Center-Authored Papers

Filters: Author is Bielinski, Suzette J  [Clear All Filters]
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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
Zubair N, Graff M, Ambite JL, Bush WS, Kichaev G, Lu Y, Manichaikul A, Sheu WH-H, Absher D, Assimes TL et al..  2016.  Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.. Human molecular genetics. 25(24):5500-5512. Abstract
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Reiner AP, Gross MD, Carlson CS, Bielinski SJ, Lange LA, Fornage M, Jenny NS, Walston J, Tracy RP, Williams DO et al..  2009.  Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascula. Circulation. Cardiovascular genetics. 2(3):244-54. 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
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Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA et al..  2014.  Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.. PLoS genetics. 10(8):e1004517. Abstract
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Kho AN, Hayes GM, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei W-Q et al..  2012.  Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.. Journal of the American Medical Informatics Association : JAMIA. 19(22):212-218. Abstract
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Franceschini N, Carty CL, Lu Y, Tao R, Sung YJ, Manichaikul A, Haessler J, Fornage M, Schwander K, Zubair N et al..  2016.  Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.. PloS one. 11(10):e0164132. Abstract
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Day FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, Stolk L, Finucane HK, Sulem P, Bulik-Sullivan B et al..  2015.  Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.. Nature genetics. 47(11):1294-1303. Abstract
Day FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, Stolk L, Finucane HK, Sulem P, Bulik-Sullivan B et al..  2015.  Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair--Editorial Comment. Obstetrical & Gynecological Survey. 70(12):758-762.
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Bielinski SJ, Reiner AP, Nickerson D, Carlson CS, Bailey KR, Thyagarajan B, Lange LA, Boerwinkle EA, Jacobs DR, Gross MD.  2011.  Polymorphisms in the ICAM1 gene predict circulating soluble intercellular adhesion molecule-1(sICAM-1).. Atherosclerosis. 216(2):390-4. Abstract
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Avery CL, Wassel CL, Richard MA, Highland HM, Bien S, Zubair N, Soliman EZ, Fornage M, Bielinski SJ, Tao R et al..  2016.  Fine-mapping of QT regions in global populations refines previously identified QT loci and identifies signals unique to african and hispanic descent populations.. Heart rhythm. Abstract