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Bryony A Thompson

Showing results (31-40 of 45) with videos related to

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International Journal of Cancer|June 4, 2017
Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysisGardenia M Vargas-Parra, Maribel González-Acosta, Bryony A Thompson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndromeMark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
Human Mutation|September 6, 2012
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutionsBryony A Thompson, Marc S Greenblatt, Maxime P Vallee, et al.
Journal of Medical Genetics|January 5, 2023
Optimising clinical care through <i>CDH1</i>-specific germline variant curation: improvement of clinical assertions and updated curation guidelinesXi Luo, Jamie L Maciaszek, Bryony A Thompson, et al.
Cancers|July 9, 2020
Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like IndividualsEstela Dámaso, Maribel González-Acosta, Gardenia Vargas-Parra, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 11, 2013
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testingDaniel D Buchanan, Yen Y Tan, Michael D Walsh, et al.
Cancers|July 24, 2021
Genomic Risk Prediction for Breast Cancer in Older WomenPaul Lacaze, Andrew Bakshi, Moeen Riaz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 2, 2020
Medically actionable pathogenic variants in a population of 13,131 healthy elderly individualsPaul Lacaze, Robert Sebra, Moeen Riaz, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2025
Scalable automated reanalysis of genomic data in research and clinical rare disease cohortsMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
Nature Medicine|June 24, 2026
Automated reanalysis of genomic data for rare disease diagnostics at scaleMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
International Journal of Cancer|June 4, 2017
Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysisGardenia M Vargas-Parra, Maribel González-Acosta, Bryony A Thompson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndromeMark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
Human Mutation|September 6, 2012
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutionsBryony A Thompson, Marc S Greenblatt, Maxime P Vallee, et al.
Journal of Medical Genetics|January 5, 2023
Optimising clinical care through <i>CDH1</i>-specific germline variant curation: improvement of clinical assertions and updated curation guidelinesXi Luo, Jamie L Maciaszek, Bryony A Thompson, et al.
Cancers|July 9, 2020
Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like IndividualsEstela Dámaso, Maribel González-Acosta, Gardenia Vargas-Parra, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 11, 2013
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testingDaniel D Buchanan, Yen Y Tan, Michael D Walsh, et al.
Cancers|July 24, 2021
Genomic Risk Prediction for Breast Cancer in Older WomenPaul Lacaze, Andrew Bakshi, Moeen Riaz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 2, 2020
Medically actionable pathogenic variants in a population of 13,131 healthy elderly individualsPaul Lacaze, Robert Sebra, Moeen Riaz, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2025
Scalable automated reanalysis of genomic data in research and clinical rare disease cohortsMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
Nature Medicine|June 24, 2026
Automated reanalysis of genomic data for rare disease diagnostics at scaleMatthew J Welland, K D Ahlquist, Paul De Fazio, et al.
Pageof 5