Annick Massacrier

SRPX2 mutations in disorders of language cortex and cognition

Patrice Roll, Gabrielle Rudolf, Sandrine Pereira et al. · Human Molecular Genetics · 2006 · 257 citations

Life Sciences, Genetics, Neuroscience +17

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Philippe Jay, Claire Rougeulle, Annick Massacrier et al. · Nature Genetics · 1997 · 245 citations

Life Sciences, Genetics, Molecular Genetics +9

A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene

Fabienne Schaller, Françoise Watrin, Rachel Sturny et al. · Human Molecular Genetics · 2010 · 233 citations · Full text

Life Sciences, Developmental Biology, Neuroscience +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 · 115 citations · Full text

Life Sciences, Genetics, Neuroscience +16

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

Life Sciences, Molecular Biology, Neuroscience +16