Colas Chrystelle

Colas Chrystelle

Génétique médicale

Clcc Institut Curie
Paris, France

166 Activités

160 Followers

Scientifique

Digital

Production scientifique

Activités par an

Expertise

Sujets de recherche

Prédisposition génétique à une maladie Tumeurs colorectales Tumeurs du sein Tumeurs colorectales héréditaires sans polypose Polypose adénomateuse colique Tumeurs de l'ovaire Tumeurs du cerveau Instabilité des microsatellites Syndromes néoplasiques héréditaires

Collaborateurs

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Coulet Florence

Hôpital Pitie Salpetriere, Paris, France

Stoppa-Lyonnet Dominique

Clcc Institut Curie, Paris, France

Clcc Institut Curie, Paris, France

Clcc Institut Curie, Paris, France

Industries

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AstraZeneca

9 collaboration(s)

Dernière en 2023

Amgen

3 collaboration(s)

Dernière en 2022

PUBLICLIN

2 collaboration(s)

Dernière en 2022

Pfizer

2 collaboration(s)

Dernière en 2021

Dernières activités

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Cerebral dural arteriovenous fistulas in patients with PTEN-related hamartoma tumor syndrome.

Clinical genetics 29 février 2024

Adaptive Nanopore Sequencing as a preeminent tool to elucidate structural variants in cancer predisposition genes

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

Cancer prognosis in PTEN Hamartoma Tumor Syndrome - a European cohort study

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

CTNNA1 germline variants with a premature termination codon are a risk factor for development of early-onset Diffuse Gastric Cancer

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

Lifestyle factors and breast cancer risk in females with PTEN Hamartoma Tumor Syndrome

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

Mismatch repair deficiency and Lynch syndrome among 1225 adult patients with glioma

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

Adaptive Nanopore sequencing to determine pathogenicity of BRCA1 exonic duplication

Abstracts from the 56th European Society of Human Genetics (ESHG) Conference 01 janvier 2024

PHYTOCHEMICAL STUDY OF BIOACTIVE PLANTS CULTIVATED IN CENTRE-VAL DE LOIRE, FRANCE

International journal of cosmetic science Congress 2023 12 décembre 2023

HAIRY ROOT CULTURES OF POPLAR: A POTENTIAL SOURCE OF COSMECEUTICALS

International journal of cosmetic science Congress 2023 12 décembre 2023