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Bio
Dr. Hagerman's research focuses on the clinical and molecular underpinnings of disorders of the fragile X (FMR1) gene, mutations of which are responsible for fragile X syndrome (FXS) - the leading heritable form of intellectual impairment, fragile X-associated primary ovarian insufficiency (FXPOI) - the leading heritable form of early menopause, and fragile X-associated tremor/ataxia syndrome (FXTAS) - one of the leading single-gene forms of neurodegeneration. The Hagerman lab is particularly interested in the "RNA toxicity" model for FXTAS, both in terms of identifying the key players in the pathogenesis of this disorder and for therapeutic targeting of the pathogenic mechanism.
Research Interests
Papers共 301 篇Author StatisticsCo-AuthorSimilar Experts
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Yeeun Tak,Andrea Schneider,Ellery Santos, Jamie Leah Randol,Flora Tassone,Paul Hagerman,Randi J. Hagerman
GENESno. 3 (2024): 331
Jamie L. Randol,Kyoungmi Kim,Matthew D. Ponzini,Flora Tassone, Alexandria K. Falcon,Randi J. Hagerman,Paul J. Hagerman
GENESno. 3 (2024): 356
CELLSno. 14 (2023): 1920-1920
Ellery Santos,Courtney Clark, Hazel Maridith B. Biag,Si Jie Tang,Kyoungmi Kim,Matthew D. Ponzini,Andrea Schneider,Cecilia Giulivi,Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe,Jacquelyn Dayton,Jamie L. Randol,
CELLSno. 24 (2023)
Nattaporn Tassanakijpanich,Forrest J McKenzie,Yingratana A McLennan, Elisabeth Makhoul,Flora Tassone,Mittal J Jasoliya, Christopher Romney,Ignacio Cortina Petrasic, Kaye Napalinga,Caroline B Buchanan,Paul Hagerman,Randi Hagerman,
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