Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Dyslexia and SLC2A3[original query] |
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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
Molecular psychiatry 2011 Jan 16 (1): 97-107. Roeske D, Ludwig K U, Neuhoff N, Becker J, Bartling J, Bruder J, Brockschmidt F F, Warnke A, Remschmidt H, Hoffmann P, Müller-Myhsok B, Nöthen M M, Schulte-Körne |
| Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children. NeuroImage 2015 Sep 118 414-21. Skeide Michael A, Kirsten Holger, Kraft Indra, Schaadt Gesa, Müller Bent, Neef Nicole, Brauer Jens, Wilcke Arndt, Emmrich Frank, Boltze Johannes, Friederici Angela |
| 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 |
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