Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Dyslexia and CNTNAP2[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 |
| Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of neurodevelopmental disorders 2011 Mar 3 (1): 39-49. Peter Beate, Raskind Wendy H, Matsushita Mark, Lisowski Mark, Vu Tiffany, Berninger Virginia W, Wijsman Ellen M, Brkanac Zor |
| 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 |
| 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 |
| 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 |
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- Page last updated:Jun 02, 2023
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