Dr. Akila Prashant

I am a passionate researcher and educator in the fields of Biochemistry and Medical Genetics. My research is driven to unravel the mysteries of molecular biology and genetics, particularly in the context of rare disorders. At present, I am a part of a significant multicentric project titled “National Registry for Rare and Other Inherited Disorders,” which promises to expand our knowledge in this critical area. I am actively involved in research aimed at developing affordable diagnostic tests for neurodegenerative disorders like Spinal Muscular Atrophy and Duchenne Muscular Dystrophy. Also, I am currently engaged in exploring therapeutic approaches using advanced computational and in vivo models for the above-mentioned disorders. Further, I conduct population-based screenings to detect treatable metabolic errors and understand the prevalence of these disorders in our communities. I am not only a researcher but also a mentor, having organized numerous national workshops and trained aspiring researchers. My vision is to continue pushing the boundaries of medical genetics and genomics, making a lasting impact on healthcare and genetics research.