Edinburgh Research Explorer

Ms. Stephanie Barnes

(Former employee or visitor)

  1. 2017
  2. Cell type-specific translation profiling reveals a novel strategy for treating fragile X syndrome

    Thomson, S., Seo, S., Barnes, S., Louros, S. R., Muscas, M., Dando, O., Kirby, C., Wyllie, D., Hardingham, G., Kind, P. & Osterweil, E., 2 Aug 2017, In : Neuron. 3

    Research output: Contribution to journalArticle

  3. 2016
  4. FMRP and the Pathophysiology of Fragile X Syndrome

    Barnes, S., Thomson, S., Kind, P. & Osterweil, E., 2016, Neuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability. Academic Press

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  5. 2015
  6. Convergence of hippocampal pathophysiology in Syngap+/- and Fmr1-/y mice

    Barnes, S., Wijetunge, L., Jackson, A. D., Katsanevaki, D., Osterweil, E., Komiyama, N., Grant, S., Bear, M. F., Nägerl, U. V., Kind, P. & Wyllie, D., 11 Nov 2015, In : Journal of Neuroscience. 35, 45, p. 15073-15081

    Research output: Contribution to journalArticle

  7. Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a rat model of Fragile X Syndrome

    Till, S. M., Asiminas, A., Jackson, A. D., Katsanevaki, D., Barnes, S. A., Osterweil, E. K., Bear, M. F., Chattarji, S., Wood, E. R., Wyllie, D. J. A. & Kind, P. C., 1 Nov 2015, In : Human Molecular Genetics. 24, 21, p. 5977-84 8 p.

    Research output: Contribution to journalArticle