(Q33772986)

29 July 2017

Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time (English)

1 reference

partial thromboplastin time

29 July 2017

1 reference

12

1 reference

29 July 2017

Lorna M Houlihan

1

0 references

Alan J. Gow

Alan J Gow

6

0 references

David J. Porteous

David J Porteous

9

0 references

Ian Deary

Ian J Deary

13

0 references

Dave Liewald

8

David C Liewald

1 reference

29 July 2017

10

John M Starr

1 reference

29 July 2017

4

Sarah E Harris

1 reference

29 July 2017

11

Gordon D Lowe

1 reference

29 July 2017

Gail Davies

2

1 reference

29 July 2017

Albert Tenesa

3

1 reference

29 July 2017

Michelle Luciano

5

1 reference

29 July 2017

Kevin A McGhee

7

1 reference

29 July 2017

language of work or name

English

0 references

publication date

18 March 2010

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

86

1 reference

29 July 2017

4

1 reference

29 July 2017

626-631

1 reference

Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

STRING 8--a global view on proteins and their functional interactions in 630 organisms

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

WGAViewer: software for genomic annotation of whole genome association studies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Deletion of murine kininogen gene 1 (mKng1) causes loss of plasma kininogen and delays thrombosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Histidine-rich glycoprotein: A novel adaptor protein in plasma that modulates the immune, vascular and coagulation systems

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Human non-synonymous SNPs: server and survey

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Genetic determinants of hemostasis phenotypes in Spanish families.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Gender-specific association between the kininogen 1 gene variants and essential hypertension in Chinese Han population

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Heterozygous factor XI deficiency associated with three novel mutations

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850435

Mortality from coronary heart disease and acute myocardial infarction--United States, 1998

30 October 2018

1 reference

12 December 2020

Prediction of deep vein thrombosis after elective hip replacement surgery by preoperative clinical and haemostatic variables: the ECAT DVT Study. European Concerted Action on Thrombosis

1 reference

12 December 2020

Activated protein C resistance and the FV:R506Q mutation in a random population sample--associations with cardiovascular risk factors and coagulation variables

1 reference

12 December 2020

Heritability of hemostasis phenotypes and their correlation with type 2 diabetes status in Mexican Americans

1 reference

12 December 2020

Genetic variants associated with deep vein thrombosis: the F11 locus

1 reference

12 December 2020

10.1016/J.AJHG.2010.02.016

Identifiers

DOI

1 reference

29 July 2017

1 reference

29 July 2017

1 reference