- Oshima J, Martin GM, Hisama FM. Werner Syndrome. In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (eds.) GeneReviews. [Internet]. pp. NBK1514. 2021. University of Washington, Seattle, WA. https://www.ncbi.nlm.nih.gov/books/NBK1514/.
Clinical review of Japanese Werner Syndrome cases.
- Yu CE, Oshima J, Fu YW, Hisama F, Wijsman EM, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Positional cloning of the Werner’s syndrome gene. Science 1996 272:258-262.
Identification of a gene responsible for Werner Syndrome.
- Yokote K, Chanprasert S, Lee L, Eirich K, Takemoto M, Watanabe A, Koizumi N, Lessel D, Mori T, Hisama FM, Ladd PD, Angle B, Baris H, Cefle K, Palanduz S, Ozturk S, Chateau A, Deguchi K, Easwar TK, Federico A, Fox A, Grebe TA, Hay B, Nampoothiri S, Seiter K, Streeten E, Piña-Aguilar RE, Poke G, Poot M, Posmyk R, Martin GM, Kubisch C, Schindler D, Oshima J. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects. Hum Mutat. 2017; 38(1):7-15.
WRN mutation update.
- Oshima J, Sidorova JM, Monnat RJ, Jr. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions. Ageing Res Rev. 2017;33:105-14.
Review of the pathogenesis of Werner Syndrome.
- Martin GM, Hisama FM, Oshima J. Review of how genetic research on segmental progeroid syndromes has documented genomic instability as a hallmark of aging but let us now pursue antigeroid syndromes! J Gerontol A Biol Sci Med Sci. 2021;76(2):253-259
Review of progeroid syndromes.