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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, Nicod J, Xiong L, Joober R, Enard W, Krinsky B, Nanba E, Richardson AJ, Riley BP, Martin NG, Strittmatter SM, Möller HJ, Rujescu D, St Clair D, Muglia P, Roos JL, Fisher SE, Wade-Martins R, Rouleau GA, Stein JF, Karayiorgou M, Geschwind DH, Ragoussis J, Kendler KS, Airaksinen MS, Oshimura M, DeLisi LE, Monaco AP. Francks C, et al. Among authors: monaco ap. Mol Psychiatry. 2007 Dec;12(12):1129-39, 1057. doi: 10.1038/sj.mp.4002053. Epub 2007 Jul 31. Mol Psychiatry. 2007. PMID: 17667961 Free PMC article.
Covering YAC-cloned DNA with phages and cosmids.
Ragoussis J, Monaco AP. Ragoussis J, et al. Among authors: monaco ap. Methods Mol Biol. 1996;54:157-66. doi: 10.1385/0-89603-313-9:157. Methods Mol Biol. 1996. PMID: 8597788 No abstract available.
Autism: recent molecular genetic advances.
Lamb JA, Moore J, Bailey A, Monaco AP. Lamb JA, et al. Among authors: monaco ap. Hum Mol Genet. 2000 Apr 12;9(6):861-8. doi: 10.1093/hmg/9.6.861. Hum Mol Genet. 2000. PMID: 10767308 Review.
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP. Lai CS, et al. Among authors: monaco ap. Am J Hum Genet. 2000 Aug;67(2):357-68. doi: 10.1086/303011. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10880297 Free PMC article.
706 results