Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records)
|Query Trace: Memory and DYX1C1[original query]|
| 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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- Page last updated:Jun 02, 2023
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