Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 56 Records) |
Query Trace: DCDC2[original query] |
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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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. Journal of medical genetics 2015 Dec . Powers Natalie R, Eicher John D, Miller Laura L, Kong Yong, Smith Shelley D, Pennington Bruce F, Willcutt Erik G, Olson Richard K, Ring Susan M, Gruen Jeffrey |
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 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 |
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 |
Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children. Clinical practice and epidemiology in mental health : CP & EMH 2017 10 13 104-114. Waye Mary M Y, Poo Lim K, Ho Connie S |
The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects. Journal of human genetics 2017 10 62 (11): 949-955. Trezzi Vittoria, Forni Diego, Giorda Roberto, Villa Marco, Molteni Massimo, Marino Cecilia, Mascheretti Sa |
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 |
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 |
Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes. Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence 2019 Aug 1-25. Li Miao, Truong Dongnhu T, DeMille Mellissa, Malins Jeffrey G, Lovett Maureen W, Bosson-Heenan Joan, Gruen Jeffrey R, Frijters Jan |
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, |
Do Genes Associated with Dyslexia of Chinese Characters Evolve Neutrally? Genes 2020 6 11 (6): . Nishiyama Kumiko V, Satta Yoko, Gojobori J |
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 |
Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance. Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 12 18 (10): 1797-1811. Gao Yizhe, Felsky Daniel, Reyes-Dumeyer Dolly, Sariya Sanjeev, Rentería Miguel Arce, Ma Yiyi, Klein Hans-Ulrich, Cosentino Stephanie, De Jager Philip L, Bennett David A, Brickman Adam M, Schellenberg Gerard D, Mayeux Richard, Barral Sandra, |
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 |
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults. Cerebral cortex (New York, N.Y. : 1991) 2024 4 34 (4): . Nea Rinne, Patrik Wikman, Elisa Sahari, Juha Salmi, Elisabet Einarsdóttir, Juha Kere, Kimmo Al |
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- Page last updated:May 06, 2024
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