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International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|May 20, 2017
Clinicopathologic Characteristics of Endometrial Cancer in Lynch Syndrome: A French Multicenter StudyLéa Rossi, Marie-Aude Le Frere-Belda, Pierre Laurent-Puig, et al.JAMA Ophthalmology|April 30, 2026
Prevalence of the Predisposing Gene MBD4 for Uveal MelanomaAnaïs Le Ven, Marie-Charlotte Villy, Marine Le Mentec, et al.Cancers|August 2, 2019
Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic ContinuumCeres Fernandez-Rozadilla, Miriam Alvarez-Barona, Esther Schamschula, et al.Clinical Epigenetics|July 3, 2025
Methylation-sensitive high-resolution melting technology is a simple and sensitive method to detect germline epimutation of the MLH1 gene promoterHélène Delhomelle, Olfa Trabelsi-Grati, Marie-Charlotte Villy, et al.Journal of Medical Genetics|October 21, 2022
APC germline pathogenic variants and epithelial ovarian cancer: causal or coincidental findings?Roseline Vibert, Jessica Le Gall, Bruno Buecher, et al.Ophthalmology Science|December 11, 2025
Genetic Background Predicts Uveal Melanoma Patients' OutcomesThibault Verrier, Anaïs Le Ven, Alexandre Houy, et al.Gastric Cancer : Official Journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association|December 6, 2018
Clinical implications of CTNNA1 germline mutations in asymptomatic carriersPatrick R Benusiglio, Chrystelle Colas, Erell Guillerm, et al.European Journal of Medical Genetics|October 11, 2020
National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tractMarion Dhooge, Stéphanie Baert-Desurmont, Carole Corsini, et al.Neuro-Oncology Advances|July 10, 2020
Constitutional mismatch repair deficiency-associated brain tumors: report from the European C4CMMRD consortiumLéa Guerrini-Rousseau, Pascale Varlet, Chrystelle Colas, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 14, 2020
Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriersRobert Blatter, Benjamin Tschupp, Stefan Aretz, et al.Pageof 12