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期刊名:Molecular autism

缩写:MOL AUTISM

ISSN:2040-2392

e-ISSN:2040-2392

IF/分区:5.5/Q1

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Rajaram Kshetri,James O Beavers,Romana Hyde et al. Rajaram Kshetri et al.
Background: SHANK3, a gene encoding a synaptic scaffolding protein, is implicated in autism spectrum disorder (ASD) and is disrupted in Phelan-McDermid syndrome (PMS). Despite evidence of regression or worsening of ASD-li...
Corinna Smith,Alexandra Lautarescu,Tony Charman et al. Corinna Smith et al.
Background: Very large sample sizes are often needed to capture heterogeneity in autism, necessitating data sharing across multiple studies with diverse assessment instruments. In these cases, data harmonization can be a ...
Tianhua Wang,Judith R Homberg,Laura Boreggio et al. Tianhua Wang et al.
Background: A lack of serotonin (also known as 5-hydroxytryptamine, 5-HT) in the brain due to deficiency of the rate-limiting enzyme in 5-HT synthesis, tryptophan hydroxylase 2 (TPH2), was recently reported to result in i...
Adeline Lacroix,Yoann Bennetot-Deveria,Monica Baciu et al. Adeline Lacroix et al.
Background: Autistic individuals often have difficulty flexibly adjusting their behavior. However, laboratory experiments have yielded inconsistent results, potentially due to various influencing factors, which need to be...
Rebecca R Canale,Caroline Larson,Rebecca P Thomas et al. Rebecca R Canale et al.
Background: "Frank autism," recognizable through the first minutes of an interaction, describes a behavioral presentation of a subset of autistic individuals that is closely tied to social communication challenges, and ma...
Jordan E Norris,Elizabeth M Berry-Kravis,Mark D Harnett et al. Jordan E Norris et al.
Fragile X syndrome (FXS) is a rare neurodevelopmental disorder caused by a CGG repeat expansion ≥ 200 repeats in 5' untranslated region of the FMR1 gene, leading to intellectual disability and cognitive difficulties, including in the domai...
Hannah Slevin,Fiona Kehinde,Jannath Begum-Ali et al. Hannah Slevin et al.
Background: Children with Neurofibromatosis 1 (NF1) show cognitive, behavioural and social differences compared to their peers. However, the age and sequence at which these differences begin to emerge is not fully underst...
Lukas S Schaffer,Sophie Breunig,Jeremy M Lawrence et al. Lukas S Schaffer et al.
Background: Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by atypical patterns of social functioning and repetitive/restricted behaviors. ASD commonly co-occurs with ADHD and, despite thei...
Igor Nenadić,Yvonne Schröder,Jonas Hoffmann et al. Igor Nenadić et al.
Background: Autistic-like traits (ALT) are prevalent across the general population and might be linked to some facets of a broader autism spectrum disorder (ASD) phenotype. Recent studies suggest an association of these t...
Peng Qing,Xiaodong Zhang,Qi Liu et al. Peng Qing et al.
Background: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder associated with alterations in structural and functional coupling in gray matter. However, despite the detectability and modulation of brain sign...