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Merico D

References (2)

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