Patrice Roll

Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions

Hsien-Yang Lee, Yong Huang, Nadine Bruneau et al. · Cell Reports · 2012 · 262 citations · Full text

SRPX2 mutations in disorders of language cortex and cognition

Patrice Roll, Gabrielle Rudolf, Sandrine Pereira et al. · Human Molecular Genetics · 2006 · 256 citations

Neurological Disorder, Neurolinguistics, Genetics +17

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex

Patrice Roll, Sonja C. Vernes, Nadine Bruneau et al. · Human Molecular Genetics · 2010 · 114 citations · Full text

Genetics, Gene Regulatory Network, Social Sciences +19

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR

Barbara Royer-Zemmour, Magali Ponsole-Lenfant, Hyam Gara et al. · Human Molecular Genetics · 2008 · 113 citations · Full text

Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex

Sarah Jamali, Fabrice Bartoloméi, Andrée Robaglia‐Schlupp et al. · Brain · 2006 · 99 citations · Full text

Neuropsychology, Neurotransmission, Entorhinal Cortex +22