Molecular Autism

Autism spectrum disorders, endocrine disrupting compounds, and heavy metals in amniotic fluid: a case-control study

Lower circulating endocannabinoid levels in children with autism spectrum disorder

Haploinsufficiency of autism causative gene Tbr1 impairs olfactory discrimination and neuronal activation of the olfactory system in mice

Autistic traits in adults who have attempted suicide

Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity

Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry

A ‘choice’, an ‘addiction’, a way ‘out of the lost’: exploring self-injury in autistic people without intellectual disability

Sensory over-responsivity: parent report, direct assessment measures, and neural architecture

Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism

Visual attention to faces in children with autism spectrum disorder: are there sex differences?

Latent trajectories of adaptive behaviour in infants at high and low familial risk for autism spectrum disorder

Mechanisms underlying the EEG biomarker in Dup15q syndrome

The distribution of autistic traits across the autism spectrum: evidence for discontinuous dimensional subpopulations underlying the autism continuum

The role of gender in the perception of autism symptom severity and future behavioral development

Delayed M50/M100 evoked response component latency in minimally verbal/nonverbal children who have autism spectrum disorder

Linguistic markers of autism in girls: evidence of a “blended phenotype” during storytelling

Behavioral characteristics of autism spectrum disorder in very preterm birth children

Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder

Increased Ca2+ signaling in NRXN1α+/− neurons derived from ASD induced pluripotent stem cells

CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes

Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature

Deviation from normative brain development is associated with symptom severity in autism spectrum disorder

Autism and family involvement in the right to education in the EU: policy mapping in the Netherlands, Belgium and Germany

Sex differences in brain structure: a twin study on restricted and repetitive behaviors in twin pairs with and without autism

Mutations in neuroligin-3 in male mice impact behavioral flexibility but not relational memory in a touchscreen test of visual transitive inference

The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in Nrxn2 deletion mice

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

The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons

Development of the Stanford Social Dimensions Scale: initial validation in autism spectrum disorder and in neurotypicals

Autism and the right to education in the EU: policy mapping and scoping review of Nordic countries Denmark, Finland, and Sweden

Biological motion perception in autism spectrum disorder: a meta-analysis

The oxytocin receptor gene predicts brain activity during an emotion recognition task in autism

Persistence of dysfunctional natural killer cells in adults with high-functioning autism spectrum disorders: stigma/consequence of unresolved early infectious events?

Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

Retinal alterations in a pre-clinical model of an autism spectrum disorder

Familiality of behavioral flexibility and response inhibition deficits in autism spectrum disorder (ASD)

RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation

Atypical event-related potentials revealed during the passive parts of a Go-NoGo task in autism spectrum disorder: a case-control study

Cellular and molecular characterization of multiplex autism in human induced pluripotent stem cell-derived neurons

Rigor in science and science reporting: updated guidelines for submissions to Molecular Autism

The Friendship Questionnaire, autism, and gender differences: a study revisited

A multifaceted approach for analyzing complex phenotypic data in rodent models of autism

Reproductive stoppage in autism spectrum disorder in a population of 2.5 million individuals

Correction to: Mechanisms underlying the EEG biomarker in Dup15q syndrome