Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
2020 · Nature Genetics · 551 citations
https://doi.org/10.1038/s41588-020-0609-2
M
Michael T. Parsons
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Michael T. Parsons is an academic researcher from Lunenfeld-Tanenbaum Research Institute. The author has contributed to research in topics: BRCA gene mutations in cancer & Genomics and Rare Diseases & Cancer Genomics and Diagnostics. The author has an h-index of 43, co-authored 153 publications.
ORCID: 0000-0003-3242-8477Papers by this author
worksMutational spectrum in a worldwide study of 29,700 families with<i>BRCA1</i>or<i>BRCA2</i>mutations
2018 · Human Mutation · 305 citations
https://doi.org/10.1002/humu.23406
Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls
2018 · Nature Communications · 261 citations
https://doi.org/10.1038/s41467-018-06581-8
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup
2023 · The American Journal of Human Genetics · 254 citations
https://doi.org/10.1016/j.ajhg.2023.06.002
Expansion of Cancer Risk Profile for <i>BRCA1</i> and <i>BRCA2</i> Pathogenic Variants
2022 · JAMA Oncology · 187 citations
https://doi.org/10.1001/jamaoncol.2022.0476
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
2020 · Nature Genetics · 186 citations
https://doi.org/10.1038/s41588-019-0537-1
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