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Michael Silk · SciRah

Researcher profile · Semantic Scholar

Michael Silk

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Michael Silk — researcher profile on SciRah

h-index: 8
Works: 15
Citations: 488

Most-cited papers

Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation
Josh Traynelis, Michael Silk, Quan-Li Wang, S. Berkovic +4 more
2017Genome Research170 citations Open access
Semantic Scholar
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction
J. Hildebrand, Maria Kauppi, I. Majewski, Zi-Kou Liu +66 more
2020Nature Communications77 citations Open access
Semantic Scholar
MTR-Viewer: identifying regions within genes under purifying selection
Michael Silk, S. Petrovski, D. Ascher
2019Nucleic Acids Res.63 citations Open access
Semantic Scholar
Exploring the structural distribution of genetic variation in SARS-CoV-2 with the COVID-3D online resource
Stephanie Portelli, M. Olshansky, Carlos H. M. Rodrigues, Elston N. D'souza +5 more
2020Nature Genetics56 citations Open access
Semantic Scholar
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome.
Sarah E. M. Stephenson, G. Costain, Laura E R Blok, Michael Silk +100 more
2022American Journal of Human Genetics38 citations Open access
Semantic Scholar
MTR3D: identifying regions within protein tertiary structures under purifying selection
Michael Silk, Douglas E. V. Pires, Carlos H. M. Rodrigues, Elston N. D'souza +3 more
2021Nucleic Acids Res.25 citations Open access
Semantic Scholar
EasyVS: a user-friendly web-based tool for molecule library selection and structure-based virtual screening
Douglas E. V. Pires, Wandré N P Veloso, Yoochan Myung, Carlos H. M. Rodrigues +7 more
2020Bioinform.22 citations Open access
Semantic Scholar
COVID-3D: An online resource to explore the structural distribution of genetic variation in SARS-CoV-2 and its implication on therapeutic development
Stephanie Portelli, M. Olshansky, Carlos H. M. Rodrigues, Elston N. D'souza +5 more
2020bioRxiv8 citations Open access
Semantic Scholar
MTR3D‐AF2: Expanding the coverage of spatially derived missense tolerance scores across the human proteome using AlphaFold2
Aaron S. Kovacs, Stephanie Portelli, Michael Silk, Carlos H. M. Rodrigues +1 more
2024Protein Science6 citations Open access
Semantic Scholar
Polymorphic tandem repeats influence cell type-specific gene expression across the human immune landscape
H. Tanudisastro, Anna S. E. Cuomo, B. Weisburd, M. Welland +54 more
2025bioRxiv5 citations Open access
Semantic Scholar
Identifying Genotype-Phenotype Correlations via Integrative Mutation Analysis
E. Airey, Stephanie Portelli, Joicymara S. Xavier, Yoochan Myung +12 more
2021Artificial Neural Networks, 3rd Edition5 citations
Semantic Scholar
Author Correction: Exploring the structural distribution of genetic variation in SARS-CoV-2 with the COVID-3D online resource
Stephanie Portelli, M. Olshansky, Carlos H. M. Rodrigues, D +6 more
2021Nature Genetics4 citations Open access
Semantic Scholar
Missense mutations in the MLKL ‘brace’ region lead to lethal neonatal inflammation in mice and are present in high frequency in humans
J. Hildebrand, Maria Kauppi, I. Majewski, Zi-Kou Liu +61 more
2019bioRxiv4 citations
Semantic Scholar
A Comprehensive Computational Platform to Guide Drug Development Using Graph-Based Signature Methods.
Douglas E. V. Pires, Stephanie Portelli, Pâmela M. Rezende, Wandré N P Veloso +7 more
2020Methods in molecular biology3 citations
Semantic Scholar
Insights from Spatial Measures of Intolerance to Identifying Pathogenic Variants in Developmental and Epileptic Encephalopathies
Michael Silk, A. D. de Sá, M. Olshansky, David B. Ascher
2021bioRxiv2 citations Open access
Semantic Scholar

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