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Author Details
Full Name
Rebecca L Zuvich
Affiliation
Center for Human Genetics Research, Vanderbilt University School of Medicine
ORCID
Career Start Year
2009
Papers
19
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
24952745
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Nat Genet
2014
24952745
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Nat Genet
2014
23196672
Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.
Genet Med
2013
23762230
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
PLoS One
2013
23838604
Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema.
Pharmacogenet Genomics
2013
23196672
Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.
Genet Med
2013
23463857
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation
2013
23838604
Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema.
Pharmacogenet Genomics
2013
23762230
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
PLoS One
2013
23463857
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation
2013
22329724
Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.
Pharmacogenomics
2012
22329724
Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.
Pharmacogenomics
2012
23067351
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Clin Transl Sci
2012
23067351
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Clin Transl Sci
2012
21234875
Quality control procedures for genome-wide association studies.
Curr Protoc Hum Genet
2011
21234875
Quality control procedures for genome-wide association studies.
Curr Protoc Hum Genet
2011
21833088
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
2011
21653641
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Hum Mol Genet
2011
22125226
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
Genet Epidemiol
2011
21981779
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Am J Hum Genet
2011
22125226
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
Genet Epidemiol
2011
21833088
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
2011
21981779
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Am J Hum Genet
2011
21653641
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Hum Mol Genet
2011
20112030
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.
Hum Genet
2010
20699326
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.
Hum Mol Genet
2010
20574445
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
Genes Immun
2010
20522537
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Am J Epidemiol
2010
20211854
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
Hum Mol Genet
2010
20112030
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.
Hum Genet
2010
20699326
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.
Hum Mol Genet
2010
20522537
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Am J Epidemiol
2010
20574445
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
Genes Immun
2010
20211854
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
Hum Mol Genet
2010
19775910
Genetics and pathogenesis of multiple sclerosis.
Semin Immunol
2009
19626040
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
Genes Immun
2009
19775910
Genetics and pathogenesis of multiple sclerosis.
Semin Immunol
2009
19626040
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
Genes Immun
2009
1 - 38 of 38
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Yale School of Medicine, Yale School of Public Health
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Rongling Li
National Human Genome Research Institute, National Institutes of Health
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Gail P Jarvik
University of Washington Medical Center
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