(Q37708719)

English

A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

scientific article published on 05 May 2013

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scholarly article

1 reference

Europe PubMed Central

22 August 2017

A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium (English)

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Europe PubMed Central

22 August 2017

genome-wide association study

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based on heuristic

inferred from title

venous thromboembolism

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based on heuristic

inferred from title

ageing research

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based on heuristic

inferred from title

Jean-Charles Lambert

24

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22 August 2017

James S. Pankow

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André Uitterlinden

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André G Uitterlinden

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Eric Boerwinkle

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Eric Boerwinkle

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Mark Lathrop

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Nathan Pankratz

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Nathan Pankratz

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David-Alexandre Trégouët

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David-Alexandre Trégouët

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Guillaume Paré

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Guillaume Paré

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Mary Cushman

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Christophe Tzourio

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Christophe Tzourio

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Philippe Amouyel

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Philippe Amouyel

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Jerome I Rotter

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Jerome I Rotter

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Albert Hofman

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Bruce M Psaty

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Susan R Heckbert

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Susan R Heckbert

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Joshua C Bis

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Paul M Ridker

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Daniel I Chasman

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Daniel I Chasman

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Thomas Lumley

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Lynda Rose

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Mariza de Andrade

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Mariza de Andrade

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Kenneth M Rice

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Nicole L. Glazer

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Nicole L Glazer

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Aaron R. Folsom

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Aaron R Folsom

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John A Heit

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Pierre-Emmanuel Morange

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Pierre-Emmanuel Morange

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Sebastian M Armasu

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Sebastian M Armasu

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Saonli Basu

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author name string

Weihong Tang

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Martina Teichert

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Guo Li

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Frank W Leebeek

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Rikje Ruiter

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Jacqueline C Witteman

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Edwin G Bovill

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Xiaoxiao Kong

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Russell P Tracy

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Daan W Loth

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Bruno H Ch Stricker

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Nicholas L Smith

40

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language of work or name

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publication date

5 May 2013

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Europe PubMed Central

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Genetic Epidemiology

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22 August 2017

37

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22 August 2017

512-521

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5

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22 August 2017

describes a project that uses

genome-wide association study

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An integrated map of genetic variation from 1,092 human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3990406

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A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.

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The endothelial protein C receptor (PROCR) Ser219Gly variant and risk of common thrombotic disorders: a HuGE review and meta-analysis of evidence from observational studies.

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Genetics of venous thrombosis: insights from a new genome wide association study

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Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism

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

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METAL: fast and efficient meta-analysis of genomewide association scans

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Genetics of venous thrombosis

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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

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23 August 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

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Imputation-based analysis of association studies: candidate regions and quantitative traits

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23 August 2017

Epidemiology and risk factors for venous thrombosis

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23 August 2017

GenABEL: an R library for genome-wide association analysis

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23 August 2017

Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia

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23 August 2017

Risk factors for venous thrombotic disease.

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Venous thrombosis: a multicausal disease

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The future of genetic studies of complex human diseases

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Amino acid sequence of the b subunit of human factor XIII, a protein composed of ten repetitive segments

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Association of genetic variations with nonfatal venous thrombosis in postmenopausal women.

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A novel polymorphism in the factor XIII B-subunit (His95Arg): relationship to subunit dissociation and venous thrombosis.

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Fibrinogen gamma gene 3'-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population

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Risk factors for venous thromboembolism

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Familial segregation of venous thromboembolism

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Recruitment of adults 65 years and older as participants in the cardiovascular health study

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Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen gamma' levels

1 reference

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The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23650146

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Gene variants associated with deep vein thrombosis

1 reference

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based on heuristic

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Identifiers

10.1002/GEPI.21731

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Europe PubMed Central

22 August 2017

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Europe PubMed Central

22 August 2017

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Europe PubMed Central

22 August 2017

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