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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
Sabela Conde-Pumpido Zubizarreta,Johan Isaksson,Åshild Faresjö et al. Sabela Conde-Pumpido Zubizarreta et al.
Background: Camouflaging autistic traits is suggested to increase stress and the risk of autistic burnout. However, the relationship with psychological and biological markers of stress and the influence of familial factor...
Sophie Roper,Rebecca Charlton,Francesca Happé et al. Sophie Roper et al.
Background: Suicide has been reported as a leading cause of premature death in autistic populations. Additionally, risk of suicidality is often found to increase with age in the general population. Despite this, suicidali...
Yiting Zhu,Dongyun Li,Chunchun Hu et al. Yiting Zhu et al.
Background: Fragile X Syndrome (FXS) is the most prevalent inherited intellectual disability disorder linked to the X chromosome, and currently lacks an approved specific treatment. Preclinical and some clinical studies h...
Jennifer L Bruno,Julia R Plank,Samantha Leder et al. Jennifer L Bruno et al.
Background: Despite high rates of autism spectrum disorder (ASD), understanding of pathophysiology is limited. The RAS-mitogen-activated protein kinase (RAS-MAPK) pathway plays a crucial role in ASD and is altered in chil...
Evangelia Pollali,Daniel Frías Donaire,Miguel Del Ángel et al. Evangelia Pollali et al.
Background: Fragile X syndrome (FXS) is the most common inherited intellectual disability, caused by the loss of fragile X mental retardation protein (FMRP), which regulates neuronal signaling and plasticity. FXS patients...
Eléonore Viora-Dupont,Julian Delanne,Aurore Garde et al. Eléonore Viora-Dupont et al.
Background: Specific learning disorders (SLDs) affect approximately 5% of school-age children. In France, genetic investigations of complex non-syndromic SLD cases include chromosomal microarray analysis and fragile X syn...
Kari L Hanson,Thomas Avino,Sandra L Taylor et al. Kari L Hanson et al.
Background: Neuronal connectivity is refined throughout development by the proliferation and pruning of axons in cerebral white matter, and progressive axon myelination that enables rapid communication across brain region...
Aaron J Kaat,Audrey Thurm,Cristan Farmer et al. Aaron J Kaat et al.
Objective: The dearth of tools to quantify and track growth in social communication ability has been a barrier to understanding and monitoring treatment outcomes for neurodevelopmental disorders. We undertook a multi-stag...
Chloe Alexa McGhee,Julia R Plank,Luca Pannone et al. Chloe Alexa McGhee et al.
Background: Noonan syndrome (NS) and Noonan syndrome with multiple lentigines (NSML) are neurodevelopmental conditions caused by genetic variants leading to upregulated signaling in the RAS-MAPK pathway. While previous re...
Liora Manelis-Baram,Tal Barami,Michal Ilan et al. Liora Manelis-Baram et al.
Background: Difficulties with non-verbal communication, including atypical use of facial expressions, are a core feature of autism. Quantifying atypical use of facial expressions during naturalistic social interactions in...