Genetics of mental retardation & cortical malformations

Our team

• About us...
• Composition
• Recent publications

Mental retardation

• Introduction
• Positional cloning
• Our work

Rett syndrome

• Introduction
• Clinical signs
• MeCP2 mutations
• Phenotypes
• Our work / Network

Cortical malformations

• Introduction
• Polymicrogyria
• Heterotopia
• Lissencephaly
• Classification
• Genetic causes
• Our work

Epilepsy

• The project
• Our work
• Call for collaboration

To read in march...

- Neuronal migration mechanisms in development and disease.

- A novel sex determination system in a close relative of the house mouse.

- Nup153 and megator define transcriptionally active regions in the Drosophila genome.

Composition of our team

Laurent VILLARD

Research scientist (DR2 / Professor), Inserm - Group leader

Publications / E-mail

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Jean-Christophe ROUX

Research scientist (CR1 / Assistant Professor), Inserm

Publications / E-mail

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Cécile MIGNON-RAVIX

Engineer, University

Publications / E-mail

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Nicole PHILIP

MD, Professor

Publications / E-mail

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Anne MONCLA

MD, Professor

Publications / E-mail

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Chantal MISSIRIAN

MD

Publications / E-mail

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Mathieu MILH

MD, PhD

Publications / E-mail

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Cornel POPOVICI

MD, PhD

Publications / E-mail

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Pierre CACCIAGLI

Technician, Marseille University Hospital

Publications / E-mail

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Ana BORGES

Assistant Engineer, Inserm

Publications / E-mail

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Adeline SPIGA

Assistant Engineer, Inserm

Publications / E-mail

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Nicolas PANAYOTIS

PhD student (october 2008 - october 2011)

Publications / E-mail

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Bilal EL WALY

PhD student (october 2009 - october 2012)

Publications / E-mail

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