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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.
American Journal of Hypertension|July 4, 2009
Novel genetic variants in the alpha-adducin and guanine nucleotide binding protein beta-polypeptide 3 genes and salt sensitivity of blood pressureTanika N Kelly, Treva K Rice, Dongfeng Gu, et al.
Inflammatory Bowel Diseases|February 16, 2010
NOD2 status and human ileal gene expressionChristina M Hamm, Melissa A Reimers, Casey K McCullough, et al.
Genetic Epidemiology|February 3, 2007
Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure ProgramTiffany A Greenwood, Ondrej Libiger, Sharon Kardia, et al.
BMC Genomics|September 14, 2017
Tissue-specific DNA methylation is conserved across human, mouse, and rat, and driven by primary sequence conservationJia Zhou, Renee L Sears, Xiaoyun Xing, et al.
Journal of the American Heart Association|May 1, 2014
Association of comorbidity burden with abnormal cardiac mechanics: findings from the HyperGEN studySenthil Selvaraj, Frank G Aguilar, Eva E Martinez, et al.
Journal of Hypertension and Management|March 6, 2018
Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studiesAnh N Do, Wei Zhao, Vinodh Srinivasasainagendra, et al.
Critical Care Explorations|September 27, 2023
Telemedicine Critical Care-Mediated Mortality Reductions in Lower-Performing Patient Diagnosis Groups: A Prospective, Before and After StudyWalter A Boyle, Christopher M Palmer, Lisa Konzen, et al.
Journal of Hypertension|February 25, 2017
Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestryPriyanka Nandakumar, Dongwon Lee, Melissa A Richard, et al.
Frontiers in Genetics|March 8, 2021
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify <i>MYRIP</i>, <i>TRAPPC11</i>, and <i>SLC27A6</i> of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry PopulationMarguerite R Irvin, Praful Aggarwal, Steven A Claas, et al.
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