Geoffrey Bertolone
Publications by Year
Research Areas
BRCA gene mutations in cancer, Genetic factors in colorectal cancer, Genomics and Rare Diseases, DNA Repair Mechanisms, Cancer Genomics and Diagnostics
Most-Cited Works
- → Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus(2016)94 cited
- → Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature(2018)54 cited
- → The transfer of multigene panel testing for hereditary breast and ovarian cancer to healthcare: What are the implications for the management of patients and families?(2016)46 cited
- → Incidental findings in a series of 2500 gene panel tests for a genetic predisposition to cancer: Results and impact on patients(2021)11 cited
- → A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers(2021)7 cited
- → Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study)(2024)3 cited
- → Patient satisfaction, experience and preferences in the implementation of genetics teleconsultations in the North-eastern region of France(2023)2 cited
- → The “extreme phenotype approach” applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles(2023)1 cited
- → Advancing precision oncology through systematic germline and tumor genetic analysis: The oncogenetic point of view on findings from a prospective multicenter clinical trial of 666 patients(2023)1 cited