| Title : Implication of LRRC4C and DPP6 in neurodevelopmental disorders - Maussion_2017_Am.J.Med.Genet.A_173_395 |
| Author(s) : Maussion G , Cruceanu C , Rosenfeld JA , Bell SC , Jollant F , Szatkiewicz J , Collins RL , Hanscom C , Kolobova I , de Champfleur NM , Blumenthal I , Chiang C , Ota V , Hultman C , O'Dushlaine C , McCarroll S , Alda M , Jacquemont S , Ordulu Z , Marshall CR , Carter MT , Shaffer LG , Sklar P , Girirajan S , Morton CC , Gusella JF , Turecki G , Stavropoulos DJ , Sullivan PF , Scherer SW , Talkowski ME , Ernst C |
| Ref : American Journal of Medicine Genet A , 173 :395 , 2017 |
| Abstract : |
| PubMedSearch : Maussion_2017_Am.J.Med.Genet.A_173_395 |
| PubMedID: 27759917 |
| Gene_locus related to this paper: human-DPP6 |
| Title : Donepezil enhances understanding of degraded speech in Alzheimer's disease - Hardy_2017_Ann.Clin.Transl.Neurol_4_835 |
| Author(s) : Hardy CJD , Hwang YT , Bond RL , Marshall CR , Ridha BH , Crutch SJ , Rossor MN , Warren JD |
| Ref : Ann Clin Transl Neurol , 4 :835 , 2017 |
| Abstract : |
| PubMedSearch : Hardy_2017_Ann.Clin.Transl.Neurol_4_835 |
| PubMedID: 29159197 |
| Title : Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families - Egger_2014_Neurogenetics_15_117 |
| Author(s) : Egger G , Roetzer KM , Noor A , Lionel AC , Mahmood H , Schwarzbraun T , Boright O , Mikhailov A , Marshall CR , Windpassinger C , Petek E , Scherer SW , Kaschnitz W , Vincent JB |
| Ref : Neurogenetics , 15 :117 , 2014 |
| Abstract : |
| PubMedSearch : Egger_2014_Neurogenetics_15_117 |
| PubMedID: 24643514 |
| Title : Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing - Jiang_2013_Am.J.Hum.Genet_93_249 |
| Author(s) : Jiang YH , Yuen RK , Jin X , Wang M , Chen N , Wu X , Ju J , Mei J , Shi Y , He M , Wang G , Liang J , Wang Z , Cao D , Carter MT , Chrysler C , Drmic IE , Howe JL , Lau L , Marshall CR , Merico D , Nalpathamkalam T , Thiruvahindrapuram B , Thompson A , Uddin M , Walker S , Luo J , Anagnostou E , Zwaigenbaum L , Ring RH , Wang J , Lajonchere C , Shih A , Szatmari P , Yang H , Dawson G , Li Y , Scherer SW |
| Ref : American Journal of Human Genetics , 93 :249 , 2013 |
| Abstract : |
| PubMedSearch : Jiang_2013_Am.J.Hum.Genet_93_249 |
| PubMedID: 23849776 |
| Gene_locus related to this paper: human-NLGN3 |
| 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 : |
| PubMedSearch : Lionel_2013_Hum.Mol.Genet_22_2055 |
| PubMedID: 23393157 |