In silico comprehensive analysis of coding and non-coding SNPs in human mTOR protein.
PMID:35788771
Association of a miRNA-binding site polymorphism in IL-16 gene with disease risk and clinical characteristics of rheumatoid arthritis and systemic lupus erythematosus.
PMID:35332405
Comprehensive Characterization of the Coding and Non-Coding Single Nucleotide Polymorphisms in the Tumor Protein p63 (TP63) Gene Using In Silico Tools.
PMID:34827731
A computational in silico approach to predict high-risk coding and non-coding SNPs of human PLCG1 gene.
PMID:34793541
Association between ADCY9 Gene Polymorphisms and Ritodrine Treatment Outcomes in Patients with Preterm Labor.
PMID:34683946
Molecular insights into the role of genetic determinants of congenital hypothyroidism.
PMID:34638176
Nuclear Pore Glycoprotein 62 Genetic Variant rs9523 is Associated with Clinical Outcomes of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Adenocarcinoma Patients.
PMID:34629889
Emerging Role of isomiRs in Cancer: State of the Art and Recent Advances.
PMID:34573429
Mapping the miRNA-mRNA Interactome in Human Hepatocytes and Identification of Functional mirSNPs in Pharmacogenes.
PMID:34314509
Evaluating the Effect of 3'-UTR Variants in DICER1 and DROSHA on Their Tissue-Specific Expression by miRNA Target Prediction.
PMID:34287278
Bioinformatics Accelerates the Major Tetrad: A Real Boost for the Pharmaceutical Industry.
PMID:34201152
Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions.
PMID:34149802
Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders.
PMID:34135841
Structure analysis of deleterious nsSNPs in human PALB2 protein for functional inference.
PMID:34092963
Identification of missense MAB21L1 variants in microphthalmia and aniridia.
PMID:33973683
ANGPTL3 gene variants in subjects with familial combined hyperlipidemia.
PMID:33772079
MicroRNA Expression Profiles in the Subcutaneous Adipose Tissues of Morbidly Obese Chinese Women.
PMID:33550286
Conceptualization of functional single nucleotide polymorphisms of polycystic ovarian syndrome genes: an in silico approach.
PMID:33506367
HumiR: Web Services, Tools and Databases for Exploring Human microRNA Data.
PMID:33233537
Identification of Functional Genetic Variants Associated With Alcohol Dependence and Related Phenotypes Using a High-Throughput Assay.
PMID:33119910
The effects of common variants in MDM2 and GNRH2 genes on the risk and survival of osteosarcoma in Han populations from Northwest China.
PMID:32994424
miRNASNP-v3: a comprehensive database for SNPs and disease-related variations in miRNAs and miRNA targets.
PMID:32990748
SIRT1 Gene SNP rs932658 Is Associated With Medication-Related Osteonecrosis of the Jaw.
PMID:32967053
Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences.
PMID:32867672
Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa.
PMID:32823908
Investigating the pathogenic SNPs in BLM helicase and their biological consequences by computational approach.
PMID:32704157
Association of variants in selected genes mediating host immune response with duration of Staphylococcus aureus bacteremia.
PMID:32507857
miRNet 2.0: network-based visual analytics for miRNA functional analysis and systems biology.
PMID:32484539
RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects.
PMID:32326527
dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions.
PMID:32227657
ErbB4 3'-UTR Variant (c.*3622A>G) is Associated with ER/PR Negativity and Advanced Breast Cancer.
PMID:32071504
An in silico approach to characterize nonsynonymous SNPs and regulatory SNPs in human TOX3 gene.
PMID:31819019
Reduced expression of microRNA-139-5p in hepatocellular carcinoma results in a poor outcome: An exploration the roles of microRNA-139-5p in tumorigenesis, advancement and prognosis at the molecular biological level using an integrated meta-analysis and bioinformatic investigation.
PMID:31807180
Identification and analysis of pathogenic nsSNPs in human LSP1 gene.
PMID:31787810
Tissue-specific microRNA expression alters cancer susceptibility conferred by a TP53 noncoding variant.
PMID:31699989
miRPathDB 2.0: a novel release of the miRNA Pathway Dictionary Database.
PMID:31691816
MicroRNA-744/transforming growth factor β1 relationship regulates liver cirrhosis.
PMID:31643031
In Silico Genetics Revealing 5 Mutations in CEBPA Gene Associated With Acute Myeloid Leukemia.
PMID:31621694
PopTargs: a database for studying population evolutionary genetics of human microRNA target sites.
PMID:31608947
The variability of SMCHD1 gene in FSHD patients: evidence of new mutations.
PMID:31600781
Structural, functional and molecular dynamics analysis of cathepsin B gene SNPs associated with tropical calcific pancreatitis, a rare disease of tropics.
PMID:31592339
Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders.
PMID:31477794
An Approach to Identify Individual Functional Single Nucleotide Polymorphisms and Isoform MicroRNAs.
PMID:31467902
Whole genome and transcriptome sequencing of post-mortem cardiac tissues from sudden cardiac death victims identifies a gene regulatory variant in NEXN.
PMID:31392414
SNP rs4937333 in the miRNA-5003-Binding Site of the ETS1 3'-UTR Decreases ETS1 Expression.
PMID:31275358
The Impact of Population Variation in the Analysis of microRNA Target Sites.
PMID:31234531
miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS.
PMID:31211169
Gain-of-Function Mutations: An Emerging Advantage for Cancer Biology.
PMID:31047772
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A.
PMID:30934838
A DAAM1 3'-UTR SNP mutation regulates breast cancer metastasis through affecting miR-208a-5p-DAAM1-RhoA axis.
PMID:30911286
Relationship of common variants in Interleukin 33 gene with susceptibility and prognosis of osteosarcoma in Han Chinese population.
PMID:30854122
SNPs rs10224002 in PRKAG2 may disturb gene expression and consequently affect hypertension.
PMID:30689184
Computational Methods for the Pharmacogenetic Interpretation of Next Generation Sequencing Data.
PMID:30564131
regQTLs: Single nucleotide polymorphisms that modulate microRNA regulation of gene expression in tumors.
PMID:30557297
miRNA Mediated Noise Making of 3'UTR Mutations in Cancer.
PMID:30424545
Framework for microRNA variant annotation and prioritization using human population and disease datasets.
PMID:30302893
Uncovering association networks through an eQTL analysis involving human miRNAs and lincRNAs.
PMID:30301969
MIR4532 gene variant rs60432575 influences the expression of KCNJ11 and the sulfonylureas-stimulated insulin secretion.
PMID:30242599
MicroRNA-17 as a promising diagnostic biomarker of gastric cancer: An investigation combining TCGA, GEO, meta-analysis, and bioinformatics.
PMID:30186751
Polymorphism studies on microRNA targetome of thalassemia.
PMID:30108424
Trends in the development of miRNA bioinformatics tools.
PMID:29982332
PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites.
PMID:29963077
MicroRNA-Related Genetic Variants Associated with Survival of Head and Neck Squamous Cell Carcinoma.
PMID:29880533
Integrative Analysis Identifies Genetic Variants Associated With Autoimmune Diseases Affecting Putative MicroRNA Binding Sites.
PMID:29755505
Clustering Pattern and Functional Effect of SNPs in Human miRNA Seed Regions.
PMID:29693000
A Comprehensive in Silico Analysis of Regulatory SNPs of Human CLEC7A Gene and Its Validation as Genotypic and Phenotypic Disease Marker in Recurrent Vulvovaginal Infections.
PMID:29616193
Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes.
PMID:29563329
A common variant alters SCN5A-miR-24 interaction and associates with heart failure mortality.
PMID:29457789
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
PMID:29304378
Genetic variation at the microRNA binding site of CAV1 gene is associated with lung cancer susceptibility.
PMID:29190968
Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases.
PMID:29129848
MSDD: a manually curated database of experimentally supported associations among miRNAs, SNPs and human diseases.
PMID:29106642
The rs2910164 variant is associated with reduced miR-146a expression but not cytokine levels in patients with type 2 diabetes.
PMID:29058209
A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma.
PMID:29049738
Variants in the CYP2B6 3'UTR Alter In Vitro and In Vivo CYP2B6 Activity: Potential Role of MicroRNAs.
PMID:28960269
Association between polymorphisms in microRNA target sites and survival in early-stage non-small cell lung cancer.
PMID:28922562
Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma.
PMID:28886711
The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes.
PMID:28819299
CXCL9-11 polymorphisms are associated with liver fibrosis in patients with chronic hepatitis C: a cross-sectional study.
PMID:28755163
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.
PMID:28743860
Phenotype prediction for mucopolysaccharidosis type I by in silico analysis.
PMID:28676128
Systematic Prediction of the Impacts of Mutations in MicroRNA Seed Sequences.
PMID:28637929
Genome-scale identification of microRNA-related SNPs associated with risk of head and neck squamous cell carcinoma.
PMID:28582492
An Integrating Approach for Genome-Wide Screening of MicroRNA Polymorphisms Mediated Drug Response Alterations.
PMID:28480217
SNPs in microRNA target sites and their potential role in human disease.
PMID:28381629
Functional variomics and network perturbation: connecting genotype to phenotype in cancer.
PMID:28344341
Computational Modeling of complete HOXB13 protein for predicting the functional effect of SNPs and the associated role in hereditary prostate cancer.
PMID:28272408
A functional variant in the 3'-UTR of VEGF predicts the 90-day outcome of ischemic stroke in Chinese patients.
PMID:28234972
miRNAs target databases: developmental methods and target identification techniques with functional annotations.
PMID:28204845
Cis-acting single nucleotide polymorphisms alter MicroRNA-mediated regulation of human brain-expressed transcripts.
PMID:28171541
Genome-Wide Prioritization and Transcriptomics Reveal Novel Signatures Associated With Thiazide Diuretics Blood Pressure Response.
PMID:28115488
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
PMID:27890468
A cross-ethnic survey of CFB and SLC44A4, Indian ulcerative colitis GWAS hits, underscores their potential role in disease susceptibility.
PMID:27759029
MicroRNA-related polymorphisms and non-Hodgkin lymphoma susceptibility in the Multicenter AIDS Cohort Study.
PMID:27701053
Alu-miRNA interactions modulate transcript isoform diversity in stress response and reveal signatures of positive selection.
PMID:27586304
Interaction Between Peroxisome Proliferator Activated Receptor δ and Epithelial Membrane Protein 2 Polymorphisms Influences HDL-C Levels in the Chinese Population.
PMID:27530449
A Bioinformatics Approach to Prioritize Single Nucleotide Polymorphisms in TLRs Signaling Pathway Genes.
PMID:27478803
Bioinformatics Approach for Prediction of Functional Coding/Noncoding Simple Polymorphisms (SNPs/Indels) in Human BRAF Gene.
PMID:27478437
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.
PMID:27432226
A 3'UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility.
PMID:27424220
A comprehensive in silico analysis of non-synonymous and regulatory SNPs of human MBL2 gene.
PMID:27390651
In silico analysis of deleterious single nucleotide polymorphisms in human BUB1 mitotic checkpoint serine/threonine kinase B gene.
PMID:27331020
microRNA editing in seed region aligns with cellular changes in hypoxic conditions.
PMID:27298257
Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD.
PMID:27113999
Mining of single nucleotide polymorphisms in the 3' untranslated region of liver cancer-implicated miR-122 target genes.
PMID:27047961
A polymorphism in the norepinephrine transporter gene is associated with affective and cardiovascular disease through a microRNA mechanism.
PMID:27046647
A genetic variation in microRNA target site of ETS2 is associated with clinical outcomes of paclitaxel-cisplatin chemotherapy in non-small cell lung cancer.
PMID:26893365
Bioinformatics Resources for MicroRNA Discovery.
PMID:26819547
Identification of critical variants within SLC44A4, an ulcerative colitis susceptibility gene identified in a GWAS in north Indians.
PMID:26741288
Double-strand break repair and colorectal cancer: gene variants within 3' UTRs and microRNAs binding as modulators of cancer risk and clinical outcome.
PMID:26735576
Differential gene expression levels might explain association of LAIR2 polymorphisms with pemphigus.
PMID:26721477
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.
PMID:26615194
Bioinformatic tools for microRNA dissection.
PMID:26578605
SomamiR 2.0: a database of cancer somatic mutations altering microRNA-ceRNA interactions.
PMID:26578591
Knowledge-based analysis of functional impacts of mutations in microRNA seed regions.
PMID:26564979
microRNAs as pharmacogenomic biomarkers for drug efficacy and drug safety assessment.
PMID:26501795
Altered Gene Expression Associated with microRNA Binding Site Polymorphisms.
PMID:26496489
miRVaS: a tool to predict the impact of genetic variants on miRNAs.
PMID:26384425
The genetics of human autoimmune disease: A perspective on progress in the field and future directions.
PMID:26343334
Polymorphism in microRNA-binding site in HNF1B influences the susceptibility of type 2 diabetes mellitus: a population based case-control study.
PMID:26329304
Genetic variants in microRNA genes: impact on microRNA expression, function, and disease.
PMID:26052338
An update of miRNASNP database for better SNP selection by GWAS data, miRNA expression and online tools.
PMID:25877638
Biological databases for human research.
PMID:25712261
Overview of microRNA biology.
PMID:25632930
Genetic variability of microRNA regulome in human.
PMID:25629077
Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA).
PMID:25576479
In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci.
PMID:25552398
Genetic variants in let-7/Lin28 modulate the risk of oral cavity cancer in a Chinese Han population.
PMID:25503985
Heterogeneity and individuality: microRNAs in mental disorders.
PMID:25395183
CardioGxE, a catalog of gene-environment interactions for cardiometabolic traits.
PMID:25368670
lncRNASNP: a database of SNPs in lncRNAs and their potential functions in human and mouse.
PMID:25332392
Polymorphisms in HLA-DPB1 are associated with differences in rubella virus-specific humoral immunity after vaccination.
PMID:25293367
Single-Nucleotide Polymorphisms Within MicroRNAs Sequences and Their 3' UTR Target Sites May Regulate Gene Expression in Gastrointestinal Tract Cancers.
PMID:25237569
Polymorphism in miRNA-1 target site and circulating miRNA-1 phenotype are associated with the decreased risk and prognosis of coronary artery disease.
PMID:25197382
Computational analysis of functional single nucleotide polymorphisms associated with the CYP11B2 gene.
PMID:25102047
Inflammation-related genetic variants predict toxicity following definitive radiotherapy for lung cancer.
PMID:25054431
miR-485-5p binding site SNP rs8752 in HPGD gene is associated with breast cancer risk.
PMID:25003827
Computational prediction of disease microRNAs in domestic animals.
PMID:24970281
Genetic variation in the 3'-UTR of CYP1A2, CYP2B6, CYP2D6, CYP3A4, NR1I2, and UGT2B7: potential effects on regulation by microRNA and pharmacogenomics relevance.
PMID:24926315
CREAM: a database for chemotherapy resistance-associated miRSNP.
PMID:24874743