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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1977 1
1978 2
1998 1
2000 1
2001 1
2002 2
2003 2
2004 4
2006 4
2007 5
2008 2
2009 3
2010 7
2011 5
2012 1
2013 4
2014 7
2015 2
2016 3
2017 3
2018 3
2019 7
2020 12
2021 6
2022 7
2023 6
2024 1

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87 results

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Page 1
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. 2022 Nov;54(11):1621-1629. doi: 10.1038/s41588-022-01192-y. Epub 2022 Oct 20. Nat Genet. 2022. PMID: 36266505 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.
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.
Diquigiovanni C, Bergamini C, Diaz R, Liparulo I, Bianco F, Masin L, Baldassarro VA, Rizzardi N, Tranchina A, Buscherini F, Wischmeijer A, Pippucci T, Scarano E, Cordelli DM, Fato R, Seri M, Paracchini S, Bonora E. Diquigiovanni C, et al. Among authors: paracchini s. FASEB J. 2019 Oct;33(10):11284-11302. doi: 10.1096/fj.201802722R. Epub 2019 Aug 7. FASEB J. 2019. PMID: 31314595
The genetic lexicon of dyslexia.
Paracchini S, Scerri T, Monaco AP. Paracchini S, et al. Annu Rev Genomics Hum Genet. 2007;8:57-79. doi: 10.1146/annurev.genom.8.080706.092312. Annu Rev Genomics Hum Genet. 2007. PMID: 17444811 Review.
Elevated levels of mixed-hand preference in dyslexia: Meta-analyses of 68 studies.
Packheiser J, Papadatou-Pastou M, Koufaki A, Paracchini S, Stein CC, Schmitz J, Ocklenburg S. Packheiser J, et al. Among authors: paracchini s. Neurosci Biobehav Rev. 2023 Nov;154:105420. doi: 10.1016/j.neubiorev.2023.105420. Epub 2023 Sep 30. Neurosci Biobehav Rev. 2023. PMID: 37783301 Review.
87 results