Lamey TM - Search Results

1

Analysis of the Outer Retinal Bands in ABCA4 and PRPH2-Associated Retinopathy using OCT.

Heath Jeffery RC, Lo J, Thompson JA, Lamey TM, McLaren TL, De Roach JN, Ayton LN, Vincent AL, Sharma A, Chen FK. Heath Jeffery RC, et al. Among authors: lamey tm. Ophthalmol Retina. 2024 Feb;8(2):174-183. doi: 10.1016/j.oret.2023.05.010. Epub 2023 May 18. Ophthalmol Retina. 2024. PMID: 37209970 Free article.

2

Isolation and expression analysis of a Pax group III gene from the crustacean Cherax destructor.

White RB, Lamey TM, Ziman M, Koenders A. White RB, et al. Among authors: lamey tm. Dev Genes Evol. 2005 Jun;215(6):306-12. doi: 10.1007/s00427-005-0478-9. Epub 2005 Mar 17. Dev Genes Evol. 2005. PMID: 15772827

3

Genotypic analysis of X-linked retinoschisis in Western Australia.

Lamey T, Laurin S, Chelva E, De Roach J. Lamey T, et al. Adv Exp Med Biol. 2010;664:283-91. doi: 10.1007/978-1-4419-1399-9_32. Adv Exp Med Biol. 2010. PMID: 20238027

4

Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa.

Paterson RL, De Roach JN, McLaren TL, Hewitt AW, Hoffmann L, Lamey TM. Paterson RL, et al. Among authors: lamey tm. Mol Vis. 2012;18:2043-52. Epub 2012 Jul 25. Mol Vis. 2012. PMID: 22876132 Free PMC article.

5

Establishment and evolution of the Australian Inherited Retinal Disease Register and DNA Bank.

De Roach JN, McLaren TL, Paterson RL, O'Brien EC, Hoffmann L, Mackey DA, Hewitt AW, Lamey TM. De Roach JN, et al. Among authors: lamey tm. Clin Exp Ophthalmol. 2013 Jul;41(5):476-83. doi: 10.1111/ceo.12020. Epub 2012 Dec 10. Clin Exp Ophthalmol. 2013. PMID: 23078154

6

Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.

Crowley C, Paterson R, Lamey T, McLaren T, De Roach J, Chelva E, Khan J. Crowley C, et al. Doc Ophthalmol. 2014 Aug;129(1):57-63. doi: 10.1007/s10633-014-9444-z. Epub 2014 May 24. Doc Ophthalmol. 2014. PMID: 24859690 Free PMC article.

7

Clinical and molecular characterization of females affected by X-linked retinoschisis.

Staffieri SE, Rose L, Chang A, De Roach JN, McLaren TL, Mackey DA, Hewitt AW, Lamey TM. Staffieri SE, et al. Among authors: lamey tm. Clin Exp Ophthalmol. 2015 Sep-Oct;43(7):643-7. doi: 10.1111/ceo.12541. Epub 2015 Jun 19. Clin Exp Ophthalmol. 2015. PMID: 25894957

8

Genetic analysis of choroideremia families in the Australian population.

McLaren TL, De Roach JN, Montgomery H, Hoffmann L, Kap C, Lamey TM. McLaren TL, et al. Among authors: lamey tm. Clin Exp Ophthalmol. 2015 Nov;43(8):727-34. doi: 10.1111/ceo.12542. Epub 2015 Jul 17. Clin Exp Ophthalmol. 2015. PMID: 25912515

9

Progress and prospects of next-generation sequencing testing for inherited retinal dystrophy.

Chiang JP, Lamey T, McLaren T, Thompson JA, Montgomery H, De Roach J. Chiang JP, et al. Expert Rev Mol Diagn. 2015;15(10):1269-75. doi: 10.1586/14737159.2015.1081057. Epub 2015 Aug 26. Expert Rev Mol Diagn. 2015. PMID: 26394700 Free PMC article. Review.

10

A computer-assisted method for pathogenicity assessment and genetic reporting of variants stored in the Australian Inherited Retinal Disease Register.

Huynh E, De Roach J, McLaren T, Thompson J, Montgomery H, Kap C, Hoffmann L, Lamey T. Huynh E, et al. Australas Phys Eng Sci Med. 2016 Mar;39(1):239-45. doi: 10.1007/s13246-015-0420-z. Epub 2016 Jan 4. Australas Phys Eng Sci Med. 2016. PMID: 26728880

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