Scherer SW

References (7)

Title : De Novo Genome and Transcriptome Assembly of the Canadian Beaver (Castor canadensis) - Lok_2017_G3.(Bethesda)_7_755
Author(s) : Lok S , Paton TA , Wang Z , Kaur G , Walker S , Yuen RK , Sung WW , Whitney J , Buchanan JA , Trost B , Singh N , Apresto B , Chen N , Coole M , Dawson TJ , Ho K , Hu Z , Pullenayegum S , Samler K , Shipstone A , Tsoi F , Wang T , Pereira SL , Rostami P , Ryan CA , Tong AH , Ng K , Sundaravadanam Y , Simpson JT , Lim BK , Engstrom MD , Dutton CJ , Kerr KC , Franke M , Rapley W , Wintle RF , Scherer SW
Ref : G3 (Bethesda) , 7 :755 , 2017
PubMedID: 28087693
Gene_locus related to this paper: cascn-a0a250y2s0 , cascn-a0a250y135 , cascn-a0a250y1i6 , cascn-a0a250y2u8 , cascn-a0a250xy53 , ursma-a0a384cw87 , cascn-a0a250y6h8

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
PubMedID: 27759917

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
PubMedID: 24643514

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
PubMedID: 23393157

Title : Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands - Vincent_2004_Am.J.Med.Genet.B.Neuropsychiatr.Genet_129B_82
Author(s) : Vincent JB , Kolozsvari D , Roberts WS , Bolton PF , Gurling HM , Scherer SW
Ref : American Journal of Medicine Genet B Neuropsychiatr Genet , 129B :82 , 2004
PubMedID: 15274046

Title : Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32 - Nakabayashi_2002_Hum.Mol.Genet_11_1743
Author(s) : Nakabayashi K , Bentley L , Hitchins MP , Mitsuya K , Meguro M , Minagawa S , Bamforth JS , Stanier P , Preece M , Weksberg R , Oshimura M , Moore GE , Scherer SW
Ref : Hum Mol Genet , 11 :1743 , 2002
PubMedID: 12095916
Gene_locus related to this paper: mouse-MEST

Title : Comparative analysis of the gene-dense ACHE\/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5 - Wilson_2001_Nucleic.Acids.Res_29_1352
Author(s) : Wilson MD , Riemer C , Martindale DW , Schnupf P , Boright AP , Cheung TL , Hardy DM , Schwartz S , Scherer SW , Tsui LC , Miller W , Koop BF
Ref : Nucleic Acids Research , 29 :1352 , 2001
PubMedID: 11239002
Gene_locus related to this paper: human-ACHE , mouse-ACHE