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CTNND2-a candidate gene for reading problems and mild intellectual disability.
Hofmeister W, Nilsson D, Topa A, Anderlid BM, Darki F, Matsson H, Tapia Páez I, Klingberg T, Samuelsson L, Wirta V, Vezzi F, Kere J, Nordenskjöld M, Syk Lundberg E, Lindstrand A. Hofmeister W, et al. Among authors: kere j. J Med Genet. 2015 Feb;52(2):111-22. doi: 10.1136/jmedgenet-2014-102757. Epub 2014 Dec 3. J Med Genet. 2015. PMID: 25473103
Two translocations of chromosome 15q associated with dyslexia.
Nopola-Hemmi J, Taipale M, Haltia T, Lehesjoki AE, Voutilainen A, Kere J. Nopola-Hemmi J, et al. Among authors: kere j. J Med Genet. 2000 Oct;37(10):771-5. doi: 10.1136/jmg.37.10.771. J Med Genet. 2000. PMID: 11015455 Free PMC article.
A dominant gene for developmental dyslexia on chromosome 3.
Nopola-Hemmi J, Myllyluoma B, Haltia T, Taipale M, Ollikainen V, Ahonen T, Voutilainen A, Kere J, Widén E. Nopola-Hemmi J, et al. Among authors: kere j. J Med Genet. 2001 Oct;38(10):658-64. doi: 10.1136/jmg.38.10.658. J Med Genet. 2001. PMID: 11584043 Free PMC article.
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Peyrard-Janvid M, Anthoni H, Onkamo P, Lahermo P, Zucchelli M, Kaminen N, Hannula-Jouppi K, Nopola-Hemmi J, Voutilainen A, Lyytinen H, Kere J. Peyrard-Janvid M, et al. Among authors: kere j. Hum Genet. 2004 Apr;114(5):510-6. doi: 10.1007/s00439-004-1103-0. Epub 2004 Mar 6. Hum Genet. 2004. PMID: 15007729
Global analysis of uniparental disomy using high density genotyping arrays.
Bruce S, Leinonen R, Lindgren CM, Kivinen K, Dahlman-Wright K, Lipsanen-Nyman M, Hannula-Jouppi K, Kere J. Bruce S, et al. Among authors: kere j. J Med Genet. 2005 Nov;42(11):847-51. doi: 10.1136/jmg.2005.032367. Epub 2005 May 6. J Med Genet. 2005. PMID: 15879501 Free PMC article.
608 results