A genetic cause of an inherited bone marrow failure identified Read more about A genetic cause of an inherited bone marrow failure identified
Jean-Laurent Casanova’s pioneering genetic discoveries earn him the 2025 Novo Nordisk Prize Read more about Jean-Laurent Casanova’s pioneering genetic discoveries earn him the 2025 Novo Nordisk Prize
Deciphering the genetic origin of language development disorders in children without intellectual disabilities, autism or apraxia of speech Read more about Deciphering the genetic origin of language development disorders in children without intellectual disabilities, autism or apraxia of speech
Evaluation of an innovative support programme for young patients with rare genetic epilepsies Read more about Evaluation of an innovative support programme for young patients with rare genetic epilepsies
Calls for Junior Group Leader at Institut Imagine Read more about Calls for Junior Group Leader at Institut Imagine
Amyotrophic lateral sclerosis: a defect in autophagy responsible for the disease Read more about Amyotrophic lateral sclerosis: a defect in autophagy responsible for the disease
Incontinentia Pigmenti, a rare skin disease that also predisposes to viral infections Read more about Incontinentia Pigmenti, a rare skin disease that also predisposes to viral infections
The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million Read more about The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million
The first inherited TNF deficiency in human underlies susceptibility to tuberculosis Read more about The first inherited TNF deficiency in human underlies susceptibility to tuberculosis
Innov4-ePiK: Innovative diagnostic and therapeutic approaches in potassium channel developmental and epileptic encephalopathies (K-DEEs) using 4P for medicine. Read more about Innov4-ePiK: Innovative diagnostic and therapeutic approaches in potassium channel developmental and epileptic encephalopathies (K-DEEs) using 4P for medicine.
