Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Dyslexia and ROBO1[original query] |
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| 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 |
| 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 |
| 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 |
| 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 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. Medicina (Kaunas, Lithuania) 2023 8 59 (8): . Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo, Santina Città, Concetta Federico, Luigi Vetri, Salvatore Saccone, Serafino Buo |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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