verified SJR 1,296 · Q1 • database Scopus / SJR & Web of Science & DOAJ indexed

United Kingdom · BioMed Central Ltd

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Journal of Neurodevelopmental Disorders

Journal of Neurodevelopmental Disorders is a journal indexed in SJR in Pathology and Forensic Medicine and Neurology (clinical) with an H index of 64. 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 1,296 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,296.

ISSN: 1866-1947

Publisher: BioMed Central Ltd

Category: Pathology and Forensic Medicine

Indexation: verifiedScopus / SJR verifiedWeb of Science verifiedDOAJ

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schedule CountryOfPapers database fields

SJR Impact Factor trending_up

1,296 Q1

H-index 64

Acceptance rate pie_chart

30% Selective

Source Acceptance_Rate

Time to publication hourglass_top

20 weeks

Field Average_time_publication_weeks

Publication cost (APC) payments

2.290 € Open Access

Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science DOAJ

SJR Impact

1,296

H-index

Docs (year)

Docs 3y

159

Total refs

4825

Cites 3y

723

Citable 3y

157

Cites/Doc 2y

4.03

Ref/Doc

67.96

Immediate OA

2290 €

Embargoed OA

NPD

Non OA / Submission

- €

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Best articles by citations

Attention and motor deficits index non-specific background liabilities that predict autism recurrence in siblings

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

Developmental learning impairments in a rodent model of nodular heterotopia

Cover essay

Cover art description

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

Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes

Cognitive training for children and adolescents with fragile X syndrome: a randomized controlled trial of Cogmed

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

Cerebellar-dependent delay eyeblink conditioning in adolescents with Specific Language Impairment

Autism and the broad autism phenotype: familial patterns and intergenerational transmission

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome

SHOW MORE ARTICLES

Attention deficit hyperactivity disorder (ADHD) in phenotypically similar neurogenetic conditions: Turner syndrome and the RASopathies

A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation

Associations between physical growth and general cognitive functioning in international adoptees from Eastern Europe at 30 months post-arrival

Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder

Angelman syndrome: advancing the research frontier of neurodevelopmental disorders

An experimental study of executive function and social impairment in Cornelia de Lange syndrome

An emotion recognition subtyping approach to studying the heterogeneity and comorbidity of autism spectrum disorders and attention-deficit/hyperactivity disorder

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

A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome

A multimeasure approach to investigating affective appraisal of social information in Williams syndrome

A functional polymorphism of the brain derived neurotrophic factor gene and cortical anatomy in autism spectrum disorder

A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3

FAQs

Journal of Neurodevelopmental Disorders has an SJR of 1,296 (best quartile Q1) in the CountryOfPapers database.

Immediate OA APC is 2290 EUR.

The acceptance rate recorded for Journal of Neurodevelopmental Disorders is 30%.

Journal of Neurodevelopmental Disorders

Metrics

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Researcher reviews

Best articles by citations

FAQs

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What is the acceptance rate?