Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 44 Records) |
| Query Trace: Dyslexia and KIAA0319[original query] |
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| 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 |
| Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia. Behavior genetics 2011 Jan 41 (1): 77-89. Elbert Adrienne, Lovett Maureen W, Cate-Carter Tasha, Pitch Ashley, Kerr Elizabeth N, Barr Cathy |
| 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 |
| 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 variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 Jan 32 (3): 817-25. Pinel Philippe, Fauchereau Fabien, Moreno Antonio, Barbot Alexis, Lathrop Mark, Zelenika Diana, Le Bihan Denis, Poline Jean-Baptiste, Bourgeron Thomas, Dehaene Stanisl |
| 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 |
| A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children. Behavioral and brain functions : BBF 2014 10 23. Lim Cadmon King-Poo, Wong Amabel May-Bo, Ho Connie Suk-Han, Waye Mary Mui-Y |
| 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 |
| 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 |
| 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 |
| 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, |
| 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 |
| Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population. Scientific reports 2016 07 6 30454. Shao Shanshan, Niu Yanfeng, Zhang Xiaohui, Kong Rui, Wang Jia, Liu Lingfei, Luo Xiu, Zhang Jiajia, Song Ranr |
| KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children. Journal of human genetics 2016 Apr . Zhao Hua, Chen Yun, Zhang Bao-Ping, Zuo Peng-Xia |
| 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 |
| Associations Between the KIAA0319 Dyslexia Susceptibility Gene Variants, Antenatal Maternal Stress, and Reading Ability in a Longitudinal Birth Cohort. Dyslexia (Chichester, England) 2016 Jul . D'Souza Stephanie, Backhouse-Smith Amelia, Thompson John M D, Slykerman Rebecca, Marlow Gareth, Wall Clare, Murphy Rinki, Ferguson Lynnette R, Mitchell Edwin A, Waldie Karen |
| Identification of NCAN as a candidate gene for developmental dyslexia. Scientific reports 2017 8 7 (1): 9294. Einarsdottir Elisabet, Peyrard-Janvid Myriam, Darki Fahimeh, Tuulari Jetro J, Merisaari Harri, Karlsson Linnea, Scheinin Noora M, Saunavaara Jani, Parkkola Riitta, Kantojärvi Katri, Ämmälä Antti-Jussi, Yiu-Lin Yu Nancy, Matsson Hans, Nopola-Hemmi Jaana, Karlsson Hasse, Paunio Tiina, Klingberg Torkel, Leinonen Eira, Kere Ju |
| 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 |
| Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexia. Developmental cognitive neuroscience 2018 6 34 7-17. Centanni T M, Pantazis D, Truong D T, Gruen J R, Gabrieli J D E, Hogan T |
| Association between KIAA0319 SNPs and risk of dyslexia: a meta-analysis. Journal of genetics 2019 6 98 (1): . Deng Ke-Gao, Zhao Hua, Zuo Peng-Xia |
| 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:Oct 1, 2023
- Page last updated:Dec 01, 2023
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