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1994 1
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64 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: talcott jb. 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.
Effects of maternal folic acid supplementation during the second and third trimesters of pregnancy on neurocognitive development in the child: an 11-year follow-up from a randomised controlled trial.
Caffrey A, McNulty H, Rollins M, Prasad G, Gaur P, Talcott JB, Witton C, Cassidy T, Marshall B, Dornan J, Moore AJ, Ward M, Strain JJ, Molloy AM, McLaughlin M, Lees-Murdock DJ, Walsh CP, Pentieva K. Caffrey A, et al. Among authors: talcott jb. BMC Med. 2021 Mar 10;19(1):73. doi: 10.1186/s12916-021-01914-9. BMC Med. 2021. PMID: 33750355 Free PMC article. Clinical Trial.
Language and reading impairments are associated with increased prevalence of non-right-handedness.
Abbondanza F, Dale PS, Wang CA, Hayiou-Thomas ME, Toseeb U, Koomar TS, Wigg KG, Feng Y, Price KM, Kerr EN, Guger SL, Lovett MW, Strug LJ, van Bergen E, Dolan CV, Tomblin JB, Moll K, Schulte-Körne G, Neuhoff N, Warnke A, Fisher SE, Barr CL, Michaelson JJ, Boomsma DI, Snowling MJ, Hulme C, Whitehouse AJO, Pennell CE, Newbury DF, Stein J, Talcott JB, Bishop DVM, Paracchini S. Abbondanza F, et al. Among authors: talcott jb. Child Dev. 2023 Jul-Aug;94(4):970-984. doi: 10.1111/cdev.13914. Epub 2023 Feb 13. Child Dev. 2023. PMID: 36780127 Free PMC article.
Syndromes of collateral-reported psychopathology for ages 18-59 in 18 Societies.
Ivanova MY, Achenbach TM, Rescorla LA, Turner LV, Árnadóttir HA, Au A, Caldas JC, Chaalal N, Chen YC, da Rocha MM, Decoster J, Fontaine JRJ, Funabiki Y, Guðmundsson HS, Kim YA, Leung P, Liu J, Malykh S, Marković J, Oh KJ, Petot JM, Samaniego VC, Silvares EFM, Šimulionienė R, Šobot V, Sokoli E, Sun G, Talcott JB, Vázquez N, Zasępa E. Ivanova MY, et al. Among authors: talcott jb. Int J Clin Health Psychol. 2015 Jan-Apr;15(1):18-28. doi: 10.1016/j.ijchp.2014.07.001. Epub 2014 Aug 29. Int J Clin Health Psychol. 2015. PMID: 29399019 Free PMC article.
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: talcott jb. 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: talcott jb. Transl Psychiatry. 2017 Jul 25;7(7):e1182. doi: 10.1038/tp.2017.151. Transl Psychiatry. 2017. PMID: 28742079 Free PMC article.
64 results