ISSN: 1866-1947

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Journal of Neurodevelopmental Disorders Q1 Unclaimed

BioMed Central Ltd United Kingdom

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Journal of Neurodevelopmental Disorders is a journal indexed in SJR in Pathology and Forensic Medicine and Neurology (clinical) with an H index of 61. It is an CC BY + CC0 Journal with a Single blind Peer Review review system, and It has a price of 2290 €. The scope of the journal is focused on neurobiology, genetics, cognitive neuroscience, psychiatry, psychology. It has an SJR impact factor of 1,422 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,422.

Type: Journal

Type of Copyright: CC BY + CC0

Languages: English

Open Access Policy: Open Access

Type of publications:

Publication frecuency: -

Categories: Cognitive Neuroscience (Q1) Neurology (clinical) (Q1) Pathology and Forensic Medicine (Q1) Pediatrics, Perinatology and Child Health (Q1)

Price

2290 €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

1,422

SJR Impact factor

61

H Index

42

Total Docs (Last Year)

160

Total Docs (3 years)

2547

Total Refs

755

Total Cites (3 years)

158

Citable Docs (3 years)

4.13

Cites/Doc (2 years)

60.64

Ref/Doc

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Aims and Scope

Neurobiology Genetics Cognitive neuroscience Psychiatry Psychology

Best articles by citations

Repetitive and self-injurious behaviors: associations with caudate volume in autism and fragile X syndrome

Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

Erratum to: Neural correlates of reward processing in adults with 22q11 deletion syndrome

Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene

Event-based prospective memory performance in autism spectrum disorder

The neural basis of auditory temporal discrimination in girls with fragile X syndrome

White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents

Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed

Motor function and perception in children with neuropsychiatric and conduct problems: results from a population based twin study

Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism

Prenatal exposure to beta2-adrenergic receptor agonists and risk of autism spectrum disorders

Erratum to: A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome

SHOW MORE ARTICLES

Verbal short-term memory deficits in Down syndrome: phonological, semantic, or both?

The broad autism phenotype predicts child functioning in autism spectrum disorders

Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome

Route knowledge and configural knowledge in typical and atypical development: a comparison of sparse and rich environments

Patterns of autism spectrum symptomatology in individuals with Down syndrome without comorbid autism spectrum disorder

Prader-Willi syndrome and autism spectrum disorders: an evolving story

Event-related potentials to repeated speech in 9-month-old infants at risk for autism spectrum disorder

Infant head growth in male siblings of children with and without autism spectrum disorders

Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance

A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome

Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits

The effect of intellectual ability on functional activation in a neurodevelopmental disorder: preliminary evidence from multiple fMRI studies in Williams syndrome