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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: willcutt eg. 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.
Characterizing the ADHD phenotype for genetic studies.
Stevenson J, Asherson P, Hay D, Levy F, Swanson J, Thapar A, Willcutt E. Stevenson J, et al. Dev Sci. 2005 Mar;8(2):115-21. doi: 10.1111/j.1467-7687.2005.00398.x. Dev Sci. 2005. PMID: 15720369 Review.
Attention-deficit/hyperactivity disorder endophenotypes.
Doyle AE, Willcutt EG, Seidman LJ, Biederman J, Chouinard VA, Silva J, Faraone SV. Doyle AE, et al. Among authors: willcutt eg. Biol Psychiatry. 2005 Jun 1;57(11):1324-35. doi: 10.1016/j.biopsych.2005.03.015. Biol Psychiatry. 2005. PMID: 15950005 Review.
Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.
Doyle AE, Ferreira MA, Sklar PB, Lasky-Su J, Petty C, Fusillo SJ, Seidman LJ, Willcutt EG, Smoller JW, Purcell S, Biederman J, Faraone SV. Doyle AE, et al. Among authors: willcutt eg. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1399-411. doi: 10.1002/ajmg.b.30868. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18973233 Free PMC article.
140 results