Center-Authored Papers

Filters: Author is Boerwinkle, Eric  [Clear All Filters]
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
W
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
Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen M-H, Auer PL, Floyd JS, Huang J et al..  2016.  Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.. American journal of human genetics. 99(2):481-8. 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
T
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
Liu C-T, Raghavan S, Maruthur N, Kabagambe EK, Hong J, Ng MCY, Hivert M-F, Lu Y, An P, Bentley AR et al..  2016.  Trans-ethnic Meta-Analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.. American journal of human genetics. 99(1):56-75. 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
S
Lin H, Wang M, Brody JA, Bis JC, Dupuis J, Lumley T, McKnight B, Rice KM, Sitlani CM, Reid JG et al..  2014.  Strategies to Design and Analyze Targeted Sequencing Data: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.. Circulation. Cardiovascular genetics. 7(3):335-43. Abstract
Li M, Li Y, Weeks O, Mijatovic V, Teumer A, Huffman JE, Tromp G, Fuchsberger C, Gorski M, Lyytikäinen L-P et al..  2016.  SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.. Journal of the American Society of Nephrology : JASN. Abstract
Liang J, Le TH, Edwards DVR, 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 genetics. 13(5):e1006728. Abstract
Liu C-T, Young KL, Brody JA, Olden M, Wojczynski MK, Heard-Costa N, Li G, Morrison AC, Muzny D, Gibbs RA et al..  2014.  Sequence Variation in TMEM18 in Association With Body Mass Index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.. Circulation. Cardiovascular genetics. 7(3):344-9. Abstract
R
Yu B, Pulit SL, Hwang S-J, Brody JA, Amin N, Auer PL, Bis JC, Boerwinkle E, Burke GL, Chakravarti A et al..  2015.  Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.. Circulation. Cardiovascular genetics. Abstract
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC et al..  2017.  Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.. Nature genetics. Abstract
Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C et al..  2015.  Rare coding variants and X-linked loci associated with age at menarche.. Nature communications. 6:7756. Abstract
Huffman JE, de Vries PS, Morrison AC, Sabater-Lleal M, Kacprowski T, Auer PL, Brody JA, Chasman DI, Chen M-H, Guo X et al..  2015.  Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.. Blood. 126(11):e19-e29. Abstract
Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM et al..  2017.  Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract
P
Franceschini N, Hu Y, Reiner AP, Buyske S, Nalls M, Yanek LR, Li Y, Hindorff LA, Cole SA, Howard BV et al..  2014.  Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.. PloS one. 9(12):e113203. Abstract
Ried JS, Jeff M J, Chu AY, Bragg-Gresham JL, van Dongen J, Huffman JE, Ahluwalia TS, Cadby G, Eklund N, Eriksson J et al..  2016.  A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.. Nature communications. 7:13357. 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
Carlson CS, Aldred SF, Lee PK, Tracy RP, Schwartz SM, Rieder M, Liu K, Williams DO, Iribarren C, Lewis CE et al..  2005.  Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels.. American journal of human genetics. 77(1):64-77. Abstract
Kraja AT, Chasman DI, North KE, Reiner AP, Yanek LR, Kilpeläinen TO, Smith JA, Dehghan A, Dupuis J, Johnson AD et al..  2014.  Pleiotropic genes for metabolic syndrome and inflammation.. Molecular genetics and metabolism. Abstract
Eicher JD, Chami N, Kacprowski T, Nomura A, Chen M-H, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N et al..  2016.  Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.. American journal of human genetics. 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
N
Jensen RA, Sim X, Smith AV, Li X, Jakobsdóttir J, Cheng C-Y, Brody JA, Cotch MF, McKnight B, Klein R et al..  2016.  Novel Genetic Loci Associated With Retinal Microvascular Diameter.. Circulation. Cardiovascular genetics. 9(1):45-54. Abstract
Baumert J, Huang J, McKnight B, Sabater-Lleal M, Steri M, Chu AY, Trompet S, Lopez LM, Fornage M, Teumer A et al..  2014.  No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.. PloS one. 9(12):e111156. Abstract