Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas

Alix de La Coste, Béatrice Romagnolo, Pierre Billuart, +8

Proceedings of the National Academy of Sciences

A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

Vincent des Portes, Jean Marc Pinard, Pierre Billuart, +11

Cell

Neurobiology Of DiseaseDevelopmental BiologyNeurogenomicsNeurological DisorderNeuroanatomy +11

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

Pierre Billuart, T Bienvenu, Nathalie Ronce, +14

Nature

Developmental BiologyMolecular NeuroscienceSignal TransductionPsychiatryGenetics +5

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hao Hu, Stefan A. Haas, Jamel Chelly, +81

Molecular Psychiatry

A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation

Ramzi Zemni, Thierry Bienvenu, Marie Claude Vinet, +23

Nature Genetics

Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics +10

Regulating Axon Branch Stability

Pierre Billuart, Christopher Winter, Alison Maresh, +2

Cell

Molecular PhysiologyDevelopmental BiologyCytoskeletonFunctional RegulationAxon Branch Stability +4

Loss of X-Linked Mental Retardation Gene Oligophrenin1 in Mice Impairs Spatial Memory and Leads to Ventricular Enlargement and Dendritic Spine Immaturity

Malik Khelfaoui, Cécile V. Denis, Elly van Galen, +10

Journal of Neuroscience

A Postsynaptic Signaling Pathway that May Account for the Cognitive Defect Due to IL1RAPL1 Mutation

Alice Pavlowsky, Antonella Gianfelice, Marta Pallotto, +16

Current Biology

NeuropsychologySynaptic TransmissionPostsynaptic Signaling PathwaySynaptic SignalingSocial Sciences +14

Astrocytes close the mouse critical period for visual plasticity

Jérôme Ribot, Rachel Breton, Charles‐Félix Calvo, +13

Science

Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia

Ginevra Zanni, Yoann Saillour, Majdi Nagara, +11

Neurology