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Support for EKN1 as the susceptibility locus for dyslexia on 15q21.
Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL. Wigg KG, et al. Among authors: lovett mw. Mol Psychiatry. 2004 Dec;9(12):1111-21. doi: 10.1038/sj.mp.4001543. Mol Psychiatry. 2004. PMID: 15249932 Clinical Trial.
Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.
Couto JM, Livne-Bar I, Huang K, Xu Z, Cate-Carter T, Feng Y, Wigg K, Humphries T, Tannock R, Kerr EN, Lovett MW, Bremner R, Barr CL. Couto JM, et al. Among authors: lovett mw. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):447-462. doi: 10.1002/ajmg.b.30999. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19588467 Free PMC article.
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.
Truong DT, Adams AK, Paniagua S, Frijters JC, Boada R, Hill DE, Lovett MW, Mahone EM, Willcutt EG, Wolf M, Defries JC, Gialluisi A, Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, Bosson-Heenan J, Gruen JR; Pediatric, Imaging, Neurocognition, and Genetics Consortium. Truong DT, et al. Among authors: lovett mw. J Med Genet. 2019 Aug;56(8):557-566. doi: 10.1136/jmedgenet-2018-105874. Epub 2019 Apr 17. J Med Genet. 2019. PMID: 30995994 Free PMC article.
63 results