Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Dyslexia and GRIN2B[original query] |
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| Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Jul . Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P |
| GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia. Psychiatric genetics 2015 Feb 25 (1): 9-20. Mascheretti Sara, Facoetti Andrea, Giorda Roberto, Beri Silvana, Riva Valentina, Trezzi Vittoria, Cellino Maria R, Marino Cecil |
| 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 |
| 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 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 |
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