Kolexia
Caron Olivier Génétique médicale
Caron Olivier
Génétique médicale
Gustave-Roussy
Villejuif, France
205 Activités
602 Followers
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{{person.topmesh1.name}} Tumeurs du sein Prédisposition génétique à une maladie Tumeurs de l'ovaire Carcinomes Tumeurs colorectales héréditaires sans polypose Tumeurs colorectales Syndrome de Li-Fraumeni Néphrocarcinome Syndromes néoplasiques héréditaires

Collaborateurs

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Stoppa-Lyonnet Dominique
Stoppa-Lyonnet Dominique
Clcc Institut Curie, Paris, France
Nogues Catherine
Nogues Catherine
Centre Paoli-Calmettes, Marseille, France
Lasset Christine
Lasset Christine
Centre Léon-Bérard, Lyon, France
Frebourg Thierry
Frebourg Thierry
Hôpital Charles Nicolle, Rouen, France

Industries

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A+A
48 collaboration(s)
Dernière en 2022
MSD
2 collaboration(s)
Dernière en 2022
Janssen
2 collaboration(s)
Dernière en 2022
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Dernières activités

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COVAR: Study of Family COsegregation of Nucleotide VARiants in the Panel of Genes to Validate Their Use in Genetic Counseling
Essai Clinique (Institut Curie)   16 janvier 2024
Hereditary and familial forms of pancreatic adenocarcinoma: Genetic determinism, patients eligible for systematic screening, screening methods and results.
Bulletin du cancer   19 décembre 2023
1734P Early impact of a personalized lung cancer interception program for heavy smokers
Abstract Book of the ESMO Congress 2023, 20 - 24 October 2023.   01 octobre 2023
Features of colorectal adenomas among young patients with Lynch syndrome according to path_MMR: Results from the PRED-IdF registry.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver   25 septembre 2023
Cancer : une prévention sur-mesure pour les personnes à risque
Essentiel Santé Magazine   07 juillet 2023
TUMOSPEC: Investigation of Tumour Spectrum, Penetrance and Clinical Utility of Germline Mutations in New Breast and Ovarian Cancer Susceptibility Genes.
Essai Clinique (Unicancer)   10 mai 2023
163P Long-term assessment of secondary malignancies (2ndM) in women with breast cancer (BC) and germline TP53 mutations (gTP53m) treated with radiation therapy (RT)
Abstract Book of ESMO Breast Cancer 2023, Berlin, Germany, 11-13 May 2023   01 mai 2023
Short and long read targeted RNAseq approaches to detect complex abnormalities for cancer susceptibility genes
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference   01 mai 2023
171MO Inflammatory profiling of individuals with germline TP53 mutations (gTP53m) and its relationship to subsequent cancer development
Abstract Book of ESMO Breast Cancer 2023, Berlin, Germany, 11-13 May 2023   01 mai 2023
172P Early impact of a personalised cancer interception programme for women at non-genetic high risk of breast cancer (BC)
Abstract Book of ESMO Breast Cancer 2023, Berlin, Germany, 11-13 May 2023   01 mai 2023