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Author Details

Frederick P Roth
University of Toronto
1998
158
63
Prashant Mali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36217029A proteome-scale map of the SARS-CoV-2-human contactome.Nat Biotechnol2023
37478847Genome-scale mapping of DNA damage suppressors through phenotypic CRISPR-Cas9 screens.Mol Cell2023
37729906Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation.Am J Hum Genet2023
37394429An Atlas of Variant Effects to understand the genome at nucleotide resolution.Genome Biol2023
37061542Next-generation large-scale binary protein interaction network for Drosophila melanogaster.Nat Commun2023
37081510satmut_utils: a simulation and variant calling package for multiplexed assays of variant effect.Genome Biol2023
37267226A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection.G3 (Bethesda)2023
37426450Minimum information and guidelines for reporting a Multiplexed Assay of Variant Effect.ArXiv2023
37292969Characterizing glucokinase variant mechanisms using a multiplexed abundance assay.bioRxiv2023
36716194Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.Circ Genom Precis Med2023
36798224Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation.bioRxiv2023
36732511Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2023
36865234Pacybara: Accurate long-read sequencing for barcoded mutagenized allelic libraries.bioRxiv2023
36055970Scalable Functional Assays for the Interpretation of Human Genetic Variation.Annu Rev Genet2022
36710959Quantitative proteomics and biological activity of extracellular vesicles engineered to express SARS-CoV-2 spike protein.J Extracell Biol2022
33300982Prioritizing genes for systematic variant effect mapping.Bioinformatics2021
34861178Improved pathogenicity prediction for rare human missense variants.Am J Hum Genet2021
34551312Improved pathogenicity prediction for rare human missense variants.Am J Hum Genet2021
34214447Shifting landscapes of human MTHFR missense-variant effects.Am J Hum Genet2021
34293323Seeds of their own destruction: Dominant-negative peptide screening yields functional insight and therapeutic leads.Cell Syst2021
32251504MaveQuest: a web resource for planning experimental tests of human variant effects.Bioinformatics2020
32000841A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase.Genome Med2020
31668799Highly Combinatorial Genetic Interaction Analysis Reveals a Multi-Drug Transporter Influence Network.Cell Syst2020
33060198Interrogation of kinase genetic interactions provides a global view of PAK1-mediated signal transduction pathways.J Biol Chem2020
32939983Systematic analysis of bypass suppression of essential genes.Mol Syst Biol2020
32763951A Comprehensive, Flexible Collection of SARS-CoV-2 Coding Regions.G3 (Bethesda)2020
32870157Multiplexed measurement of variant abundance and activity reveals VKOR topology, active site and human variant impact.Elife2020
32392905Yeast-Based Genetic Interaction Analysis of Human Kinome.Cells2020
32203420Systems analysis of RhoGEF and RhoGAP regulatory proteins reveals spatially organized RAC1 signalling from integrin adhesions.Nat Cell Biol2020
32296183A reference map of the human binary protein interactome.Nature2020
30649215A web application and service for imputing and visualizing missense variant effect maps.Bioinformatics2019
31679514MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect.Genome Biol2019
31344031Quantifying immune-based counterselection of somatic mutations.PLoS Genet2019
31283071Assessing predictions on fitness effects of missense variants in calmodulin.Hum Mutat2019
31105571Characterizing ABC-Transporter Substrate-Likeness Using a Clean-Slate Genetic Background.Front Pharmacol2019
30747104<i>CNTN5</i><sup>-</sup><i><sup>/+</sup></i>or <i>EHMT2</i><sup>-</sup><i><sup>/+</sup></i>human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networks.Elife2019
30006486The Impact of Oncogenic EGFRvIII on the Proteome of Extracellular Vesicles Released from Glioblastoma Cells.Mol Cell Proteomics2018
29807908Mapping DNA damage-dependent genetic interactions in yeast via party mating and barcode fusion genetics.Mol Syst Biol2018
30073413Multiplexed assays of variant effects contribute to a growing genotype-phenotype atlas.Hum Genet2018
30150706Modeling the impact of drug interactions on therapeutic selectivity.Nat Commun2018
27994090A common class of transcripts with 5'-intron depletion, distinct early coding sequence features, and <i>N</i><sup>1</sup>-methyladenosine modification.RNA2017
28346509Systematic identification of phosphorylation-mediated protein interaction switches.PLoS Comput Biol2017
29269382A framework for exhaustively mapping functional missense variants.Mol Syst Biol2017
29163459CRISPR/Cas9 System as a Valuable Genome Editing Tool for Wine Yeasts with Application to Decrease Urea Production.Front Microbiol2017
28542158Identifying pathogenicity of human variants via paralog-based yeast complementation.PLoS Genet2017
28886340Variant Interpretation: Functional Assays to the Rescue.Am J Hum Genet2017
28705884Quantitative analysis of protein interaction network dynamics in yeast.Mol Syst Biol2017
28596290Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target.Genome Res2017
28817247Assessing predictions of fitness effects of missense mutations in SUMO-conjugating enzyme UBE2I.Hum Mutat2017
26871637Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.Cell2016
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Collaborators

Blavatnik Institute, Harvard Medical School
Co-authored papers 37
Harvard Medical School
Co-authored papers 13
University of Toronto
Co-authored papers 12
University of Toronto
Co-authored papers 11
Preclinical and Translational Sciences, Inc.
Co-authored papers 11
Weill Institute for Cell and Molecular Biology, Cornell University
Co-authored papers 10
University of Toronto
Co-authored papers 10
Harvard Medical School
Co-authored papers 10
Co-authored papers 9
Institucio Catalana de Recerca i Estudis Avancats (ICREA)
Co-authored papers 9
Co-authored papers 8
Network Science Institute, Northeastern University
Co-authored papers 8
University of Colorado at Boulder
Co-authored papers 8
Harvard Medical School
Co-authored papers 8
The University of British Columbia
Co-authored papers 7
Co-authored papers 7
College of Information Engineering, Zhejiang University of Technology
Co-authored papers 6
University of Pittsburgh School of Medicine.
Co-authored papers 6
Co-authored papers 6
Co-authored papers 6
University Bordeaux, CNRS
Co-authored papers 6
Institute of Biostatistics, Fudan University
Co-authored papers 6
Lunenfeld-Tanenbaum Research Institute
Co-authored papers 6
Livestrong Cancer Institutes, Dell Medical School, The University of Texas at Austin
Co-authored papers 6
University of Washington, USA Brotman Baty Institute for Precision Medicine
Co-authored papers 5
Co-authored papers 5
University of Minnesota - Twin Cities
Co-authored papers 5
Co-authored papers 5
Co-authored papers 5
The University of Texas MD Anderson Cancer Center
Co-authored papers 5