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Author Details
Full Name
Frederick P Roth
Affiliation
University of Toronto
ORCID
Career Start Year
1998
Papers
158
H Index
63
Expertise
CM4AI Collaborator
Prashant Mali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36217029
A proteome-scale map of the SARS-CoV-2-human contactome.
Nat Biotechnol
2023
37478847
Genome-scale mapping of DNA damage suppressors through phenotypic CRISPR-Cas9 screens.
Mol Cell
2023
37729906
Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation.
Am J Hum Genet
2023
37394429
An Atlas of Variant Effects to understand the genome at nucleotide resolution.
Genome Biol
2023
37061542
Next-generation large-scale binary protein interaction network for Drosophila melanogaster.
Nat Commun
2023
37081510
satmut_utils: a simulation and variant calling package for multiplexed assays of variant effect.
Genome Biol
2023
37267226
A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection.
G3 (Bethesda)
2023
37426450
Minimum information and guidelines for reporting a Multiplexed Assay of Variant Effect.
ArXiv
2023
37292969
Characterizing glucokinase variant mechanisms using a multiplexed abundance assay.
bioRxiv
2023
36716194
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.
Circ Genom Precis Med
2023
36798224
Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation.
bioRxiv
2023
36732511
Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
Nat Commun
2023
36865234
Pacybara: Accurate long-read sequencing for barcoded mutagenized allelic libraries.
bioRxiv
2023
36055970
Scalable Functional Assays for the Interpretation of Human Genetic Variation.
Annu Rev Genet
2022
36710959
Quantitative proteomics and biological activity of extracellular vesicles engineered to express SARS-CoV-2 spike protein.
J Extracell Biol
2022
33300982
Prioritizing genes for systematic variant effect mapping.
Bioinformatics
2021
34861178
Improved pathogenicity prediction for rare human missense variants.
Am J Hum Genet
2021
34551312
Improved pathogenicity prediction for rare human missense variants.
Am J Hum Genet
2021
34214447
Shifting landscapes of human MTHFR missense-variant effects.
Am J Hum Genet
2021
34293323
Seeds of their own destruction: Dominant-negative peptide screening yields functional insight and therapeutic leads.
Cell Syst
2021
32251504
MaveQuest: a web resource for planning experimental tests of human variant effects.
Bioinformatics
2020
32000841
A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase.
Genome Med
2020
31668799
Highly Combinatorial Genetic Interaction Analysis Reveals a Multi-Drug Transporter Influence Network.
Cell Syst
2020
33060198
Interrogation of kinase genetic interactions provides a global view of PAK1-mediated signal transduction pathways.
J Biol Chem
2020
32939983
Systematic analysis of bypass suppression of essential genes.
Mol Syst Biol
2020
32763951
A Comprehensive, Flexible Collection of SARS-CoV-2 Coding Regions.
G3 (Bethesda)
2020
32870157
Multiplexed measurement of variant abundance and activity reveals VKOR topology, active site and human variant impact.
Elife
2020
32392905
Yeast-Based Genetic Interaction Analysis of Human Kinome.
Cells
2020
32203420
Systems analysis of RhoGEF and RhoGAP regulatory proteins reveals spatially organized RAC1 signalling from integrin adhesions.
Nat Cell Biol
2020
32296183
A reference map of the human binary protein interactome.
Nature
2020
30649215
A web application and service for imputing and visualizing missense variant effect maps.
Bioinformatics
2019
31679514
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect.
Genome Biol
2019
31344031
Quantifying immune-based counterselection of somatic mutations.
PLoS Genet
2019
31283071
Assessing predictions on fitness effects of missense variants in calmodulin.
Hum Mutat
2019
31105571
Characterizing ABC-Transporter Substrate-Likeness Using a Clean-Slate Genetic Background.
Front Pharmacol
2019
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.
Elife
2019
30006486
The Impact of Oncogenic EGFRvIII on the Proteome of Extracellular Vesicles Released from Glioblastoma Cells.
Mol Cell Proteomics
2018
29807908
Mapping DNA damage-dependent genetic interactions in yeast via party mating and barcode fusion genetics.
Mol Syst Biol
2018
30073413
Multiplexed assays of variant effects contribute to a growing genotype-phenotype atlas.
Hum Genet
2018
30150706
Modeling the impact of drug interactions on therapeutic selectivity.
Nat Commun
2018
27994090
A common class of transcripts with 5'-intron depletion, distinct early coding sequence features, and <i>N</i><sup>1</sup>-methyladenosine modification.
RNA
2017
28346509
Systematic identification of phosphorylation-mediated protein interaction switches.
PLoS Comput Biol
2017
29269382
A framework for exhaustively mapping functional missense variants.
Mol Syst Biol
2017
29163459
CRISPR/Cas9 System as a Valuable Genome Editing Tool for Wine Yeasts with Application to Decrease Urea Production.
Front Microbiol
2017
28542158
Identifying pathogenicity of human variants via paralog-based yeast complementation.
PLoS Genet
2017
28886340
Variant Interpretation: Functional Assays to the Rescue.
Am J Hum Genet
2017
28705884
Quantitative analysis of protein interaction network dynamics in yeast.
Mol Syst Biol
2017
28596290
Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target.
Genome Res
2017
28817247
Assessing predictions of fitness effects of missense mutations in SUMO-conjugating enzyme UBE2I.
Hum Mutat
2017
26871637
Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
Cell
2016
1 - 50 of 158
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University of Pittsburgh School of Medicine.
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