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List of works by Sara Mascheretti

A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples

scientific article published on 24 April 2017

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

scientific article published on 24 November 2012

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

scientific article

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

scientific article

Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.

scientific article published on 8 August 2016

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

scientific article published on 01 March 2019

DCDC2 genetic variants and susceptibility to developmental dyslexia

scientific article

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

scientific article published in February 2015

GRIN2B predicts attention problems among disadvantaged children.

scientific article published on 16 October 2014

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

scientific article published on 16 January 2014

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

scientific article published on 9 October 2015

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

scientific article

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

scientific article published on 11 June 2013

Strong motion deficits in dyslexia associated with DCDC2 gene alteration

scientific article published on May 2015

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

scientific article published on 30 September 2014

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

scientific article

The evolutionary history of genes involved in spoken and written language: beyond FOXP2.

scientific article

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

scientific article published on 3 August 2017

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