Kolexia
Mortemousque Isabelle
Génétique médicale
Centre hospitalier de Tours
Tours, France
39 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Tumeurs du sein Prédisposition génétique à une maladie Déficience intellectuelle Syndrome de Down Syndrome héréditaire de cancer du sein et de l'ovaire Tumeurs de l'ovaire Maladies génétiques liées au chromosome X Syndromes néoplasiques héréditaires Tumeurs de l'utérus

Industries

AstraZeneca
8 collaboration(s)
Dernière en 2023
Lilly
1 collaboration(s)
Dernière en 2020
Pfizer
1 collaboration(s)
Dernière en 2020
{{person.topindus4.name}}
{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

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
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
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Breast cancer research : BCR   03 août 2021
Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
International journal of cancer   09 janvier 2021
Women at Risk of Breast Cancer and OLFM4: Evaluation of the Circulating Concentration of Olfactomédine 4 (OLFM4) in Women With a BRCA1 or 2 Gene Mutation or at High Risk of Developing Breast Cancer, According to the Imaging
Essai Clinique (Institut Cancerologie de l'Ouest)   23 mars 2020
of DICER1 syndrome: a retrospective study of 204 analyses
Abstracts from the 50th European Society of Human Genetics Conference   01 juillet 2019
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
International journal of cancer   13 novembre 2018
GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in and Pathogenic Variant Carriers.
Frontiers in oncology   31 octobre 2018
New insight in ARX-mutated patients' language specific impairment and underlying FOXP1 dysregulation
Abstracts of EPNS 2017 - 12th European Paediatric Neurology Society Congress   01 juin 2017
A Novel Analog Reasoning Paradigm: New Insights in Intellectually Disabled Patients.
PloS one   26 février 2016