Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Learning and DYX1C1[original query] |
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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 |
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations. Behavior genetics 2011 Jan 41 (1): 134-40. Matsson Hans, Tammimies Kristiina, Zucchelli Marco, Anthoni Heidi, Onkamo Päivi, Nopola-Hemmi Jaana, Lyytinen Heikki, Leppanen Paavo H T, Neuhoff Nina, Warnke Andreas, Schulte-Körne Gert, Schumacher Johannes, Nöthen Markus M, Kere Juha, Peyrard-Janvid Myri |
An examination of candidate gene SNPs for dyslexia in an Indian sample. Behavior genetics 2011 Jan 41 (1): 105-9. Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur |
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family. Human genetics 2015 Sep . Einarsdottir Elisabet, Svensson Idor, Darki Fahimeh, Peyrard-Janvid Myriam, Lindvall Jessica M, Ameur Adam, Jacobsson Christer, Klingberg Torkel, Kere Juha, Matsson Ha |
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 |
ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR. Brain and behavior 2017 11 7 (11): e00851. Müller Bent, Schaadt Gesa, Boltze Johannes, Emmrich Frank, , Skeide Michael A, Neef Nicole E, Kraft Indra, Brauer Jens, Friederici Angela D, Kirsten Holger, Wilcke Arn |
Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. European journal of human genetics : EJHG 2017 1 25 (4): 452-460. Carrion-Castillo Amaia, Maassen Ben, Franke Barbara, Heister Angelien, Naber Marlies, van der Leij Aryan, Francks Clyde, Fisher Simon |
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