Kolexia
Maugard Christine Génétique médicale
Maugard Christine
Génétique médicale
Hôpital Hautepierre
Strasbourg, France
54 Activités
289 Followers
Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Tumeurs du sein Prédisposition génétique à une maladie Carcinomes Tumeurs de l'ovaire Néphrocarcinome Tumeurs du rein Syndromes néoplasiques héréditaires Polypose adénomateuse colique Instabilité des microsatellites

Collaborateurs

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Stoppa-Lyonnet Dominique
Stoppa-Lyonnet Dominique
Clcc Institut Curie, Paris, France
Caron Olivier
Caron Olivier
Gustave-Roussy, Villejuif, France
Bonadona Valerie
Bonadona Valerie
Centre Léon-Bérard, Lyon, France
Lasset Christine
Lasset Christine
Centre Léon-Bérard, Lyon, France

Industries

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AstraZeneca
6 collaboration(s)
Dernière en 2022
MSD
3 collaboration(s)
Dernière en 2023
GSK
2 collaboration(s)
Dernière en 2020
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{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

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
French college of gynecologists and obstetricians (CNGOF) recommendations for clinical practice: Place of breast self-examination in screening strategies
Breast (Edinburgh, Scotland)   03 janvier 2024
Place of breast self-examination in screening strategies. French College of Gynecologists and Obstetricians (CNGOF) recommendations for clinical practice.
Gynecologie, obstetrique, fertilite & senologie   29 août 2023
Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease.
European journal of cancer (Oxford, England : 1990)   13 novembre 2022
A novel germline pathogenic variant MET c.3389T>C p.(Leu1130Ser) identified in french population
Abstracts from the 54th European Society of Human Genetics (ESHG) Conference   01 avril 2022
Specific phenotype of germline MET mutations in papillary renal cell carcinoma type 1: about a large french series of 158 patients
Abstracts from the 54th European Society of Human Genetics (ESHG) Conference   01 avril 2022
Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type I.
Human mutation   19 janvier 2022
Techniques and complications of non-genetic risk reducing mastectomies: Guidelines of the National College of French Gynecologists and Obstetricians (CNGOF).
Gynecologie, obstetrique, fertilite & senologie   16 décembre 2021
Non-genetic indications for risk reducing mastectomies: Guidelines of the National College of French Gynecologists and Obstetricians (CNGOF).
Gynecologie, obstetrique, fertilite & senologie   14 décembre 2021
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
American journal of human genetics   30 septembre 2021