Lista de obras - Cecilia Marino - Dominio Público Uruguay

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

artículo científico publicado en 2005

A genetic linkage study of schizophrenia to chromosome 5 markers in a Northern Italian population

article

Amino acid patterns in schizophrenia: Some new findings

artículo científico publicado en 1990

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

artículo científico publicado en 2012

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

artículo científico publicado en 2015

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

artículo científico publicado en 2004

Analysis of the D4 Dopamine Receptor Gene Variant in an Italian Schizophrenia Kindred

article

Auditory discrimination predicts linguistic outcome in Italian infants with and without familial risk for language learning impairment.

artículo científico publicado en 2016

Cautionary note: complex (dys)function of the serotonin transporter

artículo científico publicado en 2000

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

DCDC2 genetic variants and susceptibility to developmental dyslexia

artículo científico publicado en 2012

Do insomnia and/or sleep disturbances predict the onset, relapse or worsening of depression in community and clinical samples of children and youth? Protocol for a systematic review and meta-analysis

scientific article published on 30 August 2020

Effect of the catechol-O-methyltransferase val(158)met genotype on children's early phases of facial stimuli processing.

artículo científico publicado en 2006

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

artículo científico publicado en 2015

GRIN2B predicts attention problems among disadvantaged children.

artículo científico publicado en 2014

Gene-environment interaction and behavioral disorders: a developmental perspective based on endophenotypes

artículo científico publicado en 2008

Influence of the serotonin transporter promoter gene and shyness on children's cerebral responses to facial expressions

artículo científico publicado en 2005

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

artículo científico publicado en 2014

Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms

artículo científico publicado en 2017

Phenotypic and genetic associations between reading comprehension, decoding skills, and ADHD dimensions: evidence from two population-based studies

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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

artículo científico publicado en 2013

Shared neurocognitive dysfunctions in young offspring at extreme risk for schizophrenia or bipolar disorder in eastern quebec multigenerational families

artículo científico publicado en 2008

Strong motion deficits in dyslexia associated with DCDC2 gene alteration

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

The Italian preadolescent mental health project (PrISMA): rationale and methods.

artículo científico publicado en 2006

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

artículo científico publicado en 2008

The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.

artículo científico publicado en 2014

Variants in SNAP25 are targets of natural selection and influence verbal performances in women.

artículo científico publicado en 2011

Verbal and visual memory impairments among young offspring and healthy adult relatives of patients with schizophrenia and bipolar disorder: selective generational patterns indicate different developmental trajectories

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Young offspring at genetic risk of adult psychoses: the form of the trajectory of IQ or memory may orient to the right dysfunction at the right time

artículo científico publicado en 2011

Lista de obras de Cecilia Marino

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

A genetic linkage study of schizophrenia to chromosome 5 markers in a Northern Italian population

Amino acid patterns in schizophrenia: Some new findings

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

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

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

Analysis of the D4 Dopamine Receptor Gene Variant in an Italian Schizophrenia Kindred

Auditory discrimination predicts linguistic outcome in Italian infants with and without familial risk for language learning impairment.

Cautionary note: complex (dys)function of the serotonin transporter

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

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

DCDC2 genetic variants and susceptibility to developmental dyslexia

Do insomnia and/or sleep disturbances predict the onset, relapse or worsening of depression in community and clinical samples of children and youth? Protocol for a systematic review and meta-analysis

Effect of the catechol-O-methyltransferase val(158)met genotype on children's early phases of facial stimuli processing.

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

GRIN2B predicts attention problems among disadvantaged children.

Gene-environment interaction and behavioral disorders: a developmental perspective based on endophenotypes

Influence of the serotonin transporter promoter gene and shyness on children's cerebral responses to facial expressions

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

Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms

Phenotypic and genetic associations between reading comprehension, decoding skills, and ADHD dimensions: evidence from two population-based studies

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

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

Shared neurocognitive dysfunctions in young offspring at extreme risk for schizophrenia or bipolar disorder in eastern quebec multigenerational families

Strong motion deficits in dyslexia associated with DCDC2 gene alteration

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

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

The Italian preadolescent mental health project (PrISMA): rationale and methods.

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

The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.

Variants in SNAP25 are targets of natural selection and influence verbal performances in women.

Verbal and visual memory impairments among young offspring and healthy adult relatives of patients with schizophrenia and bipolar disorder: selective generational patterns indicate different developmental trajectories

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

Young offspring at genetic risk of adult psychoses: the form of the trajectory of IQ or memory may orient to the right dysfunction at the right time