Latest AI and machine learning research in autism for healthcare professionals.
Early identification of cerebral palsy (CP) remains a major challenge due to the reliance on expert ...
This study provides a comprehensive medical ecology analysis of gut microbiome alterations in four n...
Over 30 international studies are exploring newborn sequencing (NBSeq) to expand the range of geneti...
Long QT syndrome (LQTS) is a life-threatening genetic disorder characterized by prolonged QT interva...
Time-to-event data in disease occurrence is often right-censored, requiring survival models for accu...
Inborn errors of immunity (IEI), formerly known as primary immune deficiencies (PID), are a group of...
Gestational diabetes mellitus (GDM), a heritable metabolic disorder and the most common pregnancy-re...
Recent advances in large language models (LLMs) have prompted a frenzy in utilizing them as universa...
Chromosomal aneuploidy, a condition characterized by an abnormal number of chromosomes, is a major g...
Traditional subjective measures are limited in the insight they provide into underlying behavioral d...
The growing use of large language models for health communication raises important questions about p...
Acute Hepatic Porphyria (AHP) is a rare genetic disease characterized by unpredictable life-threaten...
To prevent clozapine-induced agranulocytosis (CIA), patients’ white blood cell counts are closely mo...
Recent work leveraging artificial intelligence has offered promise to dissect disease heterogeneity ...
Autism subtypes, including general Autism Spectrum Disorder (ASD) and Asperger Syndrome (AS), exhibi...
Autism spectrum disorder(ASD) is a neurological condition marked by impaired communication abilities...
The polygenic risk score genetic quantitative ultrasound speed of sound (gSOS) was developed using m...
Introduction: Achieving equity in translational precision medicine requires the integration of genom...
A variety of common and rare genetic factors have been implicated in the development of amyotrophic ...
Although genetic variant effects often interact non-additively, strategies to uncover epistasis rema...
Rare diseases collectively affect 5% of the population. However, fewer than 50% of rare disease pati...