Tanja Obermeier

Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies

H. Mefford, U. Stephani, A. Franke, 2014, Epilepsy Research.

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.

C. Baker, H. Mefford, E. Eichler, 2010, Brain : a journal of neurology.

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.

I. Scheffer, H. Mefford, E. Eichler, 2009, Human molecular genetics.

Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome

H. Mefford, E. Eichler, U. Stephani, 2011, Epilepsia.