HuGE Literature Finder
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| White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant. Experimental brain research 2021 Jul . Perani Daniela, Scifo Paola, Cicchini Guido M, Rosa Pasquale Della, Banfi Chiara, Mascheretti Sara, Falini Andrea, Marino Cecilia, Morrone Maria Concet |
| 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 |
| The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects. Neuropsychologia 2018 May . Riva Valentina, Mozzi Alessandra, Forni Diego, Trezzi Vittoria, Giorda Roberto, Riva Stefania, Villa Marco, Sironi Manuela, Cagliani Rachele, Mascheretti Sa |
| A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children. NPJ science of learning 2018 3 20. Li Miao, Malins Jeffrey G, DeMille Mellissa M C, Lovett Maureen W, Truong Dongnhu T, Epstein Katherine, Lacadie Cheryl, Mehta Chintan, Bosson-Heenan Joan, Gruen Jeffrey R, Frijters Jan C, |
| DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children. Neural regeneration research 2017 Feb 12 (2): 259-266. Chen Yun, Zhao Hua, Zhang Yi-Xin, Zuo Peng-Xia |
| Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population. PloS one 2016 11 (4): e0153603. Zhang Yuping, Li Jun, Song Shuang, Tardif Twila, Burmeister Margit, Villafuerte Sandra M, Su Mengmeng, McBride Catherine, Shu H |
| Dyslexia susceptibility genes influence brain atrophy in frontotemporal dementia. Neurology. Genetics 2015 Oct 1 (3): e24. Paternicó Donata, Premi Enrico, Alberici Antonella, Archetti Silvana, Bonomi Elisa, Gualeni Vera, Gasparotti Roberto, Padovani Alessandro, Borroni Barba |
| 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 |
| The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants. Molecular neurobiology 2015 Jul . Shao Shanshan, Kong Rui, Zou Li, Zhong Rong, Lou Jiao, Zhou Jie, Guo Shengnan, Wang Jia, Zhang Xiaohui, Zhang Jiajia, Song Ranr |
| Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. Brain imaging and behavior 2015 May . Eicher John D, Montgomery Angela M, Akshoomoff Natacha, Amaral David G, Bloss Cinnamon S, Libiger Ondrej, Schork Nicholas J, Darst Burcu F, Casey B J, Chang Linda, Ernst Thomas, Frazier Jean, Kaufmann Walter E, Keating Brian, Kenet Tal, Kennedy David, Mostofsky Stewart, Murray Sarah S, Sowell Elizabeth R, Bartsch Hauke, Kuperman Joshua M, Brown Timothy T, Hagler Donald J, Dale Anders M, Jernigan Terry L, Gruen Jeffrey R, |
| Strong motion deficits in dyslexia associated with DCDC2 gene alteration. The Journal of neuroscience : the official journal of the Society for Neuroscience 2015 May 35 (21): 8059-64. Cicchini Guido Marco, Marino Cecilia, Mascheretti Sara, Perani Daniela, Morrone Maria Concet |
| The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems. European child & adolescent psychiatry 2015 Mar 24 (3): 309-18. Riva Valentina, Marino Cecilia, Giorda Roberto, Molteni Massimo, Nobile Mar |
| 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 |
| 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 |
| Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population. Journal of human genetics 2013 Aug 58 (8): 531-8. Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur |
| Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. American journal of human genetics 2013 Jul 93 (1): 19-28. Powers Natalie R, Eicher John D, Butter Falk, Kong Yong, Miller Laura L, Ring Susan M, Mann Matthias, Gruen Jeffrey |
| Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia. Molecular neurobiology 2013 Feb 47 (1): 435-42. Zhong Rong, Yang Beifang, Tang Hui, Zou Li, Song Ranran, Zhu Ling-Qiang, Miao Xiaopi |
| 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 |
| 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 |
| Association of polymorphisms in the DCDC2 gene with developmental dyslexia in the Han Chinese. Chinese medical journal 2012 Feb 125 (4): 622-5. Zuo Peng-xiang, Wu Han-rong, Li Zeng-chun, Cao Xu-dong, Pang Li-juan, Yang Lan, Liu Fan, Zhao Fe |
| DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatric genetics 2012 Feb 22 (1): 25-30. Marino Cecilia, Meng Haiying, Mascheretti Sara, Rusconi Marianna, Cope Natalie, Giorda Roberto, Molteni Massimo, Gruen Jeffrey |
| DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biological psychiatry 2011 Aug 70 (3): 237-45. Scerri Tom S, Morris Andrew P, Buckingham Lyn-Louise, Newbury Dianne F, Miller Laura L, Monaco Anthony P, Bishop Dorothy V M, Paracchini Silv |
| 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 |
| Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behavior genetics 2011 Jan 41 (1): 110-9. Czamara Darina, Bruder Jennifer, Becker Jessica, Bartling Jürgen, Hoffmann Per, Ludwig Kerstin Urte, Müller-Myhsok Bertram, Schulte-Körne Ge |
| 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 |
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- Page last updated:Jun 28, 2022
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