(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

PMC publication ID

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)

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

genome-wide association study

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1 reference

based on heuristic

inferred from title

venous thromboembolism

1 reference

based on heuristic

inferred from title

ageing research

1 reference

based on heuristic

inferred from title

Jean-Charles Lambert

24

1 reference

Europe PubMed Central

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22 August 2017

James S. Pankow

26

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22 August 2017

André Uitterlinden

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object named as

André G Uitterlinden

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Eric Boerwinkle

33

object named as

Eric Boerwinkle

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object named as

Mark Lathrop

1 reference

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22 August 2017

Nathan Pankratz

7

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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

1

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22 August 2017

Martina Teichert

2

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22 August 2017

Guo Li

6

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Frank W Leebeek

8

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Rikje Ruiter

14

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Jacqueline C Witteman

27

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Edwin G Bovill

30

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Xiaoxiao Kong

31

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Russell P Tracy

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Daan W Loth

36

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Bruno H Ch Stricker

37

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Nicholas L Smith

40

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22 August 2017

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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22 August 2017

Genetic Epidemiology

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22 August 2017

37

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22 August 2017

5

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22 August 2017

512-521

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22 August 2017

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

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

23 August 2017

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

1 reference

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

23 August 2017

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.

1 reference

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23 August 2017

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

1 reference

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

23 August 2017

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

1 reference

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23 August 2017

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

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23 August 2017

Factor XIII: novel structural and functional aspects

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

1 reference

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23 August 2017

The Rotterdam Study: 2010 objectives and design update

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23 August 2017

Genotype imputation

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23 August 2017

Genetics of venous thrombosis

1 reference

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23 August 2017

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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23 August 2017

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

1 reference

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23 August 2017

Epidemiology and risk factors for venous thrombosis

1 reference

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

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

1 reference

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23 August 2017

Risk factors for venous thrombotic disease.

1 reference

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23 August 2017

Venous thrombosis: a multicausal disease

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23 August 2017

The future of genetic studies of complex human diseases

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23 August 2017

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

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23 August 2017

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

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Structure of transglutaminases.

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The Cardiovascular Health Study: design and rationale

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

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Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women

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Management of deep vein thrombosis and pulmonary embolism. A statement for healthcare professionals. Council on Thrombosis (in consultation with the Council on Cardiovascular Radiology), American Heart Association

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A population-based perspective of the hospital incidence and case-fatality rates of deep vein thrombosis and pulmonary embolism. The Worcester DVT Study.

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1 September 2018

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

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Major genetic susceptibility for venous thromboembolism in men: a study of Danish twins.

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1 September 2018

Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.

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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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Fibrinogen alpha and gamma genes and factor VLeiden in children with thromboembolism: results from 2 family-based association studies

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Risk factors for venous thromboembolism

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based on heuristic

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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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based on heuristic

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An asymptotic analysis of the logrank test

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene variants associated with deep vein thrombosis

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/GEPI.21731

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

ResearchGate publication ID

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