Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
about
Human genetics and genomics a decade after the release of the draft sequence of the human genomeFine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritabilityPersonalized medicine: hope or hype?Triglyceride-Rich Lipoproteins and Remnants: Targets for Therapy?Hypertriglyceridemia and Cardiovascular Diseases: RevisitedApolipoprotein A-V gene therapy for disease prevention / treatment:a critical analysisRare-variant association analysis: study designs and statistical testsRole of lipotoxicity in endothelial dysfunctionGenetic susceptibility and neurotransmitters in Tourette syndromeStructural Basis for Regulation of Human Glucokinase by Glucokinase Regulatory ProteinMapping asthma-associated variants in admixed populationsApolipoprotein A-V dependent modulation of plasma triacylglycerol: a puzzlementResequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseA rare variant in MYH6 is associated with high risk of sick sinus syndromeA panel of diverse assays to interrogate the interaction between glucokinase and glucokinase regulatory protein, two vital proteins in human diseaseSequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyStrategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyGenome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmiasA genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysisRisk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.Human genetics as a model for target validation: finding new therapies for diabetes.Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseAssociation of the rs7395662 SNP in the MADD-FOLH1 and several environmental factors with serum lipid levels in the Mulao and Han populations.INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.Variant association tools for quality control and analysis of large-scale sequence and genotyping array dataApplying personal genetic data to injury risk assessment in athletes.Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung CancerEfficient Software for Multi-marker, Region-Based Analysis of GWAS Data.An NGS Workflow Blueprint for DNA Sequencing Data and Its Application in Individualized Molecular Oncology.Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels.Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's diseaseThe next generation of complex lung genetic studies.A powerful association test of multiple genetic variants using a random-effects model.Evaluation of common type 2 diabetes risk variants in a South Asian population of Sri Lankan descentInterrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipidsAmerindian-specific regions under positive selection harbour new lipid variants in Latinos.Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.Genome-wide association studies and genetic architecture of common human diseases
P2860
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P2860
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
description
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 2010
@ast
im August 2010 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2010/08/01)
@nl
наукова стаття, опублікована в серпні 2010
@uk
مقالة علمية (نشرت في أغسطس 2010)
@ar
name
Excess of rare variants in gen ...... study of hypertriglyceridemia
@ast
Excess of rare variants in gen ...... study of hypertriglyceridemia
@en
type
label
Excess of rare variants in gen ...... study of hypertriglyceridemia
@ast
Excess of rare variants in gen ...... study of hypertriglyceridemia
@en
prefLabel
Excess of rare variants in gen ...... study of hypertriglyceridemia
@ast
Excess of rare variants in gen ...... study of hypertriglyceridemia
@en
P2093
P2860
P50
P3181
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P1433
P1476
Excess of rare variants in gen ...... study of hypertriglyceridemia
@en
P2093
Adam D. McIntyre
Brooke A. Kennedy
Christopher J. O'Donnell
Christopher T. Johansen
Geesje M. Dallinga-Thie
Henian Cao
Maartje E. Visser
Matthew B. Lanktree
Matthew R. Ban
P2860
P2888
P304
P3181
P356
10.1038/NG.628
P407
P577
2010-08-01T00:00:00Z