Center-Authored Papers

Filters: Author is Durda, Peter  [Clear All Filters]
Journal Article
Ilkhanoff L, Arking DE, Lemaitre RN, Alonso A, Chen LY, Durda P, Hesselson SE, Kerr KF, Magnani JW, Marcus GM et al..  2014.  A Common SCN5A Variant is Associated with PR Interval and Atrial Fibrillation among African Americans.. Journal of cardiovascular electrophysiology. Abstract
Ben-Avraham D, Govindaraju DR, Budagov T, Fradin D, Durda P, Liu B, Ott S, Gutman D, Sharvit L, Kaplan R et al..  2017.  The GH receptor exon 3 deletion is a marker of male-specific exceptional longevity associated with increased GH sensitivity and taller stature.. Science advances. 3(6):e1602025. Abstract
Ellis J, Lange EM, Li J, Dupuis J, Baumert J, Walston JD, Keating BJ, Durda P, Fox ER, Palmer CD et al..  2014.  Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans.. Human genetics. Abstract
Kocarnik JM, Pendergrass SA, Carty CL, Pankow JS, Schumacher FR, Cheng I, Durda P, Ambite JL, Deelman E, Cook NR et al..  2014.  Multi-Ancestral Analysis of Inflammation-Related Genetic Variants and C-Reactive Protein in the Population Architecture using Genomics and Epidemiology (PAGE) Study.. Circulation. Cardiovascular genetics. 7(2):178-88. Abstract
Durda P, Sabourin J, Lange EM, Nalls MA, Mychaleckyj JC, Swords Jenny N, Li J, Walston J, Harris TB, Psaty BM et al..  2015.  Plasma Levels of Soluble IL-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan.. Arteriosclerosis, thrombosis, and vascular biology. Abstract
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang Z-Z, Bizon C, Lange EM, Smith JD, Turner EH et al..  2014.  Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.. American journal of human genetics. 94(2):233-45. Abstract