Kearns LS - Search Results

1

Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.

Siggs OM, Souzeau E, Pasutto F, Dubowsky A, Smith JEH, Taranath D, Pater J, Rait JL, Narita A, Mauri L, Del Longo A, Reis A, Chappell A, Kearns LS, Staffieri SE, Elder JE, Ruddle JB, Hewitt AW, Burdon KP, Mackey DA, Craig JE. Siggs OM, et al. Among authors: kearns ls. JAMA Ophthalmol. 2019 Apr 1;137(4):348-355. doi: 10.1001/jamaophthalmol.2018.5646. JAMA Ophthalmol. 2019. PMID: 30653210 Free PMC article.

2

Introducing a new retinitis pigmentosa patient information website.

Smallcombe KA, Kearns LS, Mackey DA. Smallcombe KA, et al. Among authors: kearns ls. Clin Exp Ophthalmol. 2005 Apr;33(2):227. doi: 10.1111/j.1442-9071.2005.00983.x. Clin Exp Ophthalmol. 2005. PMID: 15807840 No abstract available.

3

Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.

Cohn AC, Kearns LS, Savarirayan R, Ryan J, Craig JE, Mackey DA. Cohn AC, et al. Among authors: kearns ls. Ophthalmic Genet. 2005 Mar;26(1):45-53. doi: 10.1080/13816810590918398. Ophthalmic Genet. 2005. PMID: 15823925 Review.

4

Post-cycloplegia myopic shift in an older population.

Toh T, Kearns LS, Scotter LW, Mackey DA. Toh T, et al. Among authors: kearns ls. Ophthalmic Epidemiol. 2005 Jun;12(3):215-9. doi: 10.1080/09286580590964784. Ophthalmic Epidemiol. 2005. PMID: 16036481

5

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. Among authors: kearns ls. Arch Ophthalmol. 2007 Jan;125(1):112-6. doi: 10.1001/archopht.125.1.112. Arch Ophthalmol. 2007. PMID: 17210861

6

PAX6 mutations may be associated with high myopia.

Hewitt AW, Kearns LS, Jamieson RV, Williamson KA, van Heyningen V, Mackey DA. Hewitt AW, et al. Among authors: kearns ls. Ophthalmic Genet. 2007 Sep;28(3):179-82. doi: 10.1080/13816810701356676. Ophthalmic Genet. 2007. PMID: 17896318

7

Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q.

Zhu G, Hewitt AW, Ruddle JB, Kearns LS, Brown SA, Mackinnon JR, Chen CY, Hammond CJ, Craig JE, Montgomery GW, Martin NG, Mackey DA. Zhu G, et al. Among authors: kearns ls. Ophthalmology. 2008 Jun;115(6):1053-1057.e2. doi: 10.1016/j.ophtha.2007.08.013. Epub 2007 Oct 26. Ophthalmology. 2008. PMID: 17964656

8

The association between maternal smoking in pregnancy, other early life characteristics and childhood vision: the Twins Eye Study in Tasmania.

Ponsonby AL, Brown SA, Kearns LS, MacKinnon JR, Scotter LW, Cochrane JA, Mackey DA. Ponsonby AL, et al. Among authors: kearns ls. Ophthalmic Epidemiol. 2007 Nov-Dec;14(6):351-9. doi: 10.1080/01658100701486467. Ophthalmic Epidemiol. 2007. PMID: 18161608

9

How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania.

Green CM, Kearns LS, Wu J, Barbour JM, Wilkinson RM, Ring MA, Craig JE, Wong TL, Hewitt AW, Mackey DA. Green CM, et al. Among authors: kearns ls. Clin Exp Ophthalmol. 2007 Dec;35(9):793-9. doi: 10.1111/j.1442-9071.2007.01612.x. Clin Exp Ophthalmol. 2007. PMID: 18173405

10

The natural history of OPA1-related autosomal dominant optic atrophy.

Cohn AC, Toomes C, Hewitt AW, Kearns LS, Inglehearn CF, Craig JE, Mackey DA. Cohn AC, et al. Among authors: kearns ls. Br J Ophthalmol. 2008 Oct;92(10):1333-6. doi: 10.1136/bjo.2007.134726. Epub 2008 Jul 24. Br J Ophthalmol. 2008. PMID: 18653586

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