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Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B; 23andMe Research Team; Quantitative Trait Working Group of the GenLang Consortium; Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, DeFries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M. Doust C, et al. Among authors: paracchini s. Nat Genet. 2023 Mar;55(3):520. doi: 10.1038/s41588-023-01336-8. Nat Genet. 2023. PMID: 36823321 Free PMC article. No abstract available.
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.
Human handedness: A meta-analysis.
Papadatou-Pastou M, Ntolka E, Schmitz J, Martin M, Munafò MR, Ocklenburg S, Paracchini S. Papadatou-Pastou M, et al. Among authors: paracchini s. Psychol Bull. 2020 Jun;146(6):481-524. doi: 10.1037/bul0000229. Epub 2020 Apr 2. Psychol Bull. 2020. PMID: 32237881 Review.
Handedness in twins: meta-analyses.
Pfeifer LS, Schmitz J, Papadatou-Pastou M, Peterburs J, Paracchini S, Ocklenburg S. Pfeifer LS, et al. Among authors: paracchini s. BMC Psychol. 2022 Jan 15;10(1):11. doi: 10.1186/s40359-021-00695-3. BMC Psychol. 2022. PMID: 35033205 Free PMC article.
88 results