Similar articles for PMID: 11535458

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1

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier.

Craig JE, Baird PN, Healey DL, McNaught AI, McCartney PJ, Rait JL, Dickinson JL, Roe L, Fingert JH, Stone EM, Mackey DA. Craig JE, et al. Ophthalmology. 2001 Sep;108(9):1607-20. doi: 10.1016/s0161-6420(01)00654-6. Ophthalmology. 2001. PMID: 11535458

2

Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation.

Mackey DA, Healey DL, Fingert JH, Coote MA, Wong TL, Wilkinson CH, McCartney PJ, Rait JL, de Graaf AP, Stone EM, Craig JE. Mackey DA, et al. Arch Ophthalmol. 2003 Aug;121(8):1172-80. doi: 10.1001/archopht.121.8.1172. Arch Ophthalmol. 2003. PMID: 12912696

3

Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucoma.

Allingham RR, Wiggs JL, De La Paz MA, Vollrath D, Tallett DA, Broomer B, Jones KH, Del Bono EA, Kern J, Patterson K, Haines JL, Pericak-Vance MA. Allingham RR, et al. Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2288-95. Invest Ophthalmol Vis Sci. 1998. PMID: 9804137

4

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. 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

5

Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucoma.

Angius A, Spinelli P, Ghilotti G, Casu G, Sole G, Loi A, Totaro A, Zelante L, Gasparini P, Orzalesi N, Pirastu M, Bonomi L. Angius A, et al. Arch Ophthalmol. 2000 May;118(5):674-9. doi: 10.1001/archopht.118.5.674. Arch Ophthalmol. 2000. PMID: 10815160

6

A case-control comparison of the clinical characteristics of glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutation.

Graul TA, Kwon YH, Zimmerman MB, Kim CS, Sheffield VC, Stone EM, Alward WL. Graul TA, et al. Am J Ophthalmol. 2002 Dec;134(6):884-90. doi: 10.1016/s0002-9394(02)01754-3. Am J Ophthalmol. 2002. PMID: 12470758

7

Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registry.

Souzeau E, Burdon KP, Dubowsky A, Grist S, Usher B, Fitzgerald JT, Crawford A, Hewitt AW, Goldberg I, Mills RA, Ruddle JB, Landers J, Mackey DA, Craig JE. Souzeau E, et al. Ophthalmology. 2013 Jun;120(6):1135-43. doi: 10.1016/j.ophtha.2012.11.029. Epub 2013 Feb 28. Ophthalmology. 2013. PMID: 23453510

8

A myocilin Gln368STOP homozygote does not exhibit a more severe glaucoma phenotype than heterozygous cases.

Hewitt AW, Bennett SL, Dimasi DP, Craig JE, Mackey DA. Hewitt AW, et al. Am J Ophthalmol. 2006 Feb;141(2):402-3. doi: 10.1016/j.ajo.2005.08.073. Am J Ophthalmol. 2006. PMID: 16458712

9

Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees.

Bennett SL, Hewitt AW, Poulsen JL, Kearns LS, Morgan JE, Craig JE, Mackey DA. Bennett SL, et al. Arch Ophthalmol. 2007 Jan;125(1):112-6. doi: 10.1001/archopht.125.1.112. Arch Ophthalmol. 2007. PMID: 17210861

10

A GLC1A gene Gln368Stop mutation in a patient with normal-tension open-angle glaucoma.

Mardin CY, Velten I, Ozbey S, Rautenstrauss B, Michels-Rautenstrauss K. Mardin CY, et al. J Glaucoma. 1999 Apr;8(2):154-6. doi: 10.1097/00061198-199904000-00012. J Glaucoma. 1999. PMID: 10209734

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