LocusZoom: regional visualization of genome-wide association scan results - Test2 - elhamkhani - TriplyDB

LocusZoom: regional visualization of genome-wide association scan results

LocusZoom: regional visualization of genome-wide association scan results

http://www.wikidata.org/entity/Q29614868

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Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures Tandem RNA chimeras contribute to transcriptome diversity in human population and are associated with intronic genetic variants DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease Genome-wide association scan of dental caries in the permanent dentition.Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease Genetic studies of body mass index yield new insights for obesity biology Candidate gene-environment interaction research: reflections and recommendations.A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy PCSK6 is associated with handedness in individuals with dyslexia Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia Tribbles-1: a novel regulator of hepatic lipid metabolism in humans Statistical analysis for genome-wide association study SLC2A9 Genotype Is Associated with SLC2A9 Gene Expression and Urinary Uric Acid Concentration Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features Sparse whole-genome sequencing identifies two loci for major depressive disorder Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms Pedigree based DNA sequencing pipeline for germline genomes of cancer families APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema.Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types Genome-Wide Meta-Analysis of Sciatica in Finnish Population Association between Stress Response Genes and Features of Diurnal Cortisol Curves in the Multi-Ethnic Study of Atherosclerosis: A New Multi-Phenotype Approach for Gene-Based Association Tests Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma Genome-wide association study of blood lead shows multiple associations near ALAD Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin A meta-analysis of gene expression signatures of blood pressure and hypertension Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon Genetic regulation of expression of leukotriene A4 hydrolase

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LocusZoom: regional visualization of genome-wide association scan results

http://www.wikidata.org/entity/Q29614868

description

2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

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2010年論文

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2010年论文

@wuu

name

LocusZoom: regional visualization of genome-wide association scan results

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LocusZoom: regional visualization of genome-wide association scan results

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type

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LocusZoom: regional visualization of genome-wide association scan results

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LocusZoom: regional visualization of genome-wide association scan results

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LocusZoom: regional visualization of genome-wide association scan results

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LocusZoom: regional visualization of genome-wide association scan results

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LocusZoom: regional visualization of genome-wide association scan results

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P2093

Michael Boehnke

http://www.w3.org/2001/XMLSchema#string

Peter S Chines

http://www.w3.org/2001/XMLSchema#string

Randall J Pruim

http://www.w3.org/2001/XMLSchema#string

Ryan P Welch

http://www.w3.org/2001/XMLSchema#string

Tanya M Teslovich

http://www.w3.org/2001/XMLSchema#string

Terry P Gliedt

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P2860

Finding the missing heritability of complex diseases

Common variants at 30 loci contribute to polygenic dyslipidemia

Common variants near MC4R are associated with fat mass, weight and risk of obesity

The human genome browser at UCSC

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

Visualizing SNP statistics in the context of linkage disequilibrium using LD-Plus.

VALID: visualization of association study results and linkage disequilibrium.

CandiSNPer: a web tool for the identification of candidate SNPs for causal variants.

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2336-2337

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scholarly article

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75186

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10.1093/BIOINFORMATICS/BTQ419

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18

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26

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Gonçalo Abecasis

Cristen J. Willer

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2010-07-15T00:00:00Z

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45199778

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20634204

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genome-wide association study

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2935401

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