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Browsing by Author Hewitt, Alex W

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PreviewIssue DateTitleAuthor(s)
2010Mortality in primary open-angle glaucoma: 'two cupped discs and a funeral'.Hewitt, Alex W; Sanfilippo, Paul G; Ring, Maree A; Mackey, David A; Craig, Jamie
2008Myocilin allele-specific glaucoma phenotype databaseCraig, Jamie E; Hewitt, Alex W; Mackey, David A
2006A myocilin Gln368STOP homozygote does not exhibit a more severe glaucoma phenotype than heterozygous casesHewitt, Alex W; Bennett, Sonya L; Dimasi, David Paul; Craig, Jamie E; Mackey, David A
2007Myocilin Gly252Arg mutation and glaucoma of intermediate severity in caucasian individualsHewitt, 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
2010Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesChen, Jern Yee; Dimasi, David Paul; Hewitt, Alex W; Klebe, Sonja; Davey, Richard; Stirling, John W; Thompson, E; Forbes, Robin; Tan, Tiong Y; Savarirayan, Ravi; Mackey, David A; Healey, Paul R; Mitchell, Paul; Burdon, Kathryn Penelope; Craig, Jamie
2007The optic nerve head in myocilin glaucomaHewitt, Alex W; Bennett, Sonya L; Fingert, John H; Cooper, Richard L; Stone, Edwin M; Craig, Jamie E; Mackey, David A
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
2010The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ration, and central corneal thicknessDyer, Thomas D; Diego, Victor; Samples, John R; Craig, Jamie; Mackey, David A; Hewitt, Alex W; Blangero, John; Wirtz, Mary K; Charlesworth, Jac C; Kramer, Patricia L
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
2009Primary open angle glaucoma in subjects harbouring the predicted GLC1L haplotype reveals a normotensive phenotypeCraig, Jamie; Mackey, David A; Bennett, Sonya L; Baird, Paul N; Sherwin, Justin C; Hewitt, Alex W
2009Quantitative genetic analysis of the retinal vascular caliber: the Australian twins eye studyYoung, Terri L; Hammond, Christopher J; Craig, Jamie; Zhu, Gu; Martin, Nicholas G; Wong, Tien Y; Hewitt, Alex W; Ruddle, Jonathan; Hodgson, Lauren; Montgomery, Grant; He, Mingguang; Mackey, David A; Sun, Cong
2009Rapid inexpensive genome-wide association using pooled whole bloodCraig, Jamie; Sharma, Shiwani; Hewitt, Alex W; McMellon, Amy E; Henders, Anjali K; Wallace, Leanne; Ma, Lingjun; Burdon, Kathryn Penelope; Visscher, Peter; Montgomery, Grant; Macgregor, Stuart
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
2009Sensitivity of confocal laser tomography versus optical coherence tomography in detecting advanced glaucomaHewitt, Alex W; Straga, Tania; Landers, John A; Chappell, Angela J.; Mills, Richard Arthur; Craig, Jamie
2009A systematic meta-analysis of genetic association studies for diabetic retinopathyAbhary, Sotoodeh; Hewitt, Alex W; Craig, Jamie; Burdon, Kathryn Penelope
2010Systemic disease association of familial and sporadic glaucome: the glaucoma inheritance study inTasmaniaLai, Tze; Green, Catherine M; Wu, Johnny; Mackey, David A; Kearns, Lisa A; Craig, Jamie; Hewitt, Alex W
2010Tag SNPs detect association of teh CYP1B1 gene with primary open angle glaucomaBurdon, Kathryn Penelope; Hewitt, Alex W; Mackey, David A; Craig, Jamie; Mitchell, Paul
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
Showing results 31 to 49 of 49
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