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 august...

- Role of Olig1 and Olig2 in Down syndrome.

- TUBA1A mutations cause wide spectrum lissencephaly.

- Cell cloning-based transcriptome analysis in Rett patients.

Composition of our team

Laurent VILLARD

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

Publications / E-mail

---

Jean-Christophe ROUX

Research scientist (CR1 / Assistant Professor), Inserm

Publications / E-mail

---

Cécile MIGNON-RAVIX

Engineer, University

Publications / E-mail

---

Nicole PHILIP

MD, Professor

Publications / E-mail

---

Mathieu MILH

MD, PhD

Publications / E-mail

---

Cornel POPOVICI

MD, PhD

Publications / E-mail

---

Pierre CACCIAGLI

Technician, Marseille University Hospital

Publications / E-mail

---

Ana BORGES

Assistant Engineer, Inserm

Publications / E-mail

---

Adeline GHATA

Assistant Engineer, Inserm

Publications / E-mail

---

Nicolas PANAYOTIS

PhD student (october 2008 - october 2011)

Publications / E-mail

---

Bilal EL WALY

PhD student (october 2009 - october 2012)

Publications / E-mail

---