The regulation of genetic information is an essential mechanism for the survival of an organism. I have dedicated my research work to the study of the molecular mechanisms that govern genetic expression and the establishment of the epigenome in a healthy and pathological context, and more particularly now in the context of rare diseases.

Mini CV :

Since 2021 : Permanent researcher INSERM

2020-2021 : Project Manager Nomenclature maladies Rare, Banque Nationale des Données Maladies Rares, APHP, Paris BNDMR

2015-2020 : Post-doc @UMR7216 Epigenetics and cell fate and @Institut Cochin, Paris

2011-2014 : Post-doc @ULB, Free University of Brussels, Belgium

2006-2010 : Thesis, CEA Saclay, Gif-sur-Yvette PhD

Research projects :

1. Epigenetics and growth disorders: A better epigenomic description and molecular understanding of rare growth pathologies to improve diagnosis for patients.
2. iPS and rare diseases: A new dynamic tool to better understand the molecular mechanisms involved during the development of a rare growth pathology.
3. Autoantibodies and autoimmune diseases: Use of existing data to improve the description and understanding of autoimmune diseases and associated clinical signs (MAKAAO Project: MApping elements of Knowledge about Autoimmune disease, Auto antibodies and other clinical signs).

Keywords :

Epigenetics, pluripotent stem cells, rare diseases, epigenomics, diagnosis, ChIP-seq, EPIC array, iPS cells.

Useful links :

Researchgate

ORCID