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| Title : Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability - Mittal_2016_J.Hum.Genet_61_867 |
| Author(s) : Mittal K , Rafiq MA , Rafiullah R , Harripaul R , Ali H , Ayaz M , Aslam M , Naeem F , Amin-Ud-Din M , Waqas A , So J , Rappold GA , Vincent JB , Ayub M |
| Ref : J Hum Genet , 61 :867 , 2016 |
| Abstract : Mittal_2016_J.Hum.Genet_61_867 |
| ESTHER : Mittal_2016_J.Hum.Genet_61_867 |
| PubMedSearch : Mittal_2016_J.Hum.Genet_61_867 |
| PubMedID: 27305979 |
| Gene_locus related to this paper: human-TG |
| 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 : Egger_2014_Neurogenetics_15_117 |
| ESTHER : Egger_2014_Neurogenetics_15_117 |
| PubMedSearch : Egger_2014_Neurogenetics_15_117 |
| PubMedID: 24643514 |
| Title : Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder - |
| Author(s) : Mikhailov A , Fennell A , Plong-on O , Sripo T , Hansakunachai T , Roongpraiwan R , Sombuntham T , Ruangdaraganon N , Vincent JB , Limprasert P |
| Ref : Psychiatr Genet , 24 :42 , 2014 |
| PubMedID: 24362370 |
| 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 : 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 |
| Abstract : Vincent_2004_Am.J.Med.Genet.B.Neuropsychiatr.Genet_129B_82 |
| ESTHER : Vincent_2004_Am.J.Med.Genet.B.Neuropsychiatr.Genet_129B_82 |
| PubMedSearch : Vincent_2004_Am.J.Med.Genet.B.Neuropsychiatr.Genet_129B_82 |
| PubMedID: 15274046 |