Center-Authored Papers

Filters: Author is Kullo, Iftikhar J  [Clear All Filters]
2011
Zuvich RL, Armstrong LL, Bielinski SJ, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL et al..  2011.  Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.. Genetic epidemiology. 35(8):887-98. Abstract
Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G et al..  2011.  Quality control procedures for genome-wide association studies.. Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.]. Chapter 1:Unit1.19. Abstract
2012
Crosslin DR, McDavid A, Weston N, Nelson SC, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF et al..  2012.  Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.. Human genetics. 131(4):639-652. Abstract
Rasmussen-Torvik LJ, Pacheco JA, Wilke RA, Thompson WK, Ritchie MD, Kho AN, Muthalagu A, Hayes GM, Armstrong LL, Scheftner DA et al..  2012.  High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.. Clinical and translational science. 5(5):394-9. Abstract
2013
Ritchie MD, Denny JC, Zuvich RL, Crawford DC, Schildcrout JS, Bastarache L, Ramirez AH, Mosley JD, Pulley JM, Basford MA et al..  2013.  Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.. Circulation. 127(13):1377-85. Abstract
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
2014
Jarvik GP, Amendola LM, Berg JS, Brothers K, Clayton EW, Chung W, Evans BJ, Evans JP, Fullerton SM, Gallego CJ et al..  2014.  Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between.. American journal of human genetics. Abstract
Stitziel NO, Won H-H, Morrison AC, Peloso GM, Do R, Lange LA, Fontanillas P, Gupta N, Duga S, Goel A et al..  2014.  Inactivating mutations in NPC1L1 and protection from coronary heart disease.. The New England journal of medicine. 371(22):2072-82. Abstract
2016
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
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