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  1. Home
  2. Our Research
  3. Kevin Gregory-Evans

Kevin Gregory-Evans

Research Focus
Eyes and Vision
Degrees / Designations

1982: BSc (Hons), 2:1. Physiology, University of London, UK. 1985: MBBS, St. Bartholomew's Medical School, University of London, UK. 1988: Diploma of Ophthalmology, Royal College of Surgeons, London, UK. 1989: FRCS, Royal College of Surgeons and Physicians, Glasgow, UK. 1990: FRCOphth, Royal College of Ophthalmologists, London, UK. 1994: MD (Res), Molecular Genetics, University of London, UK. 2009: PhD, Cell Biology, University of London, UK. 2009: DIC, Imperial College London. UK. 2011: FRCSC, Royal College of Physicians and Surgeons of Canada.

Contact Info
http://ophthalmology.ubc.ca/faculty_pages/k-gregory-evans.html
kge30@mail.ubc.ca
604.875.5275

Biography

n/a

Research Studies

Eye Disorders

Study of Ataluren in Patients With Aniridia (STAR)

News and Awards

ASK AN EXPERT: ARE SUNGLASSES REALLY NECESSARY FOR PROTECTING MY EYES?

Aug 14, 2014

Publications

  • Cell transplantation -

    Focused magnetic stem cell targeting to the retina using superparamagnetic iron oxide nanoparticles.

    Yanai A, Häfeli UO, Metcalfe AL, Soema P, Addo L, Gregory-Evans CY, Po K, Shan X, Moritz OL, Gregory-Evans K
  • Human molecular genetics -

    Pax2 regulates a fadd-dependent molecular switch that drives tissue fusion during eye development.

    Viringipurampeer IA, Ferreira T, DeMaria S, Yoon JJ, Shan X, Moosajee M, Gregory-Evans K, Ngai J, Gregory-Evans CY
  • Ophthalmic research -

    Pharmacological enhancement of ex vivo gene therapy neuroprotection in a rodent model of retinal degeneration.

    Gregory-Evans K, Po K, Chang F, Gregory-Evans CY
  • Current biology : CB -

    Short-wavelength light sensitivity of circadian, pupillary, and visual awareness in humans lacking an outer retina.

    Zaidi FH, Hull JT, Peirson SN, Wulff K, Aeschbach D, Gooley JJ, Brainard GC, Gregory-Evans K, Rizzo JF, Czeisler CA, Foster RG, Moseley MJ, Lockley SW
  • Human molecular genetics -

    SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

    Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K
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