Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Dyslexia and DYX1C1[original query] |
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| No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy. Journal of molecular neuroscience : MN 2005 27 (3): 311-4. Bellini Giulia, Bravaccio Carmela, Calamoneri Filippo, Donatella Cocuzza Maria, Fiorillo Pasquale, Gagliano Antonella, Mazzone Domenico, del Giudice Emanuele Miraglia, Scuccimarra Geoffredo, Militerni Roberto, Pascotto Anton |
| Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jun 144B (4): 556-60. Brkanac Zoran, Chapman Nicola H, Matsushita Mark M, Chun Lani, Nielsen Kathleen, Cochrane Elizabeth, Berninger Virginia W, Wijsman Ellen M, Raskind Wendy |
| 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 |
| 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 |
| 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 |
| Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population. Genes, brain, and behavior 2011 Mar 10 (2): 158-65. Paracchini S, Ang Q W, Stanley F J, Monaco A P, Pennell C E, Whitehouse A J |
| 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 |
| Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behavior genetics 2011 Jan 41 (1): 67-76. Marino Cecilia, Mascheretti Sara, Riva Valentina, Cattaneo Francesca, Rigoletto Catia, Rusconi Marianna, Gruen Jeffrey R, Giorda Roberto, Lazazzera Claudio, Molteni Massi |
| 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 |
| Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure. Biological psychiatry 2012 Oct 72 (8): 671-6. Darki Fahimeh, Peyrard-Janvid Myriam, Matsson Hans, Kere Juha, Klingberg Tork |
| 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 |
| Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population. PloS one 2012 7 (9): 9. Zhang Y, Li J, Tardif T, Burmeister M, Villafuerte SM, McBride-Chang C, Li H, Shi B, Liang W, Zhang Z, Shu H |
| 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 |
| 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 |
| Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population. Psychiatric genetics 2014 Feb 24 (1): 10-20. Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur |
| 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 |
| 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 |
| DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development. The Journal of neuroscience : the official journal of the Society for Neuroscience 2014 Oct 34 (43): 14455-62. Darki Fahimeh, Peyrard-Janvid Myriam, Matsson Hans, Kere Juha, Klingberg Tork |
| 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 |
| 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 |
| [Genome-wide association studies on the developmental dyslexia children]. Wei sheng yan jiu = Journal of hygiene research 2015 Sep 44 (5): 767-70, 779. Wang Zhichao, Cui Guangcheng, Zhao Ameng, Li Ping, Liu Deshui, Shen Li, Li D |
| 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 |
| 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 |
| Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1. Genetics and molecular biology 2018 Feb 0. Müller Bent, Boltze Johannes, Czepezauer Ivonne, Hesse Volker, , Wilcke Arndt, Kirsten Holg |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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