Skip to Main Content

Author Details

Jack A Kosmicki
Regeneron Pharmaceuticals
2012
35
28
PMIDPaper TitleJournal TitlePublished Year
36807635Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2023
36807635Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2023
35219277Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical Trial.Clin Infect Dis2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36450978Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2022
35219277Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical Trial.Clin Infect Dis2022
36450978Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34373650Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
34017140Computationally efficient whole-genome regression for quantitative and binary traits.Nat Genet2021
33536625Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum 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
34210852Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.Science2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
34727153ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers.Invest Ophthalmol Vis Sci2021
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
34373650Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
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
33536625Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
34727153ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers.Invest Ophthalmol Vis Sci2021
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
34017140Computationally efficient whole-genome regression for quantitative and binary traits.Nat Genet2021
34210852Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.Science2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
32433464Loss of heterozygosity of essential genes represents a widespread class of potential cancer vulnerabilities.Nat Commun2020
32433464Loss of heterozygosity of essential genes represents a widespread class of potential cancer vulnerabilities.Nat Commun2020
31932770Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.Nat Neurosci2020
32461654The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2020
31932770Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.Nat Neurosci2020
32461654The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2020
30661751Predicting Splicing from Primary Sequence with Deep Learning.Cell2019
30559491Author Correction: Predicting the clinical impact of human mutation with deep neural networks.Nat Genet2019
31292440Paternal-age-related de novo mutations and risk for five disorders.Nat Commun2019
31004148Applicability of the Mutation-Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in Humans.Mol Biol Evol2019
30661751Predicting Splicing from Primary Sequence with Deep Learning.Cell2019
31292440Paternal-age-related de novo mutations and risk for five disorders.Nat Commun2019
31004148Applicability of the Mutation-Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in Humans.Mol Biol Evol2019
30559491Author Correction: Predicting the clinical impact of human mutation with deep neural networks.Nat Genet2019
30038395Predicting the clinical impact of human mutation with deep neural networks.Nat Genet2018
30038395Predicting the clinical impact of human mutation with deep neural networks.Nat Genet2018
29942082De novo variants in neurodevelopmental disorders with epilepsy.Nat Genet2018
29942082De novo variants in neurodevelopmental disorders with epilepsy.Nat Genet2018
28504703Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.Nat Genet2017
28504703Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.Nat Genet2017
28191890Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.Nat Genet2017
28191890Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.Nat Genet2017
26998691Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.Nat Genet2016
27221085Discovery of rare variants for complex phenotypes.Hum Genet2016
  • 1 - 50 of 70

Recommended Authors

Donders Institute for Brain, Radboud University Medical Center
Career Start Year 2017
Number of shared co-authors 3
The Institute for Computational Medicine, The Johns Hopkins University
Career Start Year 2016
Number of shared co-authors 2
Boston Children's Hospital
Career Start Year 2015
Number of shared co-authors 11
Center for Applied Genomics, Children's Hospital of Philadelphia
Career Start Year 2012
Number of shared co-authors 9
Invitae Corporation
Career Start Year 2012
Number of shared co-authors 3
Center for Biomedical Research in Rare Diseases Network
Career Start Year 2010
Number of shared co-authors 17
Berlin Institute of Health of Health at Charite - Universitatsmedizin Berlin
Career Start Year 2010
Number of shared co-authors 5
Wellcome Sanger Institute
Career Start Year 2010
Number of shared co-authors 13
Radboud University Medical Center
Career Start Year 2009
Number of shared co-authors 14
Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
Career Start Year 2008
Number of shared co-authors 23
Harvard Medical School.
Career Start Year 2008
Number of shared co-authors 20
Boston Children's Hospital
Career Start Year 2007
Number of shared co-authors 1
Duke University School of Medicine and Duke Health System
Career Start Year 2007
Number of shared co-authors 5
Washington University School of Medicine
Career Start Year 2006
Number of shared co-authors 2
Kidney Research Institute and Division of Nephrology, University of Washington
Career Start Year 2006
Number of shared co-authors 8
Boston Children's Hospital
Career Start Year 2005
Number of shared co-authors 7
Institute for Genomic Medicine, Nationwide Children's Hospital
Career Start Year 2005
Number of shared co-authors 18
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 8
Knight Cancer Institute, Oregon Health & Science University
Career Start Year 2004
Number of shared co-authors 21
The Huck Institutes of Life Sciences, University Park, Pennsylvania State University
Career Start Year 2003
Number of shared co-authors 10
Imperial College London
Career Start Year 2003
Number of shared co-authors 11
Feinstein Institutes for Medical Research
Career Start Year 2003
Number of shared co-authors 2
University of Exeter, Royal Devon and Exeter Hospital
Career Start Year 2003
Number of shared co-authors 9
Columbia University
Career Start Year 2002
Number of shared co-authors 20
Institute for Genomic Medicine, Columbia University
Career Start Year 2001
Number of shared co-authors 3
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 33
University of California San Diego
Career Start Year 2000
Number of shared co-authors 27
The Center for Applied Genomics, Children's Hospital of Philadelphia
Career Start Year 1995
Number of shared co-authors 74
Boston Children's Hospital, Harvard Medical School
Career Start Year 1993
Number of shared co-authors 45
Center for Applied Genomics (CAG), Children's Hospital of Philadelphia
Career Start Year 1987
Number of shared co-authors 19

Collaborators

Massachusetts General Hospital
Co-authored papers 15
Massachusetts General Hospital
Co-authored papers 11
Co-authored papers 11
Co-authored papers 10
Regeneron Pharmaceuticals
Co-authored papers 8
University of Maryland School of Medicine
Co-authored papers 7
Co-authored papers 7
Co-authored papers 6
Co-authored papers 6
Stanford University
Co-authored papers 6
Regeneron Pharmaceuticals, Inc.
Co-authored papers 6
Broad Institute of MIT and Harvard
Co-authored papers 6
Regeneron Pharmaceuticals Inc
Co-authored papers 6
Regeneron Pharmaceuticals Inc.
Co-authored papers 6
Broad Institute of MIT and Harvard
Co-authored papers 6
Broad Institute of MIT and Harvard
Co-authored papers 6
Broad Institute of MIT and Harvard
Co-authored papers 5
Co-authored papers 5
Co-authored papers 5
Co-authored papers 5
Icahn School of Medicine at Mount Sinai
Co-authored papers 4
Institute for Molecular Medicine Finland (FIMM), University of Helsinki
Co-authored papers 4
Co-authored papers 4
Broad Institute of MIT and Harvard
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Broad Institute of MIT and Harvard
Co-authored papers 4
Co-authored papers 4