Skip to Main Content

Author Details

Nicole L Washington
Renaissance Computing Institute, University of North Carolina
1997
43
26
PMIDPaper TitleJournal TitlePublished Year
36637017Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation.Genet Med2023
36637017Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation.Genet Med2023
37389415KG-Hub-building and exchanging biological knowledge graphs.Bioinformatics2023
37389415KG-Hub-building and exchanging biological knowledge graphs.Bioinformatics2023
35005651HLA-Aâ¿¿03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination.HGG Adv2022
35442193The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice.Genet Med2022
35798029Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission.Nature2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35474739SARS-CoV-2 variant Delta rapidly displaced variant Alpha in the United States and led to higher viral loads.Cell Rep Med2022
35005651HLA-Aâ¿¿03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination.HGG Adv2022
35442193The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice.Genet Med2022
35474739SARS-CoV-2 variant Delta rapidly displaced variant Alpha in the United States and led to higher viral loads.Cell Rep Med2022
35798029Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission.Nature2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34385667Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records.Genet Med2021
33861950Emergence and rapid transmission of SARS-CoV-2 B.1.1.7 in the United States.Cell2021
33930192Comprehensive Allele Genotyping in Critical Pharmacogenes Reduces Residual Clinical Risk in Diverse Populations.Clin Pharmacol Ther2021
33763119Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population.Front Genet2021
34385667Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records.Genet Med2021
33763119Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population.Front Genet2021
33861950Emergence and rapid transmission of SARS-CoV-2 B.1.1.7 in the United States.Cell2021
33930192Comprehensive Allele Genotyping in Critical Pharmacogenes Reduces Residual Clinical Risk in Diverse Populations.Clin Pharmacol Ther2021
33046911Pathogenic variants in actionable MODY genes are associated with type 2 diabetes.Nat Metab2020
31992710Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.Nat Commun2020
33046911Pathogenic variants in actionable MODY genes are associated with type 2 diabetes.Nat Metab2020
31992710Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.Nat Commun2020
30964579Genetic counseling, 2030: An on-demand service tailored to the needs of a price conscious, genetically literate, and busy world.J Genet Couns2019
30964579Genetic counseling, 2030: An on-demand service tailored to the needs of a price conscious, genetically literate, and busy world.J Genet Couns2019
27899636The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.Nucleic Acids Res2017
28603714Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.Front Med (Lausanne)2017
28662064Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data.PLoS Biol2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
27899636The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.Nucleic Acids Res2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28662064Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data.PLoS Biol2017
28603714Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.Front Med (Lausanne)2017
27569544A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.Am J Hum Genet2016
26562225Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.Genet Med2016
26599696The Resource Identification Initiative: A Cultural Shift in Publishing.J Comp Neurol2016
26589523The Resource Identification Initiative: A Cultural Shift in Publishing.Neuroinformatics2016
27569544A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.Am J Hum Genet2016
27516611Navigating the Phenotype Frontier: The Monarch Initiative.Genetics2016
26599696The Resource Identification Initiative: A Cultural Shift in Publishing.J Comp Neurol2016
26589523The Resource Identification Initiative: A Cultural Shift in Publishing.Neuroinformatics2016
26562225Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.Genet Med2016
27516611Navigating the Phenotype Frontier: The Monarch Initiative.Genetics2016
26092691Disease insights through cross-species phenotype comparisons.Mamm Genome2015
27110440The Resource Identification Initiative: a cultural shift in publishing.Brain Behav2015
26562621Next-generation diagnostics and disease-gene discovery with the Exomiser.Nat Protoc2015
26092691Disease insights through cross-species phenotype comparisons.Mamm Genome2015
  • 1 - 50 of 86

Recommended Authors

University of Southampton
Career Start Year 2014
Number of shared co-authors 16
Aerospace Center Hospital
Career Start Year 2011
Number of shared co-authors 3
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Career Start Year 2010
Number of shared co-authors 8
Harvard Medical School, Brigham and Women's Hospital
Career Start Year 2009
Number of shared co-authors 19
Vanderbilt University Medical Center
Career Start Year 2009
Number of shared co-authors 7
Regeneron Pharmaceuticals
Career Start Year 2008
Number of shared co-authors 23
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 28
Institute for Next Generation Healthcare
Career Start Year 2006
Number of shared co-authors 17
Cleveland Institute for Computational Biology, Case Western Reserve University
Career Start Year 2006
Number of shared co-authors 7
Sanford School of Medicine, University of South Dakota
Career Start Year 2005
Number of shared co-authors 19
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 16
University of Groningen, University Medical Center Groningen
Career Start Year 2004
Number of shared co-authors 47
Regeneron Pharmaceuticals Inc.
Career Start Year 2004
Number of shared co-authors 14
Broad Institute of MIT and Harvard
Career Start Year 2003
Number of shared co-authors 81
European Bioinformatics Institute
Career Start Year 2003
Number of shared co-authors 44
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Career Start Year 2002
Number of shared co-authors 7
Baylor College of Medicine
Career Start Year 2002
Number of shared co-authors 14
Columbia University
Career Start Year 2002
Number of shared co-authors 15
Broad Institute of MIT and Harvard
Career Start Year 2002
Number of shared co-authors 28
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 45
University of Washington
Career Start Year 2001
Number of shared co-authors 16
University of Toronto
Career Start Year 1998
Number of shared co-authors 16
Heersink School of Medicine, The University of Alabama at Birmingham
Career Start Year 1995
Number of shared co-authors 12
Institute for Systems Biology
Career Start Year 1995
Number of shared co-authors 10
University of Utah
Career Start Year 1994
Number of shared co-authors 30
University of Missouri School of Medicine
Career Start Year 1989
Number of shared co-authors 13
Institute for Systems Biology
Career Start Year 1988
Number of shared co-authors 28
Baylor College of Medicine
Career Start Year 1988
Number of shared co-authors 64
Massachusetts General Hospital
Career Start Year 1987
Number of shared co-authors 83
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1985
Number of shared co-authors 45

Collaborators

American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 23
Co-authored papers 23
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 17
International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences
Co-authored papers 16
Lawrence Berkeley National Laboratory
Co-authored papers 15
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 14
Division of Emergency Medicine University of Calgary Calgary Alberta Canada.
Co-authored papers 12
Duke University
Co-authored papers 10
The Rockefeller University
Co-authored papers 8
NV Center for Genomic Medicine, Desert Research Institute
Co-authored papers 8
Critical Path Institute
Co-authored papers 8
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 8
Uppsala University
Co-authored papers 6
University of Colorado Anschutz Medical Campus
Co-authored papers 6
University Medical School
Co-authored papers 6
University of Colorado Anschutz Medical Campus
Co-authored papers 5
University of Pittsburgh
Co-authored papers 5
Perth Children's Hospital
Co-authored papers 5
University of Colorado - Anschutz Medical Campus
Co-authored papers 4
The Hospital for Sick Children
Co-authored papers 4
University of British Columbia
Co-authored papers 4
Ontario Institute for Cancer Research, University Avenue
Co-authored papers 4
Ontario Institute for Cancer Research
Co-authored papers 4
DATA Team and Techna Institute, University Health Network
Co-authored papers 4
University of Toronto
Co-authored papers 4
University of Pennsylvania - Perelman School of Medicine
Co-authored papers 4
university of california san diego
Co-authored papers 4
Lawrence Berkeley National Laboratory
Co-authored papers 4
Institute for Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin
Co-authored papers 3
College of Physicians and Surgeons, Columbia University
Co-authored papers 3