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Query Trace: Dyslexia and CNTNAP2[original query]

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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed