Center-Authored Papers

Filters: Author is Lin, Dan-Yu  [Clear All Filters]
Journal Article
Franceschini N, Carty C, Buzková P, Reiner AP, Garrett T, Lin Y, Vöckler J-S, Hindorff LA, Cole SA, Boerwinkle E et al..  2011.  Association of genetic variants and incident coronary heart disease in multi-ethnic cohorts. The PAGE Study.. Circulation. Cardiovascular genetics. 4(69):661-672. Abstract
Avery CL, Sethupathy P, Buyske S, He Q, Lin D-Y, Arking DE, Carty CL, Duggan D, Fesinmeyer MD, Hindorff LA et al..  2012.  Fine-mapping and initial characterization of QT interval loci in African Americans.. PLoS genetics. 8(8):e1002870. Abstract
He Q, Avery CL, Lin D-Y.  2013.  A general framework for association tests with multivariate traits in large-scale genomics studies.. Genetic epidemiology. 37(8):759-67. Abstract
Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR et al..  2013.  Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.. Nature genetics. 45(5):501-12. 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
Crosby J, Peloso GM, Auer PL, Crosslin DR, Stitziel NO, Lange LA, Lu Y, Tang Z-Z, Zhang H, Hindy G et al..  2014.  Loss-of-function mutations in APOC3, triglycerides, and coronary disease.. The New England journal of medicine. 371(1):22-31. Abstract
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
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
He Q, Lin D-Y.  2011.  A variable selection method for genome-wide association studies.. Bioinformatics (Oxford, England). 27(1):1-8. 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