Sara Mascheretti

Sara Mascheretti

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Sara Mascheretti

Sara Mascheretti

Publications by authors named "Sara Mascheretti"

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19Publications

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The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects.

Neuropsychologia 2019 Jul 24;130:52-58. Epub 2018 May 24.

Child Psychopathology Unit, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.neuropsychologia.2018.05.021DOI Listing
July 2019

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

Neuropsychologia 2019 Jul 23;130:44-51. Epub 2018 Aug 23.

Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA; Haskins Laboratories, New Haven, CT, USA. Electronic address:

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http://dx.doi.org/10.1016/j.neuropsychologia.2018.07.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542718PMC
July 2019

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

Br J Psychiatry 2019 03;214(3):137-145

Associate Professor,School of Criminology,University of Montreal and The Montreal Mental Health University Institute,Canada.

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http://dx.doi.org/10.1192/bjp.2018.251DOI Listing
March 2019

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

Res Dev Disabil 2018 Nov 19;82:147-152. Epub 2018 Mar 19.

Vita-Salute San Raffaele University, Milano, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08914222183005
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http://dx.doi.org/10.1016/j.ridd.2018.03.005DOI Listing
November 2018

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

J Hum Genet 2017 Nov 3;62(11):949-955. Epub 2017 Aug 3.

Child Psychopathology Unit, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Italy.

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http://dx.doi.org/10.1038/jhg.2017.80DOI Listing
November 2017

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

Neuropsychology 2017 Jul 6;31(5):475-485. Epub 2017 Apr 6.

Department of Child Psychiatry, Scientific Institute, IRCCS Eugenio Medea.

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http://dx.doi.org/10.1037/neu0000376DOI Listing
July 2017

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

Am J Med Genet B Neuropsychiatr Genet 2017 Jul 24;174(5):578-586. Epub 2017 Apr 24.

Scientific Institute, IRCCS Eugenio Medea, Child Psychopathology Unit, Bosisio Parini, Italy.

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http://dx.doi.org/10.1002/ajmg.b.32546DOI Listing
July 2017

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

J Child Psychol Psychiatry 2017 01 8;58(1):75-82. Epub 2016 Aug 8.

Child Psychopathology Unit, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Italy.

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http://dx.doi.org/10.1111/jcpp.12612DOI Listing
January 2017

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

J Learn Disabil 2015 Mar-Apr;48(2):120-9. Epub 2013 Jun 11.

Centre de recherche de l'Institut universitaire en santé mentale de Québec, Québec, Canada Université Laval, Québec, Canada.

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http://ldx.sagepub.com/content/early/2013/06/10/002221941349
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http://ldx.sagepub.com/cgi/doi/10.1177/0022219413492853
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http://dx.doi.org/10.1177/0022219413492853DOI Listing
December 2016

GRIN2B predicts attention problems among disadvantaged children.

Eur Child Adolesc Psychiatry 2015 Jul 16;24(7):827-36. Epub 2014 Oct 16.

Child Psychopathology Unit, Scientific Institute 'Eugenio Medea', Don L. Monza 20, Bosisio Parini (LC), Italy.

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http://dx.doi.org/10.1007/s00787-014-0627-7DOI Listing
July 2015

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

Cereb Cortex 2015 Jun 30;25(6):1685-95. Epub 2014 Sep 30.

Child Psychopathology Unit, Scientific Institute, IRCCS Eugenio Medea, 23842 Bosisio Parini, Lecco, Italy Centre de Recherche de L'Institut Universitaire en Santé Mentale de Québec, Québec, QC, Canada G1J 2G3 Département de Psychiatrie et Neurosciences, Faculté de Médecine, Université Laval, Québec, QC, Canada G1V 0A6.

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http://dx.doi.org/10.1093/cercor/bhu234DOI Listing
June 2015

Strong motion deficits in dyslexia associated with DCDC2 gene alteration.

J Neurosci 2015 May;35(21):8059-64

Department of Translational Research on New Technologies in Medicine and Surgery, University of Pisa, 56127 Pisa, Italy, and Scientific Institute Stella Maris, 56128 Pisa, Italy

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http://dx.doi.org/10.1523/JNEUROSCI.5077-14.2015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888943PMC
May 2015

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

Psychiatr Genet 2015 Feb;25(1):9-20

aChild Psychopathology Unit, Department of Child Psychiatry bMolecular Biology Laboratory, Scientific Institute 'Eugenio Medea', Bosisio Parini (Lecco) cDevelopmental and Cognitive Neuroscience Lab, Department of General Psychology, University of Padua, Padua dRegional Reference Center for the Specific Learning Disability, ULSS 20, Verona, Italy eCentre de recherche de l'Institut universitaire en santé mentale de Québec fDepartment of Psychiatry and Neuroscience, Laval University, Québec, Canada.

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http://dx.doi.org/10.1097/YPG.0000000000000068DOI Listing
February 2015

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

Cortex 2014 Aug 9;57:227-43. Epub 2014 May 9.

C.E.R.M.A.C. (Centro di Risonanza Magnetica ad Alto Campo), Milan, Italy; Department of Nuclear Medicine San Raffaele Hospital and Division of Neuroscience, Scientific Institute San Raffaele, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00109452140013
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http://dx.doi.org/10.1016/j.cortex.2014.04.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975637PMC
August 2014

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

J Hum Genet 2014 Apr 16;59(4):189-97. Epub 2014 Jan 16.

1] Centre de recherche de l'Institut universitaire en santé mentale de Québec, Québec, QC, Canada [2] Département de Psychiatrie et Neurosciences, Faculté de Médecine, Université Laval, Québec, QC, Canada.

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http://dx.doi.org/10.1038/jhg.2013.141DOI Listing
April 2014

DCDC2 genetic variants and susceptibility to developmental dyslexia.

Psychiatr Genet 2012 Feb;22(1):25-30

Department of Child Psychiatry, Scientific Institute Eugenio Medea, Bosisio Parini, Italy.

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http://dx.doi.org/10.1097/YPG.0b013e32834acdb2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232293PMC
February 2012