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Michael A. Province

Researcher at Washington University in St. Louis

Publications -  409
Citations -  40871

Michael A. Province is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 79, co-authored 396 publications receiving 37334 citations. Previous affiliations of Michael A. Province include Jewish Hospital & Harvard University.

Papers
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Fibrinogen, Plasminogen Activator Inhibitor-1, and Carotid Intima-Media Wall Thickness in the NHLBI Family Heart Study

TL;DR: The data suggest 1) elevated fibrinogen and PAI-1 do not explain clustering of CHD in families and 2) fibr inogen andPAi-1 may partly mediate the effects of other risk factors on carotid atherosclerosis, though the data are also consistent with them playing no causal role.
Book

Genetic dissection of complex traits

TL;DR: The present work presents a meta-analysis of Model-free methods for Linkage Analysis and classification Methods for Confronting Heterogeneity for Complex Inheritance, which aims to clarify the genetic architecture of a Multivariate Phenotype.
Journal ArticleDOI

A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

Yun Ju Sung, +317 more
TL;DR: A genome-wide gene-smoking interaction study of mean arterial pressure (MAP) and pulse pressure (PP) in 129 913 individuals in stage 1 and follow-up analysis in 480 178 additional individuals in stages 2 identified 136 loci significantly associated with MAP and/or PP and identified nine new signals near known loci.
Journal ArticleDOI

Meta-analysis of genome-wide scans for blood pressure in African American and Nigerian samples. The National Heart, Lung, and Blood Institute GeneLink Project.

TL;DR: Follow-up studies involving positional cloning efforts of the combined families showing linkage evidence in these regions (particularly 2p and 7p) may be warranted to verify these findings and identify the genes and causative variants.