(Q30419337)

English

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

scientific article published on 2 September 2012

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scholarly article

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Europe PubMed Central

16 August 2017

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Common variants at 6p21.1 are associated with large artery atherosclerotic stroke (English)

1 reference

Europe PubMed Central

16 August 2017

atherosclerosis

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based on heuristic

inferred from title

35

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Matthew Traylor

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Matthew Traylor

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Jim Jannes

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Martin D Lewis

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Giorgio B Boncoraglio

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Simon Andrea Koblar

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Simon A Koblar

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Graeme J. Hankey

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Cathie Sudlow

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Christopher Oldmeadow

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Christopher Levi

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Christopher Levi

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Jonathan Golledge

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Jonathan Golledge

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Wellcome Trust Case Control Consortium 2

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Wellcome Trust Case Control Consortium 2

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Andreas Gschwendtner

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Andreas Gschwendtner

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Rainer Malik

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Peter M. Rothwell

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Peter M Rothwell

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Thomas G Brott

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Thomas H Mosley

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Thomas H Mosley

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Joshua C Bis

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James F Meschia

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James F Meschia

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International Stroke Genetics Consortium

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International Stroke Genetics Consortium

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Karen L Furie

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Elizabeth Holliday

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Elizabeth G Holliday

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Jonathan W Sturm

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Jonathan W Sturm

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Simona Barlera

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Bradford B Worrall

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W T Longstreth

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Mark McEvoy

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author name string

Jane M Maguire

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Tiffany-Jane Evans

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Ross Baker

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Mark W Parsons

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Erik Biros

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Roseanne Peel

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Wayne Smith

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Robert D Brown

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Yu-Ching Cheng

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John W Cole

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Ioana Cotlarciuc

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William J Devan

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Sólveig Grétarsdóttir

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Michael A Nalls

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Pankaj Sharma

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Benjamin F J Verhaaren

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Hugh S Markus

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Rodney J Scott

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Australian Stroke Genetics Collaborative

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language of work or name

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publication date

2 September 2012

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Nature Genetics

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44

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1147-1151

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Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

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Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

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LocusZoom: regional visualization of genome-wide association scan results

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Common SNPs explain a large proportion of the heritability for human height

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Association between 9p21 genomic markers and heart disease: a meta-analysis

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Genotype imputation

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Genetic control of human brain transcript expression in Alzheimer disease

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Histone modifications at human enhancers reflect global cell-type-specific gene expression

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Worldwide stroke incidence and early case fatality reported in 56 population-based studies: a systematic review

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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

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Practical aspects of imputation-driven meta-analysis of genome-wide association studies

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Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data

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Potential confounding by intermediate phenotypes in studies of the genetics of ischaemic stroke

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Haploview: analysis and visualization of LD and haplotype maps

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Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke

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The apolipoprotein L gene cluster has emerged recently in evolution and is expressed in human vascular tissue

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The human apolipoprotein L gene cluster: identification, classification, and sites of distribution

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Plasma apolipoprotein L concentrations correlate with plasma triglycerides and cholesterol levels in normolipidemic, hyperlipidemic, and diabetic subjects

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Vascular endothelial genes that are responsive to tumor necrosis factor-alpha in vitro are expressed in atherosclerotic lesions, including inhibitor of apoptosis protein-1, stannin, and two novel genes

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Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

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Preventing stroke: saving lives around the world.

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21 January 2018

Risk factors for ischaemic and intracerebral haemorrhagic stroke in 22 countries (the INTERSTROKE study): a case-control study

1 reference

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21 January 2018

Evaluating the genetic component of ischemic stroke subtypes: a family history study.

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21 January 2018

Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families

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Heritability of leukoaraiosis in hypertensive sibships

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Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins.

1 reference

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Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.

1 reference

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Genetic and Environmental Contributions to Atherosclerosis Phenotypes in Men and Women

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Microarray analysis of primary endothelial cells challenged with different inflammatory and immune cytokines.

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Genetic and environmental contributions to atherosclerosis phenotypes in men and women: heritability of carotid intima-media thickness in the Framingham Heart Study

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Cumulative association of five genetic variants with prostate cancer

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based on heuristic

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Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22941190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/NG.2397

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

ResearchGate publication ID

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Springer Nature article ID

10.1038/ng.2397

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