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A Whole-Genome Scan for Stroke or Myocardial Infarction in Family Blood Pressure Program Families
Author(s) -
Richard Sherva,
Michael B. Miller,
James S. Pankow,
Steven C. Hunt,
Eric Boerwinkle,
Thomas H. Mosley,
Alan B. Weder,
J. David Curb,
Amy Luke,
Alanna C. Morrison,
Myriam Fornage,
Donna K. Arnett
Publication year - 2008
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.107.490433
Subject(s) - medicine , stroke (engine) , blood pressure , myocardial infarction , cardiology , ischemic stroke , genome , genetics , gene , ischemia , mechanical engineering , biology , engineering
Atherothrombotic diseases, including stroke and myocardial infarction, share a common pathogenesis. Chromosomal regions have been linked to atherothrombotic diseases in family studies, and association studies have identified candidate gene polymorphisms that affect the risk of stroke and/or myocardial infarction. Using data from the Family Blood Pressure Program, we tested for chromosomal regions linked to the composite phenotype of stroke or myocardial infarction in a large set of hypertensive families.

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