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615 results

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Page 1
The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.
Anthoni H, Sucheston LE, Lewis BA, Tapia-Páez I, Fan X, Zucchelli M, Taipale M, Stein CM, Hokkanen ME, Castrén E, Pennington BF, Smith SD, Olson RK, Tomblin JB, Schulte-Körne G, Nöthen M, Schumacher J, Müller-Myhsok B, Hoffmann P, Gilger JW, Hynd GW, Nopola-Hemmi J, Leppanen PH, Lyytinen H, Schoumans J, Nordenskjöld M, Spencer J, Stanic D, Boon WC, Simpson E, Mäkelä S, Gustafsson JÅ, Peyrard-Janvid M, Iyengar S, Kere J. Anthoni H, et al. Among authors: kere j. Behav Genet. 2012 Jul;42(4):509-27. doi: 10.1007/s10519-012-9532-3. Epub 2012 Mar 17. Behav Genet. 2012. PMID: 22426781 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.
Upregulation of CFTR expression but not SLC26A3 and SLC9A3 in ulcerative colitis.
Lohi H, Mäkelä S, Pulkkinen K, Höglund P, Karjalainen-Lindsberg ML, Puolakkainen P, Kere J. Lohi H, et al. Among authors: kere j. Am J Physiol Gastrointest Liver Physiol. 2002 Sep;283(3):G567-75. doi: 10.1152/ajpgi.00356.2001. Am J Physiol Gastrointest Liver Physiol. 2002. PMID: 12181169 Free article.
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, Muller K, Kaaranen M, Lindsberg PJ, Hannula-Jouppi K, Kere J. Taipale M, et al. Among authors: kere j. Proc Natl Acad Sci U S A. 2003 Sep 30;100(20):11553-8. doi: 10.1073/pnas.1833911100. Epub 2003 Sep 3. Proc Natl Acad Sci U S A. 2003. PMID: 12954984 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
Transgenic mouse models support HCR as an effector gene in the PSORS1 locus.
Elomaa O, Majuri I, Suomela S, Asumalahti K, Jiao H, Mirzaei Z, Rozell B, Dahlman-Wright K, Pispa J, Kere J, Saarialho-Kere U. Elomaa O, et al. Among authors: kere j. Hum Mol Genet. 2004 Aug 1;13(15):1551-61. doi: 10.1093/hmg/ddh178. Epub 2004 Jun 9. Hum Mol Genet. 2004. PMID: 15190014
Family-based association study of DYX1C1 variants in autism.
Ylisaukko-Oja T, Peyrard-Janvid M, Lindgren CM, Rehnström K, Vanhala R, Peltonen L, Järvelä I, Kere J. Ylisaukko-Oja T, et al. Among authors: kere j. Eur J Hum Genet. 2005 Jan;13(1):127-30. doi: 10.1038/sj.ejhg.5201272. Eur J Hum Genet. 2005. PMID: 15470369
615 results