ANRS CO22 HEPATHER

Therapeutic options for hepatitis B and C: a French cohort

BANCCO+

A CNV database to reduce diagnostic wandering, identify new genes, and expand our knowledge of the human genome

• Genetics/Heredity
• Rare diseases
• Families

CDE.ai

Using Artificial Intelligence to create minimum data sets for rare diseases

CKD-REIN

Cohort of patients with chronic kidney disease

• Chronic diseases
• Adults

COBLANCE

Bladder Cancer Research Cohort

CONSTANCES

Cohort of health examination center consultants

E3N-Générations

Epidemiological study with E3N women and their families

ELFE

French Longitudinal Study from Childhood.

EPIPAGE 2

Epidemiological study on young gestational ages

FACE.S-4-KIDS

A deep-phenotyping database using artificial intelligence to study craniofacial anomalies during development

• Rare diseases
• Genetics/Heredity
• Families

FG-CoALS

Franco-German cohort study on factors associated with weight loss in amyotrophic lateral sclerosis (ALS)

• Rare diseases
• Adults

HOPE-EPI / CCOP

Childhood Cancer Observation Platform

MARIANNE

National cohort dedicated to research on the biological and environmental determinants of autism and neurodevelopmental disorders

MITOMICS

Mitochondrial Disease database: An integrated multi-OMICS approach

PAMPERO

Towards personalized medicine in a rare genetic vascular disease: Rendu-Osler disease

• Genetics/Heredity
• Rare diseases
• Families

PROGRESS FSHD

Remote assessment and artificial intelligence to validate new measures, biomarkers, and therapeutic targets for facioscapulohumeral muscular dystrophy (FSHD)

• Rare diseases
• Databases

PSY-COH

French cohort of patients suffering from bipolar disorder or schizophrenia

RaDiCo

Rare Disease Cohort Program

• Families
• Genetics/Heredity
• Rare diseases

RaDiCo - ECYSCO

European cystinosis cohort: new biomarkers and new therapeutic approaches

• Genetics/Heredity
• Rare diseases
• Families

RASores

Preclinical approaches for the treatment of RASopathy patients through a multi-omic study of their pathophysiology using a deeply phenotyped cohort in a dedicated European registry

• Rare diseases
• Databases
• Genetics/Heredity