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Author Details

Anurag Verma
Corporal Michael J Crescenz VA Medical Center Philadelphia
2010
71
22
PMIDPaper TitleJournal TitlePublished Year
36350094How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT).Clin Pharmacol Ther2023
37425708Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.medRxiv2023
37365631Development of complemented comprehensive networks for rapid screening of repurposable drugs applicable to new emerging disease outbreaks.J Transl Med2023
37293013Uncovering genetic associations in the human diseasome using an endophenotype-augmented disease network.medRxiv2023
36541008HIGH-PERFORMANCE COMPUTING MEETS HIGH-PERFORMANCE MEDICINE.Pac Symp Biocomput2023
36571484Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data.Bioinformatics2023
36041210Reply to: Sookaromdee and Wiwanitkit.Am J Respir Crit Care Med2023
35166337NETMAGE: A human disease phenotype map generator for the network-based visualization of phenome-wide association study results.Gigascience2022
35771531A <i>MUC5B</i> Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.Am J Respir Crit Care Med2022
35410495Schizophrenia Imaging Signatures and Their Associations With Cognition, Psychopathology, and Genetics in the General Population.Am J Psychiatry2022
35580180Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection.Proc Natl Acad Sci U S A2022
35835913Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries.Nat Genet2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35759254Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait.JAMA Intern Med2022
35752651Dissecting the clinical relevance of polygenic risk score for obesity-a cross-sectional, longitudinal analysis.Int J Obes (Lond)2022
35654975A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.Nat Genet2022
35482673A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.PLoS Genet2022
36443877Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population.J Transl Med2022
36513072Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank.Cell Rep Med2022
36556195The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population.J Pers Med2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34890160netCRS: Network-based comorbidity risk score for prediction of myocardial infarction using biobank-scaled PheWAS data.Pac Symp Biocomput2022
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
35027740Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.Nat Genet2022
33469597SARS-CoV-2 seropositivity and seroconversion in patients undergoing active cancer-directed therapy.medRxiv2021
33655282Targeting the Coronavirus Nucleocapsid Protein through GSK-3 Inhibition.medRxiv2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
33791713Alternative splicing of OAS1 alters the risk for severe COVID-19.medRxiv2021
33901188Tissue specificity-aware TWAS (TSA-TWAS) framework identifies novel associations with metabolic, immunologic, and virologic traits in HIV-positive adults.PLoS Genet2021
33619501Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease.medRxiv2021
33554040Rates of COVID-19-Related Outcomes in Cancer Compared With Noncancer Patients.JNCI Cancer Spectr2021
33631096Seasonal human coronavirus antibodies are boosted upon SARS-CoV-2 infection but not associated with protection.Cell2021
34593624Targeting the coronavirus nucleocapsid protein through GSK-3 inhibition.Proc Natl Acad Sci U S A2021
34341784Impact of natural selection on global patterns of genetic variation, and association with clinical phenotypes, at genes involved in SARS-CoV-2 infection.Res Sq2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
34140684A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts.Nat Genet2021
33432171Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.Nat Med2021
31306493Pharmacogenomics Clinical Annotation Tool (PharmCAT).Clin Pharmacol Ther2020
33200143Seasonal human coronavirus antibodies are boosted upon SARS-CoV-2 infection but not associated with protection.medRxiv2020
32676623SARS-CoV-2 Seroprevalence Among Parturient Women.medRxiv2020
32817956Rates of COVID-19-related Outcomes in Cancer compared to non-Cancer Patients.medRxiv2020
32727884SARS-CoV-2 seroprevalence among parturient women in Philadelphia.Sci Immunol2020
30598166Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals.Am J Hum Genet2019
31216868Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.Circulation2019
30864331Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.Pac Symp Biocomput2019
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
29218873Session Introduction: Challenges of Pattern Recognition in Biomedical Data.Pac Symp Biocomput2018
29847509Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events.Pharmacogenet Genomics2018
30353015Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide.Sci Rep2018
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Collaborators

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VA Boston Healthcare System
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McGill University
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Columbia University
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VA Boston Healthcare System
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Mayo Clinic
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Brigham and Women's Hospital, Harvard Medical School
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Biomedical Research Institute, Stellenbosch University.
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Stanford University School of Medicine.
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Center for Precision Medicine Research, Marshfield Clinic Research Institute
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Corporal Michael J Crescenz VA Medical Center
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University of Pennsylvania
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