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Author Details

Rebecca L Zuvich
Center for Human Genetics Research, Vanderbilt University School of Medicine
2009
19
17
PMIDPaper TitleJournal TitlePublished Year
24952745Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Nat Genet2014
24952745Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Nat Genet2014
23196672Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.Genet Med2013
23762230Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.PLoS One2013
23838604Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema.Pharmacogenet Genomics2013
23196672Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.Genet Med2013
23463857Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.Circulation2013
23838604Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema.Pharmacogenet Genomics2013
23762230Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.PLoS One2013
23463857Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.Circulation2013
22329724Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.Pharmacogenomics2012
22329724Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.Pharmacogenomics2012
23067351High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.Clin Transl Sci2012
23067351High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.Clin Transl Sci2012
21234875Quality control procedures for genome-wide association studies.Curr Protoc Hum Genet2011
21234875Quality control procedures for genome-wide association studies.Curr Protoc Hum Genet2011
21833088Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.Nature2011
21653641Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.Hum Mol Genet2011
22125226Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.Genet Epidemiol2011
21981779Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.Am J Hum Genet2011
22125226Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.Genet Epidemiol2011
21833088Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.Nature2011
21981779Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.Am J Hum Genet2011
21653641Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.Hum Mol Genet2011
20112030Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.Hum Genet2010
20699326Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.Hum Mol Genet2010
20574445A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.Genes Immun2010
20522537Variation within DNA repair pathway genes and risk of multiple sclerosis.Am J Epidemiol2010
20211854CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.Hum Mol Genet2010
20112030Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.Hum Genet2010
20699326Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.Hum Mol Genet2010
20522537Variation within DNA repair pathway genes and risk of multiple sclerosis.Am J Epidemiol2010
20574445A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.Genes Immun2010
20211854CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.Hum Mol Genet2010
19775910Genetics and pathogenesis of multiple sclerosis.Semin Immunol2009
19626040Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.Genes Immun2009
19775910Genetics and pathogenesis of multiple sclerosis.Semin Immunol2009
19626040Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.Genes Immun2009
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Collaborators

Cleveland Institute for Computational Biology, Case Western Reserve University
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Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 9
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Columbia University Medical Center
Co-authored papers 7
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University of Pennsylvania
Co-authored papers 7
Yale School of Medicine, Yale School of Public Health
Co-authored papers 7
Vanderbilt University
Co-authored papers 7
University of Minnesota Medical School, 1035 University Drive duluth
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Mayo Clinic
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Brigham and Women's Hospital
Co-authored papers 6
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Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 6
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
University of Washington Medical Center
Co-authored papers 6
Vanderbilt University Medical Center
Co-authored papers 5
National Human Genome Research Institute
Co-authored papers 5
University of Washington
Co-authored papers 5
Mayo Clinic
Co-authored papers 4
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University of South Dakota Sanford School of Medicine
Co-authored papers 4
Northwestern University Feinberg School of Medicine
Co-authored papers 4
Feinberg School of Medicine, Northwestern University
Co-authored papers 4
University of Washington
Co-authored papers 3
University of Washington School of Medicine.
Co-authored papers 3
Vanderbilt University Medical Center
Co-authored papers 3