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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 |
| Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular psychiatry 2020 Oct . Gialluisi Alessandro, Andlauer Till F M, Mirza-Schreiber Nazanin, Moll Kristina, Becker Jessica, Hoffmann Per, Ludwig Kerstin U, Czamara Darina, Pourcain Beate St, Honbolygó Ferenc, Tóth Dénes, Csépe Valéria, Huguet Guillaume, Chaix Yves, Iannuzzi Stephanie, Demonet Jean-Francois, Morris Andrew P, Hulslander Jacqueline, Willcutt Erik G, DeFries John C, Olson Richard K, Smith Shelley D, Pennington Bruce F, Vaessen Anniek, Maurer Urs, Lyytinen Heikki, Peyrard-Janvid Myriam, Leppänen Paavo H T, Brandeis Daniel, Bonte Milene, Stein John F, Talcott Joel B, Fauchereau Fabien, Wilcke Arndt, Kirsten Holger, Müller Bent, Francks Clyde, Bourgeron Thomas, Monaco Anthony P, Ramus Franck, Landerl Karin, Kere Juha, Scerri Thomas S, Paracchini Silvia, Fisher Simon E, Schumacher Johannes, Nöthen Markus M, Müller-Myhsok Bertram, Schulte-Körne Ge |
| The associations of zinc and GRIN2B genetic polymorphisms with the risk of dyslexia. Environmental research 2020 Sep 110207. Liu Qi, Zhu Bing, Xue Qi, Xie Xinyan, Zhou Yu, Zhu Kaiheng, Wan Zihao, Wu Hao, Zhang Jiajia, Song Ranr |
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Cortex; a journal devoted to the study of the nervous system and behavior 2019 Nov 124 137-153. Carrion-Castillo Amaia, Pepe Antonietta, Kong Xiang-Zhen, Fisher Simon E, Mazoyer Bernard, Tzourio-Mazoyer Nathalie, Crivello Fabrice, Francks Cly |
| Dyslexia associated functional variants in Europeans are not associated with dyslexia in Chinese. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019 Jul . Liu Lingfei, Gu Huaiting, Hou Fang, Xie Xinyan, Li Xin, Zhu Bing, Zhang Jiajia, Wei Wen-Hua, Song Ranr |
| Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Translational psychiatry 2019 02 9 (1): 77. Gialluisi Alessandro, Andlauer Till F M, Mirza-Schreiber Nazanin, Moll Kristina, Becker Jessica, Hoffmann Per, Ludwig Kerstin U, Czamara Darina, St Pourcain Beate, Brandler William, Honbolygó Ferenc, Tóth Dénes, Csépe Valéria, Huguet Guillaume, Morris Andrew P, Hulslander Jacqueline, Willcutt Erik G, DeFries John C, Olson Richard K, Smith Shelley D, Pennington Bruce F, Vaessen Anniek, Maurer Urs, Lyytinen Heikki, Peyrard-Janvid Myriam, Leppänen Paavo H T, Brandeis Daniel, Bonte Milene, Stein John F, Talcott Joel B, Fauchereau Fabien, Wilcke Arndt, Francks Clyde, Bourgeron Thomas, Monaco Anthony P, Ramus Franck, Landerl Karin, Kere Juha, Scerri Thomas S, Paracchini Silvia, Fisher Simon E, Schumacher Johannes, Nöthen Markus M, Müller-Myhsok Bertram, Schulte-Körne Ge |
| 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 |
| Genetic variants in the CNTNAP2 gene are associated with gender differences among dyslexic children in China. EBioMedicine 2018 Jul . Gu Huaiting, Hou Fang, Liu Lingfei, Luo Xiu, Nkomola Pauline Denis, Xie Xinyan, Li Xin, Song Ranr |
| The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age. Behavior genetics 2018 Jun . Luciano Michelle, Gow Alan J, Pattie Alison, Bates Timothy C, Deary Ian |
| 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 |
| 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 |
| 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, |
| Association study of FGF18 with developmental dyslexia in Chinese population. Psychiatric genetics 2018 02 28 (1): 8-11. Chen Huan, Zhou Yuxi, Ge Zeng, Li Qian, Sun Qinsheng, Zheng Liyuan, Lv Hong, Tan Li-Hai, Sun Yim |
| Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. Genome medicine 2017 Nov 9 (1): 105. Lowther Chelsea, Merico Daniele, Costain Gregory, Waserman Jack, Boyd Kerry, Noor Abdul, Speevak Marsha, Stavropoulos Dimitri J, Wei John, Lionel Anath C, Marshall Christian R, Scherer Stephen W, Bassett Anne |
| Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. Human genetics 2017 Sep . Adams Andrew K, Smith Shelley D, Truong Dongnhu T, Willcutt Erik G, Olson Richard K, DeFries John C, Pennington Bruce F, Gruen Jeffrey |
| 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 |
| A method for integrating neuroimaging into genetic models of learning performance. Genetic epidemiology 2017 Jan 41 (1): 4-17. Mehta Chintan M, Gruen Jeffrey R, Zhang Hepi |
| 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 |
| Genetic polymorphism of nonsyndromic cleft lip with or without cleft palate is associated with developmental dyslexia in Chinese school-aged populations. Journal of human genetics 2016 Oct . Wang Bin, Zhou Yuxi, Leng Song, Zheng Liyuan, Lv Hong, Wang Fei, Tan Li-Hai, Sun Yim |
| 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 |
| Neuroimaging genetic analyses of novel candidate genes associated with reading and language. Brain and language 2016 Jul . Gialluisi Alessandro, Guadalupe Tulio, Francks Clyde, Fisher Simon |
| 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 |
| 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 |
| 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 |
| 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 |
| Working-memory endophenotype and dyslexia-associated genetic variant predict dyslexia phenotype. Cortex; a journal devoted to the study of the nervous system and behavior 2015 Oct 71 291-305. Männel Claudia, Meyer Lars, Wilcke Arndt, Boltze Johannes, Kirsten Holger, Friederici Angela |
| [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 |
| 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 |
| CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders. Journal of neurodevelopmental disorders 2015 7 (1): 26. Hu Jie, Liao Jun, Sathanoori Malini, Kochmar Sally, Sebastian Jessica, Yatsenko Svetlana A, Surti Urvas |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 28, 2022
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