Similar articles for PMID: 20846247

Year	Number of Results
2001	1
2002	1
2003	2
2004	3
2005	6
2006	4
2007	5
2008	6
2009	8
2010	12
2011	13
2012	13
2013	10
2014	7
2015	7
2016	11
2017	6
2018	5
2019	5
2020	3
2022	2
2023	1
2024	0

1

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.

Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ. Paracchini S, et al. Genes Brain Behav. 2011 Mar;10(2):158-65. doi: 10.1111/j.1601-183X.2010.00651.x. Epub 2010 Oct 19. Genes Brain Behav. 2011. PMID: 20846247 Free PMC article.

2

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.

Anthoni H, Zucchelli M, Matsson H, Müller-Myhsok B, Fransson I, Schumacher J, Massinen S, Onkamo P, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Schulte-Körne G, Kere J, Nöthen MM, Peyrard-Janvid M. Anthoni H, et al. Hum Mol Genet. 2007 Mar 15;16(6):667-77. doi: 10.1093/hmg/ddm009. Epub 2007 Feb 19. Hum Mol Genet. 2007. PMID: 17309879

3

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.

Bates TC, Lind PA, Luciano M, Montgomery GW, Martin NG, Wright MJ. Bates TC, et al. Mol Psychiatry. 2010 Dec;15(12):1190-6. doi: 10.1038/mp.2009.120. Epub 2009 Nov 10. Mol Psychiatry. 2010. PMID: 19901951

4

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.

Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH. Brkanac Z, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):556-60. doi: 10.1002/ajmg.b.30471. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17450541

5

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.

Scerri TS, Morris AP, Buckingham LL, Newbury DF, Miller LL, Monaco AP, Bishop DV, Paracchini S. Scerri TS, et al. Biol Psychiatry. 2011 Aug 1;70(3):237-45. doi: 10.1016/j.biopsych.2011.02.005. Epub 2011 Mar 31. Biol Psychiatry. 2011. PMID: 21457949 Free PMC article.

6

Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.

Marino C, Citterio A, Giorda R, Facoetti A, Menozzi G, Vanzin L, Lorusso ML, Nobile M, Molteni M. Marino C, et al. Genes Brain Behav. 2007 Oct;6(7):640-6. doi: 10.1111/j.1601-183X.2006.00291.x. Epub 2007 Feb 13. Genes Brain Behav. 2007. PMID: 17309662 Free article.

7

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, Scerri T, Stein J, Pembrey ME, Ragoussis J, Golding J, Monaco AP. Paracchini S, et al. Am J Psychiatry. 2008 Dec;165(12):1576-84. doi: 10.1176/appi.ajp.2008.07121872. Epub 2008 Oct 1. Am J Psychiatry. 2008. PMID: 18829873

8

Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.

Carrion-Castillo A, Maassen B, Franke B, Heister A, Naber M, van der Leij A, Francks C, Fisher SE. Carrion-Castillo A, et al. Eur J Hum Genet. 2017 Apr;25(4):452-460. doi: 10.1038/ejhg.2016.194. Epub 2017 Jan 11. Eur J Hum Genet. 2017. PMID: 28074887 Free PMC article.

9

A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.

Tran C, Gagnon F, Wigg KG, Feng Y, Gomez L, Cate-Carter TD, Kerr EN, Field LL, Kaplan BJ, Lovett MW, Barr CL. Tran C, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):146-56. doi: 10.1002/ajmg.b.32123. Epub 2013 Jan 22. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23341075 Free PMC article.

10

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.

Ludwig KU, Roeske D, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Ziegler A, Remschmidt H, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. J Neural Transm (Vienna). 2008 Nov;115(11):1587-9. doi: 10.1007/s00702-008-0124-6. Epub 2008 Sep 23. J Neural Transm (Vienna). 2008. PMID: 18810304

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