about
DCDC2 genetic variants and susceptibility to developmental dyslexiaCharacterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQYoung 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 timeNeurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanismsThe DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.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 trajectoriesStrong motion deficits in dyslexia associated with DCDC2 gene alteration.Shared neurocognitive dysfunctions in young offspring at extreme risk for schizophrenia or bipolar disorder in eastern quebec multigenerational familiesPleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.The Italian preadolescent mental health project (PrISMA): rationale and methods.Auditory discrimination predicts linguistic outcome in Italian infants with and without familial risk for language learning impairment.Phenotypic and genetic associations between reading comprehension, decoding skills, and ADHD dimensions: evidence from two population-based studies.Putative risk factors in developmental dyslexia: a case-control study of Italian children.The influence of family structure, the TPH2 G-703T and the 5-HTTLPR serotonergic genes upon affective problems in children aged 10-14 years.An assessment of transmission disequilibrium between quantitative measures of childhood problem behaviors and DRD2/Taql and DRD4/48bp-repeat polymorphisms.Influence of the serotonin transporter promoter gene and shyness on children's cerebral responses to facial expressions.GRIN2B predicts attention problems among disadvantaged children.Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia.The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.Effect of the catechol-O-methyltransferase val(158)met genotype on children's early phases of facial stimuli processing.An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia.The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability.KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.Variants in SNAP25 are targets of natural selection and influence verbal performances in women.Analysis of the D4 Dopamine Receptor Gene Variant in an Italian Schizophrenia KindredA genetic linkage study of schizophrenia to chromosome 5 markers in a Northern Italian populationAmino acid patterns in schizophrenia: Some new findingsCautionary note: complex (dys)function of the serotonin transporterGene-Environment Interaction and Behavioral Disorders: A Developmental Perspective Based on Endophenotypes
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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type
label
Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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Cecilia Marino
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P106
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7102632247
P21
P31
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0000-0001-9308-5610