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European Journal of Cancer (Oxford, England : 1990)|May 11, 2021
Response to systemic therapy in fumarate hydratase-deficient renal cell carcinomaLucia Carril-Ajuria, Emeline Colomba, Luigi Cerbone, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|September 27, 2023
Features of colorectal adenomas among young patients with Lynch syndrome according to path_MMR: Results from the PRED-IdF registryHadrien Alric, Elise Coffin, Celine Lekhal, et al.
Human Mutation|May 18, 2026
<i>MLH1</i> 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.
Journal of Medical Genetics|April 26, 2015
A germline mutation in PBRM1 predisposes to renal cell carcinomaPatrick R Benusiglio, Sophie Couvé, Brigitte Gilbert-Dussardier, 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.
Genes, Chromosomes & Cancer|December 11, 2022
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancerJulie Leclerc, Marie Beaumont, Roseline Vibert, et al.
JCO Precision Oncology|June 1, 2023
Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With GliomaPatrick R Benusiglio, Fikret Elder, Mehdi Touat, et al.
Annals of Surgery|July 20, 2022
Management of Pathogenic CDH1 Variant Carriers Within the FREGAT Network: A Multicentric Retrospective StudyCapucine Bres, Thibault Voron, Leonor Benhaim, et al.
Cancer Research|November 6, 2014
Genetic evidence of a precisely tuned dysregulation in the hypoxia signaling pathway during oncogenesisSophie Couvé, Charline Ladroue, Elodie Laine, et al.
Journal of Medical Genetics|June 29, 2022
Cancer risk and tumour spectrum in 172 patients with a germline <i>SUFU</i> pathogenic variation: a collaborative study of the SIOPE Host Genome Working GroupLéa Guerrini-Rousseau, Julien Masliah-Planchon, Sebastian M Waszak, et al.
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