Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism.

about

Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism.

Item

http://www.wikidata.org/entity/Q47120217

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Whole exome sequencing in thro ...... rs for venous thromboembolism.

@en

Whole exome sequencing in thro ...... rs for venous thromboembolism.

@nl

type

Item

label

Whole exome sequencing in thro ...... rs for venous thromboembolism.

@en

Whole exome sequencing in thro ...... rs for venous thromboembolism.

@nl

prefLabel

Whole exome sequencing in thro ...... rs for venous thromboembolism.

@en

Whole exome sequencing in thro ...... rs for venous thromboembolism.

@nl

P1476

Whole exome sequencing in thro ...... ors for venous thromboembolism

@en

P2093

Astrid van Hylckama Vlieg

http://www.w3.org/2001/XMLSchema#string

Frits R Rosendaal

http://www.w3.org/2001/XMLSchema#string

Joost C M Meijers

http://www.w3.org/2001/XMLSchema#string

Pieter H Reitsma

http://www.w3.org/2001/XMLSchema#string

Saskia Middeldorp

http://www.w3.org/2001/XMLSchema#string

P2860

Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13)

Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis

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

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

Common variants at 30 loci contribute to polygenic dyslipidemia

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Biological, clinical and population relevance of 95 loci for blood lipids

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

Common variants in the trichohyalin gene are associated with straight hair in Europeans

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

P304

e0187699

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0187699

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Marisa L R Cunha

P577

2017-11-08T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29117201

http://www.w3.org/2001/XMLSchema#string

P921

thrombophilia

P932

5695603

http://www.w3.org/2001/XMLSchema#string