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Shefali S Verma

Showing results (41-50 of 70) with videos related to

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BMC Medical Genomics|August 19, 2016
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variantsAnurag Verma, Shefali S Verma, Sarah A Pendergrass, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Genes|September 16, 2020
Effect of <i>CYP3A4</i>*22 and <i>PPAR-α</i> Genetic Variants on Platelet Reactivity in Patients Treated with Clopidogrel and Lipid-Lowering Drugs Undergoing Elective Percutaneous Coronary InterventionThomas O Bergmeijer, Alfi Yasmina, Gerrit J A Vos, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 19, 2016
INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIESAnurag Verma, Joseph B Leader, Shefali S Verma, et al.
American Journal of Human Genetics|April 7, 2023
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasetsPankhuri Singhal, Yogasudha Veturi, Scott M Dudek, et al.
Plos Genetics|June 4, 2021
Novel EDGE encoding method enhances ability to identify genetic interactionsMolly A Hall, John Wallace, Anastasia M Lucas, et al.
Biodata Mining|December 18, 2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)Rishika De, Shefali S Verma, Fotios Drenos, et al.
Journal of Personalized Medicine|December 23, 2022
The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse PopulationAnurag Verma, Scott M Damrauer, Nawar Naseer, et al.
Science (New York, N.Y.)|February 26, 2016
The phenotypic legacy of admixture between modern humans and NeandertalsCorinne N Simonti, Benjamin Vernot, Lisa Bastarache, et al.
Molecular Vision|October 30, 2014
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility lociMarylyn D Ritchie, Shefali S Verma, Molly A Hall, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
BMC Medical Genomics|August 19, 2016
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variantsAnurag Verma, Shefali S Verma, Sarah A Pendergrass, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Genes|September 16, 2020
Effect of <i>CYP3A4</i>*22 and <i>PPAR-α</i> Genetic Variants on Platelet Reactivity in Patients Treated with Clopidogrel and Lipid-Lowering Drugs Undergoing Elective Percutaneous Coronary InterventionThomas O Bergmeijer, Alfi Yasmina, Gerrit J A Vos, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 19, 2016
INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIESAnurag Verma, Joseph B Leader, Shefali S Verma, et al.
American Journal of Human Genetics|April 7, 2023
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasetsPankhuri Singhal, Yogasudha Veturi, Scott M Dudek, et al.
Plos Genetics|June 4, 2021
Novel EDGE encoding method enhances ability to identify genetic interactionsMolly A Hall, John Wallace, Anastasia M Lucas, et al.
Biodata Mining|December 18, 2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)Rishika De, Shefali S Verma, Fotios Drenos, et al.
Journal of Personalized Medicine|December 23, 2022
The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse PopulationAnurag Verma, Scott M Damrauer, Nawar Naseer, et al.
Science (New York, N.Y.)|February 26, 2016
The phenotypic legacy of admixture between modern humans and NeandertalsCorinne N Simonti, Benjamin Vernot, Lisa Bastarache, et al.
Molecular Vision|October 30, 2014
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility lociMarylyn D Ritchie, Shefali S Verma, Molly A Hall, et al.
Pageof 7