Lamey TM - Search Results

1

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. 2023 Dec;7(12):e20-e21. doi: 10.1016/j.oret.2023.07.028. Epub 2023 Aug 28. Ophthalmol Retina. 2023. PMID: 37642631 No abstract available.

2

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

3

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.

4

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

5

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.

6

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

7

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

8

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.

9

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

10

Enhanced Visualization of Subtle Outer Retinal Pathology by En Face Optical Coherence Tomography and Correlation with Multi-Modal Imaging.

Sampson DM, Alonso-Caneiro D, Chew AL, Lamey T, McLaren T, De Roach J, Chen FK. Sampson DM, et al. PLoS One. 2016 Dec 13;11(12):e0168275. doi: 10.1371/journal.pone.0168275. eCollection 2016. PLoS One. 2016. PMID: 27959968 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

62 results

Search Page