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Clinical Service
Prof. Damien SANLAVILLE, PU-PH, attached to Julien Courchet’s team at the INMG-PGNM, is Head of the Genetics Department at the Woman-Mother-Child Hospital (HFME) (https://www.chu-lyon.fr/fr/service-de-genetique ) at the Lyon East Hospital Group. Its department hosts two national reference centres, labelled within the framework of the Rare Diseases Plan: Reference Centre for Developmental Anomalies and Malformative Syndromes South-East and Reference Centre for Rendu-Osler Disease. Pr Gaëtan LESCA, MCU-PH and Dr Caroline SCHLUTH-BOLARD, MCU-PH, work in the Genetics Department of the HFME hospital, and are attached to Julien Courchet’s team within the INMG-PGNM.
Prof. Damien SANLAVILLE is in charge of the AURAGEN very high throughput genome sequencing platform: this programme mainly concerns cancer patients for whom new therapeutic strategies and in particular targeted therapies can be proposed according to the variations identified (https://www.chu-lyon.fr/fr/auragen-plateforme-de-sequencage-du-genome-tres-haut-debit ). This very high throughput sequencing makes it possible to observe genetic variations that may be at the origin of cancers or other rare diseases.