Huda Y. Zoghbi
Papers
1
Total Citations
300
H-Index
1
About
Dr. Huda Y. Zoghbi is a pioneering neuroscientist and geneticist renowned for her transformative work on neurodevelopmental and neurodegenerative disorders. Her research primarily focuses on the genetic and molecular mechanisms underlying conditions such as Rett syndrome, spinocerebellar ataxias, and autism spectrum disorders. Zoghbi’s landmark discovery of the MECP2 gene as the cause of Rett syndrome revolutionized the field, providing a foundation for understanding how disruptions in gene regulation affect brain development and function. Her work on the role of Math1 (Atoh1) in intestinal cellular homeostasis, as highlighted in her 2007 study with over 300 citations, exemplifies her broad impact on developmental biology and tissue-specific gene regulation. With over 40,000 total citations, Zoghbi’s contributions have earned her numerous accolades, including the Breakthrough Prize in Life Sciences and the Kavli Prize in Neuroscience. Her dedication to mentoring the next generation of scientists and her leadership at the Jan and Dan Duncan Neurological Research Institute underscore her legacy as a visionary who has fundamentally reshaped our understanding of neurological disease.
Research Focus
Key Achievements
Top Papers
- 1