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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: tannock r. 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: tannock r. 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.
Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.
Barr CL, Xu C, Kroft J, Feng Y, Wigg K, Zai G, Tannock R, Schachar R, Malone M, Roberts W, Nöthen MM, Grünhage F, Vandenbergh DJ, Uhl G, Sunohara G, King N, Kennedy JL. Barr CL, et al. Among authors: tannock r. Biol Psychiatry. 2001 Feb 15;49(4):333-9. doi: 10.1016/s0006-3223(00)01053-2. Biol Psychiatry. 2001. PMID: 11239904
193 results