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Author Details

Shefali S Verma
University of Pennsylvania
2013
75
24
PMIDPaper TitleJournal TitlePublished Year
36350094How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT).Clin Pharmacol Ther2023
38072966Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts.Sci Rep2023
37345113Genome-Wide Association Study of Breast Density among Women of African Ancestry.Cancers (Basel)2023
37248299Polygenic prediction of preeclampsia and gestational hypertension.Nat Med2023
37342866Leveraging electronic health record data for endometriosis research.Front Digit Health2023
37308786Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.Nat Genet2023
37196359Gene Interactions in Human Disease Studies-Evidence Is Mounting.Annu Rev Biomed Data Sci2023
37028392Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.Am J Hum Genet2023
36846987Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.J Am Heart Assoc2023
36540998Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.Pac Symp Biocomput2023
36540995Session Introduction: SALUD: Scalable Applications of cLinical risk Utility and preDiction.Pac Symp Biocomput2023
36824881Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia.medRxiv2023
34611967Genetic liability for substance use associated with medical comorbidities in electronic health records of African- and European-ancestry individuals.Addict Biol2022
36443877Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population.J Transl Med2022
36441943Quality Control Procedures for Genome-Wide Association Studies.Curr Protoc2022
36556195The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population.J Pers Med2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35121771Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits.Sci Rep2022
34906489Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank.Genet Med2022
33469597SARS-CoV-2 seropositivity and seroconversion in patients undergoing active cancer-directed therapy.medRxiv2021
33850243Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.NPJ Digit Med2021
33720771Genetically Downregulated Interleukin-6 Signaling Is Associated With a Favorable Cardiometabolic Profile: A Phenome-Wide Association Study.Circulation2021
34086673Novel EDGE encoding method enhances ability to identify genetic interactions.PLoS Genet2021
32472697Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium.Clin Pharmacol Ther2020
32034279Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer.Sci Rep2020
33031386Genetics of height and risk of atrial fibrillation: A Mendelian randomization study.PLoS Med2020
32932966Effect 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 Intervention.Genes (Basel)2020
32981348Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.Circulation2020
30864329Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network.Pac Symp Biocomput2019
31748686An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer.Sci Rep2019
31821430Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry.JAMA2019
31311600GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.BMC Med2019
30988330Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.Sci Rep2019
30864331Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.Pac Symp Biocomput2019
29218873Session Introduction: Challenges of Pattern Recognition in Biomedical Data.Pac Symp Biocomput2018
30038396Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.Nat Genet2018
29847509Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events.Pharmacogenet Genomics2018
30166544A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.Nat Commun2018
30353015Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide.Sci Rep2018
29618318A simulation study investigating power estimates in phenome-wide association studies.BMC Bioinformatics2018
29606303PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.Am J Hum Genet2018
29545597Rare variants in drug target genes contributing to complex diseases, phenome-wide.Sci Rep2018
29713383Collective feature selection to identify crucial epistatic variants.BioData Min2018
29370075Another Round of "Clue" to Uncover the Mystery of Complex Traits.Genes (Basel)2018
29218904Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.Pac Symp Biocomput2018
27897004IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR.Pac Symp Biocomput2017
28198095Genetic risk models: Influence of model size on risk estimates and precision.Genet Epidemiol2017
28099408Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.Pharmacogenet Genomics2017
28448694The joint effect of air pollution exposure and copy number variation on risk for autism.Autism Res2017
29079728PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.Nat Commun2017
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Collaborators

Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 64
Anurag Verma
Corporal Michael J Crescenz VA Medical Center Philadelphia
Co-authored papers 22
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 21
Sarah A Pendergrass
Biomedical and Translational Informatics Institute
Co-authored papers 19
David R Crosslin
University of Washington Medical Center
Co-authored papers 18
Yuki Bradford
University of Pennsylvania
Co-authored papers 16
Iftikhar J Kullo
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Co-authored papers 15
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers 14
Peggy L Peissig
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Co-authored papers 14
Joshua C Denny
Vanderbilt University
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Gerard Tromp
Biomedical Research Institute, Stellenbosch University.
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Catherine A McCarty
University of Minnesota Medical School, 1035 University Drive duluth
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Eric B Larson
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Murray H Brilliant
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Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
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Scott M Damrauer
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 8
Dana C Crawford
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 8
Renae Judy
Co-authored papers 8
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 8
Mariza de Andrade
Mayo Clinic
Co-authored papers 7
Jason H Moore
Cedars-Sinai Medical Center
Co-authored papers 7
John B Harley
US Department of Veterans Affairs Medical Center
Co-authored papers 7
John R Wallace
The University of Alabama at Birmingham
Co-authored papers 7
Bahram Namjou
Cincinnati Children's Hospital
Co-authored papers 7
Rongling Li
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 7
Daniel J Rader
Co-authored papers 7
Kenneth M Borthwick
Hood Center for Health Research
Co-authored papers 6
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 6
Brendan J Keating
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Co-authored papers 6
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