| Title : Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia - Gauthier_2011_Hum.Genet_130_563 |
| Author(s) : Gauthier J , Siddiqui TJ , Huashan P , Yokomaku D , Hamdan FF , Champagne N , Lapointe M , Spiegelman D , Noreau A , Lafreniere RG , Fathalli F , Joober R , Krebs MO , DeLisi LE , Mottron L , Fombonne E , Michaud JL , Drapeau P , Carbonetto S , Craig AM , Rouleau GA |
| Ref : Hum Genet , 130 :563 , 2011 |
| Abstract : |
| PubMedSearch : Gauthier_2011_Hum.Genet_130_563 |
| PubMedID: 21424692 |
| Title : De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia - Gauthier_2010_Proc.Natl.Acad.Sci.U.S.A_107_7863 |
| Author(s) : Gauthier J , Champagne N , Lafreniere RG , Xiong L , Spiegelman D , Brustein E , Lapointe M , Peng H , Cote M , Noreau A , Hamdan FF , Addington AM , Rapoport JL , DeLisi LE , Krebs MO , Joober R , Fathalli F , Mouaffak F , Haghighi AP , Neri C , Dube MP , Samuels ME , Marineau C , Stone EA , Awadalla P , Barker PA , Carbonetto S , Drapeau P , Rouleau GA |
| Ref : Proc Natl Acad Sci U S A , 107 :7863 , 2010 |
| Abstract : |
| PubMedSearch : Gauthier_2010_Proc.Natl.Acad.Sci.U.S.A_107_7863 |
| PubMedID: 20385823 |
| Title : Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis - Daoud_2010_Amyotroph.Lateral.Scler_11_389 |
| Author(s) : Daoud H , Valdmanis PN , Dion PA , Rouleau GA |
| Ref : Amyotroph Lateral Scler , 11 :389 , 2010 |
| Abstract : |
| PubMedSearch : Daoud_2010_Amyotroph.Lateral.Scler_11_389 |
| PubMedID: 20001489 |
| Title : NLGN3\/NLGN4 gene mutations are not responsible for autism in the Quebec population - Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74 |
| Author(s) : Gauthier J , Bonnel A , St-Onge J , Karemera L , Laurent S , Mottron L , Fombonne E , Joober R , Rouleau GA |
| Ref : American Journal of Medicine Genet B Neuropsychiatr Genet , 132B :74 , 2005 |
| Abstract : |
| PubMedSearch : Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74 |
| PubMedID: 15389766 |
| Gene_locus related to this paper: human-NLGN4X |