High impact projects funded

EPITHYR-ONENA

Identifying genetic risk factors of differentiated thyroid cancer in Oceanians of Non-European, Non-Asian Descent (ONENA) by whole genome sequencing and low pass sequencing

Therese Truong and Florent de Vathaire
Exposome and Heredity/ Epidemiology of Radiations CESP-Gustave Roussy , Villejuif

MITOCHONGEVITY

Association of germline variants, somatic mutations and DNA methylation of the mitochondrial genome to human longevity

Alexandre How Kit
Fondation Jean Dausset - CEPH, Paris

CHIKGENE

Genotyping of patients from La Réunion island by low coverage sequencing and imputation for search of
new variants associated with long-term Chikungunya manifestations

Jean-François Zagury
GBCM, Conservatoire National des Arts et Métiers, Paris

DIVA

Diversity, community replacement, and perturbations in the vaginal microbiota

Samuel ALIZON
CIRB, UMR CNRS 7241- INSERM U1050 - Collège de France, Paris

CAT-SEQ

Molecular characterization offelinelow grade alimentary lymphoma, a spontaneous animal model of human indolent T-cell lymphoproliferative disorder of the gastrointestinal tract

Lucile Couronné
Unité INSERM-Intitut Imagine Paris

GENTAUMIX

GENomic and Transcriptomic Analysis of Undiagnosed Myalgia Induced by eXercise

Fabrice Rannou
Physiology Department- CHRU Cavale Blanche Brest

Mitral Valve-Seq

A sequencing-based genome-wide association study on Mitral Valve Disease

Jean-Jacques Schott
Inserm-Institut du Thorax Nantes

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