Neurogenetics is the study of how genes influence the development and function of the nervous system. It plays a critical role in understanding inherited neurological disorders, such as Huntington’s disease, epilepsy, muscular dystrophies, and certain forms of dementia. Genomics goes a step further, analyzing the entire genetic makeup to identify disease-causing mutations and guide personalized treatment strategies. The Neurogenetics and Genomics session will explore groundbreaking research on gene mapping, molecular mechanisms, and targeted therapies. With advancements in genome sequencing and bioinformatics, this session will focus on how genetic knowledge can lead to early detection, prevention, and precise interventions for neurological diseases.

Genetic researchers, neurologists, neuroscientists, bioinformaticians, and students interested in genomics conferences will greatly benefit from this session. It also caters to professionals developing gene-based therapies and diagnostic tools for neurological disorders. By attending, participants will gain in-depth knowledge of genetic influences on neurological conditions and learn how genomics is shaping the future of precision medicine in neurology.