| Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms S Mascheretti, A De Luca, V Trezzi, D Peruzzo, A Nordio, C Marino, ... Translational psychiatry 7 (1), e987-e987, 2017 | 159 | 2017 |
| An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypes S Mascheretti, A Bureau, M Battaglia, D Simone, E Quadrelli, J Croteau, ... Genes, Brain and Behavior 12 (1), 47-55, 2013 | 96 | 2013 |
| DCDC2 genetic variants and susceptibility to developmental dyslexia C Marino, H Meng, S Mascheretti, M Rusconi, N Cope, R Giorda, ... Psychiatric genetics 22 (1), 25-30, 2012 | 96 | 2012 |
| The DCDC2 Intron 2 Deletion Impairs Illusory Motion Perception Unveiling the Selective Role of Magnocellular-Dorsal Stream in Reading (Dis)ability S Gori, S Mascheretti, E Giora, L Ronconi, M Ruffino, E Quadrelli, ... Cerebral Cortex 25 (6), 1685-1695, 2015 | 81 | 2015 |
| The evolutionary history of genes involved in spoken and written language: beyond FOXP2 A Mozzi, D Forni, M Clerici, U Pozzoli, S Mascheretti, FR Guerini, S Riva, ... Scientific reports 6 (1), 1-12, 2016 | 74 | 2016 |
| KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia S Mascheretti, V Riva, R Giorda, S Beri, LFE Lanzoni, MR Cellino, ... Journal of Human Genetics 59 (4), 189-197, 2014 | 70 | 2014 |
| Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia C Marino, S Mascheretti, V Riva, F Cattaneo, C Rigoletto, M Rusconi, ... Behavior genetics 41, 67-76, 2011 | 68 | 2011 |
| The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia C Marino, P Scifo, PA Della Rosa, S Mascheretti, A Facoetti, ML Lorusso, ... Cortex 57, 227-243, 2014 | 61 | 2014 |
| Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ JD Eicher, NR Powers, LL Miller, KL Mueller, S Mascheretti, C Marino, ... Human Genetics 133, 869-881, 2014 | 58 | 2014 |
| Beyond genes: A systematic review of environmental risk factors in specific reading disorder S Mascheretti, C Andreola, S Scaini, S Sulpizio Research in Developmental Disabilities 82, 147-152, 2018 | 49 | 2018 |
| Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples S Mascheretti, V Trezzi, R Giorda, M Boivin, V Plourde, F Vitaro, ... Journal of Child Psychology and Psychiatry 58 (1), 75-82, 2017 | 49 | 2017 |
| Strong motion deficits in dyslexia associated with DCDC2 gene alteration GM Cicchini, C Marino, S Mascheretti, D Perani, MC Morrone Journal of Neuroscience 35 (21), 8059-8064, 2015 | 43 | 2015 |
| The heritability of reading and reading-related neurocognitive components: A multi-level meta-analysis C Andreola, S Mascheretti, R Belotti, A Ogliari, C Marino, M Battaglia, ... Neuroscience & Biobehavioral Reviews 121, 175-200, 2021 | 41 | 2021 |
| GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia S Mascheretti, A Facoetti, R Giorda, S Beri, V Riva, V Trezzi, MR Cellino, ... Psychiatric genetics 25 (1), 9-20, 2015 | 40 | 2015 |
| Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia S Mascheretti, S Gori, V Trezzi, M Ruffino, A Facoetti, C Marino Genes, Brain and Behavior 17 (1), 70-81, 2018 | 34 | 2018 |
| Putative risk factors in developmental dyslexia: A case-control study of Italian children S Mascheretti, C Marino, D Simone, E Quadrelli, V Riva, MR Cellino, ... Journal of learning disabilities 48 (2), 120-129, 2015 | 27 | 2015 |
| Working memory mediates the effects of gestational age at birth on expressive language development in children. V Riva, C Cantiani, G Dionne, A Marini, S Mascheretti, M Molteni, ... Neuropsychology 31 (5), 475, 2017 | 26 | 2017 |
| Sluggish dorsally-driven inhibition of return during orthographic processing in adults with dyslexia S Franceschini, S Mascheretti, S Bertoni, V Trezzi, C Andreola, S Gori, ... Brain and language 179, 1-10, 2018 | 25 | 2018 |
| An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia S Mascheretti, A Bureau, V Trezzi, R Giorda, C Marino Human genetics 134, 749-760, 2015 | 25 | 2015 |
| A common genetic variant in FOXP2 is associated with language‐based learning (dis)abilities: Evidence from two Italian independent samples A Mozzi, V Riva, D Forni, M Sironi, C Marino, M Molteni, S Riva, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 …, 2017 | 23 | 2017 |
