Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Memory and Dyx1c1[original query] |
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| Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes, brain, and behavior 2007 Oct 6 (7): 640-6. Marino C, Citterio A, Giorda R, Facoetti A, Menozzi G, Vanzin L, Lorusso M L, Nobile M, Molteni |
| Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Psychiatric genetics 2009 Apr 19 (2): 59-63. Dahdouh Faten, Anthoni Heidi, Tapia-Páez Isabel, Peyrard-Janvid Myriam, Schulte-Körne Gerd, Warnke Andreas, Remschmidt Helmut, Ziegler Andreas, Kere Juha, Müller-Myhsok Bertram, Nöthen Markus M, Schumacher Johannes, Zucchelli Mar |
| Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Molecular psychiatry 2010 Dec 15 (12): 1190-6. Bates T C, Lind P A, Luciano M, Montgomery G W, Martin N G, Wright M |
| Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children. Behavioral and brain functions : BBF 2011 7 (1): 16. Lim Cadmon K P, Ho Connie S H, Chou Crystal H N, Waye Mary M |
| An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes. Genes, brain, and behavior 2012 Nov . Mascheretti S, Bureau A, Battaglia M, Simone D, Quadrelli E, Croteau J, Cellino MR, Giorda R, Beri S, Maziade M, Marino C |
| Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1. Brain and language 2015 May . Rendall Amanda R, Tarkar Aarti, Contreras-Mora Hector M, LoTurco Joseph J, Fitch R Hol |
| An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia. Human genetics 2015 Jul 134 (7): 749-60. Mascheretti S, Bureau A, Trezzi V, Giorda R, Marino |
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