Skip to Main Content

Author Details

Michael C Zody
Broad Institute of Harvard and MIT
2001
96
55
Christopher Churas (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36671517Genetic Predisposition to Neurological Complications in Patients with COVID-19.Biomolecules2023
37745577Multi-OMIC analysis of Huntington disease reveals a neuroprotective astrocyte state.bioRxiv2023
37632041Molecular and Clinical Epidemiology of SARS-CoV-2 Infection among Vaccinated and Unvaccinated Individuals in a Large Healthcare Organization from New Jersey.Viruses2023
37961520Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.Res Sq2023
36671517Genetic Predisposition to Neurological Complications in Patients with COVID-19.Biomolecules2023
37632041Molecular and Clinical Epidemiology of SARS-CoV-2 Infection among Vaccinated and Unvaccinated Individuals in a Large Healthcare Organization from New Jersey.Viruses2023
37961520Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.Res Sq2023
37745577Multi-OMIC analysis of Huntington disease reveals a neuroprotective astrocyte state.bioRxiv2023
35233546System-wide transcriptome damage and tissue identity loss in COVID-19 patients.Cell Rep Med2022
35647563Accounting for population structure in genetic studies of cystic fibrosis.HGG Adv2022
35997285Genomic Epidemiology and Serology Associated with a SARS-CoV-2 R.1 Variant Outbreak in New Jersey.mBio2022
35410384Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes.Nat Genet2022
36192399Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.Nat Commun2022
36055201High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.Cell2022
35290762Familial long-read sequencing increases yield of de novo mutations.Am J Hum Genet2022
35036860Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19.iScience2022
35233546System-wide transcriptome damage and tissue identity loss in COVID-19 patients.Cell Rep Med2022
35347136Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.Nat Commun2022
35410384Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes.Nat Genet2022
35647563Accounting for population structure in genetic studies of cystic fibrosis.HGG Adv2022
35347136Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.Nat Commun2022
35997285Genomic Epidemiology and Serology Associated with a SARS-CoV-2 R.1 Variant Outbreak in New Jersey.mBio2022
36055201High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.Cell2022
36192399Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.Nat Commun2022
35290762Familial long-read sequencing increases yield of de novo mutations.Am J Hum Genet2022
35036860Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19.iScience2022
33241313Somatic variant analysis of linked-reads sequencing data with Lancet.Bioinformatics2021
33632895Haplotype-resolved diverse human genomes and integrated analysis of structural variation.Science2021
33626341Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway.Cell Rep2021
34256850Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.Hum Genomics2021
33605984The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans.Invest Ophthalmol Vis Sci2021
33977858A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations.Emerg Microbes Infect2021
33758858Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps.bioRxiv2021
34312540Recent ultra-rare inherited variants implicate new autism candidate risk genes.Nat Genet2021
33241313Somatic variant analysis of linked-reads sequencing data with Lancet.Bioinformatics2021
34787439Postvaccination SARS-COV-2 among Health Care Workers in New Jersey: A Genomic Epidemiological Study.Microbiol Spectr2021
34431691Emergence of Multiple SARS-CoV-2 Antibody Escape Variants in an Immunocompromised Host Undergoing Convalescent Plasma Treatment.mSphere2021
33626341Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway.Cell Rep2021
33758858Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps.bioRxiv2021
33632895Haplotype-resolved diverse human genomes and integrated analysis of structural variation.Science2021
33605984The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans.Invest Ophthalmol Vis Sci2021
34431691Emergence of Multiple SARS-CoV-2 Antibody Escape Variants in an Immunocompromised Host Undergoing Convalescent Plasma Treatment.mSphere2021
34787439Postvaccination SARS-COV-2 among Health Care Workers in New Jersey: A Genomic Epidemiological Study.Microbiol Spectr2021
33977858A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations.Emerg Microbes Infect2021
34312540Recent ultra-rare inherited variants implicate new autism candidate risk genes.Nat Genet2021
34256850Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.Hum Genomics2021
32511326Type 2 and interferon inflammation strongly regulate SARS-CoV-2 related gene expression in the airway epithelium.bioRxiv2020
32459537Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth.Am J Respir Crit Care Med2020
32327564Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand <i>KITLG/SCF</i> and Gene-By-Air-Pollution Interaction.Genetics2020
33046696Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium.Nat Commun2020
  • 1 - 50 of 192

Recommended Authors

Fritz J Sedlazeck
Baylor College of Medicine
Career Start Year 2012
Number of shared co-authors 46
Ryan M Layer
Boulder and BioFrontiers Institute, University of Colorado Boulder
Career Start Year 2011
Number of shared co-authors 7
Marta Gut
Universitat de Barcelona (UB)
Career Start Year 2010
Number of shared co-authors 41
Jared T Simpson
Ontario Institute for Cancer Research
Career Start Year 2009
Number of shared co-authors 42
Martin Kircher
Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin
Career Start Year 2008
Number of shared co-authors 18
Aakrosh Ratan
Center for Public Health Genomics, University of Virginia
Career Start Year 2008
Number of shared co-authors 38
Jeffrey G Reid
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 47
Aaron R Quinlan
University of Utah
Career Start Year 2007
Number of shared co-authors 19
Stephan Ossowski
Institute of Medical Genetics and Applied Genomics, University of Tubingen
Career Start Year 2006
Number of shared co-authors 7
Gabriel Renaud
Technical University of Denmark
Career Start Year 2006
Number of shared co-authors 14
James G D Prendergast
The Roslin Institute, The University of Edinburgh
Career Start Year 2005
Number of shared co-authors 10
Ziad Khan
Baylor College of Medicine
Career Start Year 2005
Number of shared co-authors 90
Vikas Bansal
University of California San Diego
Career Start Year 2004
Number of shared co-authors 10
Shane McCarthy
Wellcome Sanger Institute
Career Start Year 2004
Number of shared co-authors 57
Jeffrey A Rosenfeld
Cancer Institute of New Jersey
Career Start Year 2004
Number of shared co-authors 29
Ali Bashir
Google Accelerated Science Team, Google Inc
Career Start Year 2003
Number of shared co-authors 31
Lachlan J M Coin
The Peter Doherty Institute for Infection and Immunity, The University of Melbourne
Career Start Year 2003
Number of shared co-authors 24
Fuli Yu
East China University of Science and Technology
Career Start Year 2002
Number of shared co-authors 88
Brent S Pedersen
Center for Molecular Medicine, University Medical Center Utrecht
Career Start Year 2001
Number of shared co-authors 3
Can Alkan
Bilkent University
Career Start Year 2001
Number of shared co-authors 77
Michael Brudno
University of Toronto
Career Start Year 2000
Number of shared co-authors 66
Sarah J Wheelan
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1998
Number of shared co-authors 28
Matthew E Hurles
Wellcome Sanger Institute
Career Start Year 1998
Number of shared co-authors 98
Anton Nekrutenko
The Pennsylvania State University, University Park
Career Start Year 1998
Number of shared co-authors 64
Colin A Semple
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year 1997
Number of shared co-authors 23
Guillaume Bourque
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Career Start Year 1997
Number of shared co-authors 68
Jay Shendure
University of Washington
Career Start Year 1996
Number of shared co-authors 71
Ian T Fiddes
Liver Center and Diabetes Center, University of California san francisco
Career Start Year 1996
Number of shared co-authors 47
Jared C Roach
Institute for Systems Biology
Career Start Year 1995
Number of shared co-authors 15
Kelly A Frazer
University of California, USA Institute for Genomic Medicine
Career Start Year 1967
Number of shared co-authors 75

Collaborators

Eric S Lander
Vanderbilt-Ingram Cancer Center, Vanderbilt University
Co-authored papers 20
Kerstin Lindblad-Toh
Uppsala University
Co-authored papers 16
Chad Nusbaum
Co-authored papers 14
Bruce W Birren
Broad Institute of MIT and Harvard
Co-authored papers 14
Evan E Eichler
University of Washington
Co-authored papers 13
David B Jaffe
Co-authored papers 13
Toby Bloom
Co-authored papers 11
Jean L Chang
Co-authored papers 10
Manuel Garber
Co-authored papers 10
Kanika Arora
Co-authored papers 9
Matthew R Henn
Co-authored papers 9
Deborah A Nickerson
University of Washington
Co-authored papers 8
Niall J Lennon
Broad Institute of MIT and Harvard.
Co-authored papers 8
Nicolas Robine
Sloan-Kettering Institute
Co-authored papers 8
Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
Co-authored papers 8
Michele Clamp
Harvard University
Co-authored papers 7
Richard K Wilson
The Ohio State University
Co-authored papers 7
Hyun Min Kang
Co-authored papers 7
Minita Shah
Co-authored papers 7
Tina Graves
McDonnell Genome Institute, Washington University
Co-authored papers 7
Mark J Daly
Massachusetts General Hospital
Co-authored papers 7
Robert B Darnell
Co-authored papers 6
Vladimir Vacic
Stanley Institute for Cognitive Genomics
Co-authored papers 6
Esteban G Burchard
University of California San Francisco (UCSF)
Co-authored papers 6
Richard A Gibbs
Baylor College of Medicine
Co-authored papers 6
Elaine R Mardis
The Ohio State University
Co-authored papers 6
Jennifer Baldwin
Co-authored papers 6
Stephen M J Searle
Wellcome Trust Sanger Institute
Co-authored papers 6
Jane Rogers
The Wellcome Trust Sanger Institute
Co-authored papers 6
Andrew Zimmer
Co-authored papers 6
Release 1.2