Baird PN - Search Results

1

A genome-wide association study of corneal astigmatism: The CREAM Consortium.

Shah RL, Li Q, Zhao W, Tedja MS, Tideman JWL, Khawaja AP, Fan Q, Yazar S, Williams KM, Verhoeven VJM, Xie J, Wang YX, Hess M, Nickels S, Lackner KJ, Pärssinen O, Wedenoja J, Biino G, Concas MP, Uitterlinden A, Rivadeneira F, Jaddoe VWV, Hysi PG, Sim X, Tan N, Tham YC, Sensaki S, Hofman A, Vingerling JR, Jonas JB, Mitchell P, Hammond CJ, Höhn R, Baird PN, Wong TY, Cheng CY, Teo YY, Mackey DA, Williams C, Saw SM, Klaver CCW, Guggenheim JA, Bailey-Wilson JE; CREAM Consortium. Shah RL, et al. Among authors: baird pn. Mol Vis. 2018 Feb 5;24:127-142. eCollection 2018. Mol Vis. 2018. PMID: 29422769 Free PMC article.

2

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

3

Evidence for a novel glaucoma locus at chromosome 3p21-22.

Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Baird PN, et al. Hum Genet. 2005 Jul;117(2-3):249-57. doi: 10.1007/s00439-005-1296-x. Epub 2005 May 20. Hum Genet. 2005. PMID: 15906098

4

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

5

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

6

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.

Hewitt AW, Sharma S, Burdon KP, Wang JJ, Baird PN, Dimasi DP, Mackey DA, Mitchell P, Craig JE. Hewitt AW, et al. Among authors: baird pn. Hum Mol Genet. 2008 Mar 1;17(5):710-6. doi: 10.1093/hmg/ddm342. Epub 2007 Nov 23. Hum Mol Genet. 2008. PMID: 18037624

7

A tag-single nucleotide polymorphisms approach to the vascular endothelial growth factor-A gene in age-related macular degeneration.

Richardson AJ, Islam FM, Guymer RH, Cain M, Baird PN. Richardson AJ, et al. Among authors: baird pn. Mol Vis. 2007 Nov 26;13:2148-52. Mol Vis. 2007. PMID: 18079689

8

Assessment of TGIF as a candidate gene for myopia.

Pertile KK, Schäche M, Islam FM, Chen CY, Dirani M, Mitchell P, Baird PN. Pertile KK, et al. Among authors: baird pn. Invest Ophthalmol Vis Sci. 2008 Jan;49(1):49-54. doi: 10.1167/iovs.07-0896. Invest Ophthalmol Vis Sci. 2008. PMID: 18172074

9

Primary open angle glaucoma in subjects harbouring the predicted GLC1L haplotype reveals a normotensive phenotype.

Sherwin JC, Hewitt AW, Bennett SL, Baird PN, Craig JE, Mackey DA. Sherwin JC, et al. Among authors: baird pn. Clin Exp Ophthalmol. 2009 Mar;37(2):201-7. doi: 10.1111/j.1442-9071.2009.02002.x. Epub 2009 Feb 3. Clin Exp Ophthalmol. 2009. PMID: 19723129

10

Role of the hepatocyte growth factor gene in refractive error.

Veerappan S, Pertile KK, Islam AF, Schäche M, Chen CY, Mitchell P, Dirani M, Baird PN. Veerappan S, et al. Among authors: baird pn. Ophthalmology. 2010 Feb;117(2):239-45.e1-2. doi: 10.1016/j.ophtha.2009.07.002. Epub 2009 Dec 14. Ophthalmology. 2010. PMID: 20005573

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