single molecule and amplification based sequencing of cancer transcriptomes. PMID:21390249
Assessing quality and completeness of human transcriptional regulatory pathways on a genome-wide scale. PMID:21356087
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Identifying regulators for EAG1 channels with a novel electrophysiology and tryptophan fluorescence based screen. PMID:20824064
Curating the innate immunity interactome. PMID:20727158
Update of human and mouse forkhead box (FOX) gene families. PMID:20650821
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Coregulation mapping based on individual phenotypic variation in response to virus infection. PMID:20298589
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A MOD(ern) perspective on literature curation. PMID:20221640
Antiviral response dictated by choreographed cascade of transcription factors. PMID:20164420
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The Chicken Gene Nomenclature Committee report. PMID:19607656
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes. PMID:19498102
Hyperlink Management System and ID Converter System: enabling maintenance-free hyperlinks among major biological databases. PMID:19454601
Insights into the regulation of intrinsically disordered proteins in the human proteome by analyzing sequence and gene expression data. PMID:19432952
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Planning the human variome project: the Spain report. PMID:19306394
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Genome and proteome annotation: organization, interpretation and integration. PMID:19019817
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Petabyte-scale innovations at the European Nucleotide Archive. PMID:18978013
The database of experimentally supported targets: a functional update of TarBase. PMID:18957447
Localization and targeting of voltage-dependent ion channels in mammalian central neurons. PMID:18923186
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Analysis of Omics Data Reveals Nucleotide Excision Repair-Related Genes Signature in Highly-Grade Serous Ovarian Cancer to Predict Prognosis. PMID:35769257
The Human Proteoform Atlas: a FAIR community resource for experimentally derived proteoforms. PMID:34986596
Development and Verification of an Autophagy-Related lncRNA Signature to Predict Clinical Outcomes and Therapeutic Responses in Ovarian Cancer. PMID:34671615
Downregulation of exhausted cytotoxic T cells in gene expression networks of multisystem inflammatory syndrome in children. PMID:34381049
Generating real-world evidence from unstructured clinical notes to examine clinical utility of genetic tests: use case in BRCAness. PMID:33407429
Cytotoxic lymphocytes are dysregulated in multisystem inflammatory syndrome in children. PMID:32909006
Data-driven Sublanguage Analysis for Cancer Genomics Knowledge Modeling: Applications in Mining Oncological Genetics Information from Patients' Genetic Reports. PMID:32477695
Integrated analysis of lymphocyte infiltration-associated lncRNA for ovarian cancer via TCGA, GTEx and GEO datasets. PMID:32419983
Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years. PMID:32417790
Pharmacological target-focused transcriptomic analysis of native vs cultured human and mouse dorsal root ganglia. PMID:32197039
Portrait of Tissue-Specific Coexpression Networks of Noncoding RNAs (miRNA and lncRNA) and mRNAs in Normal Tissues. PMID:31565069
A quantitative analysis of heterogeneities and hallmarks in acute myelogenous leukaemia. PMID:30988472
Biological Interpretation of Complex Genomic Data. PMID:30649721
Prediction of candidate RNA signatures for recurrent ovarian cancer prognosis by the construction of an integrated competing endogenous RNA network. PMID:30226545
Platforms for Investigating LncRNA Functions. PMID:29945466
Recurrent Patterns of Protein Expression Signatures in Pediatric Acute Lymphoblastic Leukemia: Recognition and Therapeutic Guidance. PMID:29669823
Recognition of Recurrent Protein Expression Patterns in Pediatric Acute Myeloid Leukemia Identified New Therapeutic Targets. PMID:29669821
DeepARG: a deep learning approach for predicting antibiotic resistance genes from metagenomic data. PMID:29391044
From word models to executable models of signaling networks using automated assembly. PMID:29175850
The impact of the protein interactome on the syntenic structure of mammalian genomes. PMID:28910296
Histone deacetylase 3 prepares brown adipose tissue for acute thermogenic challenge. PMID:28614293
Functional proteogenomics reveals biomarkers and therapeutic targets in lymphomas. PMID:28607076
snpGeneSets: An R Package for Genome-Wide Study Annotation. PMID:27807048
A Pathway Proteomic Profile of Ischemic Stroke Survivors Reveals Innate Immune Dysfunction in Association with Mild Symptoms of Depression - A Pilot Study. PMID:27379006
ToxEvaluator: an integrated computational platform to aid the interpretation of toxicology study-related findings. PMID:27161010
LEIGC long non-coding RNA acts as a tumor suppressor in gastric carcinoma by inhibiting the epithelial-to-mesenchymal transition. PMID:25496320
Pregnancy-induced gingivitis and OMICS in dentistry: in silico modeling and in vivo prospective validation of estradiol-modulated inflammatory biomarkers. PMID:24983467
Jointly creating digital abstracts: dealing with synonymy and polysemy. PMID:23110757
Gene expression profiles of the NCI-60 human tumor cell lines define molecular interaction networks governing cell migration processes. PMID:22570691
Functional categories associated with clusters of genes that are co-expressed across the NCI-60 cancer cell lines. PMID:22291933
SNOntology: Myriads of novel snoRNAs or just a mirage? PMID:22047601
Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers. PMID:21992066
Chemical structural novelty: on-targets and off-targets. PMID:21916467
Cx31.1 acts as a tumour suppressor in non-small cell lung cancer (NSCLC) cell lines through inhibition of cell proliferation and metastasis. PMID:21777377
The Booly aliasing resource: a database of grouped biological identifiers. PMID:21544171
Modeling and characterization of disease associated subnetworks in the human interactome using machine learning. PMID:21347156
Biomolecular Systems of Disease Buried Across Multiple GWAS Unveiled by Information Theory and Ontology. PMID:21347143
Gene set enrichment analysis of microarray data from Pimephales promelas (Rafinesque), a non-mammalian model organism. PMID:21269471
Unifying candidate gene and GWAS Approaches in Asthma. PMID:21103062
SCLD: a Stem Cell Lineage Database for the annotation of cell types and developmental lineages. PMID:20972216
Robust assignment of cancer subtypes from expression data using a uni-variate gene expression average as classifier. PMID:20925936
BACE1 gene variants do not influence BACE1 activity, levels of APP or Aβ isoforms in CSF in Alzheimer's disease. PMID:20849576
The characterization of twenty sequenced human genomes. PMID:20838461
Negative energy balance and hepatic gene expression patterns in high-yielding dairy cows during the early postpartum period: a global approach. PMID:20716645
Identification, classification and evolution of owl monkeys (Aotus, Illiger 1811). PMID:20704725
Literature-based discovery of IFN-gamma and vaccine-mediated gene interaction networks. PMID:20625487
i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study. PMID:20435672
High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity. PMID:20351689
An extended nomenclature for mammalian V-ATPase subunit genes and splice variants. PMID:20224822
Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information. PMID:20092628
Single-nucleotide polymorphism bioinformatics: a comprehensive review of resources. PMID:20031630
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. PMID:20010835
The Protein Naming Utility: a rules database for protein nomenclature. PMID:20007151
Graphle: Interactive exploration of large, dense graphs. PMID:20003429
PDbase: a database of Parkinson's disease-related genes and genetic variation using substantia nigra ESTs. PMID:19958497
GIFtS: annotation landscape analysis with GeneCards. PMID:19852797
Proteomics analysis of A33 immunoaffinity-purified exosomes released from the human colon tumor cell line LIM1215 reveals a tissue-specific protein signature. PMID:19837982
Knowledge-based characterization of similarity relationships in the human protein-tyrosine phosphatase family for rational inhibitor design. PMID:19810703
Mapping the human membrane proteome: a majority of the human membrane proteins can be classified according to function and evolutionary origin. PMID:19678920
HAPPI: an online database of comprehensive human annotated and predicted protein interactions. PMID:19594875
DDEC: Dragon database of genes implicated in esophageal cancer. PMID:19580656
Pleiotropic effects of negative energy balance in the postpartum dairy cow on splenic gene expression: repercussions for innate and adaptive immunity. PMID:19567785
A chemogenomics view on protein-ligand spaces. PMID:19534738
Probabilistic retrieval and visualization of biologically relevant microarray experiments. PMID:19477980
Immunome knowledge base (IKB): an integrated service for immunome research. PMID:19134210
An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases. PMID:19091018
Genes and social behavior. PMID:18988841
IUPHAR-DB: the IUPHAR database of G protein-coupled receptors and ion channels. PMID:18948278
PMAP: databases for analyzing proteolytic events and pathways. PMID:18842634
PhyloPat: an updated version of the phylogenetic pattern database contains gene neighborhood. PMID:18832367
PharmGKB: an integrated resource of pharmacogenomic data and knowledge. PMID:18819074
Integrating high dimensional bi-directional parsing models for gene mention tagging. PMID:18586726
The SWAN biomedical discourse ontology. PMID:18583197
A searchable database of genetic evidence for psychiatric disorders. PMID:18548508
ConTra: a promoter alignment analysis tool for identification of transcription factor binding sites across species. PMID:18453628
Overlapping genes in the human and mouse genomes. PMID:18410680
MethCancerDB--aberrant DNA methylation in human cancer. PMID:18253128
Genome-wide analysis reveals regulatory role of G4 DNA in gene transcription. PMID:18096746
A comparison study on algorithms of detecting long forms for short forms in biomedical text. PMID:18047706
Xenbase: a Xenopus biology and genomics resource. PMID:17984085
The HGNC Database in 2008: a resource for the human genome. PMID:17984084
Integration of biological networks and gene expression data using Cytoscape. PMID:17947979
The Edinburgh human metabolic network reconstruction and its functional analysis. PMID:17882155
PepBank--a database of peptides based on sequence text mining and public peptide data sources. PMID:17678535
Variability in the kinesin light chain 1 gene may influence risk of age-related cataract. PMID:17653041
Semantic classification of biomedical concepts using distributional similarity. PMID:17460124
Pathways and genes differentially expressed in the motor cortex of patients with sporadic amyotrophic lateral sclerosis. PMID:17244347
DiscoverySpace: an interactive data analysis application. PMID:17210078
CYCLONET--an integrated database on cell cycle regulation and carcinogenesis. PMID:17202170
UniHI: an entry gate to the human protein interactome. PMID:17158159
CutDB: a proteolytic event database. PMID:17142225
The UCSC genome browser database: update 2007. PMID:17142222
methBLAST and methPrimerDB: web-tools for PCR based methylation analysis. PMID:17094804
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LPInsider: a webserver for lncRNA-protein interaction extraction from the literature. PMID:35428172
The Genomic Organization of the LILR Region Remained Largely Conserved Throughout Primate Evolution: Implications for Health And Disease. PMID:34737739
The Thyroid Na+/I- Symporter: Molecular Characterization and Genomic Regulation. PMID:28117294
Genenames.org: the HGNC and VGNC resources in 2017. PMID:27799471
Human Prostate Cancer Hallmarks Map. PMID:27476486
A Systems Biology Approach to Reveal Putative Host-Derived Biomarkers of Periodontitis by Network Topology Characterization of MMP-REDOX/NO and Apoptosis Integrated Pathways. PMID:26793622
The Transporter Classification Database (TCDB): recent advances. PMID:26546518
Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia. PMID:25398481
Genenames.org: the HGNC resources in 2015. PMID:25361968
Altered expression of Alzheimer's disease-related genes in the cerebellum of autistic patients: a model for disrupted brain connectome and therapy. PMID:24853428
Major components of energy drinks (caffeine, taurine, and guarana) exert cytotoxic effects on human neuronal SH-SY5Y cells by decreasing reactive oxygen species production. PMID:23766861
Genenames.org: the HGNC resources in 2013. PMID:23161694
IMGT-ONTOLOGY 2012. PMID:22654892
Evolutionary plasticity determination by orthologous groups distribution. PMID:21586164
Meta-analysis of muscle transcriptome data using the MADMuscle database reveals biologically relevant gene patterns. PMID:21324190
Automated recognition of brain region mentions in neuroscience literature. PMID:19750194
Perturbation of interaction networks for application to cancer therapy. PMID:19390668
A controlled challenge study on di(2-ethylhexyl) phthalate (DEHP) in house dust and the immune response in human nasal mucosa of allergic subjects. PMID:19057701
Overview of BioCreative II gene normalization. PMID:18834494
Evolutionary origins of human apoptosis and genome-stability gene networks. PMID:18832373
Identifying gene-disease associations using centrality on a literature mined gene-interaction network. PMID:18586725
Hereditary spastic paraplegia caused by the novel mutation 1047insC in the SPG7 gene. PMID:18563470
Conserved co-expression for candidate disease gene prioritization. PMID:18433471
Comparative molecular biological analysis of membrane transport genes in organisms. PMID:18293089
A genomic view of the NOD-like receptor family in teleost fish: identification of a novel NLR subfamily in zebrafish. PMID:18254971
RGST - Rat Gene Symbol Tracker, a database for defining official rat gene symbols. PMID:18215257
Spectrum of disease-causing mutations in protein secondary structures. PMID:17727703
The functional modulation of epigenetic regulators by alternative splicing. PMID:17651478
Using contextual and lexical features to restructure and validate the classification of biomedical concepts. PMID:17650333
CAG-encoded polyglutamine length polymorphism in the human genome. PMID:17519034
IDR knowledge base for primary immunodeficiencies. PMID:17394641
MCEF is localized to the nucleus by protein sequences encoded within three distinct exons, where it represses HIV-1 Tat-transactivation of LTR-directed transcription. PMID:17389929
SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis. PMID:17338820
Impaired expression of NER gene network in sporadic solid tumors. PMID:17332015
Standard mutation nomenclature in molecular diagnostics: practical and educational challenges. PMID:17251329
Dynamic role of postsynaptic caspase-3 and BIRC4 in zebra finch song-response habituation. PMID:17178408
Structural and biochemical characterization of human orphan DHRS10 reveals a novel cytosolic enzyme with steroid dehydrogenase activity. PMID:17067289
Analysis of cytoskeletal and motility proteins in the sea urchin genome assembly. PMID:17027957
Gene and protein nomenclature in public databases. PMID:16899134
TreeFam: a curated database of phylogenetic trees of animal gene families. PMID:16381935
TRANSPATH: an information resource for storing and visualizing signaling pathways and their pathological aberrations. PMID:16381929
pSTIING: a 'systems' approach towards integrating signalling pathways, interaction and transcriptional regulatory networks in inflammation and cancer. PMID:16381926
FLIGHT: database and tools for the integration and cross-correlation of large-scale RNAi phenotypic datasets. PMID:16381916
The HUGO Gene Nomenclature Database, 2006 updates. PMID:16381876
TCDB: the Transporter Classification Database for membrane transport protein analyses and information. PMID:16381841
RNAi Codex: a portal/database for short-hairpin RNA (shRNA) gene-silencing constructs. PMID:16381835
TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes. PMID:16381825
HCOP: the HGNC comparison of orthology predictions search tool. PMID:16284797
GeneSeer: a sage for gene names and genomic resources. PMID:16176584
L2L: a simple tool for discovering the hidden significance in microarray expression data. PMID:16168088
Distribution of immunodeficiency fact files with XML--from Web to WAP. PMID:15978138
Evaluation of BioCreAtIvE assessment of task 2. PMID:15960828
A simple approach for protein name identification: prospects and limits. PMID:15960827
CoPub Mapper: mining MEDLINE based on search term co-publication. PMID:15760478
Linking disease-associated genes to regulatory networks via promoter organization. PMID:15701758
The Vertebrate Genome Annotation (Vega) database. PMID:15608237
Biomedical term mapping databases. PMID:15608198
UTRdb and UTRsite: a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs. PMID:15608165
An overview of Ensembl. PMID:15078858
Tags:
Tags
More detailed information about this field from each metasource.
gene
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
gene name
metasource: Fairsharing.org
version: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
bioinformatics
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
gene family
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
genetics
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
human genes
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
phenotype
metasource: re3data.org
version: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
human biology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
genomics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
ontology and terminology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:27:09.518324
Tags
More detailed information about this field from each metasource.
gene
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
gene name
metasource: Fairsharing.orgversion: FAIRsharing.org: HGNC; HUGO Gene Nomenclature Committee; DOI: https://doi.org/10.25504/FAIRsharing.29we0s; Last edited: March 2, 2020, 6:53 p.m.; Last accessed: Jan 03 2022 7:06 p.m.
bioinformatics
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
gene family
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
genetics
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
human genes
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
phenotype
metasource: re3data.orgversion: re3data.org: HUGO Gene Nomenclature Committee; editing status 2019-04-09; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3XC80 last accessed: 2022-11-04
human biology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
genomics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
ontology and terminology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:27:09.518324
gene gene name bioinformatics gene family genetics human genes phenotype human genomics ontology and terminology
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