Baird PN - Search Results

1

Analysis of the Y402H variant of the complement factor H gene in age-related macular degeneration.

Baird PN, Islam FM, Richardson AJ, Cain M, Hunt N, Guymer R. Baird PN, et al. Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4194-8. doi: 10.1167/iovs.05-1285. Invest Ophthalmol Vis Sci. 2006. PMID: 17003406

2

Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration.

Guymer RH, McNeil R, Cain M, Tomlin B, Allen PJ, Dip CL, Baird PN. Guymer RH, et al. Among authors: baird pn. Clin Exp Ophthalmol. 2002 Dec;30(6):419-23. doi: 10.1046/j.1442-9071.2002.00572.x. Clin Exp Ophthalmol. 2002. PMID: 12427233

3

Identification of a mutation in the PKD2 gene in a family with age-related macular degeneration.

Narendran N, Guymer RH, Cain M, Baird PN. Narendran N, et al. Among authors: baird pn. Am J Med Genet A. 2004 Jun 1;127A(2):208-10. doi: 10.1002/ajmg.a.20673. Am J Med Genet A. 2004. PMID: 15108213 No abstract available.

4

The epsilon2 and epsilon4 alleles of the apolipoprotein gene are associated with age-related macular degeneration.

Baird PN, Guida E, Chu DT, Vu HT, Guymer RH. Baird PN, et al. Invest Ophthalmol Vis Sci. 2004 May;45(5):1311-5. doi: 10.1167/iovs.03-1121. Invest Ophthalmol Vis Sci. 2004. PMID: 15111582

5

Association of the M55L and Q192R paraoxonase gene polymorphisms with age-related macular degeneration.

Baird PN, Chu D, Guida E, Vu HT, Guymer R. Baird PN, et al. Am J Ophthalmol. 2004 Oct;138(4):665-6. doi: 10.1016/j.ajo.2004.04.053. Am J Ophthalmol. 2004. PMID: 15488805

6

Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye Study.

Baird PN, Richardson AJ, Craig JE, Mackey DA, Rochtchina E, Mitchell P. Baird PN, et al. Clin Exp Ophthalmol. 2004 Oct;32(5):518-22. doi: 10.1111/j.1442-9071.2004.00886.x. Clin Exp Ophthalmol. 2004. PMID: 15498064

7

HMG CoA reductase inhibitors (statins): do they have a role in age-related macular degeneration?

Guymer RH, Chiu AW, Lim L, Baird PN. Guymer RH, et al. Among authors: baird pn. Surv Ophthalmol. 2005 Mar-Apr;50(2):194-206. doi: 10.1016/j.survophthal.2004.12.002. Surv Ophthalmol. 2005. PMID: 15749309 Review.

8

The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye Study.

Baird PN, Richardson AJ, Craig JE, Rochtchina E, Mackey DA, Mitchell P. Baird PN, et al. Am J Ophthalmol. 2005 Jun;139(6):1125-6. doi: 10.1016/j.ajo.2004.11.061. Am J Ophthalmol. 2005. PMID: 15953455

9

A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families.

Baird PN, Richardson AJ, Mackey DA, Craig JE, Faucher M, Raymond V. Baird PN, et al. Am J Ophthalmol. 2005 Oct;140(4):760-2. doi: 10.1016/j.ajo.2005.04.043. Am J Ophthalmol. 2005. PMID: 16226543

10

Heritability of macular thickness determined by optical coherence tomography.

Chamberlain MD, Guymer RH, Dirani M, Hopper JL, Baird PN. Chamberlain MD, et al. Among authors: baird pn. Invest Ophthalmol Vis Sci. 2006 Jan;47(1):336-40. doi: 10.1167/iovs.05-0599. Invest Ophthalmol Vis Sci. 2006. PMID: 16384982

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