Kearns LS - Search Results

1

The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohort.

Siggs OM, Awadalla MS, Souzeau E, Staffieri SE, Kearns LS, Laurie K, Kuot A, Qassim A, Edwards TL, Coote MA, Mancel E, Walland MJ, Dondey J, Galanopoulous A, Casson RJ, Mills RA, MacArthur DG, Ruddle JB, Burdon KP, Craig JE. Siggs OM, et al. Among authors: kearns ls. Clin Genet. 2020 May;97(5):764-769. doi: 10.1111/cge.13722. Epub 2020 Mar 5. Clin Genet. 2020. PMID: 32052405 Free PMC article.

2

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.

3

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

4

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

5

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

6

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

7

Effect of birth parameters on retinal vascular caliber: the Twins Eye Study in Tasmania.

Sun C, Ponsonby AL, Wong TY, Brown SA, Kearns LS, Cochrane J, MacKinnon JR, Ruddle JB, Hewitt AW, Liew G, Dwyer T, Scurrah K, Mackey DA. Sun C, et al. Among authors: kearns ls. Hypertension. 2009 Mar;53(3):487-93. doi: 10.1161/HYPERTENSIONAHA.108.125914. Epub 2009 Jan 12. Hypertension. 2009. PMID: 19139377

8

RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population.

Ruddle JB, Ebenezer ND, Kearns LS, Mulhall LE, Mackey DA, Hardcastle AJ. Ruddle JB, et al. Among authors: kearns ls. Br J Ophthalmol. 2009 Sep;93(9):1151-4. doi: 10.1136/bjo.2008.153908. Epub 2009 May 7. Br J Ophthalmol. 2009. PMID: 19429592

9

Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twins.

Mackey DA, Mackinnon JR, Brown SA, Kearns LS, Ruddle JB, Sanfilippo PG, Sun C, Hammond CJ, Young TL, Martin NG, Hewitt AW. Mackey DA, et al. Among authors: kearns ls. Twin Res Hum Genet. 2009 Oct;12(5):441-54. doi: 10.1375/twin.12.5.441. Twin Res Hum Genet. 2009. PMID: 19803772 Free PMC article.

10

Systemic disease associations of familial and sporadic glaucoma: the Glaucoma Inheritance Study in Tasmania.

Hewitt AW, Wu J, Green CM, Lai T, Kearns LS, Craig JE, Mackey DA. Hewitt AW, et al. Among authors: kearns ls. Acta Ophthalmol. 2010 Feb;88(1):70-4. doi: 10.1111/j.1755-3768.2009.01786.x. Epub 2009 Dec 16. Acta Ophthalmol. 2010. PMID: 19958295 Free article.

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