Geneimprint
Catalogue of genes (from different species including human) that contains general information about a gene as well as whether it is imprinted and which allele is expressed.
Description
More detailed information about this field from each metasource.
Catalogue of genes (from different species including human) that contains general information about a gene as well as whether it is imprinted and which allele is expressed.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
Webpage:
http://www.geneimprint.com/site/genes-by-speciesWebpage
More detailed information about this field from each metasource.
http://www.geneimprint.com/site/genes-by-species
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
Publications:
Publications
More detailed information about this field from each metasource.
Genomic imprinting: implications for human disease
PMID: 10079240
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
Genomic imprinting and cancer
PMID: 10094809
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
Publications
More detailed information about this field from each metasource.
Genomic imprinting: implications for human disease
PMID: 10079240
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
Genomic imprinting and cancer
PMID: 10094809
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
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Genomic imprinting: implications for human disease
PubMed citations: 98.
98 articles citing: Genomic imprinting: implications for human disease
A guide for the diagnosis of rare and undiagnosed disease: beyond the exome. PMID:35220969
Detection of CRISPR-mediated genome modifications through altered methylation patterns of CpG islands. PMID:33267773
A robust test for X-chromosome genetic association accounting for X-chromosome inactivation and imprinting. PMID:32234109
Insulin-like growth factor-II and bioactive proteins containing a part of the E-domain of pro-insulin-like growth factor-II. PMID:32026557
Clinical utility of genomic sequencing. PMID:31693580
Monitoring of switches in heterochromatin-induced silencing shows incomplete establishment and developmental instabilities. PMID:31527269
PRISM: methylation pattern-based, reference-free inference of subclonal makeup. PMID:31510697
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree. PMID:30675526
Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions. PMID:30204804
Long Non-Coding RNAs in Obesity-Induced Cancer. PMID:30154386
PHLDA2 is a key oncogene-induced negative feedback inhibitor of EGFR/ErbB2 signaling via interference with AKT signaling. PMID:29861842
Early prenatal alcohol exposure alters imprinted gene expression in placenta and embryo in a mouse model. PMID:29763474
Placental lncRNA Expression Is Associated With Prenatal Phthalate Exposure. PMID:29385630
A powerful parent-of-origin effects test for qualitative traits on X chromosome in general pedigrees. PMID:29304743
Estimation of Trait-Model Parameters in a MOD Score Linkage Analysis. PMID:29131067
Generalized disequilibrium test for association in qualitative traits incorporating imprinting effects based on extended pedigrees. PMID:29037145
Genome-wide random regression analysis for parent-of-origin effects of body composition allometries in mouse. PMID:28338098
Intrafamily and intragenomic conflicts in human warfare. PMID:28228515
The quest for an effective and safe personalized cell therapy using epigenetic tools. PMID:27891192
A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3. PMID:27876814
Paternal chronic colitis causes epigenetic inheritance of susceptibility to colitis. PMID:27538787
DNA Methylation Variation Trends during the Embryonic Development of Chicken. PMID:27438711
DNA methylation signature of human fetal alcohol spectrum disorder. PMID:27358653
Genomic Imprinting. PMID:27275355
Incorporating parent-of-origin effects in whole-genome prediction of complex traits. PMID:27091137
Identification of allelic expression imbalance genes in human hepatocellular carcinoma through massively parallel DNA and RNA sequencing. PMID:27000824
Epigenetic modulators, modifiers and mediators in cancer aetiology and progression. PMID:26972587
Epigenetic alteration of imprinted genes during neural differentiation of germline-derived pluripotent stem cells. PMID:26962997
The Molecular Karyotype of 25 Clinical-Grade Human Embryonic Stem Cell Lines. PMID:26607962
Characterization of SLC22A18 as a tumor suppressor and novel biomarker in colorectal cancer. PMID:26196590
Pyrosequencing for accurate imprinted allele expression analysis. PMID:25581900
A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data. PMID:25518739
An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins. PMID:25502755
Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease. PMID:25391383
Hybrid mice reveal parent-of-origin and Cis- and trans-regulatory effects in the retina. PMID:25340786
Genomic imprinting variations in the mouse type 3 deiodinase gene between tissues and brain regions. PMID:25232934
Detection of parent-of-origin effects for quantitative traits using general pedigree data. PMID:25189228
Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data. PMID:25119724
Investigating Epigenetic Effects of Prenatal Exposure to Toxic Metals in Newborns: Challenges and Benefits. PMID:24955086
Mapping of imprinted quantitative trait loci using immortalized F2 populations. PMID:24676330
Statistical dissection of cyto-nuclear epistasis subject to genomic imprinting in line crosses. PMID:24643065
Pyrosequencing for the rapid and efficient quantification of allele-specific expression. PMID:23973940
Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer. PMID:23756864
Joint detection of association, imprinting and maternal effects using all children and their parents. PMID:23531864
The fibromyalgia family study: a genome-wide linkage scan study. PMID:23280346
A multi-locus likelihood method for assessing parent-of-origin effects using case-control mother-child pairs. PMID:23184538
Gene therapy for colorectal cancer by an oncolytic adenovirus that targets loss of the insulin-like growth factor 2 imprinting system. PMID:23171475
dsPIG: a tool to predict imprinted genes from the deep sequencing of whole transcriptomes. PMID:23083219
Male reprotoxicity and endocrine disruption. PMID:22945574
Role of ART in imprinting disorders. PMID:22549709
Characterization, tissue expression, and imprinting analysis of the porcine CDKN1C and NAP1L4 genes. PMID:22500112
Lack of genomic imprinting of DNA primase, polypeptide 2 (PRIM2) in human term placenta and white blood cells. PMID:22437878
Evolutionary approaches to autism- an overview and integration. PMID:22363193
Bayesian mapping of genome-wide epistatic imprinted loci for quantitative traits. PMID:22350088
A powerful test of parent-of-origin effects for quantitative traits using haplotypes. PMID:22174922
A powerful approach for association analysis incorporating imprinting effects. PMID:21798962
Detection of parent-of-origin effects for quantitative traits in complete and incomplete nuclear families with multiple children. PMID:21633117
Novel retrotransposed imprinted locus identified at human 6p25. PMID:21421564
Number and mode of inheritance of QTL influencing backfat thickness on SSC2p in Sino-European pig pedigrees. PMID:21375775
Biology of FGFRL1, the fifth fibroblast growth factor receptor. PMID:21080029
Environmental epigenetics and allergic diseases: recent advances. PMID:20718778
Epigenetic effects of endocrine-disrupting chemicals on female reproduction: an ovarian perspective. PMID:20609371
Parents' ages at birth and risk of adult-onset hematologic malignancies among female teachers in California. PMID:20507900
Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation. PMID:20009564
Imprinting evolution and human health. PMID:19830403
Detection of parent-of-origin effects using general pedigree data. PMID:19676055
Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data. PMID:19671182
The role of epigenetics in aging and autoimmunity. PMID:19653133
Sex-specific genetic architecture of human disease. PMID:19002143
Detection of parent-of-origin effects based on complete and incomplete nuclear families with multiple affected children. PMID:18931505
Liver insulin-like growth factor 2 methylation in hepatitis C virus cirrhosis and further occurrence of hepatocellular carcinoma. PMID:18803353
Environmental studies of schizophrenia through the prism of epigenetics. PMID:18703665
Epigenetics, aging, and autoimmunity. PMID:18432411
Environmental epigenetics and asthma: current concepts and call for studies. PMID:18187692
Structure and functional analysis of the IGF-II/IGF2R interaction. PMID:18046459
Evidence for transgenerational transmission of epigenetic tumor susceptibility in Drosophila. PMID:17845077
Environmental epigenomics and disease susceptibility. PMID:17363974
An extension of the transmission disequilibrium test incorporating imprinting. PMID:17194789
Human embryonic stem cell stability. PMID:17142848
A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15. PMID:17075716
Comparative phylogenetic analysis reveals multiple non-imprinted isoforms of opossum Dlk1. PMID:16465595
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder. PMID:16380918
Conservation of genomic imprinting at the XIST, IGF2, and GTL2 loci in the bovine. PMID:15599555
Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region. PMID:15590938
Phylogenetic footprint analysis of IGF2 in extant mammals. PMID:15342558
Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies. PMID:15123827
Transcriptional activities of the zinc finger protein Zac are differentially controlled by DNA binding. PMID:12529403
Imprinting disorders: non-Mendelian mechanisms affecting growth. PMID:12510981
Glutamate receptor genes: susceptibility factors in schizophrenia and depressive disorders? PMID:11936559
Methylome profiling of cancer cells by amplification of inter-methylated sites (AIMS). PMID:11917034
Structure of a functional IGF2R fragment determined from the anomalous scattering of sulfur. PMID:11867533
Likelihood formulation of parent-of-origin effects on segregation analysis, including ascertainment. PMID:11741195
Coeliac disease in the father affects the newborn. PMID:11454790
Unequal expression of allelic kainate receptor GluR7 mRNAs in human brains. PMID:11124978
Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation. PMID:11076856
Rare etiology of autosomal recessive disease in a child with noncarrier parents. PMID:10915611
Imprinted genes as potential genetic and epigenetic toxicologic targets. PMID:10698719
Paternal monoallelic expression of the paired immunoglobulin-like receptors PIR-A and PIR-B. PMID:10359805 -
Genomic imprinting and cancer
PubMed citations: 27.
27 articles citing: Genomic imprinting and cancer
Pregnancy exposure to synthetic phenols and placental DNA methylation - An epigenome-wide association study in male infants from the EDEN cohort. PMID:34523531
Simultaneous profiling of chromatin accessibility and methylation on human cell lines with nanopore sequencing. PMID:33230324
Immediate and durable effects of maternal tobacco consumption alter placental DNA methylation in enhancer and imprinted gene-containing regions. PMID:33023569
Allelic Switching of DLX5, GRB10, and SVOPL during Colorectal Cancer Tumorigenesis. PMID:31093489
Allele-specific RNA-seq expression profiling of imprinted genes in mouse isogenic pluripotent states. PMID:30767785
The quest for an effective and safe personalized cell therapy using epigenetic tools. PMID:27891192
HIN-1: a New Epigenetic Biomarker Crucial for Therapy Selection in Glioblastoma Multiforme. PMID:25752997
Pyrosequencing for the rapid and efficient quantification of allele-specific expression. PMID:23973940
Similarities in the Age-Specific Incidence of Colon and Testicular Cancers. PMID:23840520
Integrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancer. PMID:22637570
Small nucleolar RNAs in cancer. PMID:22498252
Biological Basis of Differential Susceptibility to Hepatocarcinogenesis among Mouse Strains. PMID:22271974
Toxin-based therapeutic approaches. PMID:22069564
The tumorigenicity of human embryonic and induced pluripotent stem cells. PMID:21390058
Modeling the aneuploidy control of cancer. PMID:20594351
Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data. PMID:19671182
Clinical significance of loss of heterozygosity for M6P/IGF2R in patients with primary hepatocellular carcinoma. PMID:18322954
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight. PMID:17180344
Molecular cytogenetics in haematological malignancy: current technology and future prospects. PMID:16003502
Molecular pathogenesis of oligodendroglial tumors. PMID:15674476
M6P/IGF2R loss of heterozygosity in head and neck cancer associated with poor patient prognosis. PMID:12589712
Tissue-specific inactivation of murine M6P/IGF2R. PMID:12507915
Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality. PMID:11884600
Methylation matters. PMID:11333864
RNA-directed DNA methylation. PMID:10999405
Genomic imprinting and environmental disease susceptibility. PMID:10706535
Imprinted genes as potential genetic and epigenetic toxicologic targets. PMID:10698719
Tags:
Tags
More detailed information about this field from each metasource.
epigenetics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
pathology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
gene expression
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
gene transcripts
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
human biology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
rare diseases
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:43.873620
Tags
More detailed information about this field from each metasource.
epigenetics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
pathology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
gene expression
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
gene transcripts
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
human biology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
rare diseases
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:43.873620
epigenetics pathology gene expression gene transcripts human rare diseases
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