IRIS
MASCHERETTI, SARA
 Distribuzione geografica
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Continente #
NA - Nord America 164
AS - Asia 62
EU - Europa 61
Totale 287
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Nazione #
US - Stati Uniti d'America 164
CN - Cina 42
FI - Finlandia 25
IT - Italia 22
SG - Singapore 20
DE - Germania 4
CZ - Repubblica Ceca 3
FR - Francia 3
IE - Irlanda 2
PT - Portogallo 2
Totale 287
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Città #
Ashburn 54
Boardman 41
Helsinki 25
Shanghai 19
Singapore 11
Dallas 7
Milan 4
Washington 4
Cerignola 3
Aveiro 2
Beijing 2
Brno 2
Dublin 2
Frankfurt am Main 2
Genoa 2
Jiaxing 2
Jinan 2
Los Angeles 2
Pavia 2
Perugia 2
Piscataway 2
Reggio Emilia 2
Sassari 2
Seattle 2
Udine 2
Council Bluffs 1
Huangshi 1
Jilin City 1
Liaocheng 1
Mountain View 1
Olomouc 1
Xiangtan 1
Yantai 1
Totale 208
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Nome #
Working memory mediates the effects of gestational age at birth on expressive language development in children 19
Action video games normalise the phonemic awareness in pre-readers at risk for developmental dyslexia 16
From BDNF to reading: Neural activation and phonological processing as multiple mediators 15
Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation 14
GRIN2B predicts attention problems among disadvantaged children 14
Beyond genes: A systematic review of environmental risk factors in specific reading disorder 13
DCDC2 genetic variants and susceptibility to developmental dyslexia 11
Continuity and change of genetic and environmental influences on reading and reading-related neurocognitive skills: A systematic review of longitudinal twin studies 11
An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes 11
Animal models of developmental dyslexia: Where we are and what we are missing 11
Genetic and phenotypic evidence of the predictive validity of preschool parent reports of hyperactivity/impulsivity and inattention 11
GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia 10
Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples 9
An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia 9
A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples 8
White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant 8
The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia 8
Strong motion deficits in dyslexia associated with DCDC2 gene alteration 8
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ 8
KIAA0319 and ROBO1: Evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia 7
Sluggish dorsally-driven inhibition of return during orthographic processing in adults with dyslexia 7
The heritability of reading and reading-related neurocognitive components: A multi-level meta-analysis 7
Long-Lasting Effects of Changes in Daily Routine during the Pandemic-Related Lockdown on Preschoolers’ Language and Emotional–Behavioral Development: A Moderation Analysis 7
Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion 7
Cumulative risk and protection effect of serotonergic genes on male antisocial behaviour: Results from a prospective cohort assessed in adolescence and early adulthood 7
Neurogenetics of developmental dyslexia: From genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms 7
Putative Risk Factors in Developmental Dyslexia: A Case-Control Study of Italian Children 7
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia 6
Brain Alteration Patterns in Children with Duchenne Muscular Dystrophy: A Machine Learning Approach to Magnetic Resonance Imaging 6
Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia 5
Monoamine oxidase A polymorphism moderates stability of attention problems and susceptibility to life stress during adolescence 5
Illusory Motion Perception Is Impaired in individuals with DCDC2 Intron 2 Deletion showing the Selective Role of Magnocellular-Dorsal Stream in Dyslexia 5
Selecting the most relevant brain regions to classify children with developmental dyslexia and typical readers by using complex magnocellular stimuli and multiple kernel learning 5
The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: Testing main and interactive effects 4
The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects 4
The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (Dis)ability 4
Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis 4
New Digital Technologies for Diagnosis and Rehabilitation of Neurodevelopmental Disorders 3
The mediation role of dynamic multisensory processing using molecular genetic data in dyslexia 3
The Benefits of Playing Action-Like Video Games on Salience Processing 3
The evolutionary history of genes involved in spoken and written language: Beyond FOXP2 3
Totale 330
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Categoria #
all - tutte 2.998
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.998
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202335 0 0 0 0 0 0 0 0 0 0 34 1
2023/2024223 30 11 19 12 25 37 4 9 0 10 32 34
2024/202572 22 50 0 0 0 0 0 0 0 0 0 0
Totale 330