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| Title : Genome-wide copy number variation analysis in attention-deficit\/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree - Lesch_2011_Mol.Psychiatry_16_491 |
| Author(s) : Lesch KP , Selch S , Renner TJ , Jacob C , Nguyen TT , Hahn T , Romanos M , Walitza S , Shoichet S , Dempfle A , Heine M , Boreatti-Hummer A , Romanos J , Gross-Lesch S , Zerlaut H , Wultsch T , Heinzel S , Fassnacht M , Fallgatter A , Allolio B , Schafer H , Warnke A , Reif A , Ropers HH , Ullmann R |
| Ref : Mol Psychiatry , 16 :491 , 2011 |
| Abstract : Lesch_2011_Mol.Psychiatry_16_491 |
| ESTHER : Lesch_2011_Mol.Psychiatry_16_491 |
| PubMedSearch : Lesch_2011_Mol.Psychiatry_16_491 |
| PubMedID: 20308990 |
| Title : X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family - Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| Author(s) : Laumonnier F , Bonnet-Brilhault F , Gomot M , Blanc R , David A , Moizard MP , Raynaud M , Ronce N , Lemonnier E , Calvas P , Laudier B , Chelly J , Fryns JP , Ropers HH , Hamel BC , Andres C , Barthelemy C , Moraine C , Briault S |
| Ref : American Journal of Human Genetics , 74 :552 , 2004 |
| Abstract : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| ESTHER : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| PubMedSearch : Laumonnier_2004_Am.J.Hum.Genet_74_552 |
| PubMedID: 14963808 |
| Gene_locus related to this paper: human-NLGN4X |
| Title : Molecular cloning and characterization of the Fugu rubripes MEST\/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis - Brunner_2000_Chromosome.Res_8_465 |
| Author(s) : Brunner B , Grutzner F , Yaspo ML , Ropers HH , Haaf T , Kalscheuer VM |
| Ref : Chromosome Res , 8 :465 , 2000 |
| Abstract : Brunner_2000_Chromosome.Res_8_465 |
| ESTHER : Brunner_2000_Chromosome.Res_8_465 |
| PubMedSearch : Brunner_2000_Chromosome.Res_8_465 |
| PubMedID: 11032317 |
| Gene_locus related to this paper: fugru-MEST |
| Title : Evidence against a major role of PEG1\/MEST in Silver-Russell syndrome - Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| Author(s) : Riesewijk AM , Blagitko N , Schinzel AA , Hu L , Schulz U , Hamel BC , Ropers HH , Kalscheuer VM |
| Ref : Eur J Hum Genet , 6 :114 , 1998 |
| Abstract : Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| ESTHER : Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| PubMedSearch : Riesewijk_1998_Eur.J.Hum.Genet_6_114 |
| PubMedID: 9781054 |
| Title : Monoallelic expression of human PEG1\/MEST is paralleled by parent-specific methylation in fetuses - Riesewijk_1997_Genomics_42_236 |
| Author(s) : Riesewijk AM , Hu L , Schulz U , Tariverdian G , Hoglund P , Kere J , Ropers HH , Kalscheuer VM |
| Ref : Genomics , 42 :236 , 1997 |
| Abstract : Riesewijk_1997_Genomics_42_236 |
| ESTHER : Riesewijk_1997_Genomics_42_236 |
| PubMedSearch : Riesewijk_1997_Genomics_42_236 |
| PubMedID: 9192843 |
| Gene_locus related to this paper: human-MEST |