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François Cambien

Researcher at Institute of Chartered Accountants of Nigeria

Publications -  6
Citations -  610

François Cambien is an academic researcher from Institute of Chartered Accountants of Nigeria. The author has contributed to research in topics: Population & Linkage disequilibrium. The author has an hindex of 5, co-authored 6 publications receiving 553 citations. Previous affiliations of François Cambien include French Institute of Health and Medical Research & University of Virginia.

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Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism

Marine Germain, +61 more
TL;DR: A meta-analysis of genome-wide association studies to identify additional VTE susceptibility genes uncovered unexpected actors of VTE etiology and pave the way for novel mechanistic concepts of V TE pathophysiology.
Journal Article

Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.

TL;DR: Ten new polymorphisms were identified, among which 8 were genotyped in 95 healthy nuclear families, in addition to the I/D polymorphism, which suggests the existence of two quantitative trait loci acting additively on ACE levels.
Journal Article

Testing for association between disease and linked marker loci: a log-linear-model analysis.

TL;DR: The log-linear model offers a stepwise method of identification of the parameters causing the difference between populations, and can be extended to any number of loci, alleles, or populations.
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Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2

Jie Huang, +103 more
TL;DR: A meta-analysis of genome-wide association studies to identify novel correlates of circulating levels of tPA found no associations of the 3 lead SNPs with coronary artery disease or stroke, and implicate a novel role for STXBP5 and STX2 in regulating tPA release.
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Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities.

TL;DR: The association between aldosterone synthase (CYP11B2) gene polymorphism and white matter hyperintensities seen on cerebral MRI was studied in a population-based sample of 829 individuals aged 63 to 75 years and the T allele was associated with the risk of severe white matterhyperintENSities.