Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
《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。
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
