Center-Authored Papers

Filters: Author is Rotter, Jerome I  [Clear All Filters]
2011
O'Donnell CJ, Kavousi M, Smith AV, Kardia SLR, Feitosa MF, Hwang S-J, Sun YV, Province MA, Aspelund T, Dehghan A et al..  2011.  Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction.. Circulation. 124(25):2855-2864. Abstract
Avery CL, He Q, North KE, Ambite JL, Boerwinkle E, Fornage M, Hindorff LA, Kooperberg C, Meigs JB, Pankow JS et al..  2011.  A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains.. PLoS genetics. 7(10):e1002322. Abstract
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang S-J et al..  2011.  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
2012
Elbers CC, Guo Y, Tragante V, van Iperen EPA, Lanktree MB, Castillo BA, Chen F, Yanek LR, Wojczynski MK, Li YR et al..  2012.  Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.. PloS one. 7(12):e50198. Abstract
Estrada K, Styrkarsdottir U, Evangelou E, Hsu Y-H, Duncan EL, Ntzani EE, Oei L, Albagha OME, Amin N, Kemp JP et al..  2012.  Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.. Nature genetics. 44(5):491-501. Abstract
Smith GJ, Avery CL, Evans DS, Nalls MA, Meng YA, Smith EN, Palmer C, Tanaka T, Mehra R, Butler AM et al..  2012.  Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.. Circulation. Cardiovascular genetics. 5(6):647-655. Abstract
Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR et al..  2012.  Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.. American journal of human genetics. 90(3):410-25. Abstract
Asselbergs FW, Guo Y, van Iperen EPA, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J et al..  2012.  Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci.. American journal of human genetics. 91(5):823-38. Abstract
2013
Sim X, Jensen RA, Ikram KM, Cotch MF, Li X, Macgregor S, Xie J, Smith AV, Boerwinkle E, Mitchell P et al..  2013.  Genetic loci for retinal arteriolar microcirculation.. PloS one. 8(6):e65804. Abstract
Jensen RA, Sim X, Li X, Cotch MF, Ikram KM, Holliday EG, Eiriksdottir G, Harris TB, Jonasson F, Klein BEK et al..  2013.  Genome-Wide Association Study of Retinopathy in Individuals without Diabetes.. PloS one. 8(2):e54232. Abstract
Holliday EG, Smith AV, Cornes BK, Buitendijk GHS, Jensen RA, Sim X, Aspelund T, Aung T, Baird PN, Boerwinkle E et al..  2013.  Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.. PloS one. 8(1):e53830. Abstract
Liu C-T, Monda KL, Taylor KC, Lange L, Demerath EW, Palmas W, Wojczynski MK, Ellis JC, Vitolins MZ, Liu S et al..  2013.  Genome-wide association of body fat distribution in African ancestry populations suggests new loci.. PLoS genetics. 9(8):e1003681. Abstract
Wu Y, Waite LL, Jackson AU, Sheu WH-H, Buyske S, Absher D, Arnett DK, Boerwinkle E, Bonnycastle LL, Carty CL et al..  2013.  Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.. PLoS genetics. 9(3):e1003379. Abstract
Lin H, Sinner MF, Brody JA, Arking DE, Lunetta KL, Rienstra M, Lubitz SA, Magnani JW, Sotoodehnia N, McKnight B et al..  2013.  Targeted sequencing in candidate genes for atrial fibrillation: The Cohorts for Heart and Aging Research in Genomic Epidemiology Targeted Sequencing Study.. Heart rhythm : the official journal of the Heart Rhythm Society. Abstract
Gordon AS, Tabor HK, Johnson AD, Snively BM, Assimes TL, Auer PL, Ioannidis JPA, Peters U, Robinson JG, Sucheston LE et al..  2013.  Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.. Human molecular genetics. Abstract
Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD, Teumer A, Reiner AP, Folkersen L, Basu S et al..  2013.  Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.. Circulation. 128(12):1310-24. Abstract
Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A et al..  2013.  Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.. American journal of human genetics. 93(3):545-54. Abstract
2014
Keller MF, Reiner AP, Okada Y, van Rooij FJA, Johnson AD, Chen M-H, Smith AV, Morris AP, Tanaka T, Ferrucci L et al..  2014.  Trans-ethnic Meta-analysis of White Blood Cell Phenotypes.. Human molecular genetics. 23(25):6944-60. Abstract
Du M, Auer PL, Jiao S, Haessler J, Altshuler D, Boerwinkle E, Carlson CS, Carty CL, Chen Y-DI, Curtis K et al..  2014.  Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.. Human molecular genetics. 23(24):6607-15. Abstract
Holmes MV, Dale CE, Zuccolo L, Silverwood RJ, Guo Y, Ye Z, Prieto-Merino D, Dehghan A, Trompet S, Wong A et al..  2014.  Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.. BMJ (Clinical research ed.). 349:g4164. Abstract
Suchy-Dicey A, Heckbert SR, Smith NL, McKnight B, Rotter JI, Chen YI, Psaty BM, Enquobahrie DA.  2014.  Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes.. International journal of molecular epidemiology and genetics. 5(1):22-30. Abstract
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
Ibrahim-Verbaas CA, Fornage M, Bis JC, Choi SH, Psaty BM, Meigs JB, Rao M, Nalls M, Fontes JD, O'Donnell CJ et al..  2014.  Predicting Stroke Through Genetic Risk Functions: The CHARGE Risk Score Project.. Stroke; a journal of cerebral circulation. 45(2):403-12. Abstract
Peloso GM, Auer PL, Bis JC, Voorman A, Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M et al..  2014.  Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.. American journal of human genetics. 94(2):223-32. 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