Marino C - Search Results

1

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.

2

An assessment of transmission disequilibrium between quantitative measures of childhood problem behaviors and DRD2/Taql and DRD4/48bp-repeat polymorphisms.

Marino C, Vanzin L, Giorda R, Frigerio A, Lorusso ML, Nobile M, Molteni M, Battaglia M. Marino C, et al. Behav Genet. 2004 Sep;34(5):495-502. doi: 10.1023/B:BEGE.0000038487.80597.7e. Behav Genet. 2004. PMID: 15319572

3

A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.

Marino C, Giorda R, Luisa Lorusso M, Vanzin L, Salandi N, Nobile M, Citterio A, Beri S, Crespi V, Battaglia M, Molteni M. Marino C, et al. Eur J Hum Genet. 2005 Apr;13(4):491-9. doi: 10.1038/sj.ejhg.5201356. Eur J Hum Genet. 2005. PMID: 15702132

4

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.

5

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.

6

No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes.

Marino C, Giorda R, Vanzin L, Molteni M, Lorusso ML, Nobile M, Baschirotto C, Alda M, Battaglia M. Marino C, et al. Eur Child Adolesc Psychiatry. 2003 Aug;12(4):198-202. doi: 10.1007/s00787-003-0332-4. Eur Child Adolesc Psychiatry. 2003. PMID: 14505070

7

Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia.

Mascheretti S, Gori S, Trezzi V, Ruffino M, Facoetti A, Marino C. Mascheretti S, et al. Among authors: marino c. Genes Brain Behav. 2018 Jan;17(1):70-81. doi: 10.1111/gbb.12409. Epub 2017 Sep 14. Genes Brain Behav. 2018. PMID: 28834383 Free article.

8

A case-control and family-based association study of the 5-HTTLPR in pediatric-onset depressive disorders.

Nobile M, Cataldo MG, Giorda R, Battaglia M, Baschirotto C, Bellina M, Marino C, Molteni M. Nobile M, et al. Among authors: marino c. Biol Psychiatry. 2004 Aug 15;56(4):292-5. doi: 10.1016/j.biopsych.2004.05.018. Biol Psychiatry. 2004. PMID: 15312818

9

Socioeconomic status mediates the genetic contribution of the dopamine receptor D4 and serotonin transporter linked promoter region repeat polymorphisms to externalization in preadolescence.

Nobile M, Giorda R, Marino C, Carlet O, Pastore V, Vanzin L, Bellina M, Molteni M, Battaglia M. Nobile M, et al. Among authors: marino c. Dev Psychopathol. 2007 Fall;19(4):1147-60. doi: 10.1017/S0954579407000594. Dev Psychopathol. 2007. PMID: 17931440

10

The influence of family structure, the TPH2 G-703T and the 5-HTTLPR serotonergic genes upon affective problems in children aged 10-14 years.

Nobile M, Rusconi M, Bellina M, Marino C, Giorda R, Carlet O, Vanzin L, Molteni M, Battaglia M. Nobile M, et al. Among authors: marino c. J Child Psychol Psychiatry. 2009 Mar;50(3):317-25. doi: 10.1111/j.1469-7610.2008.01958.x. Epub 2008 Nov 1. J Child Psychol Psychiatry. 2009. PMID: 19175813

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