Center-Authored Papers

Filters: Author is Carrell, David S  [Clear All Filters]
2013
Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E et al..  2013.  Genetic variation associated with circulating monocyte count in the eMERGE Network.. Human molecular genetics. 22(10):2119-2127. Abstract
2016
Farjah F, Halgrim S, Buist DSM, Gould MK, Zeliadt SB, Loggers ET, Carrell DS.  2016.  An Automated Method for Identifying Individuals with a Lung Nodule Can Be Feasibly Implemented Across Health Systems.. EGEMS (Washington, DC). 4(1):1254. Abstract
De R, Verma SS, Holzinger E, Hall M, Burt A, Carrell DS, Crosslin DR, Jarvik GP, Kuivaniemi H, Kullo IJ et al..  2016.  Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.. Human genetics. Abstract
Schmidt AF, Swerdlow DI, Holmes MV, Patel RS, Fairhurst-Hunter Z, Lyall DM, Hartwig FP, Horta BL, Hyppönen E, Power C et al..  2016.  PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.. The lancet. Diabetes & endocrinology. Abstract
2017
Holzinger ER, Verma SS, Moore CB, Hall M, De R, Gilbert-Diamond D, Lanktree MB, Pankratz N, Amuzu A, Burt A et al..  2017.  Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.. BioData mining. 10:25. Abstract