Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Dyslexia and ATP2C2[original query] |
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| Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior genetics 2011 Jan 41 (1): 90-104. Newbury D F, Paracchini S, Scerri T S, Winchester L, Addis L, Richardson Alex J, Walter J, Stein J F, Talcott J B, Monaco A |
| 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 |
| Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders. Autism research : official journal of the International Society for Autism Research 2015 Apr 8 (2): 229-34. Eicher John D, Gruen Jeffrey |
| 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 |
| A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Human molecular genetics 2021 4 30 (12): 1160-1171. Martinelli Angela, Rice Mabel L, Talcott Joel B, Diaz Rebeca, Smith Shelley, Raza Muhammad Hashim, Snowling Margaret J, Hulme Charles, Stein John, Hayiou-Thomas Marianna E, Hawi Ziarih, Kent Lindsey, Pitt Samantha J, Newbury Dianne F, Paracchini Silv |
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- Page last updated:May 22, 2023
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