相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Epidemiology of lower extremity peripheral artery disease in veterans
James Willey et al.
JOURNAL OF VASCULAR SURGERY (2018)
Rivaroxaban with or without aspirin in patients with stable peripheral or carotid artery disease: an international, randomised, double-blind, placebo-controlled trial
Sonia S. Anand et al.
LANCET (2018)
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Rainer Malik et al.
NATURE GENETICS (2018)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila et al.
SCIENCE (2018)
Race and Socioeconomic Status Independently Affect Risk of Major Amputation in Peripheral Artery Disease
Shipra Arya et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2018)
Genomic atlas of the human plasma proteome
Benjamin B. Sun et al.
NATURE (2018)
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft et al.
NATURE (2018)
Genetics of blood lipids among ∼300,000 multi-ethnic participants of the Million Veteran Program
Derek Klarin et al.
NATURE GENETICS (2018)
Global, regional, and national age-sex specific mortality for 264 causes of death, 1980-2016: a systematic analysis for the Global Burden of Disease Study 2016
Mohsen Naghavi et al.
LANCET (2017)
Efficiency and safety of varying the frequency of whole blood donation (INTERVAL): a randomised trial of 45 000 donors
Emanuele Di Angelantonio et al.
LANCET (2017)
Genetic effects on gene expression across human tissues
Francois Aguet et al.
NATURE (2017)
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
F. E. Dewey et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor
Derek Klarin et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2017)
PhenoScanner: a database of human genotype-phenotype associations
James R. Staley et al.
BIOINFORMATICS (2016)
Million Veteran Program: A mega-biobank to study genetic influences on health and disease
John Michael Gaziano et al.
JOURNAL OF CLINICAL EPIDEMIOLOGY (2016)
Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels
Connor A. Emdin et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent
Craig L. Hyde et al.
NATURE GENETICS (2016)
Fast and accurate long-range phasing in a UK Biobank cohort
Po-Ru Loh et al.
NATURE GENETICS (2016)
Integrative approaches for large-scale transcriptome-wide association studies
Alexander Gusev et al.
NATURE GENETICS (2016)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Nathan O. Stitziel et al.
NEW ENGLAND JOURNAL OF MEDICINE (2016)
Society for Vascular Surgery practice guidelines for atherosclerotic occlusive disease of the lower extremities: Management of asymptomatic disease and claudication
Michael S. Conte et al.
JOURNAL OF VASCULAR SURGERY (2015)
A global reference for human genetic variation
David M. Altshuler et al.
NATURE (2015)
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Majid Nikpay et al.
NATURE GENETICS (2015)
An atlas of genetic correlations across human diseases and traits
Brendan Bulik-Sullivan et al.
NATURE GENETICS (2015)
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population
Mitsuru Matsukura et al.
PLOS ONE (2015)
R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment
Robert J. Carroll et al.
BIOINFORMATICS (2014)
Quality control and conduct of genome-wide association meta-analyses
Thomas W. Winkler et al.
NATURE PROTOCOLS (2014)
Billing code algorithms to identify cases of peripheral artery disease from administrative data
Jin Fan et al.
JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION (2013)
Comparison of global estimates of prevalence and risk factors for peripheral artery disease in 2000 and 2010: a systematic review and analysis
F. Gerald R. Fowkes et al.
LANCET (2013)
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
Joshua C. Denny et al.
NATURE BIOTECHNOLOGY (2013)
Polygenic Modeling with Bayesian Sparse Linear Mixed Models
Xiang Zhou et al.
PLOS GENETICS (2013)
Current and Former Smoking and Risk for Venous Thromboembolism: A Systematic Review and Meta-Analysis
Yun-Jiu Cheng et al.
PLOS MEDICINE (2013)
A robust clustering algorithm for identifying problematic samples in genome-wide association studies
Celine Bellenguez et al.
BIOINFORMATICS (2012)
Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies
Joanne M. Murabito et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2012)
What makes UK Biobank special?
Rory Collins
LANCET (2012)
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
Bryan Howie et al.
NATURE GENETICS (2012)
Genetic Influences on Peripheral Arterial Disease in a Twin Population
Carl Magnus Wahlgren et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2011)
Robust relationship inference in genome-wide association studies
Ani Manichaikul et al.
BIOINFORMATICS (2010)
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations
Joshua C. Denny et al.
BIOINFORMATICS (2010)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
Risk Factors for Venous Thromboembolism Results From the Copenhagen City Heart Study
Anders G. Holst et al.
CIRCULATION (2010)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich et al.
NATURE (2010)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight et al.
NATURE GENETICS (2010)
Exome Sequencing, ANGPTL3 Mutations, and Familial Combined Hypolipidemia
Kiran Musunuru et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Fast model-based estimation of ancestry in unrelated individuals
David H. Alexander et al.
GENOME RESEARCH (2009)
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Thorgeir E. Thorgeirsson et al.
NATURE (2008)
COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke
Igor Sibon et al.
ANNALS OF NEUROLOGY (2007)
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
Paul I. W. de Bakker et al.
NATURE GENETICS (2006)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
M Swanberg et al.
NATURE GENETICS (2005)