Latest AI and machine learning research in autism for healthcare professionals.
This study investigates the potential of artificial intelligence, particularly Natural Language Processing and large-scale language models, to improve resource management and service access for individuals with autism in Alabama. The research aims to explore and evaluate the potential of AI-driven tools to address challenges in navigating complex datasets and supporting social work practices. We d...
Disruptions in chromatin remodelers and synaptic proteins represent major genetic risk factors for autism spectrum disorder (ASD), yet how these distinct gene classes converge to impair circuit function remains unclear. CHD2, a chromatin remodeler linked to ASD, epilepsy, and intellectual disability, regulates gene expression through epigenetic mechanisms. In Drosophila, its homologue Chd1 functio...
Epilepsy is a chronic neurological disorder causing recurrent seizures. Improved diagnosis and management, including high-resolution imaging, genetic ...
BACKGROUND: Genetic aberrations are among the critical driving factors of lung cancer. Importantly, the impact of genetic variations on proteomic dysr...
Psoriatic arthritis is a heterogeneous disease where delayed diagnosis and variable treatment responses remain significant challenges. This review add...
Efforts to predict schizophrenia risk using biological data have been hampered by the heterogeneity of current "clinical-high-risk" (CHR-P) criteria, ...
BACKGROUND: Tacrolimus is a first-line immunosuppressant essential for preventing graft rejection after liver transplantation, but its narrow therapeu...
Glioblastoma (GBM) is an aggressive brain tumor with a poor prognosis, yet its molecular mechanisms remain incompletely understood. Olfactomedin 1 (OL...
INTRODUCTION: Residual feed intake (RFI) is a key indicator of feed efficiency in poultry and is regulated by coordinated physiological processes acro...
Restful sleep is essential for health, yet many children with Attention Deficit Hyperactivity Disorder (ADHD) experience disturbances such as delayed ...
BRAF inhibitors (BRAFi) have transformed the treatment of BRAF mutant melanoma, but inherent and acquired resistance remains a major barrier to curati...
Cell-free DNA (cfDNA) is an emerging biomarker detectable in various bodily fluids, with promising implications across a wide range of clinical domain...
RASopathies are a group of genetic disorders caused by pathogenic variants in the RAS-mitogen-activated protein kinase (RAS-MAPK) signaling pathway, o...
Oxidative stress (OS) is a hallmark of Alzheimer's disease (AD), yet the cell type-specific mechanisms remain unclear. We analyzed a single-cell RNA s...
STUDY OBJECTIVES: Manual sleep staging in pediatric populations is challenging due to developmental variability and limited scoring consistency, espec...
BACKGROUND: Neurodevelopmental disorders (NDDs), such as autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD), often eme...
Major depressive disorder (MDD) is a highly heterogeneous condition that limits the reliability of symptom-based diagnosis and treatment selection. In...
Preimplantation genetic testing (PGT) is a critical tool in reproductive medicine for selecting genetically healthy embryos, thereby reducing the risk...
Predicting phenotypes from genomic mutations remains a major genetic challenge. Traditional statistical methods (such as GBLUP and BayesR) have limita...
KBG syndrome (KBGS, OMIM #148050) is a rare genetic disorder caused by heterozygous truncating or missense variants in the ANKRD11 gene or a deletion ...