New Research Expands List of Genes Associated with Autism Spectrum Disorder
New analyses have more than tripled the number of genes associated with autism, offering deeper insights into genetic susceptibility and the complex biology of ASD.
Rare SH2B1 Gene Variants Linked to Neurodevelopmental Disorders and Metabolic Features
A study links rare SH2B1 gene variants to neurodevelopmental disorders with metabolic symptoms, expanding understanding of their clinical impact.
Genetic Variants in Na+,K+-ATPase Linked to Diverse Neurological Disorders: A Comprehensive Review
A systematic review has identified 123 genetic variants in Na+,K+-ATPase subunits linked to a range of neurological disorders, including epilepsy, migraines, and neurodevelopmental conditions.
CACNA1C Genetic Variants Influence Neuronal Networks Through Distinct Mechanisms
New research reveals that different genetic variants in CACNA1C affect neuronal networks and development through distinct pathways, influencing conditions like autism and epilepsy.
Study Explores Shared Genetic Factors in Childhood Heart Defects and Neurodevelopmental Disorders
A recent study using multiomic profiling highlights shared genetic and epigenetic factors in children with congenital heart disease and neurodevelopmental disorders, offering new insights into their co-occurrence.