Shamita Sanga
Scientist-C |
Decision Unit-1: Genomics and Genome Biology
Professor |
Academy of Scientific and Innovative Research
Shamita is focused on understanding the genetic and molecular basis of rare diseases with a particular emphasis on neurodegenerative and undiagnosed disorders. Using next-generation sequencing and bioinformatic analysis, she aims to improve diagnostic accuracy, uncover novel pathogenic variants, and facilitate precision medicine. Her work integrates patient-derived data and functional validation to bridge the gap between discovery and clinical impact for rare disease communities.
Specific Interests
- Identifying molecular underpinnings of rare neuro-degenerative disorders
- Genotype-phenotype correlation
- Variant interpretation and functional validation