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2018

Beyond genes: A systematic review of environmental risk factors in specific reading disorder

Mascheretti, S., Andreola, C., Scaini, S. & Sulpizio, S., 2018, In : Research in Developmental Disabilities. 82, p. 147-152 6 p.

Research output: Contribution to journalArticle

Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation

Perdue, M. V., Mascheretti, S., Kornilov, S. A., Jasińska, K. K., Ryherd, K., Einar Mencl, W., Frost, S. J., Grigorenko, E. L., Pugh, K. R. & Landi, N., 2018, In : Neuropsychologia.

Research output: Contribution to journalArticle

Cumulative risk and protection effect of serotonergic genes on male antisocial behaviour: results from a prospective cohort assessed in adolescence and early adulthood

Langevin, S., Mascheretti, S., Cote, S., Vitaro, F., Boivin, M., Turecki, G., Tremblay, R. T. & Ouellett-Morin, I., 2018, In : British Journal of Psychiatry. 9 p.

Research output: Contribution to journalArticle

Sluggish dorsally-driven inhibition of return during orthographic processing in adults with dyslexia

Franceschini, S., Mascheretti, S., Bertoni, S., Trezzi, V., Andreola, C., Gori, S. & Facoetti, A., Apr 1 2018, In : Brain and Language. 179, p. 1-10 10 p.

Research output: Contribution to journalArticle

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

Mascheretti, S., Gori, S., Trezzi, V., Ruffino, M., Facoetti, A. & Marino, C., Jan 1 2018, In : Genes, Brain and Behavior. 17, 1, p. 70-81 12 p.

Research output: Contribution to journalArticle

Open Access

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., 2017, In : Journal of Child Psychology and Psychiatry and Allied Disciplines. 58, 1, p. 75-82

Research output: Contribution to journalArticle

Working memory mediates the effects of gestational age at birth on expressive language development in children

Riva, V., Cantiani, C., Dionne, G., Marini, A., Mascheretti, S., Molteni, M. & Marino, C., Jul 1 2017, In : Neuropsychology. 31, 5, p. 475-485 11 p.

Research output: Contribution to journalArticle

2016
2015

An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia

Mascheretti, S., Bureau, A., Trezzi, V., Giorda, R. & Marino, C., Apr 28 2015, In : Human Genetics. 134, 7, p. 749-760 12 p.

Research output: Contribution to journalArticle

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, M. R. & Marino, C., Feb 3 2015, In : Psychiatric Genetics. 25, 1, p. 9-20 12 p.

Research output: Contribution to journalArticle

Monoamine oxidase A polymorphism moderates stability of attention problems and susceptibility to life stress during adolescence

Zohsel, K., Bianchi, V., Mascheretti, S., Hohm, E., Schmidt, M. H., Esser, G., Brandeis, D., Banaschewski, T., Nobile, M. & Laucht, M., Nov 1 2015, In : Genes, Brain and Behavior. 14, 8, p. 565-572 8 p.

Research output: Contribution to journalArticle

Putative Risk Factors in Developmental Dyslexia: A Case-Control Study of Italian Children

Mascheretti, S., Marino, C., Simone, D., Quadrelli, E., Riva, V., Cellino, M. R., Maziade, M., Brombin, C. & Battaglia, M., Mar 13 2015, In : Journal of Learning Disabilities. 48, 2, p. 120-129 10 p.

Research output: Contribution to journalArticle

Strong motion deficits in dyslexia associated with DCDC2 gene alteration

Cicchini, G. M., Marino, C., Mascheretti, S., Perani, D. & Morrone, M. C., May 27 2015, In : Journal of Neuroscience. 35, 21, p. 8059-8064 6 p.

Research output: Contribution to journalArticle

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., Jun 1 2015, In : Cerebral Cortex. 25, 6, p. 1685-1695 11 p.

Research output: Contribution to journalArticle

2014

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

Eicher, J. D., Powers, N. R., Miller, L. L., Mueller, K. L., Mascheretti, S., Marino, C., Willcutt, E. G., DeFries, J. C., Olson, R. K., Smith, S. D., Pennington, B. F., Tomblin, J. B., Ring, S. M. & Gruen, J. R., 2014, In : Human Genetics. 133, 7, p. 869-881 13 p.

Research output: Contribution to journalArticle

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., Oct 16 2014, In : European Child and Adolescent Psychiatry. 24, 7, p. 827-836 10 p., A009.

Research output: Contribution to journalArticle

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, L. F. E., Cellino, M. R. & Marino, C., 2014, In : Journal of Human Genetics. 59, 4, p. 189-197 9 p.

Research output: Contribution to journalArticle

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

Marino, C., Scifo, P., Della Rosa, P. A., Mascheretti, S., Facoetti, A., Lorusso, M. L., Giorda, R., Consonni, M., Falini, A., Molteni, M., Gruen, J. R. & Perani, D., 2014, In : Cortex. 57, p. 227-243 17 p.

Research output: Contribution to journalArticle

2013

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, M. R., Giorda, R., Beri, S., Maziade, M. & Marino, C., Feb 2013, In : Genes, Brain and Behavior. 12, 1, p. 47-55 9 p.

Research output: Contribution to journalArticle

2012

DCDC2 genetic variants and susceptibility to developmental dyslexia

Marino, C., Meng, H., Mascheretti, S., Rusconi, M., Cope, N., Giorda, R., Molteni, M. & Gruen, J. R., Feb 2012, In : Psychiatric Genetics. 22, 1, p. 25-30 6 p.

Research output: Contribution to journalArticle

2011

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, J. R., Giorda, R., Lazazzera, C. & Molteni, M., Jan 2011, In : Behavior Genetics. 41, 1, p. 67-76 10 p.

Research output: Contribution to journalArticle