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  • Education

    Call for applications 2021 MD, PharmD, VetD-PhD Program Imagine Institute

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    Laboratoires de recherche
    Sigolène Meilhac
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    Imagine is certified as Institut Carnot

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    Pass on all or part of your estate to research for the benefit of sick children

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    Let's speed up the diagnosis of genetic diseases

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    Teddy Riner supports Imagine in a national fundraising campaign

  • Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders.

    Vincent Cantagrel

    Source :

    Am. J. Hum. Genet.

    2020 Feb 28

    Pmid / DOI:

    32109419

  • Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance.

    Valérie Malan

    Source :

    Eur. J. Hum. Genet.

    2019 Feb 21

    Pmid / DOI:

    29483668

  • AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability.

    Patrick Nitschké, Karine Siquier

    Source :

    Nat Commun

    2018 Dec 11

    Pmid / DOI:

    28675162

  • Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival

    Lydie Burglen

    Source :

    Genet Med.

    Pmid / DOI:

    32103185

  • Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.

    Edor Kabashi

    Source :

    Hum. Mutat.

    2019 Dec 24

    Pmid / DOI:

    31513310