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Author Details

Gundula Povysil
Institute for Genomic Medicine, Columbia University Medical Center
2016
27
13
PMIDPaper TitleJournal TitlePublished Year
36758113Clinical and Genetic Characteristics of CKD Patients with High-Risk APOL1 Genotypes.J Am Soc Nephrol2023
37904125Prevalence and significance of clonal hematopoiesis of indeterminate potential in lung transplant recipients.BMC Pulm Med2023
36645932Genetic insights into childhood-onset schizophrenia: The yield of clinical exome sequencing.Schizophr Res2023
34799694The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders.Mol Psychiatry2022
35666822Genome-wide Enrichment of <i>TERT</i> Rare Variants in Idiopathic Pulmonary Fibrosis Patients of Latino Ancestry.Am J Respir Crit Care Med2022
35417304Rare and Common Variants in <i>KIF15</i> Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis.Am J Respir Crit Care Med2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36028256Utility of whole genome sequencing in assessing risk and clinically relevant outcomes for pulmonary fibrosis.Eur Respir J2022
33326012Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.JAMA Cardiol2021
33575654Increased yields of duplex sequencing data by a series of quality control tools.NAR Genom Bioinform2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
33709076Erratum: Increased yields of duplex sequencing data by a series of quality control tools.NAR Genom Bioinform2021
33757430ATAV: a comprehensive platform for population-scale genomic analyses.BMC Bioinformatics2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34156980Association of rare predicted loss-of-function variants of influenza-related type I IFN genes with critical COVID-19 pneumonia. Reply.J Clin Invest2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
32131723Family reunion via error correction: an efficient analysis of duplex sequencing data.BMC Bioinformatics2020
31898838Further delineation of putative ACTB loss-of-function variants: A 4-patient series.Hum Mutat2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
32807983Rare genetic causes of complex kidney and urological diseases.Nat Rev Nephrol2020
32786180Causal Genetic Variants in Stillbirth.N Engl J Med2020
31023833The impact of poly-A microsatellite heterologies in meiotic recombination.Life Sci Alliance2019
31605095Rare-variant collapsing analyses for complex traits: guidelines and applications.Nat Rev Genet2019
31085678Exome-Based Rare-Variant Analyses in CKD.J Am Soc Nephrol2019
28881961Rectified factor networks for biclustering of omics data.Bioinformatics2017
28449315panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnostics.Hum Mutat2017
28158547IBD Sharing between Africans, Neandertals, and Denisovans.Genome Biol Evol2016
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Collaborators

David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 16
Krzysztof Kiryluk
Columbia University
Co-authored papers 8
Ali G Gharavi
Columbia University College of Physicians and Surgeons
Co-authored papers 6
Guillaume Butler-Laporte
McGill University
Co-authored papers 6
John Brent Richards
Lady Davis Institute for Medical Research, Jewish General Hospital
Co-authored papers 5
Mark Lathrop
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Co-authored papers 5
Mathieu Bourgey
McGill University
Co-authored papers 3
John Kenneth Baillie
Roslin Institute, University of Edinburgh
Co-authored papers 3
Vincenzo Forgetta
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Ning Shang
Columbia University Irving Medical Center
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Qatar Foundation Research, Qatar Foundation
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King Faisal Specialist Hospital & Research Centre
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Emory School of Medicine
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Said I Ismail
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Jack A Kosmicki
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Robert Eveleigh
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
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Hamdi Mbarek
Vrije Universiteit
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Yaseen M Arabi
King Saud bin Abdulaziz Medical City for Science and Technology
Co-authored papers 3
Guillaume Bourque
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
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Manal Alaamery
National Centre for Genomic Technologies
Co-authored papers 3
Salam Massadeh
National Centre for Genomic Technologies
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Andrew S Allen
Duke University School of Medicine
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Vincent Mooser
McGill University
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Anton Nekrutenko
The Pennsylvania State University, University Park
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Pierre Lepage
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Alison Meynert
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Aris Baras
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Maddalena Marasa
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