Rebecca L. Zuvich, Ph.D.

Vanderbilt University, Nashville, TN 
"Rebecca Zuvich"
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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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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
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