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• Tackling the greatest challenge in cataract surgery.

  Chang DF. Chang DF. Br J Ophthalmol. 2005 Sep;89(9):1073-4. doi: 10.1136/bjo.2005.068213. Br J Ophthalmol. 2005. PMID: 16113349 Free PMC article. No abstract available.
• A deletion mutation in the betaA1/A3 crystallin gene ( CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family.

  Qi Y, Jia H, Huang S, Lin H, Gu J, Su H, Zhang T, Gao Y, Qu L, Li D, Li Y. Qi Y, et al. Hum Genet. 2004 Jan;114(2):192-7. doi: 10.1007/s00439-003-1049-7. Epub 2003 Nov 4. Hum Genet. 2004. PMID: 14598164
• Prevalence and causes of blindness and visual impairment in Bangladeshi adults: results of the National Blindness and Low Vision Survey of Bangladesh.

  Dineen BP, Bourne RR, Ali SM, Huq DM, Johnson GJ. Dineen BP, et al. Br J Ophthalmol. 2003 Jul;87(7):820-8. doi: 10.1136/bjo.87.7.820. Br J Ophthalmol. 2003. PMID: 12812875 Free PMC article.
• Prevalence of blindness in people over 40 years in the volta region of ghana.

  Guzek JP, Anyomi FK, Fiadoyor S, Nyonator F. Guzek JP, et al. Ghana Med J. 2005 Jun;39(2):55-62. doi: 10.4314/gmj.v39i2.35983. Ghana Med J. 2005. PMID: 17299544 Free PMC article.
• A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.

  Héon E, Paterson AD, Fraser M, Billingsley G, Priston M, Balmer A, Schorderet DF, Verner A, Hudson TJ, Munier FL. Héon E, et al. Am J Hum Genet. 2001 Mar;68(3):772-7. doi: 10.1086/318798. Epub 2001 Feb 5. Am J Hum Genet. 2001. PMID: 11179024 Free PMC article.