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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, Loturco J, Monaco AP. Paracchini S, et al. Hum Mol Genet. 2006 May 15;15(10):1659-66. doi: 10.1093/hmg/ddl089. Epub 2006 Apr 6. Hum Mol Genet. 2006. PMID: 16600991
Impaired dopamine release in Parkinson's disease.
Cramb KML, Beccano-Kelly D, Cragg SJ, Wade-Martins R. Cramb KML, et al. Brain. 2023 Aug 1;146(8):3117-3132. doi: 10.1093/brain/awad064. Brain. 2023. PMID: 36864664 Free PMC article. Review.
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. 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.
175 results