| 1 | DYX1C1, ICS26
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| DYX1C1 is required for axonemal dynein assembly and ciliary motility.
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| Tarkar A, Loges NT, Slagle CE, Francis R, Dougherty GW, Tamayo JV, Shook B, Cantino M, Schwartz D, Jahnke C, Olbrich H, Werner C, Raidt J, Pennekamp P, Abouhamed M, Hjeij R, Köhler G, Griese M, Li Y, Lemke K, Klena N, Liu X, Gabriel G, Tobita K, Jaspers M, Morgan LC, Shapiro AJ, Letteboer SJ, Mans DA, Carson JL, Leigh MW, Wolf WE, Chen S, Lucas JS, Onoufriadis A, Plagnol V, Schmidts M, Boldt K; UK10K, Roepman R, Zariwala MA, Lo CW, Mitchison HM, Knowles MR, Burdine RD, Loturco JJ, Omran H.
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| Nat Genet 45(9):995-1003. doi: 10.1038/ng.2707. Epub 2013 Jul 21.
2013
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| 2 | DYX1C1
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| The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function.
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| Chandrasekar G, Vesterlund L, Hultenby K, Tapia-Páez I, Kere J.
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| PLoS One 8(5):e63123. doi: 10.1371/journal.pone.0063123. Print 2013.
2013
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| 3 | DCDC2, DYX1C1
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| Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.
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| Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JR, Giorda R, Lazazzera C, Molteni M.
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| Behav Genet 41(1):67-76. doi: 10.1007/s10519-010-9412-7. Epub 2010 Nov 3.
2011
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| 4 | DYX1C1
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| Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.
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| Bates TC, Lind PA, Luciano M, Montgomery GW, Martin NG, Wright MJ.
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| Mol Psychiatry 15(12):1190-6. doi: 10.1038/mp.2009.120. Epub 2009 Nov 10.
2010
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| 5 | DYX1C1
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| Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
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| Massinen S, Tammimies K, Tapia-Páez I, Matsson H, Hokkanen ME, Söderberg O, Landegren U, Castrén E, Gustafsson JA, Treuter E, Kere J.
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| Hum Mol Genet 18(15):2802-12. Epub 2009 May 7.
2009
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| 6 | DYX1C1
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| Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
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| Dahdouh F, Anthoni H, Tapia-Páez I, Peyrard-Janvid M, Schulte-Körne G, Warnke A, Remschmidt H, Ziegler A, Kere J, Müller-Myhsok B, Nöthen MM, Schumacher J, Zucchelli M.
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| Psychiatr Genet 19(2):59-63. doi: 10.1097/YPG.0b013e32832080e1.
2009
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| 7 | DYX1C1
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| Molecular characterization of the DYX1C1 gene and its application as a cancer biomarker.
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| Kim YJ, Huh JW, Kim DS, Bae MI, Lee JR, Ha HS, Ahn K, Kim TO, Song GA, Kim HS.
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| J Cancer Res Clin Oncol 135(2):265-70. doi: 10.1007/s00432-008-0445-8. Epub 2008 Jul 10.
2009
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| 8 | DYX1C1, GTF2I, PARP1, SFPQ
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| The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.
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| Tapia-Páez I, Tammimies K, Massinen S, Roy AL, Kere J.
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| FASEB J 22(8):3001-9. Epub 2008 Apr 29.
2008
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| 9 | DCDC2, DYX1, DYX1C1, DYX2, DYX3, KIAA0319, ROBO1
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| The genetic lexicon of dyslexia.
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| Paracchini S, Scerri T, Monaco AP.
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| Annu Rev Genomics Hum Genet 8:57-79. Review.
2007
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| 10 | DYX1C1
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| DYX1C1 functions in neuronal migration in developing neocortex.
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| Wang Y, Paramasivam M, Thomas A, Bai J, Kaminen-Ahola N, Kere J, Voskuil J, Rosen GD, Galaburda AM, Loturco JJ.
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| Neuroscience 143(2):515-22. Epub 2006 Sep 20.
2006
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| 11 | DYX1C1
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| Family-based association study of DYX1C1 variants in autism.
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| Ylisaukko-Oja T, Peyrard-Janvid M, Lindgren CM, Rehnstrom K, Vanhala R, Peltonen L, Jarvela I, Kere J.
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| Eur J Hum Genet 13(1):127-30. 2005
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| 12 | DYX1, DYX1C1
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| Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.
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| Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH.
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| Am J Med Genet 131B(1):67-75. 2004
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| 13 | DYX1C1
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| Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
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| Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP.
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| J Med Genet 41(11):853-7. No abstract available. 2004
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| 14 | DYX1C1
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| A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
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| Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, Muller K, Kaaranen M, Lindsberg PJ, Hannula-Jouppi K, Kere J.
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| Proc Natl Acad Sci U S A 100(20):11553-8. Epub 2003 Sep 03. 2003
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