Marino C - Search Results

1

Putative risk factors in developmental dyslexia: a case-control study of Italian children.

Mascheretti S, Marino C, Simone D, Quadrelli E, Riva V, Cellino MR, Maziade M, Brombin C, Battaglia M. Mascheretti S, et al. Among authors: marino c. J Learn Disabil. 2015 Mar-Apr;48(2):120-9. doi: 10.1177/0022219413492853. Epub 2013 Jun 11. J Learn Disabil. 2015. PMID: 23757350

2

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. Mascheretti S, et al. Among authors: marino c. J Hum Genet. 2014 Apr;59(4):189-97. doi: 10.1038/jhg.2013.141. Epub 2014 Jan 16. J Hum Genet. 2014. PMID: 24430574

3

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. Mascheretti S, et al. Among authors: marino c. Psychiatr Genet. 2015 Feb;25(1):9-20. doi: 10.1097/YPG.0000000000000068. Psychiatr Genet. 2015. PMID: 25426763

4

An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.

Mascheretti S, Bureau A, Battaglia M, Simone D, Quadrelli E, Croteau J, Cellino MR, Giorda R, Beri S, Maziade M, Marino C. Mascheretti S, et al. Among authors: marino c. Genes Brain Behav. 2013 Feb;12(1):47-55. doi: 10.1111/gbb.12000. Epub 2012 Nov 24. Genes Brain Behav. 2013. PMID: 23176554 Free article.

5

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. Marino C, et al. Behav Genet. 2011 Jan;41(1):67-76. doi: 10.1007/s10519-010-9412-7. Epub 2010 Nov 3. Behav Genet. 2011. PMID: 21046216 Free PMC article.

6

DCDC2 genetic variants and susceptibility to developmental dyslexia.

Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR. Marino C, et al. Psychiatr Genet. 2012 Feb;22(1):25-30. doi: 10.1097/YPG.0b013e32834acdb2. Psychiatr Genet. 2012. PMID: 21881542 Free PMC article.

7

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. Gori S, et al. Among authors: marino c. Cereb Cortex. 2015 Jun;25(6):1685-95. doi: 10.1093/cercor/bhu234. Epub 2014 Sep 30. Cereb Cortex. 2015. PMID: 25270309

8

GRIN2B predicts attention problems among disadvantaged children.

Riva V, Battaglia M, Nobile M, Cattaneo F, Lazazzera C, Mascheretti S, Giorda R, Mérette C, Émond C, Maziade M, Marino C. Riva V, et al. Among authors: marino c. Eur Child Adolesc Psychiatry. 2015 Jul;24(7):827-36. doi: 10.1007/s00787-014-0627-7. Epub 2014 Oct 16. Eur Child Adolesc Psychiatry. 2015. PMID: 25316095

9

Strong motion deficits in dyslexia associated with DCDC2 gene alteration.

Cicchini GM, Marino C, Mascheretti S, Perani D, Morrone MC. Cicchini GM, et al. Among authors: marino c. J Neurosci. 2015 May 27;35(21):8059-64. doi: 10.1523/JNEUROSCI.5077-14.2015. J Neurosci. 2015. PMID: 26019324 Free PMC article.

10

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. Mascheretti S, et al. Among authors: marino c. J Child Psychol Psychiatry. 2017 Jan;58(1):75-82. doi: 10.1111/jcpp.12612. Epub 2016 Aug 8. J Child Psychol Psychiatry. 2017. PMID: 27501527

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