Publications by authors named "Nadia Bahi"

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Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).
Karine Poirier, David A Keays, Fiona Francis, Yoann Saillour, Nadia Bahi

Hum Mutat· November 2007

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IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongation.
Frédéric Gambino, Alice Pavlowsky, Aurélie Béglé, Jean-Luc Dupont, Nadia Bahi

Proc Natl Acad Sci U S A· May 2007

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Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes.
Gaëlle Friocourt, Caroline Kappeler, Yoann Saillour, Fabien Fauchereau, Manuel S Rodriguez, Nadia Bahi

Mol Cell Neurosci· January 2005

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High prevalence of SLC6A8 deficiency in X-linked mental retardation.
Efraim H Rosenberg, Ligia S Almeida, Tjitske Kleefstra, Rose S deGrauw, Helger G Yntema, Nadia Bahi

Am J Hum Genet· July 2004

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Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons.
Karine Poirier, Hilde Van Esch, Gaëlle Friocourt, Yoann Saillour, Nadia Bahi

Brain Res Mol Brain Res· March 2004

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Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin-1 gene.
Vincent des Portes, Nathalie Boddaert, Silvia Sacco, Sylvain Briault, Kim Maincent, Nadia Bahi

Am J Med Genet A· February 2004

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IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis.
Nadia Bahi, Gaelle Friocourt, Alain Carrié, Margaret E Graham, Jamie L Weiss

Hum Mol Genet· June 2003

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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.
Thierry Bienvenu, Karine Poirier, Gaelle Friocourt, Nadia Bahi, Delphine Beaumont

Hum Mol Genet· April 2002

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