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Items: 1 to 20 of 100

1.

The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects.

Riva V, Mozzi A, Forni D, Trezzi V, Giorda R, Riva S, Villa M, Sironi M, Cagliani R, Mascheretti S.

Neuropsychologia. 2019 Jul;130:52-58. doi: 10.1016/j.neuropsychologia.2018.05.021. Epub 2018 May 24.

PMID:
29803723
2.

The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects.

Trezzi V, Forni D, Giorda R, Villa M, Molteni M, Marino C, Mascheretti S.

J Hum Genet. 2017 Nov;62(11):949-955. doi: 10.1038/jhg.2017.80. Epub 2017 Aug 3.

PMID:
29066855
3.

DCDC2 genetic variants and susceptibility to developmental dyslexia.

Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR.

Psychiatr Genet. 2012 Feb;22(1):25-30. doi: 10.1097/YPG.0b013e32834acdb2.

4.

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
5.

The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.

Riva V, Marino C, Giorda R, Molteni M, Nobile M.

Eur Child Adolesc Psychiatry. 2015 Mar;24(3):309-18. doi: 10.1007/s00787-014-0580-5. Epub 2014 Jul 11.

PMID:
25012462
6.

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
7.

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
8.

Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children.

Waye MMY, Poo LK, Ho CS.

Clin Pract Epidemiol Ment Health. 2017 Aug 21;13:104-114. doi: 10.2174/1745017901713010104. eCollection 2017.

9.

Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.

Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JR, Giorda R, Lazazzera C, Molteni M.

Behav Genet. 2011 Jan;41(1):67-76. doi: 10.1007/s10519-010-9412-7. Epub 2010 Nov 3.

10.

KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.

Mascheretti S, Riva V, Giorda R, Beri S, Lanzoni LF, Cellino MR, Marino C.

J Hum Genet. 2014 Apr;59(4):189-97. doi: 10.1038/jhg.2013.141. Epub 2014 Jan 16.

PMID:
24430574
11.

The role of gene DCDC2 in German dyslexics.

Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P.

Ann Dyslexia. 2009 Jun;59(1):1-11. doi: 10.1007/s11881-008-0020-7. Epub 2009 Feb 24.

PMID:
19238550
12.

The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability.

Gori S, Mascheretti S, Giora E, Ronconi L, Ruffino M, Quadrelli E, Facoetti A, Marino C.

Cereb Cortex. 2015 Jun;25(6):1685-95. doi: 10.1093/cercor/bhu234. Epub 2014 Sep 30.

PMID:
25270309
13.

Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample.

Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC.

Eur J Hum Genet. 2010 Jun;18(6):668-73. doi: 10.1038/ejhg.2009.237. Epub 2010 Jan 13.

14.

The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.

Marino C, Scifo P, Della Rosa PA, Mascheretti S, Facoetti A, Lorusso ML, Giorda R, Consonni M, Falini A, Molteni M, Gruen JR, Perani D.

Cortex. 2014 Aug;57:227-43. doi: 10.1016/j.cortex.2014.04.016. Epub 2014 May 9.

15.

DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.

Chen Y, Zhao H, Zhang YX, Zuo PX.

Neural Regen Res. 2017 Feb;12(2):259-266. doi: 10.4103/1673-5374.200809.

16.

A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.

Devasenapathy S, Midha R, Naskar T, Mehta A, Prajapati B, Ummekulsum M, Sagar R, Singh NC, Sinha S.

Asian J Psychiatr. 2018 Oct;37:121-129. doi: 10.1016/j.ajp.2018.08.020. Epub 2018 Aug 25.

PMID:
30199849
17.

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.

18.

GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia.

Mascheretti S, Facoetti A, Giorda R, Beri S, Riva V, Trezzi V, Cellino MR, Marino C.

Psychiatr Genet. 2015 Feb;25(1):9-20. doi: 10.1097/YPG.0000000000000068.

PMID:
25426763
19.

The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.

Powers NR, Eicher JD, Miller LL, Kong Y, Smith SD, Pennington BF, Willcutt EG, Olson RK, Ring SM, Gruen JR.

J Med Genet. 2016 Mar;53(3):163-71. doi: 10.1136/jmedgenet-2015-103418. Epub 2015 Dec 11.

20.

Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia.

Zhong R, Yang B, Tang H, Zou L, Song R, Zhu LQ, Miao X.

Mol Neurobiol. 2013 Feb;47(1):435-42. doi: 10.1007/s12035-012-8381-7. Epub 2012 Dec 11.

PMID:
23229871

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