Neurogenetics and Neurological Disorders: From Genes to Clinical Practice

Neurogenetics is a rapidly advancing field that bridges the gap between genetic research and clinical practice in the context of neurological disorders. This track will explore the comprehensive journey from genetic discoveries to their application in clinical settings, emphasizing how genetic insights are transforming the diagnosis, management, and treatment of neurological diseases. Overview of recent genetic findings related to various neurological disorders, including epilepsy, autism spectrum disorders, Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS). Insights from GWAS that identify genetic risk factors and susceptibility loci for complex neurological conditions. Application of NGS technologies, such as whole-exome sequencing (WES) and whole-genome sequencing (WGS), in uncovering rare genetic mutations and novel disease genes. Techniques to study the functional impact of genetic variants on neuronal function and brain development, including CRISPR-Cas9 gene editing, RNA sequencing, and proteomics

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