Patricia N. Tonin

Montreal, QC H3A0C7, Canada

Last Updated: 09/26/2026

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Found 47 publications

ATM c.7374_7375insAlu is a French-Canadian founder pathogenic variant associated with predisposition to pancreatic and breast cancer.

ATM c.7374_7375insAlu is a French-Canadian founder pathogenic variant associated with predisposition to pancreatic and breast cancer.

Journal: Journal of medical genetics

Published: December 31, 2025

The Genetic and Molecular Analyses of Rare Candidate Germline BRIP1/FANCJ Variants Implicated in Hereditary Breast and Ovarian Cancers.

The Genetic and Molecular Analyses of Rare Candidate Germline BRIP1/FANCJ Variants Implicated in Hereditary Breast and Ovarian Cancers.

Journal: International journal of molecular sciences

Published: October 03, 2025

Co-occurring rare germline DNA repair gene variants in BRCA1/BRCA2 implicated hereditary breast cancer families.

Co-occurring rare germline DNA repair gene variants in BRCA1/BRCA2 implicated hereditary breast cancer families.

Journal: NPJ breast cancer

Published: June 23, 2025

Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene.

Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene.

Journal: Genes

Published: December 01, 2022

Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.

Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.

Journal: Frontiers in oncology

Published: November 29, 2022

Single-cell DNA sequencing-a potential dosimetric tool.

Single-cell DNA sequencing-a potential dosimetric tool.

Journal: Radiation protection dosimetry

Published: July 28, 2022

The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population.

The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population.

Journal: Cancers

Published: March 18, 2022

Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1 and BRCA2 Variants.

Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1 and BRCA2 Variants.

Journal: Genes

Published: March 08, 2022

The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families.

The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families.

Journal: Cancers

Published: May 19, 2021

Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families.

Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families.

Journal: NPJ breast cancer

Published: February 12, 2021

Candidate Markers of Olaparib Response from Genomic Data Analyses of Human Cancer Cell Lines.

Candidate Markers of Olaparib Response from Genomic Data Analyses of Human Cancer Cell Lines.

Journal: Cancers

Published: January 31, 2021

Investigating the causal role of MRE11A p.E506* in breast and ovarian cancer.

Investigating the causal role of MRE11A p.E506* in breast and ovarian cancer.

Journal: Scientific reports

Published: September 30, 2020

Showing 1-12 of 47

Last Updated: 09/26/2026