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Flinders Academic Commons >
Browsing by Author Craig, Jamie E
Showing results 19 to 38 of 38
| Issue Date | Title | Author(s) | | 2008 | Investigation of eight candidate genes on
chromosome 1p36 for autosomal dominant total congenital cataract | Mackey, David A; Craig, Jamie E; Burdon, Kathryn Penelope; Lachke, Salil A; Hattersely, Kathryn; Laurie, Kate; Maas, Richard L |
| 2005 | Lack of association of p53 polymorphisms and
haplotypes in high and normal tension open angle glaucoma | Dimasi, David Paul; Hewitt, Alex W; Green, Catherine M; Mackey, David A; Craig, Jamie E |
| 2005 | Linkage to 10q22 for maximum intraocular pressure
and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma
pedigree | Charlesworth, Jac C; Dyer, Thomas D; Stankovich, Jim M; Blangero, John; Mackey, David A; Craig, Jamie E; Green, Catherine M; Baird, Paul N; Sale, Michele M; Foote, Simon J |
| 2003 | Mutations in a novel gene, NHS, cause the
pleiotropic effects of Nance-Horan Syndrome including severe congenital cataract, dental
anomalies and mental retardation | Thomas, P; Thomas, T; Voss, A K; Sharma, Shiwani; Russell-Eggit, Isabelle M; Craig, Jamie E; Sale, Michele M; Mackey, David A; Wirth, M Gabriela; Gajovic, S; Clarke, M P; Gecz, Jozef; Elder, James E; Gruss, P; Fitzgerald, Liesel M; McKay, James D; Shaw, Marie A; Nicholl, A; Ross, S; Stankich, J M; Burdon, Kathryn Penelope |
| 2006 | Mutations in the NDP gene: contribution to Norrie
disease, familial exudative vitreoretinopathy and retinopathy of prematurity | Dickinson, Joanne L; Sale, Michele M; Passmore, Abraham; Fitzgerald, Liesel M; Wheatley, Catherine M; Burdon, Kathryn Penelope; Craig, Jamie E; Tengtrisorn, Supaporn; Carden, Susan M; Maclean, Hector; Mackey, David A |
| 2008 | Myocilin allele-specific glaucoma phenotype
database | Craig, Jamie E; Hewitt, Alex W; Mackey, David A |
| 2006 | A myocilin Gln368STOP homozygote does not exhibit
a more severe glaucoma phenotype than heterozygous cases | Hewitt, Alex W; Bennett, Sonya L; Dimasi, David Paul; Craig, Jamie E; Mackey, David A |
| 2007 | Myocilin Gly252Arg mutation and glaucoma of
intermediate severity in caucasian individuals | Hewitt, Alex W; Bennett, Sonya L; Richards, J E; Dimasi, David Paul; Booth, Adam P; Inglehearn, Chris; Anwar, Rashida; Yamamoto, Tetsuya; Fingert, John H; Heon, Elise; Craig, Jamie E; Mackey, David A |
| 2006 | Nance-Horan syndrome protein, NHS, associates with
epithelial cell junctions | Sharma, Shiwani; Ang, Sharyn; Shaw, Marie A; Mackey, David A; Gecz, Jozef; McAvoy, J; Craig, Jamie E |
| 2008 | Novel causative mutations in patients with
Nance-Horan Syndrome and altered localization of the mutant NHS-A protein
isoform | Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Dave, Alpana; Jamieson, Robyn; Yaron, Yuval; Billson, Frank; Maldergem, Lionel; Lorenz, Birgit; Gecz, Jozef |
| 2007 | A novel deletion in the FTL gene causes hereditary
hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start
site | Burdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia S |
| 2008 | A novel locus for X-lined congenital cataract on
Xq24 | Craig, Jamie E; Friend, K; Gecz, Jozef; Rattray, K M; Troski, Mark; Mackey, David A; Burdon, Kathryn Penelope |
| 2004 | A novel mutation in the Connexin 46 Gene causes
autosomal dominant congenital cataract with incomplete penetrance | Craig, Jamie E; Sale, Michele M; Mackey, David A; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Dickinson, Joanne L; Elder, James E; Burdon, Kathryn Penelope |
| 2007 | The optic nerve head in myocilin
glaucoma | Hewitt, Alex W; Bennett, Sonya L; Fingert, John H; Cooper, Richard L; Stone, Edwin M; Craig, Jamie E; Mackey, David A |
| 26-Sep-2012 | The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucoma | Wiggs, Janey L; Hewitt, Alex W; Fan, Bao Jian; Wang, Dan Yi; O'Brien, Colm; Realini, Anthony; Craig, Jamie E; Dimasi, David Paul; Mackey, David A; Haines, Jonathan L; Pasquale, Louis R; Figueiredo Sena, Dayse R |
| 2006 | The PITX3 gene in posterior polar congenital
cataract in Australia | Burdon, Kathryn Penelope; McKay, James D; Wirth, M Gabriela; Ruddle, Jonathan; Russell-Eggit, Isabelle M; Bhatti, Samira; Dimasi, David Paul; Mackey, David A; Craig, Jamie E |
| 2007 | Prevalence of CYP1B1 mutations in Australian
patients with primary congenital glaucoma | Elder, James E; Casey, T; Mackey, David A; Craig, Jamie E; MacKinnon, Jane R; Hewitt, Alex W; Dimasi, David Paul; Pater, John Brian; Straga, Tania |
| 2006 | The role of the Met98Lys optineurin variant in
inherited optic nerve diseases | Craig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A |
| Jul-2005 | The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes. | McKay, James D; Patterson, B; Craig, Jamie E; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Hewitt, Alex W; Cohn, Amy C; Kerdraon, Y; Mackey, David A |
| 2005 | The telomere of human chromosome 1p contains at
least two independent autosomal dominant congenital cataract genes | McKay, James D; Patterson, B; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Cohn, Amy C; Kerdraon, Y; Mackey, David A; Craig, Jamie E; Hewitt, Alex W |
Showing results 19 to 38 of 38
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