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Author Details

Suzanna E Lewis
Lawrence Berkeley National Laboratory
1996
97
58
PMIDPaper TitleJournal TitlePublished Year
35411350Wastewater sequencing uncovers early, cryptic SARS-CoV-2 variant transmission.medRxiv2022
35411350Wastewater sequencing uncovers early, cryptic SARS-CoV-2 variant transmission.medRxiv2022
34697637OBO Foundry in 2021: operationalizing open data principles to evaluate ontologies.Database (Oxford)2021
34697637OBO Foundry in 2021: operationalizing open data principles to evaluate ontologies.Database (Oxford)2021
30726205Apollo: Democratizing genome annotation.PLoS Comput Biol2019
30726205Apollo: Democratizing genome annotation.PLoS Comput Biol2019
31548717Gene Ontology Causal Activity Modeling (GO-CAM) moves beyond GO annotations to structured descriptions of biological functions and systems.Nat Genet2019
31548717Gene Ontology Causal Activity Modeling (GO-CAM) moves beyond GO annotations to structured descriptions of biological functions and systems.Nat Genet2019
28968857Gearing up to handle the mosaic nature of life in the quest for orthologs.Bioinformatics2018
28968857Gearing up to handle the mosaic nature of life in the quest for orthologs.Bioinformatics2018
30224793Model organism data evolving in support of translational medicine.Lab Anim (NY)2018
30224793Model organism data evolving in support of translational medicine.Lab Anim (NY)2018
27812951The Vision and Challenges of the Gene Ontology.Methods Mol Biol2017
27899636The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.Nucleic Acids Res2017
27812951The Vision and Challenges of the Gene Ontology.Methods Mol Biol2017
27899636The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.Nucleic Acids Res2017
27043882Standardized benchmarking in the quest for orthologs.Nat Methods2016
27043882Standardized benchmarking in the quest for orthologs.Nat Methods2016
27412096MSAViewer: interactive JavaScript visualization of multiple sequence alignments.Bioinformatics2016
27072794JBrowse: a dynamic web platform for genome visualization and analysis.Genome Biol2016
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
28025345Large-scale inference of gene function through phylogenetic annotation of Gene Ontology terms: case study of the apoptosis and autophagy cellular processes.Database (Oxford)2016
27664130The environment ontology in 2016: bridging domains with increased scope, semantic density, and interoperation.J Biomed Semantics2016
28025345Large-scale inference of gene function through phylogenetic annotation of Gene Ontology terms: case study of the apoptosis and autophagy cellular processes.Database (Oxford)2016
27664130The environment ontology in 2016: bridging domains with increased scope, semantic density, and interoperation.J Biomed Semantics2016
27412096MSAViewer: interactive JavaScript visualization of multiple sequence alignments.Bioinformatics2016
27516611Navigating the Phenotype Frontier: The Monarch Initiative.Genetics2016
27569544A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.Am J Hum Genet2016
27072794JBrowse: a dynamic web platform for genome visualization and analysis.Genome Biol2016
25562316Finding our way through phenotypes.PLoS Biol2015
25562316Finding our way through phenotypes.PLoS Biol2015
25957950The Confidence Information Ontology: a step towards a standard for asserting confidence in annotations.Database (Oxford)2015
26713234Emerging semantics to link phenotype and environment.PeerJ2015
26092691Disease insights through cross-species phenotype comparisons.Mamm Genome2015
26269093Use of model organism and disease databases to support matchmaking for human disease gene discovery.Hum Mutat2015
26133389Quest for Orthologs Entails Quest for Tree of Life: In Search of the Gene Stream.Genome Biol Evol2015
26119816The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease.Am J Hum Genet2015
26153621Anatomy of BioJS, an open source community for the life sciences.Elife2015
26269093Use of model organism and disease databases to support matchmaking for human disease gene discovery.Hum Mutat2015
26713234Emerging semantics to link phenotype and environment.PeerJ2015
26133389Quest for Orthologs Entails Quest for Tree of Life: In Search of the Gene Stream.Genome Biol Evol2015
26153621Anatomy of BioJS, an open source community for the life sciences.Elife2015
26119816The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease.Am J Hum Genet2015
26092691Disease insights through cross-species phenotype comparisons.Mamm Genome2015
25957950The Confidence Information Ontology: a step towards a standard for asserting confidence in annotations.Database (Oxford)2015
24217912The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.Nucleic Acids Res2014
25315429Deletions of chromosomal regulatory boundaries are associated with congenital disease.Genome Biol2014
24217912The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.Nucleic Acids Res2014
24162188Improved exome prioritization of disease genes through cross-species phenotype comparison.Genome Res2014
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Collaborators

International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences
Co-authored papers 42
University of Cambridge
Co-authored papers 24
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 18
Co-authored papers 18
Division of Emergency Medicine University of Calgary Calgary Alberta Canada.
Co-authored papers 16
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 16
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 15
Renaissance Computing Institute, University of North Carolina
Co-authored papers 15
The University of Florida
Co-authored papers 13
Co-authored papers 12
Ontario Institute for Cancer Research, University Avenue
Co-authored papers 11
Lawrence Berkely National Laboratory, Massachusetts Institute of Technology, Princeton University
Co-authored papers 10
University at Buffalo
Co-authored papers 9
University of Geneva
Co-authored papers 9
University of Southern California
Co-authored papers 9
Lawrence Berkeley National Laboratory
Co-authored papers 8
University of Cambridge
Co-authored papers 8
Stanford University
Co-authored papers 7
European Bioinformatics Institute
Co-authored papers 7
Institute of Neuroscience, University of Oregon
Co-authored papers 7
Institute of Cancer and Genomic Sciences, University of Birmingham
Co-authored papers 7
Lawrence Berkeley National Laboratory
Co-authored papers 7
University of California berkeley
Co-authored papers 6
University of Southern California
Co-authored papers 6
Renaissance Computing Institute, University of North Carolina
Co-authored papers 6
Oxford e-Research Centre, University of Oxford
Co-authored papers 6
University of Utah
Co-authored papers 5
Lawrence Berkeley National Laboratory
Co-authored papers 5
University of Oxford
Co-authored papers 5
University of Utah
Co-authored papers 5