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Annales De Pathologie|February 13, 2020
[Clinical Cancer Genetics: A guide for the pathologist]Noémie Basset, Camille Desseignés, Christilla Boucher, et al.
European Journal of Human Genetics : EJHG|July 18, 2020
Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspringErell Guillerm, Magali Svrcek, Armelle Bardier-Dupas, et al.
European Journal of Human Genetics : EJHG|March 18, 2025
Pathogenic germline variants in patients with early-onset colorectal cancer according to phenotypeAntoine Dardenne, Marion Dhooge, Noémie Basset, et al.
European Journal of Human Genetics : EJHG|March 12, 2022
Detection of a pathogenic Alu element insertion in PALB2 gene from targeted NGS diagnostic dataMélanie Eyries, Olivier Ariste, Gaelle Legrand, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 24, 2020
Everolimus and Octreotide for Patients with Recurrent Meningioma: Results from the Phase II CEVOREM TrialThomas Graillon, Marc Sanson, Chantal Campello, et al.
European Journal of Human Genetics : EJHG|April 23, 2023
Lynch syndrome: influence of additional susceptibility variants on cancer riskRoseline Vibert, Jasmine Hasnaoui, Alexandre Perrier, et al.
Human Mutation|May 18, 2026
MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation LevelCédric Facon, Catherine Vermaut, Lucie Delattre, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 27, 2023
Validation of the Clinical Use of GIScar, an Academic-developed Genomic Instability Score Predicting Sensitivity to Maintenance Olaparib for Ovarian CancerRaphaël Leman, Etienne Muller, Angelina Legros, et al.
International Journal of Cancer|June 12, 2025
Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratoriesEdwige Kasper, Flavie Boulouard, Noémie Basset, et al.
American Journal of Human Genetics|October 1, 2021
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approachSandrine M Caputo, Lisa Golmard, Mélanie Léone, et al.
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