Publications and ressources

De novo monoallelic Reelin missense variants act in a dominant-negative manner causing neuronal migration disorders.

Martina Riva, Sofia Ferreira, Yoann Saillour, Vera Medvedeva, Frédéric Causeret, Nadia Bahi-Buisson, Alessandra Pierani

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Repurposing of the multiciliation gene regulatory network in fate specification of Cajal-Retzius neurons

Matthieu Moreau, Yoann Saillour, Vicente Elorriaga, Amaia OCHANDORENA SAA , Alessandra Pierani, Frédéric Causeret

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Diversity within olfactory sensory derivatives revealed by the contribution of Dbx1 lineages

Frédéric Causeret, Alessandra Pierani

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Aberrant survival of hippocampal Cajal-Retzius cells leads to memory deficits, gamma rhythmopathies and susceptibility to seizures in adult mice

Alessandra Pierani, Martina Riva, Patrick Azzam, Francesco Dori

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Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures

Nasim Ramezanidoraki, Driss EL-OUARDI, Nadia Bahi-Buisson, Alessandra Pierani, Pierre Billuart

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Functional characterization of RELN missense mutations involved in recessive and dominant forms of Neuronal Migration Disorders

Martina Riva, Sofia Ferreira, Vera Medvedeva, Frédéric Causeret, Nadia Bahi-Buisson, Alessandra Pierani

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Evolutionary Gain of Dbx1 Expression Drives Subplate Identity in the Cerebral Cortex.

Alessandra Pierani, Andrzej W Cwetsch, Yoann Saillour

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Activity-dependent death of transient Cajal-Retzius neurons is required for functional cortical wiring.

Alessandra Pierani, Martina Riva

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Developmental cell death regulates lineage-related interneuron-oligodendroglia functional clusters and oligodendrocyte homeostasis.

Alessandra Pierani

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Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics.

Nadia Bahi-Buisson

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Kremen1-induced cell death is regulated by homo- and heterodimerization.

Frédéric Causeret, Alessandra Pierani

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Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy.

Nadia Bahi-Buisson, Camille Maillard

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Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.

Lydie Burglen, Nadia Bahi-Buisson

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Extracellular Pax6 Regulates Tangential Cajal-Retzius Cell Migration in the Developing Mouse Neocortex.

Alessandra Pierani

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Mutations in TBR1 gene leads to cortical malformations and intellectual disability.

Nadia Bahi-Buisson, Camille Maillard

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