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Browsing by Author Craig, Jamie E

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PreviewIssue DateTitleAuthor(s)
26-Sep-2012The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucomaWiggs, 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
2006The PITX3 gene in posterior polar congenital cataract in AustraliaBurdon, Kathryn Penelope; McKay, James D; Wirth, M Gabriela; Ruddle, Jonathan B; Russell-Eggit, Isabelle M; Bhatti, Samira; Dimasi, David Paul; Mackey, David A; Craig, Jamie E
2007Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucomaElder, James E; Casey, T; Mackey, David A; Craig, Jamie E; MacKinnon, Jane R; Hewitt, Alex W; Dimasi, David Paul; Pater, John Brian; Straga, Tania
22-Apr-2011The prevalence of glaucoma in indigenous Australians within Central Australia: the Central Australian Ocular Health StudyLanders, John; Henderson, Timothy R; Craig, Jamie E
26-Oct-2012The reliability of single-field fundus photography in screening for diabetic retinopathy: the Central Australian Ocular Health StudyKu, Janice J-Y; Landers, John; Henderson, Timothy R; Craig, Jamie E
30-Jul-2013Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconusBae, HA; Mills, RA; Lindsay, RG; Phillips, T; Mitchell, P; Wang, JJ; Coster, Douglas John; Craig, Jamie E; Burdon, Kathryn Penelope
2006The role of the Met98Lys optineurin variant in inherited optic nerve diseasesCraig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A
Mar-2014Screening of the COL8A2 gene in an Australian family with early-onset Fuchs’ endothelial corneal dystrophyKuot, Abraham; Mills, Richard Arthur; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope
12-Dec-2012The status of intercellular junctions in established lens epithelial cell linesDave, Alpana; Craig, Jamie E; Sharma, Shiwani
Jul-2005The 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
2005The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesMcKay, 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
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