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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-Hemmi J, Schumacher J, Neuhoff N, Warnke A, Lyytinen H, Schulte-Körne G, Nöthen MM, Leppänen PH, Peyrard-Janvid M, Kere J. Matsson H, et al. Among authors: kere j. J Hum Genet. 2015 Jul;60(7):399-401. doi: 10.1038/jhg.2015.37. Epub 2015 Apr 16. J Hum Genet. 2015. PMID: 25877001 Free PMC article.
Data mining applied to linkage disequilibrium mapping.
Toivonen HT, Onkamo P, Vasko K, Ollikainen V, Sevon P, Mannila H, Herr M, Kere J. Toivonen HT, et al. Among authors: kere j. Am J Hum Genet. 2000 Jul;67(1):133-45. doi: 10.1086/302954. Epub 2000 Jun 9. Am J Hum Genet. 2000. PMID: 10848493 Free PMC article.
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.
Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus.
Asumalahti K, Veal C, Laitinen T, Suomela S, Allen M, Elomaa O, Moser M, de Cid R, Ripatti S, Vorechovsky I, Marcusson JA, Nakagawa H, Lazaro C, Estivill X, Capon F, Novelli G, Saarialho-Kere U, Barker J, Trembath R, Kere J; Psoriasis Consortium. Asumalahti K, et al. Among authors: kere j. Hum Mol Genet. 2002 Mar 1;11(5):589-97. doi: 10.1093/hmg/11.5.589. Hum Mol Genet. 2002. PMID: 11875053
618 results