Recommended Readings: Huda Y. Zoghbi, M.D., May 10, 2024

Recommended Readings: Huda Y. Zoghbi, M.D., May 10, 2024

Hybrid Friday Lecture Series

(open to the Rockefeller and Tri-Institutional communities)

Friday, May 10, 2024

Huda Y. Zoghbi, M.D.

Distinguished Service Professor, Departments of Pediatrics, Molecular and Human Genetics, Neurology and Neuroscience, Baylor College of Medicine; Director, Jan and Dan Duncan Neurological Research Institute at Texas Children’s Hospital; Investigator, Howard Hughes Medical Institute


Molecular and Neurobiological Studies in Rett Syndrome and MECP2 Disorders

The Joshua Lederberg Distinguished Lecture in Molecular Genetics


Recommended Readings:

Zhou, Jian, et al. “A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels.” Genes & Development 37.19-20 (2023): 883-900.

Trostle, Alexander J., et al. “A Comprehensive and Integrative Approach to MeCP2 Disease Transcriptomics.” International Journal of Molecular Sciences 24.6 (2023): 5122.

Sandweiss, Alexander J., Vicky L. Brandt, and Huda Y. Zoghbi. “Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies.” The Lancet Neurology 19.8 (2020): 689-698.

Lombardi, Laura Marie, Steven Andrew Baker, and Huda Yahya Zoghbi. “MECP2 disorders: from the clinic to mice and back.” The Journal of clinical investigation 125.8 (2015): 2914-2923.

Shahbazian, Mona D., and Huda Y. Zoghbi. “Rett syndrome and MeCP2: linking epigenetics and neuronal function.” The American Journal of Human Genetics 71.6 (2002): 1259-1272.

By |2024-04-17T15:17:00+00:00April 17th, 2024|Categories: Friday Lectures, Recommended Readings|Tags: , , |Comments Off on Recommended Readings: Huda Y. Zoghbi, M.D., May 10, 2024

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