Accessibility issues or difficulties with this website?
Call 919-962-2073 or email hchsadministration@unc.edu.

Manuscripts and Publications

Filters: Keyword is Male and Author is Rotter, Jerome I  [Clear All Filters]
2017
Qi Q, Stilp AM, Sofer T, Moon J-Y, Hidalgo B, Szpiro AA, Wang T, C Y Ng M, Guo X, Chen Y-DIda et al..  2017.  Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).. Diabetes. 66(5):1419-1425.
Dunn EC, Sofer T, Gallo LC, Gogarten SM, Kerr KF, Chen C-Y, Stein MB, Ursano RJ, Guo X, Jia Y et al..  2017.  Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos.. Am J Med Genet B Neuropsychiatr Genet. 174(2):132-143.
Raffield LM, Louie T, Sofer T, Jain D, Ipp E, Taylor KD, Papanicolaou GJ, Avilés-Santa L, Lange LA, Laurie CC et al..  2017.  Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? Hum Mol Genet. 26(10):1966-1978.
Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu YMei, Auer PL et al..  2017.  Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.. PLoS Genet. 13(4):e1006760.
Noordam R, Sitlani CM, Avery CL, Stewart JD, Gogarten SM, Wiggins KL, Trompet S, Warren HR, Sun F, Evans DS et al..  2017.  A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.. J Med Genet. 54(5):313-323.
Liang J, Le TH, Edwards DRVelez, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR et al..  2017.  Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.. PLoS Genet. 13(5):e1006728.