A practical guide for the functional annotation of genetic variations using SNPnexus.
about
Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomesAn ImmunoChip study of multiple sclerosis risk in African Americans.Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.Genetics of hand grip strength in mid to late life.A pharmacogenetic candidate gene study of tenofovir-associated Fanconi syndrome.SNP characteristics predict replication success in association studies.Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) RiskA Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic PainA genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic painGenome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults.A Genome-Wide Association Study Provides New Evidence That CACNA1C Gene is Associated With Diabetic CataractGene × smoking interactions on human brain gene expression: finding common mechanisms in adolescents and adults.Integrative genomic analysis identifies epigenetic marks that mediate genetic risk for epithelial ovarian cancer.Exome-based proteogenomics of HEK-293 human cell line: Coding genomic variants identified at the level of shotgun proteome.Common Polymorphisms in IFI16 and AIM2 Genes Are Associated With Periodontal Disease.Disease Risk Assessment Using a Voronoi-Based Network Analysis of Genes and Variants Scores.Genome-wide integrative analysis identified SNP-miRNA-mRNA interaction networks in peripheral blood mononuclear cells.A multifaceted computational report on the variants effect on KIR2DL3 and IFNL3 candidate gene in HCV clearance.Pharmacogenetic Analysis of the Model-Based Pharmacokinetics of Five Anti-HIV Drugs: How Does This Influence the Effect of Aging?Protein quantitative trait locus study in obesity during weight-loss identifies a leptin regulator.A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.Molecular Correlates of In Vitro Responses to Dacomitinib and Afatinib in Bladder Cancer.A Genome-Wide Association Study Identifies a Candidate Gene Associated With Atazanavir Exposure Measured in Hair.Significant SNPs Related to Telomere Length and Hepatocellular Carcinoma Risk in Chronic Hepatitis B CarriersGenetic variants in two pathways influence serum urate levels and gout risk: a systematic pathway analysis.Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women.SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer familyConfirmation of GLRA3 as a susceptibility locus for albuminuria in Finnish patients with type 1 diabetes
P2860
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P2860
A practical guide for the functional annotation of genetic variations using SNPnexus.
description
2013 nî lūn-bûn
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2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
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@zh-my
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@zh-hant
name
A practical guide for the functional annotation of genetic variations using SNPnexus.
@en
A practical guide for the functional annotation of genetic variations using SNPnexus.
@nl
type
label
A practical guide for the functional annotation of genetic variations using SNPnexus.
@en
A practical guide for the functional annotation of genetic variations using SNPnexus.
@nl
prefLabel
A practical guide for the functional annotation of genetic variations using SNPnexus.
@en
A practical guide for the functional annotation of genetic variations using SNPnexus.
@nl
P2860
P356
P1476
A practical guide for the functional annotation of genetic variations using SNPnexus.
@en
P2093
Abu Z Dayem Ullah
P2860
P304
P356
10.1093/BIB/BBT004
P577
2013-02-08T00:00:00Z