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Items: 5

1.

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.

Transl Psychiatry. 2017 Jul 25;7(7):e1182. doi: 10.1038/tp.2017.151.

2.

Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.

Martinez-Garay I, Guidi LG, Holloway ZG, Bailey MA, Lyngholm D, Schneider T, Donnison T, Butt SJ, Monaco AP, Molnár Z, Velayos-Baeza A.

Brain Struct Funct. 2017 Apr;222(3):1367-1384. doi: 10.1007/s00429-016-1282-1. Epub 2016 Aug 10.

3.

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.

König IR, Schumacher J, Hoffmann P, Kleensang A, Ludwig KU, Grimm T, Neuhoff N, Preis M, Roeske D, Warnke A, Propping P, Remschmidt H, Nöthen MM, Ziegler A, Müller-Myhsok B, Schulte-Körne G.

Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):36-43. doi: 10.1002/ajmg.b.31135. Epub 2010 Nov 2.

PMID:
21184582
4.

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J.

Am J Hum Genet. 2006 Jan;78(1):52-62. Epub 2005 Nov 17.

5.

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J.

Am J Hum Genet. 2005 Apr;76(4):581-91. Epub 2005 Feb 16. Erratum in: Am J Hum Genet. 2005 Nov;77(5):898.

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