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Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.
Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE; SLI Consortium; Whitehouse AJ, Snowling MJ, Newbury DF, Paracchini S. Pettigrew KA, et al. Among authors: paracchini s. Genes Brain Behav. 2015 Apr;14(4):369-76. doi: 10.1111/gbb.12213. Epub 2015 Apr 1. Genes Brain Behav. 2015. PMID: 25778778 Free PMC article.
The DCDC2 deletion is not a risk factor for dyslexia.
Scerri TS, Macpherson E, Martinelli A, Wa WC, Monaco AP, Stein J, Zheng M, Suk-Han Ho C, McBride C, Snowling M, Hulme C, Hayiou-Thomas ME, Waye MMY, Talcott JB, Paracchini S. Scerri TS, et al. Among authors: paracchini s. Transl Psychiatry. 2017 Jul 25;7(7):e1182. doi: 10.1038/tp.2017.151. Transl Psychiatry. 2017. PMID: 28742079 Free PMC article.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, Demonet JF, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Kirsten H, Müller B, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G. Gialluisi A, et al. Among authors: paracchini s. Mol Psychiatry. 2021 Jul;26(7):3004-3017. doi: 10.1038/s41380-020-00898-x. Epub 2020 Oct 14. Mol Psychiatry. 2021. PMID: 33057169 Free PMC article.
88 results