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144 results found for your search

  • Research Acceleration

    Evaluation of an innovative support programme for young patients with rare genetic epilepsies

  • Research Acceleration

    Deciphering the genetic origin of language development disorders in children without intellectual disabilities, autism or apraxia of speech

  • Research Acceleration

    Jean-Laurent Casanova’s pioneering genetic discoveries earn him the 2025 Novo Nordisk Prize

  • Research Acceleration

    A genetic cause of an inherited bone marrow failure identified

  • Research Acceleration

    Enhanced bone repair with FGFR antagonists in a model of hypochondroplasia

  • Striking picture

    Research Acceleration

    Notch3, a new player in heart development and asymmetry

  • Drépanocytose

    Research Acceleration

    Sickle cell disease: gene therapy efficacy depends on degree of host inflammation

  • Research Acceleration

    A new MEDopathy caused by biallelic mutations of MED16

  • institutimagine_jean-laurent-casanova_portrait

    Research Acceleration

      Portrait

    Jean-Laurent Casanova: And if infectious diseases were in fact (also) genetic diseases?

  • Maia et sa mère

    Research Acceleration

      Portrait

    KCNB1 association: coming together in the face of disease

  • mickael-menager-portrait-blouse

    Research Acceleration

      Portrait

    Mickaël Ménager: thinking about the medicine of tomorrow

  • alainfischer_institutimagine_collegedefrance

    Research Acceleration

      Portrait

    Alain Fischer, doctor-researcher at heart and the first director of Imagine