Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
《分子孤独症》是一本同行评审、开放获取的期刊，发表高质量的基础、转化和临床研究，这些研究与孤独症和相关神经发育疾病的病因学、病理生物学或治疗相关。鼓励包括跨层级整合的研究。《分子孤独症》发表实证研究、评论和简短的通讯。
Autism prevalence in China is comparable to Western prevalence
来源期刊：Molecular AutismDOI：10.1186/s13229-018-0246-0
Selection bias on intellectual ability in autism research: a cross-sectional review and meta-analysis
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0260-x
Generalizability and reproducibility of functional connectivity in autism
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0273-5
Autism spectrum disorders, endocrine disrupting compounds, and heavy metals in amniotic fluid: a case-control study
来源期刊：Molecular AutismDOI：10.1186/s13229-018-0253-1
Lower circulating endocannabinoid levels in children with autism spectrum disorder
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0256-6
Haploinsufficiency of autism causative gene Tbr1 impairs olfactory discrimination and neuronal activation of the olfactory system in mice
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0257-5
Autistic traits in adults who have attempted suicide
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0274-4
Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0265-5
Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0281-5
A ‘choice’, an ‘addiction’, a way ‘out of the lost’: exploring self-injury in autistic people without intellectual disability
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0267-3
Sensory over-responsivity: parent report, direct assessment measures, and neural architecture
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0255-7
Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0277-1
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0271-7
Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism
来源期刊：Molecular AutismDOI：10.1186/s13229-018-0250-4
Visual attention to faces in children with autism spectrum disorder: are there sex differences?
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0276-2
Latent trajectories of adaptive behaviour in infants at high and low familial risk for autism spectrum disorder
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0264-6
Mechanisms underlying the EEG biomarker in Dup15q syndrome
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0280-6
The distribution of autistic traits across the autism spectrum: evidence for discontinuous dimensional subpopulations underlying the autism continuum
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0275-3
The role of gender in the perception of autism symptom severity and future behavioral development
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0266-4
Delayed M50/M100 evoked response component latency in minimally verbal/nonverbal children who have autism spectrum disorder
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0283-3
Linguistic markers of autism in girls: evidence of a “blended phenotype” during storytelling
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0268-2
Behavioral characteristics of autism spectrum disorder in very preterm birth children
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0282-4
Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0284-2
Increased Ca2+ signaling in NRXN1α+/− neurons derived from ASD induced pluripotent stem cells
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0303-3
CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0278-0
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0291-3
Deviation from normative brain development is associated with symptom severity in autism spectrum disorder
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0301-5
Autism and family involvement in the right to education in the EU: policy mapping in the Netherlands, Belgium and Germany
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0297-x
Sex differences in brain structure: a twin study on restricted and repetitive behaviors in twin pairs with and without autism
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0309-x
Mutations in neuroligin-3 in male mice impact behavioral flexibility but not relational memory in a touchscreen test of visual transitive inference
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0292-2
The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in Nrxn2 deletion mice
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0261-9
A meta-analysis of two high-risk prospective cohort studies reveals autism-specific transcriptional changes to chromatin, autoimmune, and environmental response genes in umbilical cord blood
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0287-z
The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0293-1
Development of the Stanford Social Dimensions Scale: initial validation in autism spectrum disorder and in neurotypicals
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0298-9
Autism and the right to education in the EU: policy mapping and scoping review of Nordic countries Denmark, Finland, and Sweden
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0290-4
Biological motion perception in autism spectrum disorder: a meta-analysis
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0299-8
The oxytocin receptor gene predicts brain activity during an emotion recognition task in autism
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0258-4
Persistence of dysfunctional natural killer cells in adults with high-functioning autism spectrum disorders: stigma/consequence of unresolved early infectious events?
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0269-1
Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0294-0
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0286-0
Retinal alterations in a pre-clinical model of an autism spectrum disorder
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0270-8
Familiality of behavioral flexibility and response inhibition deficits in autism spectrum disorder (ASD)
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0296-y
RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0285-1
Atypical event-related potentials revealed during the passive parts of a Go-NoGo task in autism spectrum disorder: a case-control study
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0259-3
Cellular and molecular characterization of multiplex autism in human induced pluripotent stem cell-derived neurons
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0306-0
Rigor in science and science reporting: updated guidelines for submissions to Molecular Autism
来源期刊：Molecular AutismDOI：10.1186/s13229-018-0249-x
The Friendship Questionnaire, autism, and gender differences: a study revisited
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0295-z
A multifaceted approach for analyzing complex phenotypic data in rodent models of autism
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0263-7
Reproductive stoppage in autism spectrum disorder in a population of 2.5 million individuals
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0300-6
Correction to: Mechanisms underlying the EEG biomarker in Dup15q syndrome
来源期刊：Molecular AutismDOI：10.1186/s13229-019-0288-y
