Rebecca L. Zuvich, Ph.D.
Affiliations: | Vanderbilt University, Nashville, TN |
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=95Google:
"Rebecca Zuvich"Mean distance: 19430.2
Parents
Sign in to add mentor| Jonathan L. Haines | grad student | 2009 | Vanderbilt | |
| (Pathway approach to decoding multiple sclerosis.) | ||||
| Marylyn D. Ritchie | post-doc | Vanderbilt (Computational Biology Tree) | ||
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Publications
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| 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 |
| Pare G, Kubo M, Byrd JB, et al. (2013) Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema. Pharmacogenetics and Genomics. 23: 470-8 |
| McDavid A, Crane PK, Newton KM, et al. (2013) Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. Plos One. 8: e63481 |
| Ritchie MD, Denny JC, Zuvich RL, et al. (2013) Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. Circulation. 127: 1377-85 |
| Rasmussen-Torvik LJ, Pacheco JA, Wilke RA, 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: 394-9 |
| Ramirez AH, Shi Y, Schildcrout JS, et al. (2012) Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record. Pharmacogenomics. 13: 407-18 |
| Zuvich RL, Armstrong LL, Bielinski SJ, 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: 887-98 |
| Denny JC, Crawford DC, Ritchie MD, et al. (2011) Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. American Journal of Human Genetics. 89: 529-42 |
| Sawcer S, et al. (2011) Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature. 476: 214-9 |
| Zuvich RL, Bush WS, McCauley JL, et al. (2011) Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. Human Molecular Genetics. 20: 3517-24 |