Craig JE - Search Results

1

A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish type.

Mullany S, Souzeau E, Klebe S, Zhou T, Knight LSW, Qassim A, Berry EC, Marshall H, Hussey M, Dubowsky A, Breen J, Hassall MM, Mills RA, Craig JE, Siggs OM. Mullany S, et al. Among authors: craig je. Hum Mutat. 2021 Jul;42(7):818-826. doi: 10.1002/humu.24214. Epub 2021 May 11. Hum Mutat. 2021. PMID: 33973672

2

Central corneal thickness of indigenous Australians within Central Australia.

Landers JA, Billing KJ, Mills RA, Henderson TR, Craig JE. Landers JA, et al. Among authors: craig je. Am J Ophthalmol. 2007 Feb;143(2):360-2. doi: 10.1016/j.ajo.2006.09.047. Epub 2006 Oct 19. Am J Ophthalmol. 2007. PMID: 17258537

3

A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.

Burdon KP, Sharma S, Chen CS, Dimasi DP, Mackey DA, Craig JE. Burdon KP, et al. Among authors: craig je. Hum Mutat. 2007 Jul;28(7):742. doi: 10.1002/humu.9501. Hum Mutat. 2007. PMID: 17579362

4

Myocilin allele-specific glaucoma phenotype database.

Hewitt AW, Mackey DA, Craig JE. Hewitt AW, et al. Among authors: craig je. Hum Mutat. 2008 Feb;29(2):207-11. doi: 10.1002/humu.20634. Hum Mutat. 2008. PMID: 17966125

5

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, Hewitt AW, Latimer P, Craig JE. Burdon KP, et al. Among authors: craig je. Hum Genet. 2008 Nov;124(4):379-86. doi: 10.1007/s00439-008-0555-z. Epub 2008 Sep 5. Hum Genet. 2008. PMID: 18795334

6

Heritability of central corneal thickness in nuclear families.

Landers JA, Hewitt AW, Dimasi DP, Charlesworth JC, Straga T, Mills RA, Savarirayan R, Mackey DA, Burdon KP, Craig JE. Landers JA, et al. Among authors: craig je. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4087-90. doi: 10.1167/iovs.08-3271. Epub 2009 May 6. Invest Ophthalmol Vis Sci. 2009. PMID: 19420341

7

Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry.

Sharma S, Chataway T, Burdon KP, Jonavicius L, Klebe S, Hewitt AW, Mills RA, Craig JE. Sharma S, et al. Among authors: craig je. Exp Eye Res. 2009 Oct;89(4):479-85. doi: 10.1016/j.exer.2009.05.001. Epub 2009 May 12. Exp Eye Res. 2009. PMID: 19442659

8

Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.

Dimasi DP, Chen JY, Hewitt AW, Klebe S, Davey R, Stirling J, Thompson E, Forbes R, Tan TY, Savarirayan R, Mackey DA, Healey PR, Mitchell P, Burdon KP, Craig JE. Dimasi DP, et al. Among authors: craig je. Hum Genet. 2010 Jan;127(1):33-44. doi: 10.1007/s00439-009-0729-3. Epub 2009 Aug 28. Hum Genet. 2010. PMID: 19714363

9

Sensitivity of confocal laser tomography versus optical coherence tomography in detecting advanced glaucoma.

Hewitt AW, Chappell AJ, Straga T, Landers J, Mills RA, Craig JE. Hewitt AW, et al. Among authors: craig je. Clin Exp Ophthalmol. 2009 Dec;37(9):836-41; quiz 903-4. doi: 10.1111/j.1442-9071.2009.02181.x. Clin Exp Ophthalmol. 2009. PMID: 20092591

10

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.

Burdon KP, Macgregor S, Hewitt AW, Sharma S, Chidlow G, Mills RA, Danoy P, Casson R, Viswanathan AC, Liu JZ, Landers J, Henders AK, Wood J, Souzeau E, Crawford A, Leo P, Wang JJ, Rochtchina E, Nyholt DR, Martin NG, Montgomery GW, Mitchell P, Brown MA, Mackey DA, Craig JE. Burdon KP, et al. Among authors: craig je. Nat Genet. 2011 Jun;43(6):574-8. doi: 10.1038/ng.824. Epub 2011 May 1. Nat Genet. 2011. PMID: 21532571

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