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Items: 1 to 20 of 113

1.

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP.

Mol Psychiatry. 2006 Dec;11(12):1085-91, 1061. Epub 2006 Oct 10.

PMID:
17033633
2.

Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.

Sun Y, Gao Y, Zhou Y, Chen H, Wang G, Xu J, Xia J, Huen MS, Siok WT, Jiang Y, Tan LH.

Am J Med Genet B Neuropsychiatr Genet. 2014 Dec;165B(8):627-34. doi: 10.1002/ajmg.b.32267. Epub 2014 Sep 17.

PMID:
25230923
3.

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.

4.

Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB.

J Hum Genet. 2013 Aug;58(8):531-8. doi: 10.1038/jhg.2013.46. Epub 2013 May 16.

PMID:
23677054
5.

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.

J Neural Transm (Vienna). 2008 Nov;115(11):1587-9. doi: 10.1007/s00702-008-0124-6. Epub 2008 Sep 23.

PMID:
18810304
6.

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.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):556-60.

PMID:
17450541
7.

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ.

Eicher JD, Powers NR, Miller LL, Mueller KL, Mascheretti S, Marino C, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Tomblin JB, Ring SM, Gruen JR.

Hum Genet. 2014 Jul;133(7):869-81. doi: 10.1007/s00439-014-1427-3. Epub 2014 Feb 9.

8.

An examination of candidate gene SNPs for dyslexia in an Indian sample.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB.

Behav Genet. 2011 Jan;41(1):105-9. doi: 10.1007/s10519-010-9441-2. Epub 2011 Jan 4.

PMID:
21203818
9.

Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.

Mascheretti S, Trezzi V, Giorda R, Boivin M, Plourde V, Vitaro F, Brendgen M, Dionne G, Marino C.

J Child Psychol Psychiatry. 2017 Jan;58(1):75-82. doi: 10.1111/jcpp.12612. Epub 2016 Aug 8.

PMID:
27501527
10.

Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia.

Elbert A, Lovett MW, Cate-Carter T, Pitch A, Kerr EN, Barr CL.

Behav Genet. 2011 Jan;41(1):77-89. doi: 10.1007/s10519-010-9434-1. Epub 2011 Jan 5.

11.

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.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):447-462. doi: 10.1002/ajmg.b.30999.

12.

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.

Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, Coggill P, Beck S, Green ED, Monaco AP.

PLoS Genet. 2009 Mar;5(3):e1000436. doi: 10.1371/journal.pgen.1000436. Epub 2009 Mar 27.

13.

Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.

Shao S, Niu Y, Zhang X, Kong R, Wang J, Liu L, Luo X, Zhang J, Song R.

Sci Rep. 2016 Jul 28;6:30454. doi: 10.1038/srep30454.

14.

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP.

Behav Genet. 2011 Jan;41(1):90-104. doi: 10.1007/s10519-010-9424-3. Epub 2010 Dec 17.

15.

Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia.

Czamara D, Bruder J, Becker J, Bartling J, Hoffmann P, Ludwig KU, Müller-Myhsok B, Schulte-Körne G.

Behav Genet. 2011 Jan;41(1):110-9. doi: 10.1007/s10519-010-9413-6. Epub 2010 Nov 21.

PMID:
21104116
16.

Study of candidate genes for dyslexia in Brazilian individuals.

Svidnicki MC, Salgado CA, Lima RF, Ciasca SM, Secolin R, Pomilio MC, Junqueira PA, Pinto MS, Pereira MM, Sartorato EL.

Genet Mol Res. 2013 Nov 7;12(4):5356-64. doi: 10.4238/2013.November.7.10.

17.

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.

Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, Hoffmann P.

Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78.

PMID:
19018237
18.

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
19.

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.

Biol Psychiatry. 2011 Aug 1;70(3):237-45. doi: 10.1016/j.biopsych.2011.02.005. Epub 2011 Mar 31.

20.

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.

Eur J Hum Genet. 2017 Apr;25(4):452-460. doi: 10.1038/ejhg.2016.194. Epub 2017 Jan 11.

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