Human Genetic

Contribution to decipher cancer heredity

Brigitte BRESSAC-de PAILLERETS et Daniel GAUTHERET
Institut Gustave Roussy – Villejuif

Identification of molecular events associated to metastatic progression of multifocal prostate cancer

Olivier CUSSENOT
Oncotype-URO, UPMC, Paris

The French Exome Project: a federative resource for the analysis of next-generation sequencing data

Emmanuelle GENIN
INSERM UMR 1078, Brest

Identification of genes responsible for monogenic frms of juvenile onset insuline dependent diabetes

Thierry ROUXEL
INRA Bioger, Grignon

Identification of innovative therapeutictargets due to aberrant splicing in msi gastrointestinal tumours

Alex DUVAL
UMRS 938, Hôpital Saint-Antoine, Paris

Integrating sequenced, genotyped and imputed data to unveil the genetic architecture of Parkinson’s diseaseris

Maria MARTINEZ
INSERM UMR 1043, Hôpital Purpan, Toulouse

Myocapture : novel genes for myopathies

Jocelyn LAPORTE
IGBMC U964, UMR7104, Université de Strasbourg

Analysis of clonal evolution of neuroblastoma by whole-genome sequencing

Gudrun SCHLEIERMACHER

From splice sequencing to drug

Marc PECHANSKI
I-Stem, UMR 861 INSERM / UEVE, Evry

Deep RNA-sequencing to assess novel therapeutics in human disease muscle cells

Denis FURLING
INSERM, UMR7215 CNRS – G.H. Pitié-Salpêtrière - Paris