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American Journal of Human Genetics|September 6, 2003
Genomewide linkage and linkage disequilibrium analyses identify COL6A1, on chromosome 21, as the locus for ossification of the posterior longitudinal ligament of the spineToshihiro Tanaka, Katsunori Ikari, Kozo Furushima, et al.
Stroke|March 8, 2008
A whole-genome scan for stroke or myocardial infarction in family blood pressure program familiesRichard Sherva, Michael B Miller, James S Pankow, et al.
Hypertension (Dallas, Tex. : 1979)|January 17, 2007
Genome-wide linkage mapping for valve calcification susceptibility loci in hypertensive sibships: the Hypertension Genetic Epidemiology Network StudyJonathan N Bella, Weihong Tang, Aldi Kraja, et al.
American Journal of Nephrology|January 21, 2009
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN studyBarry I Freedman, Jeffrey B Kopp, Cheryl A Winkler, et al.
Frontiers in Endocrinology|December 3, 2021
Corrigendum: Association of Complement-Related Proteins in Subjects With and Without Second Trimester Gestational DiabetesManjunath Ramanjaneya, Alexandra E Butler, Meis Alkasem, et al.
American Journal of Hypertension|August 2, 2005
A summary of the effects of antihypertensive medications on measured blood pressureJun Wu, Aldi T Kraja, Al Oberman, et al.
Med (New York, N.Y.)|June 16, 2022
Following Roux-en-Y gastric bypass surgery, serum ceramides demarcate patients that will fail to achieve normoglycemia and diabetes remissionAnnelise M Poss, Benjamin Krick, J Alan Maschek, et al.
Diabetes|December 29, 2006
Genotype-by-sex interaction on fasting insulin concentration: the HyperGEN studyKari E North, Nora Franceschini, Ingrid B Borecki, et al.
American Journal of Hypertension|February 1, 2003
A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure ProgramMichael A Province, Sharon L R Kardia, Koustubh Ranade, et al.
European Journal of Human Genetics : EJHG|June 16, 2011
Characterization of autosomal copy-number variation in African Americans: the HyperGEN StudyNathan E Wineinger, Nicholas M Pajewski, Richard E Kennedy, et al.
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