Alan Shiels
Department of Ophthalmology and Visual Sciences
Washington University School of Medicine
St. Louis
MO 63110
USA
Name/email consistency: high
- The EPHA2 gene is associated with cataracts linked to chromosome 1p. Shiels, A., Bennett, T.M., Knopf, H.L., Maraini, G., Li, A., Jiao, X., Hejtmancik, J.F. Mol. Vis. (2008)
- X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7. Shiels, A., Bennett, T.M., Prince, J.B., Tychsen, L. Mol. Vis. (2007)
- CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q. Shiels, A., Bennett, T.M., Knopf, H.L., Yamada, K., Yoshiura, K., Niikawa, N., Shim, S., Hanson, P.I. Am. J. Hum. Genet. (2007)
- Refractive defects and cataracts in mice lacking lens intrinsic membrane protein-2. Shiels, A., King, J.M., Mackay, D.S., Bassnett, S. Invest. Ophthalmol. Vis. Sci. (2007)
- Optical dysfunction of the crystalline lens in aquaporin-0-deficient mice. Shiels, A., Bassnett, S., Varadaraj, K., Mathias, R., Al-Ghoul, K., Kuszak, J., Donoviel, D., Lilleberg, S., Friedrich, G., Zambrowicz, B. Physiol. Genomics (2001)
- Disruption of lens fiber cell architecture in mice expressing a chimeric AQP0-LTR protein. Shiels, A., Mackay, D., Bassnett, S., Al-Ghoul, K., Kuszak, J. FASEB J. (2000)
