Journal of Neurodevelopmental Disorders
ISSN:1866-1947

Journal of Neurodevelopmental Disorders

J NEURODEV DISORD
学科领域:医学
是否预警:不在预警名单内
是否OA:
录用周期:>12周,或约稿
新锐分区:医学2区
年发文量:69
影响因子:4
JCR分区:Q1

基本信息

《 神经 发育 障碍 杂志 》 是 一 本 开放 获取 的 杂志 , 整合 了 许多 学科 的 最 新 前沿 研究 , 包括 神经 生物 学 、 遗传 学 、 认知 神经 科学 、 精神 病学 和 心理 学 。该 杂志 主要 关注 神经 发育 障碍 的 发病 机制 , 包括 自闭症 、 脆性 X 综合 征 、 结节 性 硬化 症 、 特纳 综合 征 、 22q 缺失 综合 征 、 普拉德 - 威利 和 安杰曼 综合 征 、 威廉姆斯 综合 征 、 溶酶体 贮积 病 、 诵读 困难 、 特殊 语言 障碍 和 胎儿 酒精 综合 征 。随着 神经 发育 综合 征 相关 基因 的 发现 、 神经 回路 研究 工具 的 出现 以及 分子 机制 研究 新 方法 的 发展 , 神经 发育 障碍 发病 机制 的 跨 学科 研究 日益 普遍 。《 神经 发育 障碍 杂志 》 为 研究 人员 提供 了 一 个 独特 的 场所 , 他们 有 兴趣 比较 和 对比 与 各种 神经 发育 障碍 的 发病 机制 相关 的 机制 和 特征 , 加深 我们 对 每 种 疾病 的 病因 学 和 相关 表 型 的 理解 。
1866-1947SCIE/Scopus收录/DOAJ开放期刊
4
3.4
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学2区
CLINICAL NEUROLOGY 临床神经病学
2区
NEUROSCIENCES 神经科学
2区
N/A
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科:CLINICAL NEUROLOGY
SCIE
Q1
54/286
学科:NEUROSCIENCES
SCIE
Q2
79/314
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科:CLINICAL NEUROLOGY
SCIE
Q1
61/286
学科:NEUROSCIENCES
SCIE
Q1
77/314
38
69
2%->12周,或约稿GBP2090; USD2890; EUR2490医学-临床神经学
7.5%
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
85.51%100%2.38%
CiteScore:7.00
SJR:1.296
SNIP:1.479
学科类别分区排名百分位
大类:Medicine
小类:Pediatrics, Perinatology and Child Health
Q1
24 / 342
大类:Medicine
小类:Pathology and Forensic Medicine
Q1
26 / 204
大类:Medicine
小类:Neurology (clinical)
Q1
79 / 400
大类:Medicine
小类:Cognitive Neuroscience
Q1
27 / 121

期刊高被引文献

A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9273-1
A diffusion-weighted imaging tract-based spatial statistics study of autism spectrum disorder in preschool-aged children
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9291-z
A phase 1/2, open-label assessment of the safety, tolerability, and efficacy of transdermal cannabidiol (ZYN002) for the treatment of pediatric fragile X syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9277-x
Adaptation of the Clinical Dementia Rating Scale for adults with Down syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9300-2
Adaptation to different communicative contexts: an eye tracking study of autistic adults
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9265-1
Impaired neurodevelopmental pathways in autism spectrum disorder: a review of signaling mechanisms and crosstalk
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9268-y
In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9267-z
Are there shared neural correlates between dyslexia and ADHD? A meta-analysis of voxel-based morphometry studies
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9287-8
Early white matter development is abnormal in tuberous sclerosis complex patients who develop autism spectrum disorder
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9293-x
Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9292-y
Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9275-z
Cognitive training for children and adolescents with fragile X syndrome: a randomized controlled trial of Cogmed
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9264-2
The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9289-6
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9263-3
Differentiating social preference and social anxiety phenotypes in fragile X syndrome using an eye gaze analysis: a pilot study
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9262-4
Phenotypic characterization of individuals with SYNGAP1 pathogenic variants reveals a potential correlation between posterior dominant rhythm and developmental progression
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9276-y
Refining the concept of GFAP toxicity in Alexander disease
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9290-0
STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9278-9
Developmental divergence: motor trajectories in children with fragile X syndrome with and without co-occurring autism
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9281-1
Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9282-0
Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9270-4
Vocabulary comprehension in adults with fragile X syndrome (FXS)
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9285-x
Reducing Th2 inflammation through neutralizing IL-4 antibody rescues myelination in IUGR rat brain
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9297-6
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9288-7
Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9284-y
Quantitative gait assessment in children with 16p11.2 syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9286-9
White matter as a monitoring biomarker for neurodevelopmental disorder intervention studies
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9295-8
Children with facial paralysis due to Moebius syndrome exhibit reduced autonomic modulation during emotion processing
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9272-2
Infant regulatory function acts as a protective factor for later traits of autism spectrum disorder and attention deficit/hyperactivity disorder but not callous unemotional traits
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9274-0
Spatiotemporal development of spinal neuronal and glial populations in the Ts65Dn mouse model of Down syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9294-9
Magnetoencephalographic (MEG) brain activity during a mental flexibility task suggests some shared neurobiology in children with neurodevelopmental disorders
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9280-2
Initial eye gaze to faces and its functional consequence on face identification abilities in autism spectrum disorder
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9303-z
Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9269-x
The impact of expressive language development and the left inferior longitudinal fasciculus on listening and reading comprehension
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9296-7
Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9283-z
Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9271-3
Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9301-1
Assessing general cognitive and adaptive abilities in adults with Down syndrome: a systematic review
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9279-8
Lesser suppression of response to bright visual stimuli and visual abnormality in children with autism spectrum disorder: a magnetoencephalographic study
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9266-0
White matter and neurodevelopmental disorders: honoring Jean De Vellis through the work of the NICHD-funded intellectual and developmental disabilities research centers
来源期刊:Journal of Neurodevelopmental DisordersDOI:10.1186/s11689-019-9299-4

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