معرفی
Monika Winter is an Assistant Professor in the Applied Sciences Department at Northumbria University. Her research focuses on mitochondrial genetics, genetic disorders, and molecular mechanisms underlying human diseases. She has published extensively on topics such as mitochondrial ribosome assembly, genetic variants associated with mitochondrial dysfunction, and the clinical spectrum of mitochondrial diseases.
Her recent work includes studies on DAP3 and MRPL49 variants linked to Perrault syndrome and sensorineural hearing loss, as well as the role of COA5 in mitochondrial complex IV assembly. Collaborations span multiple institutions globally, emphasizing interdisciplinary genetics and genomics research.
No scientific awards or grants are explicitly mentioned in the provided text. No advising students are listed, though her research involves collaborative teams across institutions.
