Bonnet-Brilhault F

References (3)

Title : Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level - Daoud_2009_Biol.Psychiatry_66_906
Author(s) : Daoud H , Bonnet-Brilhault F , Vedrine S , Demattei MV , Vourc'h P , Bayou N , Andres CR , Barthelemy C , Laumonnier F , Briault S
Ref : Biological Psychiatry , 66 :906 , 2009
PubMedID: 19545860

Title : X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family - Laumonnier_2004_Am.J.Hum.Genet_74_552
Author(s) : Laumonnier F , Bonnet-Brilhault F , Gomot M , Blanc R , David A , Moizard MP , Raynaud M , Ronce N , Lemonnier E , Calvas P , Laudier B , Chelly J , Fryns JP , Ropers HH , Hamel BC , Andres C , Barthelemy C , Moraine C , Briault S
Ref : American Journal of Human Genetics , 74 :552 , 2004
PubMedID: 14963808
Gene_locus related to this paper: human-NLGN4X

Title : The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit - Raux_2002_Mol.Psychiatry_7_1006
Author(s) : Raux G , Bonnet-Brilhault F , Louchart S , Houy E , Gantier R , Levillain D , Allio G , Haouzir S , Petit M , Martinez M , Frebourg T , Thibaut F , Campion D
Ref : Mol Psychiatry , 7 :1006 , 2002
PubMedID: 12399955