Elizabeth J. Rossin, Ph.D.
Affiliations: | 2012 | Biology: Medical Sciences, Division of | Harvard University, Cambridge, MA, United States |
Area:
GeneticsGoogle:
"Elizabeth Rossin"Parents
Sign in to add mentor| Joel N. Hirschhorn | grad student | 2012 | Harvard | |
| (The proteomic landscape of human disease: construction and evaluation of networks associated to complex traits.) | ||||
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Publications
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| Pollack S, Igo RP, Jensen RA, et al. (2018) Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes |
| van der Harst P, van Setten J, Verweij N, et al. (2016) 52 Genetic Loci Influencing Myocardial Mass. Journal of the American College of Cardiology. 68: 1435-48 |
| Lundby A, Rossin EJ, Steffensen AB, et al. (2014) Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics. Nature Methods. 11: 868-74 |
| Arking DE, Pulit SL, Crotti L, et al. (2014) Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature Genetics. 46: 826-36 |
| et al. (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics. 46: 234-44 |
| Anttila V, Winsvold BS, Gormley P, et al. (2013) Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nature Genetics. 45: 912-7 |
| Li G, Diogo D, Wu D, et al. (2013) Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. Plos Genetics. 9: e1003487 |
| den Hoed M, Eijgelsheim M, Esko T, et al. (2013) Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics. 45: 621-31 |
| Morris AP, Voight BF, Teslovich TM, et al. (2012) Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nature Genetics. 44: 981-90 |
| Talkowski ME, Rosenfeld JA, Blumenthal I, et al. (2012) Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 149: 525-37 |