Kolexia
Cavaille Mathias Génétique médicale
Cavaille Mathias
Génétique médicale
Hôpital Gabriel Montpied
Clermont-Ferrand, France
29 Activités
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{{person.topmesh1.name}} Tumeurs du sein Tumeurs du sein triple-négatives Prédisposition génétique à une maladie Tumeurs de l'ovaire Carcinomes Néphrocarcinome Tumeurs colorectales Carcinogenèse Récidive tumorale locale

Collaborateurs

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Gay-Bellile Mathilde
Gay-Bellile Mathilde
Centre Jean-Perrin, Clermont-Ferrand, France
Bignon Yves-Jean
Bignon Yves-Jean
Centre Jean-Perrin, Clermont-Ferrand, France
Lepage Mathis
Lepage Mathis
Centre Jean-Perrin, Clermont-Ferrand, France
Durando Xavier
Durando Xavier
Centre Jean-Perrin, Clermont-Ferrand, France

Industries

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AstraZeneca
4 collaboration(s)
Dernière en 2023
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Dernières activités

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XenoBreast: A Prospective Study of Xenografts Development From Samples Taken From Surgical Specimens of Patients With Triple Negative or Luminal B Breast Cancer
Essai Clinique (Centre Jean-Perrin)   07 février 2024
Beyond MEN1, when to think about MEN4? Retrospective study on 5600 patients in the French population & literature review.
The Journal of clinical endocrinology and metabolism   30 janvier 2024
Familial uveal melanoma and other tumours in 25 families with monoallelic germline MBD4 variants.
Journal of the National Cancer Institute   07 décembre 2023
Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer.
Genes   25 octobre 2023
Case Series of 11 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature.
Genes   25 août 2023
Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature.
BMC medical genomics   13 juillet 2023
PERCEPTION Trial Protocol: Comparison of Predictive and Prognostic Capacities of Neutrophil, Lymphocyte and Platelet Counts and Tumour-infiltrating Lymphocytes in Triple Negative Breast Cancer
Essai Clinique (Centre Jean-Perrin)   07 février 2023
Rare duplication of the CDC73 gene and atypical hyperparathyroidism-jaw tumor syndrome: A case report and review of the literature.
Molecular genetics & genomic medicine   14 janvier 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
Proposal of new candidate genes of predisposition to serous ovarian cancer using whole-exome-sequencing of 16 patients with a familial form
Abstracts from the 54th European Society of Human Genetics (ESHG) Conference   01 avril 2022