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| A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN. Asian journal of psychiatry 2018 Aug 37 121-129. Devasenapathy Subhashree, Midha Rashi, Naskar Teesta, Mehta Anuradha, Prajapati Bharat, Ummekulsum Mariam, Sagar Rajesh, Singh Nandini C, Sinha Subra |
| Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct . Kong Rui, Shao Shanshan, Wang Jia, Zhang Xiaohui, Guo Shengnan, Zou Li, Zhong Rong, Lou Jiao, Zhou Jie, Zhang Jiajia, Song Ranr |
| 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 |
| Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of human genetics 2015 Jul 60 (7): 399-401. Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo Ht, Peyrard-Janvid Myriam, Kere Ju |
| Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 627-34. Sun Yimin, Gao Yong, Zhou Yuxi, Chen Huan, Wang Guoqing, Xu Junquan, Xia Jiguang, Huen Michael S Y, Siok Wai Ting, Jiang Yuyang, Tan Li H |
| KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. Journal of human genetics 2014 Apr 59 (4): 189-97. Mascheretti Sara, Riva Valentina, Giorda Roberto, Beri Silvana, Lanzoni Lara Francesca Emilia, Cellino Maria Rosaria, Marino Cecil |
| Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia. Gene 2013 Oct 529 (2): 215-9. Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur |
| Study of candidate genes for dyslexia in Brazilian individuals. Genetics and molecular research : GMR 2013 12 (4): 5356-64. Svidnicki M C C M, Salgado C A, Lima R F, Ciasca S M, Secolin R, Pomilio M C A, Junqueira P A, Pinto M S, Pereira M M, Sartorato E |
| 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 |
| Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior genetics 2011 Jan 41 (1): 50-7. Bates Timothy C, Luciano Michelle, Medland Sarah E, Montgomery Grant W, Wright Margaret J, Martin Nicholas |
| Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior genetics 2011 Jan 41 (1): 90-104. Newbury D F, Paracchini S, Scerri T S, Winchester L, Addis L, Richardson Alex J, Walter J, Stein J F, Talcott J B, Monaco A |
| 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 |
| A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human molecular genetics 2007 Mar 16 (6): 667-77. Anthoni Heidi, Zucchelli Marco, Matsson Hans, Müller-Myhsok Bertram, Fransson Ingegerd, Schumacher Johannes, Massinen Satu, Onkamo Päivi, Warnke Andreas, Griesemann Heide, Hoffmann Per, Nopola-Hemmi Jaana, Lyytinen Heikki, Schulte-Körne Gerd, Kere Juha, Nöthen Markus M, Peyrard-Janvid Myri |
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