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Randi J. Hagerman

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Randi J. Hagerman
NationalityUnited States
Alma materStanford University
Known forFragile-X Syndrome and FXTAS
Scientific career
FieldsBehavior genetics, Autism Fragile X Syndrome, behavioral pharmacology
InstitutionsUniversity of California, Davis
Websitewww.ucdmc.ucdavis.edu/mindinstitute/ourteam/faculty/hagerman_r.html

Randi J. Hagerman, M.D. is the medical director of MIND Institute at the University of California, Davis.[1][2] She is internationally recognized researcher in the field of genetics of autism spectrum disorder with special focus on genomic instability. She has published many papers on the topic of repeat expansion and genetics of neurodevelopmental disorders (e.g. Fragile-X). She has discovered the Fragile X-associated tremor/ataxia syndrome (FXTAS), a neurological disorder that affects older male and rare female carriers of fragile X.[3][4]

Awards

  • Jerrett Cole Award, National Fragile X Foundation, 1992
  • Bonfils-Stanton Foundation Award for Science including Medicine, 1993
  • Namesake (with Paul Hagerman), Hagerman Award for Research in FXTAS, International Association for the Study of Intellectual Deficiency, 2004
  • Lifetime Achievement Award, National Fragile X Foundation, 2008

References

  1. ^ "5 Questions for Dr. Randi Hagerman: Fragile X Conditions expert". blog.sfgate.com. 30 January 2013. Retrieved 1 July 2016.
  2. ^ Megan Brooks (7 September 2010). "Minocycline Promising in Fragile X Syndrome". medscape.com. Retrieved 1 July 2016.
  3. ^ Hagerman, Randi J., et al. "Fragile-X–associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation." The American Journal of Human Genetics 74.5 (2004): 1051-1056.
  4. ^ Greco, C. M., et al. "Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)." Brain 129.1 (2006): 243-255.
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