Human Genome Epidemiology Literature Finder

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Query Trace: Dyslexia and meta-analysis and DYX1C1[original query]
Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Dec 159B (8): 970-6. Zou Li, Chen Wei, Shao Shanshan, Sun Zhao, Zhong Rong, Shi Junxin, Miao Xiaoping, Song Ranr Similar articles in PubMed
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. European journal of human genetics : EJHG 2014 May 22 (5): 675-80. Becker Jessica, Czamara Darina, Scerri Tom S, Ramus Franck, Csépe Valéria, Talcott Joel B, Stein John, Morris Andrew, Ludwig Kerstin U, Hoffmann Per, Honbolygó Ferenc, Tóth Dénes, Fauchereau Fabien, Bogliotti Caroline, Iannuzzi Stéphanie, Chaix Yves, Valdois Sylviane, Billard Catherine, George Florence, Soares-Boucaud Isabelle, Gérard Christophe-Loïc, van der Mark Sanne, Schulz Enrico, Vaessen Anniek, Maurer Urs, Lohvansuu Kaisa, Lyytinen Heikki, Zucchelli Marco, Brandeis Daniel, Blomert Leo, Leppänen Paavo H T, Bruder Jennifer, Monaco Anthony P, Müller-Myhsok Bertram, Kere Juha, Landerl Karin, Nöthen Markus M, Schulte-Körne Gerd, Paracchini Silvia, Peyrard-Janvid Myriam, Schumacher Johann Similar articles in PubMed
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jan . Tran C, Gagnon F, Wigg KG, Feng Y, Gomez L, Cate-Carter TD, Kerr EN, Field LL, Kaplan BJ, Lovett MW, Barr CL Similar articles in PubMed