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| Title : Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures - Lionel_2013_Hum.Mol.Genet_22_2055 |
| Author(s) : Lionel AC , Vaags AK , Sato D , Gazzellone MJ , Mitchell EB , Chen HY , Costain G , Walker S , Egger G , Thiruvahindrapuram B , Merico D , Prasad A , Anagnostou E , Fombonne E , Zwaigenbaum L , Roberts W , Szatmari P , Fernandez BA , Georgieva L , Brzustowicz LM , Roetzer K , Kaschnitz W , Vincent JB , Windpassinger C , Marshall CR , Trifiletti RR , Kirmani S , Kirov G , Petek E , Hodge JC , Bassett AS , Scherer SW |
| Ref : Hum Mol Genet , 22 :2055 , 2013 |
| Abstract : Lionel_2013_Hum.Mol.Genet_22_2055 |
| ESTHER : Lionel_2013_Hum.Mol.Genet_22_2055 |
| PubMedSearch : Lionel_2013_Hum.Mol.Genet_22_2055 |
| PubMedID: 23393157 |
| 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 : Gauthier_2011_Hum.Genet_130_563 |
| ESTHER : Gauthier_2011_Hum.Genet_130_563 |
| PubMedSearch : Gauthier_2011_Hum.Genet_130_563 |
| PubMedID: 21424692 |
| 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 : Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74 |
| ESTHER : Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74 |
| PubMedSearch : Gauthier_2005_Am.J.Med.Genet.B.Neuropsychiatr.Genet_132B_74 |
| PubMedID: 15389766 |
| Gene_locus related to this paper: human-NLGN4X |