High impact projects funded

FCD-Genomics

Large scale genomic, expression and epigenetic studies to better understand Genetic, molecular and cellular pathology of focal cortical dysplasia (FCD)

Jamel Chelly
IGBMC Strasbourg

ALLOGENOMICS

Whole exome sequencing inlivingDonor/Recipient kidney transplants

Laurent Mesnard
INSERM-IMR 1155-Hôpital Tenon Paris

HeHCC

Deciphering the heterogeneous genome-microenvironment interplay in hepatocellular carcinomas

Jessica Zucman-Rossi
INSERM U1162 Paris

K-Rare

Contribution of rare variants to kidney cancer genetic susceptibility Génétique Humaine

Estelle Chanudet
INSERM U1162 Paris

MARIO

Genomic characterisation of metastatic breast cancers

Fabrice Andre
INSERM-Gustave Roussy Villejuif

CIMP-DRIVE

Discovery of noncoding genetic drivers implicated in the aggressive CpG-island methylator phenotype(CIMP)in adrenocortical carcinom

Valentina Boeva
Institute Cochin-INSERM-Université Paris Descartes Paris

ALPS WGS + RNA-Seq

Comprehensive genomicand transcriptional characterization of the Autoimmune Lymphoproliferative Syndrome (ALPS): Whole Genome Sequencing and RNA-seq profiling of a representative panel offamilies withclinical incomplete penetrance

Antonio Rausell
Imagine Institute Paris

GeniLuc

Genomic analysis of inherited lung cancer

James McKay
IARC-Lyon Génétique Humaine

DISSEQT

Identify genetic determinants of the risk of drug-induced cardiac arrhythmiasby sequencing subjects with extreme phenotypes

Jean-Sébastien Hulot
Faculté de Médecine- Pitié- Salpêtrière UPMC-Paris

C-METAGENO

Combining METagenomic And GENomics in severe Obesity

Karine Clément
AP-HP-Faculté de Médecine Pitié - Salpêtrière UPMC-Paris

SIREN

Signatures of environmental exposures and lifestyle factors associated with renal cancers in European populations

Ghislaine Scélo
IARC-Lyon

HeartGenomics

The genomics of congenital heart malformation

Stanislas Lyonnet
University Paris Descartes INSERM -Hôpital Universitaire Necker- Enfants Malades-Paris

Brugada-Seq

A sequencing-based genome-wide association study on Brugada syndrome

Richard Redon
INSERM-Nantes

GePeLiN

Integrated GenomicAnalysis of Pediatric Hepatocellular Tumors

Jessica Zucman-Rossi
INSERM-Paris

CYNOMAGENVIR

Characterization of cynomolgus macaque genetic variability in the context of viral infections

Roger LE GRAND
IDMIT Infrastructure- Paris

Phaeoexplorer

Exploring the evolution of biological complexity in the brown algae through the establishment of a multi-scale genomic data resource

Mark J. Cock
CNRS / UPMC-Station Biologique de Roscoff