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Items where Subject is Socio-Economic Objective, Health, Clinical Health (Organs, Diseases and Abnormal Conditions), Hearing, Vision, Speech and Their Disorders

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Journal Article

Thompson, AJ, Combination glaucoma preparations, Prescriber, 20, (12) pp. 57-58. ISSN 0959-6682 (2009) [Letter or Note in Journal]
Sun, C and Ponsonby, AL and Wong, TY and Brown, Shayne and Kearns, LS and Cochrane, JA and MacKinnon, JR and Ruddle, JB and Hewitt, AW and Liew, G and Dwyer, T and Scurrah, K and Mackey, DA, Effect of birth parameters on retinal vascular caliber: the twins eye study in Tasmania, Hypertension, 53, (3) pp. 487-493. ISSN 0194-911X (2009) [Refereed Article] 
Sun, C and Wang, JJ and Mackey, DA and Wong, TY, Retinal vascular caliber: systemic, environmental, and genetic associations, Survey of Ophthalmology, 54, (1) pp. 74-95. ISSN 0039-6257 (2009) [Refereed Article] 
Craig, JE and Friend, KL and Gecz, J and Rattray, KM and Troski, M and Mackey, DA and Burdon, KP, A novel locus for X-linked congenital cataract on Xq24, Molecular Vision, 18, (14) pp. 721-6. ISSN 1090-0535 (2008) [Refereed Article] 
Hewitt, AW and Sharma, S and Burdon, KP and Wang, JJ and Baird, PN and Dimasi, DP and Mackey, DA and Mitchell, P and Craig, JE, Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people, Human Molecular Genetics, 17, (5) pp. 710-716. ISSN 0964-6906 (2008) [Refereed Article]
Burdon, KP and Sharma, S and Hewitt, AW and McMellon, AE and Wang, JJ and Mackey, DA and Mitchell, P and Craig, JE, Genetic analysis of the clusterin gene in pseudoexfoliation syndrome, Molecular Vision, 22, (14) pp. 1727-36. ISSN 1090-0535 (2008) [Refereed Article] 
Zhu, G and Hewitt, AW and Ruddle, JB and Kearns, LS and Brown, SA and Mackinnon, JR and Chen, CY and Hammond, CJ and Craig, JE and Montgomery, GW and Martin, NG and Mackey, DA, Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q, Ophthalmology, 115, (6) pp. 1053-1057. ISSN 0161-6420 (2008) [Refereed Article] 
He, M and Wang, D and Zheng, Y and Zhang, J and Yin, Q and Huang, W and Mackey, DA and Foster, PJ, Heritability of anterior chamber depth as an intermediate phenotype of angle-closure in Chinese: the Guangzhou Twin Eye Study, Investigative Ophthalmology & Visual Science, 49, (1) pp. 81-86. ISSN 0146-0404 (2008) [Refereed Article] 
Carbonaro, F and Andrew, T and Mackey, DA and Spector, TD and Hammond, CJ, Heritability of intraocular pressure: a classical twin study, British Journal Of Ophthalmology, 92, (8) pp. 1125-8. ISSN 0007-1161 (2008) [Refereed Article] 
He, M and Ge, J and Wang, D and Zhang, J and Hewitt, AW and Hur, Y and Mackey, DA and Foster, PJ, Heritability of the iridotrabecular angle width measured by optical coherence tomography in Chinese children: the Guangzhou twin eye study, Investigative Ophthalmology & Visual Science, 49, (4) pp. 1356-61. ISSN 0146-0404 (2008) [Refereed Article] 
Hewitt, AW and Mackey, DA and Craig, JE, Myocilin Allele-Specific Glaucoma Phenotype Database, Human Mutation, 29, (2) pp. 207-211. ISSN 1059-7794 (2008) [Refereed Article]
Carbonaro, F and Andrew, T and Mackey, DA and Spector, TD and Hammond, CJ, The Heritability of Corneal Hysteresis and Ocular Pulse Amplitude, Ophthalmology, 115, (9) pp. 1545-1549. ISSN 0161-6420 (2008) [Refereed Article] 
Cohn, AC and Toomes, C and Hewitt, AW and Kearns, LS and Inglehearn, CF and Craig, JE and Mackey, DA, The natural history of OPA1-related autosomal dominant optic atrophy, British Journal of Ophthalmology, 92, (10) pp. 1333-1336. ISSN 0007-1161 (2008) [Refereed Article] 
Mackey, DA and Green, CM and Craig, JE and Hewitt, AW, The pathogenesis of the glaucoma: nature versus nurture, Clinical and Experimental Ophthalmology pp. 297. ISSN 1442-6404 (2008) [Letter or Note in Journal] 
Burdon, KP and Sharma, S and Chen, CS and Dimasi, DP and Mackey, DA and Craig, JE, A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site, Human Mutation, 972, (7) EJ ISSN 1059-7794 (2007) [Refereed Article] 
Balaratnasingam, C and Morgan, WH and Nelson, J and Mackey, DA and Dimasi, DP and Lam, G, Abnormal iris processes may be a marker of glaucoma gene carrier status in some cases of primary infantile glaucoma, Ophthalmic Genetics, 28, (3) pp. 157-162. ISSN 1381-6810 (2007) [Refereed Article]
Cohn, AC and Toomes, C and Potter, C and Towns, KV and Hewitt, AW and Inglehearn, CF and Craig, JE and Mackey, DA, Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations, Am J Ophthalmol, 143, (4) pp. 656-662. ISSN 0002-9394 (2007) [Refereed Article]
Mackey, DA, Central corneal thickness and glaucoma in the Australian Aboriginal population, Clinical and Experimental Ophthalmology, 35 pp. 691-692. ISSN 1442-6404 (2007) [Letter or Note in Journal] 
Chen, C and Scurrah, KJ and Stankovich, J and Garoufalis, P and Dirani, M and Pertile, KK and Richardson, AJ and Mitchell, P and Baird, PN, Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study, Human Genetics, 121, (3-4) pp. 511-520. ISSN 0340-6717 (2007) [Refereed Article]
Hewitt, AW and Poulsen, JP and Alward, WLM and Bennett, SL and Budde, WM and Cooper, RL and Craig, JE and Fingert, JH and Foster, PJ and Garway-Heath, DF and Green, CM and Hammond, CJ and Hayreb, SS and Jonas, JB and Kaufman, PL and Miller, NR and Morgan, WH and Newman, NJ and Quigley, HA and Samples, JR and Spaeth, GL and Pesudovs, K and Mackey, DA, Heritable features of the optic disc: a novel twin method for determining genetic significance, Investigative Ophthalmology & Visual Science, 48, (6) pp. 0146-0404. ISSN 0009-9163 (2007) [Refereed Article]
Green, CM and Kearns, LS and Wu, J and Barbour, JM and Wilkinson, RM and Ring, M and Craig, JE and Wong, TL and Hewitt, AW and Mackey, DA, How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania, Clinical and Experimental Ophthalmology, 35, (9) pp. 793-799. ISSN 1442-6404 (2007) [Refereed Article]
Hewitt, AW and Samples, JR and Allingham, RR and Jarvela, I and Kitsos, G and Krishnadas, SR and Richards, JE and Lichter, PR and Petersen, MB and Sundaresan, P and Wiggs, JL and Mackey, DA and Wirtz, MK, Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds, Molecular Vision, 13, (March) pp. 487-492. ISSN 1090-0535 (2007) [Refereed Article]
Chen, CY and Stankovich, J and Scurrah, KJ and Garoufalis, P and Dirani, M and Pertile, KK and Richardson, AJ and Baird, PN, Linkage Replication of the MYP12 Locus in Common Myopia, Investigative Ophthalmology and Vision Science, 48, (10) pp. 4433-4439. ISSN 0146-0404 (2007) [Refereed Article]
Hewitt, AW and Bennett, SL and Richard, JE and Dimasi, DP and Booth, AP and Inglehearn, C and Anwar, R and Yamamoto, T and Fingert, JH and Heon, E and Craig, JE and Mackey, DA, Myocilin Gly252Arg Mutation and Glaucoma of Intermediate Severity in Caucasioan Individuals, Archives of Ophthalmology, 125, (January) pp. 98-104. ISSN 0003-9950 (2007) [Refereed Article]
Fingert, JH and Alward, WLM and Kwon, YH and Shankar, SP and Andorf, JL and Mackey, DA and Sheffield, VC and Stone, EM, No association between variations in the WDR36 gene and primary open-angle glaucoma, Archives of Ophthalmology, 28, (3) pp. 434-436. ISSN 0003-9950 (2007) [Other Refereed Article]
Symons, RCA and Turakulov, R and Foote, SJ and Craig, JE and McCartney, PJ and Mackey, DA, No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma, Ophthalmic Genetics, 28, (1) pp. 39-41. ISSN 1381-6810 (2007) [Letter or Note in Journal] 
Hewitt, AW and Kearns, LS and Jamieson, RV and Williamson, KA and Heyningen, VV and Mackey, DA, PAX6 mutations may be associated with high myopia, Ophthalmic Genetics, 28, (3) pp. 179-182. ISSN 1381-6810 (2007) [Other Refereed Article] 
Dimasi, DP and Hewitt, AW and Straga, T and Pater, J and MacKinnon, JR and Elder, JE and Casey, T and Mackey, DA and Craig, JE, Prevalence of CYP1B1 mutations in Australian patients with primary congenial glaucoma, Clinical Genetics, 72, (3) pp. 255-260. ISSN 0009-9163 (2007) [Refereed Article] 
Bennett, SL and Hewitt, AW and Poulsen, JL and Kearns, LS and Morgan, JE and Craig, JE and Mackey, DA, Screening for Glaucomatous Disc Changes Prior to Diagnosis of Glaucoma in Myocilin Pedifrees, Archives of Ophthalmology, 125, (January) pp. 112-116. ISSN 0003-9950 (2007) [Refereed Article]
Ponsonby, AL and Brown, SA and Kearns, LS and MacKinnon, JR and Scotter, LW and Cochrane, JA and Mackey, DA, The Association Between Maternal Smoking in Pregnancy, Other Early Life Characteristics and Childhood Vision: The Twins Eye Study in Tasmania, Ophthalmic Epidemiology, 14, (Nov - Dec 2007) pp. 351-359. ISSN 0928-6586 (2007) [Refereed Article]
Ponsonby, AL and Brown, SA and Kearns LS, T and MacKinnon, JR and Scotter, LW and Cochrane, JA and Mackey, DA, The association between maternal smoking in pregnancy, other early life characteristics and childhood vision: The twins eye study in Tasmania, Ophthalmic Epidemiology, 14, (6) pp. 351-359. ISSN 0928-6586 (2007) [Refereed Article]
Hewitt, AW and Bennett, SL and Fingert, JH and Cooper, RL and Stone, EM and Craig, JE and Mackey, DA, The Optic Nerve Head in Myocilin Glaucoma, Investigative Ophthalmology & Visual Science, 48, (1) pp. 238-243. ISSN 0146-0404 (2007) [Refereed Article]
Mackey, DA, 2005 Gregg Lecture: Congenital cataract - from rubella to genetics, Clinical and Experimental Ophthalmology, 34 pp. 199-207. ISSN 1442-6404 (2006) [Refereed Article] 
Hewitt, AW and Dimasi, DP and Mackey, DA and Craig, JE, A Glaucoma Case-Control Study of the WDR36 Gene D658G Sequence Variant, American Journal of Ophthalmology, 142, (2) pp. 324-325. ISSN 0002-9394 (2006) [Refereed Article] 
Petersen, MB and Kitos, G and Samples, JR and Gaudette, ND and Economou-Petersen, E and Sykes, R and Rust, K and Grigoriadou, M and Aperis, G and Cboi, D and Psilas, K and Craig, JE and Kramer, PL and Mackey, DA and Wirtz, MK, A Large GLC1C Greek Family with a Myocilin T377M Mutation: Inheritance and Phenotypic Variability, Investigative Ophthalmology & Visual Science, 47, (2) pp. 620-625. ISSN 0146-0404 (2006) [Refereed Article] 
Hewitt, AW and Bennett, SL and Dimasi, DP and Craig, JE and Mackey, DA, A Myocilin Gln368STOP Homozygote Does Not Exhibit a More Severe Glaucoma Phenotype than Heterozygous Cases, American Journal of Ophthalmology, 141, (2) pp. 402-403. ISSN 0002-9394 (2006) [Refereed Article] 
Hewitt, AW and Craig, JE and Mackey, DA, Complex genetics of complex traits: the case of primary open-angle glaucoma, Clinical and Experimental Ophthalmology, 34 pp. 472-484. ISSN 1442-6404 (2006) [Refereed Article] 
Petersen, MB and Kitsos, G and Samples, JR and Gaudette, ND and Economou-Petersen, E and Sykes, R and Rust, K and Grigoriadou, M and Aperis, G and Choi, D and Psilas, K and Craig, JE and Mackey, DA and Wirtz, MK, Complex Inheritance of Primary Open Angle Glaucoma Involving Myocilin and the GLCIC Gene, Investigative ophthalmology & visual science, 47 pp. 620-625. ISSN 1234-1234 (2006) [Refereed Article] 
Charlesworth, JC and Stankovich, J and Mackey, DA and Craig, JE and Haybittel, M and Westmore, RN and Sale, MM, Confirmation of the Adult-Onset Primary Open Angle Glaucoma Locus GLC1B at 2cen-q13 in an Australian Family, Ophthalmologica, 220 pp. 23-30. ISSN 0030-3755 (2006) [Refereed Article]
Slaghuis, WL and Ryan, JF, Directional motion contrast sensitivity in developmental dyslexia, Vision Research, 46, (2006) pp. 3291-3303. ISSN 0042-6989 (2006) [Refereed Article]
Wu, J and Hewitt, AW and Green, CM and Ring, M and McCartney, PJ and Craig, JE and Mackey, DA, Disease Severity of Familial Glaucoma Compared With Sporadic Glaucoma, Archives of Ophthalmology, 124, (July) pp. 930-934. ISSN 0003-9950 (2006) [Refereed Article] 
Wu, J and Hewitt, AW and Green, CM and McCartney, PJ and Craig, JE and Ring, MA and Mackey, DA, Familial glaucoma is more severe than sporadic glaucoma, Archives of Opthalmology, 124 pp. 950-954. ISSN 1234-1234 (2006) [Refereed Article] 
Hewitt, AW and MacKinnon, JR and Giubilato, A and Elder, JE and Craig, JE and Mackey, DA, Familial Transmission Risk of Infantile Glaucoma in Australia, Ophthalmic Genetics, 27 pp. 93-97. ISSN 1381-6810 (2006) [Refereed Article] 
Self, JE and Ennis, S and Collins, A and Shawkat, F and Harris, CM and Mackey, DA and Hodgkins, PR and Temple, IK and Chen, XL and Lotery, AJ, Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3, Molecular Vision, 12 pp. 1211-1216. ISSN 1090-0535 (2006) [Refereed Article] 
Nelson, MR, Managing conjunctivitis in general practice: Recommendations depend on health system, British Medical Journal, 333, (2006) pp. 446. ISSN 0959-8146 (2006) [Letter or Note in Journal] 
Dickinson, JL and Sale, MM and Passmore, A and Fitzgerald, LM and Wheatley, CM and Burdon, KP and Craig, JE and Tengtrisorn, S and Carden, SM and Franzco, HM and Mackey, DA, Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity, Clinical and Experimental Ophthalmology, 34 pp. 682-688. ISSN 1442-6404 (2006) [Refereed Article]
Mimiwati, Z and Mackey, DA and Craig, JE and MacKinnon, JR and Rait, JL and Liebelt, JE and Ayala-Lugo, R and Vollrath, D and Richards, JE, Nail-patella syndrome and its association with glaucoma: a review of eight families, British Journal of Ophthalmology, 90 pp. 1505-1511. ISSN 0007-1161 (2006) [Refereed Article] 
Sharma, S and Ang, SL and Shaw, M and Mackey, DA and Gecz, J and McAvoy, JW and Craig, JE, Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions, Human Molecular Genetics, 15, (2) pp. 1972-1983. ISSN 0964-6906 (2006) [Refereed Article] 
Burdon, KP and McKay, JD and Wirth, MG and Russell-Eggit, IM and Bhatti, S and Ruddle, JB and Dimasi, D and Mackey, DA and Craig, JE, The PITX3 gene in posterior polar congenital cataract in Australia, Molecular Vision, 12, (April) pp. 367-371. ISSN 1090-0535 (2006) [Refereed Article]
Craig, JE and Hewitt, AW and Dimasi, DP and Howell, N and Toomes, C and Cohn, AC and Mackey, DA, The role of the Met98Lys optineurin variant in inherited optic nerve diseases, British Journal of Ophthalmology, 90 pp. 1420-1424. ISSN 0007-1161 (2006) [Refereed Article] 
Hewitt, AW and Traill, A and Cooper, RL and Morgan, JE and Mackey, DA, Tools for cup:disc ratio measurement. Letters to the Editor, Clinical and Experimental Ophthalmology, 34 pp. 288-289. ISSN 1442-6404 (2006) [Letter or Note in Journal] 
Baird, PN and Richardson, AJ and Mackey, DA and Craig, JE and Faucher, M and Raymond, V, A Common Disease Haplotype for the Q368STOP Mutation of the Myocilin Gene in Australian and Canadian Glaucoma Families, American Journal of Ophthalmology , 140, (4) pp. 760-762. ISSN 0002-9394 (2005) [Refereed Article] 
Toh, TY and Liew, SHM and MacKinnon, JR and Hewitt, AW and Poulsen, JL and Spector, TD and Gilbert, CE and Craig, JE and Hammond, CJ and Mackey, DA, Central Corneal Thickness Is Highly Heritable: The Twin Eye Studies, Investigative Ophthalmology & Visual Science, 46, (10) pp. 3718-3722. ISSN 0146-0404 (2005) [Refereed Article] 
Cohn, AC and Kearns, LS and Savarirayan, R and Ryan, J and Craig, JE and Mackey, DA, Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter, Ophthalmic Genetics, 26, (1) pp. 45-53. ISSN 1381-6810 (2005) [Professional, Non Refereed Article] 
Baird, PN and Foote, SJ and Mackey, DA and Craig, JE and Speed, TP and Bureau, A, Evidence for a novel glaucoma locus at chromosome 3p21-22, Human Genetics, 117, (2-3) pp. 249-257. ISSN 0340-6717 (2005) [Refereed Article] 
Baird, PN and Foote, SJ and Mackey, DA and Craig, JE and Speed, TP and Bureau, A, Evidence for a novel glaucoma locus at chromosome 3p21-22, Human Genetics, 117, (2-3) pp. 249-257. ISSN 0340-6717 (2005) [Refereed Article] 
Hewitt, AW and Fitzgerald, LM and Scotter, LW and Mulhall, LE and McKay, JD and Mackey, DA, Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia, Clinical and Experimental Ophthalmology, 33, (3) pp. 233-239. ISSN 1442-6404 (2005) [Refereed Article] 
Dimasi, DP and Hewitt, AW and Green, CM and Mackey, DA and Craig, JE, Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma, Journal of Medical Genetics, 42, (9) pp. e55-e58. ISSN 0022-2593 (2005) [Refereed Article] 
Charlesworth, JC and Dyer, TD and Stankovich, J and Blangero, J and Mackey, DA and Craig, JE and Green, CM and Foote, SJ and Baird, PN and Sale, MM, Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree, Investigative Ophthalmology & Visual Science, 46, (10) pp. 3723-3729. ISSN 0146-0404 (2005) [Refereed Article] 
Krafchak, CM and Pawar, H and Moroi, SE and Sugar, A and Lichter, PR and Mackey, DA and Main, S and Nairus, T and Elner, V and Schteingart, MT and Downs, CA and Kijek, TG and Johnson, JM and Trager, EH and Rozsa, FW and Mandal, MN and Epstein, MP and Vollrath, D and Ayyagari, R and Boehnke, M and Richards, JE, Mutations in TCF8 Cause Posterior Polymorphous Corneal Dystrophy and Ectopic Expression of COL4A3 by Corneal Endothelial Cells, American Journal of Human Genetics, 77, (5) pp. 694-708. ISSN 0002-9297 (2005) [Refereed Article] 
Toh, TY and Kearns, LS and Scotter, LW and Mackey, DA, Post-Cycloplegia Myopic Shift in an Older Population, Ophthalmic Epidemiology, 12, (3) pp. 215-219. ISSN 0928-6586 (2005) [Refereed Article] 
Baird, PN and Richardson, AJ and Craig, JE and Rochtchina, E and Mackey, DA and Mitchell, P, The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye Study, American Journal of Ophthalmology , 139, (6) pp. 1125-1126. ISSN 0002-9394 (2005) [Refereed Article] 
McKay, JD and Patterson, B and Craig, JE and Russell-Eggitt, E and Wirth, MG and Burdon, KP and Hewitt, AW and Cohn, AC and Kerdraon, Y and Mackey, DA, The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes, British Journal of Ophthalmology, 89, (7) pp. 831-834. ISSN 0007-1161 (2005) [Refereed Article] 
Burdon, KP and Wirth, GM and Mackey, DA and Russell-Eggitt, IM and Craig, JE and Elder, J and Dickinson, JL and Sale, MM, A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance, Journal of medical genetics, 41 pp. e106. ISSN 1234-1234 (2004) [Refereed Article] 
Baird, PN and Richardson, AJ and Craig, JE and Mackey, DA and Rochtchina, E and Mitchell, P, Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye Study, Clinical and Experimental Ophthalmology, 32 pp. 518-522. ISSN 1442-6404 (2004) [Refereed Article] 
Healey, DL and Craig, JE and Wilkinson, CH and Stone, EM and Mackey, DA, Attitudes to Predictive DNA Testing for Myocilin Glaucoma Experience with a Large Australian Family, Journal of Glaucoma, 13, (4) pp. 304-311. ISSN 1057-0829 (2004) [Refereed Article] 
Burdon, KP and Wirth, MG and Mackey, DA and Russell-Eggitt, IM and Craig, JE and Elder, JE and Dickinson, JL and Sale, MM, Extended Report. Investigation of crystallin genes in familial cataract, and report of two disease associated mutations, British Journal of Ophthalmology , 41, (March) pp. 79-83. ISSN 0007-1161 (2004) [Refereed Article] 
Yamada, K and Chan, WM and Andrews, C and Bosley, TM and Sener, EC and Zwaan, JT and Mullaney, PB and Ozturk, BT and Akarsu, N and Sabol, LJ and Demer, JL and Sullivan, TJ and Gottlob, I and Roggenkaemper, P and Mackey, DA and de Uzcategui, CE and Uzcategui, N and Ben-Zeev, B and Traboulsi, EI and Magli, A and de Berardinis, T and Gagliardi, V and Awastbi-Patney, S and Vogel, MC and Rizzo III, JF and Engle, EC, Identification of KIF21A Mutations as a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 (CFEOM3), Investigative Ophthalmology & Visual Science, 45, (7) pp. 2218-2223. ISSN 0146-0404 (2004) [Refereed Article] 
Burdon, KP and Wirth, GM and Mackey, DA and Russell-Eggitt, I and Craig, JE and Elder, J and Dickinson, JL and Sale, MM, Investigation of crystallin genes in familial cataract, and report of two disease associated mutations, British Journal of Ophthalmology, 88, (1) pp. 79-83. ISSN 0007-1161 (2004) [Refereed Article] 
Wan, PYW and Howell, N and Mackey, DA and Norby, S and Rosenberg, T and Turnbull, DM and Chinnery, PF, Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees, Journal of Medical Genetics, 41 pp. e41-45. ISSN 0022-2593 (2004) [Refereed Article] 
Toomes, C and Bottomley, HM and Jackson, RM and Towns, KV and Scott, S and Mackey, DA and Craig, JE and Jiang, L and Yang, ZL and Trembath, R and Woodruff, G and Gregory-Evans, CY and Gregory-Evans, K and Parker, MJ and Downey, LM and Zhang, K and Inglehearn, CF, Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q, American Journal of Human Genetics, 74 pp. 721-730. ISSN 0002-9297 (2004) [Refereed Article] 
Burdon, KP and Wirth, MG and Mackey, DA and Russell-Eggitt, IM and Craig, JE and Elder, JE and Dickinson, JL and Sale, MM, Online Mutation Report. A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance, Journal of Medical Genetics, 41, (August) pp. e106-109. ISSN 0022-2593 (2004) [Refereed Article] 
MacKinnon, JR and Giubilato, A and Elder JE, CH and Craig, JE and Mackey, DA, Primary infantile glaucoma in an Australian population, Clinical and Experimental Ophthalmology, 32 pp. 14-18. ISSN 1442-6404 (2004) [Refereed Article] 
Connell, BJ and Wilkinson, RM and Barbour, JM and Scotter, LW and Poulsen, JL and Wirth, MG and Essex, RW and Savarirayan, R and Mackey, DA, Research Report. Are Duane syndrome and infantile esotropia allelic?, Ophthalmic Genetics, 25, (3) pp. 189-198. ISSN 1381-6810 (2004) [Refereed Article] 
Toomes, C and Bottomley, HM and Scott, S and Mackey, DA and Craig, JE and Appukuttan, B and Stout, JT and Flaxel, CJ and Zhang, K and Black, GCM and Fryer, A and Downey, LM and Inglebearn, CF, Spectrum and Frequency of FZD4 Mutations in Familial Exudative Vitreorectinopathy, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 45, (7) pp. 2083-2090. ISSN 0146-0404 (2004) [Refereed Article] 
Alward, WL and Kwon, YH and Kawase, K and Craig, JE and Hayreh, SS and Johnson, AT and Khanna, CL and Yamamoto, T and Mackey, DA and Roos, BR and Affatigato, LM and Sheffield, VC and Stone, EM, Evaluation of optineurin sequence variations in 1048 individuals with open angle glaucoma, American journal of Ophthalmology, 136 pp. 904-910. ISSN 1234-1234 (2003) [Refereed Article] 
Craig, JE and Clark, JB and McLeod, JL and Kirkland, MA and Grant, G and Elder, JE and Toohey, MG and Kowal, L and Chen, C and Wirth, MG and Mackey, DA, Hereditary Hyperferritinemia -Cataract Syndrome: Prevalence, lens morphology and spectrum of mutations and clinical presentations, Archives of Opthalmology, 121 pp. 1753-1761. ISSN 1234-1234 (2003) [Refereed Article] 
Burdon, KP and Wilkinson, RM and Barbour, JM and Dickinson, JL and Stankovich, J and Mackey, DA and Sale, MM, Investigation of albinism genes in congenital esotropia, Molecular Vision, 9 pp. 710-4. ISSN 1090-0535 (2003) [Refereed Article] 
Ruddle, JB and Mackey, DA and Downie, NA, Keratoconus developing following a Vth nerve palsy, Clinical & experimental ophthalmology, 31 pp. 363-5. ISSN 1234-1234 (2003) [Refereed Article] 
Mackey, DA and Fingert, JH and Luzhansky, JZ and McCluskey, PJ and Howell, N and Hall, AJ and Pierce, AB and Hoy, JF, Leber's Hereditary Optic Neuropathy (LHON) Triggered by Antiretroviral Therapy for Human Immunodeficiency Virus (HIV), Eye, 17 pp. 312-7. ISSN 1234-1234 (2003) [Refereed Article] 
Howell, N and Herrnstadt, C and Mackey, DA, Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mt-DNS background, American journal of medical genetics, 119 pp. 147-51. ISSN 1234-1234 (2003) [Refereed Article] 
Mackey, DA and Heon, E and Webster, AR, Management Controversy: Predictive DNA Testing in Ophthalmology, The British journal of ophthalmology, 87 pp. 633-638. ISSN 1234-1234 (2003) [Refereed Article] 
Ng, WT and Toohey, MG and Mulhall, L and Mackey, DA, Pigmentary retinopathy, macular oedema and abnormal ERG with mitotane treatment, British journal of ophthalmology, 87 pp. 500-1. ISSN 1234-1234 (2003) [Refereed Article] 
Mackey, DA and Craig, JE, Predictive DNA testing for glaucoma: Reality in 2003, Ophthalmology clinics of North America, 16 pp. 639-645. ISSN 1234-1234 (2003) [Refereed Article] 
Howell, N and Oostra, R and Bolhuis, PA and Spruijt, L and Clarke, LA and Mackey, DA and Preston, G and Herrnstadt, C, Sequence analysis of the mitochodrial genomes from Dutch LHON pedigrees, American journal of human genetics, 72 pp. 1460-1469. ISSN 1234-1234 (2003) [Refereed Article] 
Howell, N and Smejkal, CB and Mackey, DA and Chinnery, PF and Turnbull, DM and Herrnstadt, C, The Pedigree Rate of Sequence Divergence in the Human Mitochondrial Genome. There Is a Difference between Phylogenetic and Pedigree Rates, 72 pp. 659-70. ISSN 1234-1234 (2003) [Refereed Article] 
Wilkinson, C and van der Straaten, D and Craig, JE and Coote, M and McCartney, PJ and Stankovich, J and Stone, E and Mackey, DA, Tonography demonstrates reduced facility of outflow of aqueous humour in myocilin mutation carriers, Journal of Glaucoma, 12 pp. 237-242. ISSN 0000-0000 (2003) [Refereed Article] 
Mackey, DA and Healey, DL and Fingert, JH and Coote, MA and Wong, TL and Wilkinson, CH and McCartney, PJ and Rait, JL and de Graaf, AP and Stone, ME and Craig, JE, `Glaucoma phenotype in pedigrees with the Myocilin Thr377Met mutation, Archives of ophthalmology, 121 pp. 1172-1180. ISSN 1234-1234 (2003) [Refereed Article] 
Wirth, MG and Russell-Eggitt, IM and Craig, JE and Elder, JE and Mackey, DA, Aetiology of congenital and paediatric cataract in an Australian population, British journal of ophthalmology, 86 pp. 782-786. ISSN 1234-1234 (2002) [Refereed Article] 
Sale, MM and Craig, JE and Charlesworth, JC and Fitzgerald, LM and Hanson, I and Dickinson, JL and Matthews, S and van Heyningen, V and Fingert, J and Mackey, DA, Broad Phenotypic variability in a Single Pedigree With a Novel 1410delC Mutation in the PST Domain of the PAX6 Gene, Human Mutation, 20, (4) pp. 322. ISSN 1059-7794 (2002) [Refereed Article] 
Mackey, DA and Chan, W and Chan, C and Gillies, WE and Brooks, AMV and O'Day, J and Engle, EC, Congenital fibrosis of the vertically acting extraocular muscles maps to the FEOM3 locus, Human Genetics, 110 pp. 510-512. ISSN 1234-1234 (2002) [Refereed Article] 
Marchbank, NJ and Craig, JE and Leek, JP and Toohey, M and Churchill, AJ and Markham, AF and Mackey, DA and Toomes, C and Inglehearn, CF, Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease, Journal of medical genetics, 39 pp. e47. ISSN 1234-1234 (2002) [Refereed Article] 
Fullerton, J and Paprocki, P and Foote, S and Mackey, DA and Williamson, R and Forrest, S, Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia, Human Genetics, 110, (5) pp. 462-470. ISSN 0340-6717 (2002) [Refereed Article] 
Sale, MM and Fitzgerald, LM and Kagame, K and Erdmann, I and Craig, JE and Dickinson, JL and Copper, R, Investigation of the prevalence of the myocilin Q368STOP mutation in Ugandan glaucoma patients, Ophthalmic Genetics, 33, (1) pp. 67-69. ISSN 1381-6810 (2002) [Letter or Note in Journal] 
Howell, N and Miller, AR and Mackey, DA and Arnold, A and Herrnstadt, C and Williams, IM and Kubacka, I, Lightning Striking Twice: Leber Hereditary Optic Neuropathy Families with Two Pathogenic mtDNA Mutations, Journal of neuro-ophthalmology: the official journal of the North American Neuro-Ophthalmology Society, 22 pp. 262-9. ISSN 1234-1234 (2002) [Refereed Article] 
Grenness, MJ and Osborn, JE and Weller, WL, Mapping ear canal movement using area-based surface matching, Journal of the Acoustical Society of America, 111, (2) pp. 960-971. ISSN 0001-4966 (2002) [Refereed Article] 
Keen, TJ and Hims, MM and McKie, AB and Moore, AT and Doran, RM and Mackey, DA and Mansfield, DC and Mueller, RF and Bhattacharya, SS and Bird, AC and Markham, AF and Inglehearn, CF, Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa, European journal of human genetics, 10 pp. 245-9. ISSN 1234-1234 (2002) [Refereed Article] 
Wheatley, C and Dickinson, JL and Mackey, DA and Craig, JE and Sale, MM, Retinopathy of prematurity: recent advances in our understanding, British Journal of Ophthalmology, 86, (6) pp. 696-701. ISSN 0007-1161 (2002) [Refereed Article] 
Wheatley, C and Dickinson, JL and Mackey, DA and Craig, JE and Sale, MM, Retinopathy of prematurity: recent advances in our understanding, Archives of Disease in Childhood, 87, (2) pp. F78-F82. ISSN 0003-9888 (2002) [Refereed Article] 
Wheatley, CM and Dickinson, JL and Mackey, DA and Craig, JE and Sale, MM, Retinopathy of prematurity: recent advances in our understanding, Archives of disease in childhood. Fetal and neonatal edition, 87 pp. F78-82. ISSN 1234-1234 (2002) [Refereed Article] 
Vickers, JC and Craig, JE and Stankovich, J and McCormack, GH and West, AK and Dickinson, JL and McCartney, PJ and Coote, M and Healey, D and Mackey, DA, The apolipoprotein ¿4 gene is associated with elevated risk of normal tension glaucoma, Molecular Vision, 8, (October) pp. 389-393. ISSN 1090-0535 (2002) [Refereed Article] 
McLean, IM and Mueller, E and Buttery, RG and Mackey, DA, Visual field assessment and the Austroad driving standard, Clinical and experimental ophthalmology, 30 pp. 3-7. ISSN 1234-1234 (2002) [Refereed Article] 
Mitchell, P and Cumming, RG and Mackey, DA, Author's reply, Ophthalmology, 108 pp. 837. ISSN 1234-1234 (2001) [Letter or Note in Journal] 
Craig, JE and Baird, PN and Healey, DL and McNaught, AI and McCartney, PJ and Rait, JL and Dickinson, JL and Roe, L and Fingert, JH and Stone, EM and Mackey, DA, Evidence for Genetic Heterogeneity within Eight Glaucoma Families, with the GLC1A Gln368STOP Mutation Being an Important Phenotypic Modifier, Ophthalmology, 108, (9) pp. 1607-1620. ISSN 0161-6420 (2001) [Refereed Article] 
MacKinnon, JR and Challis, DR and Mackey, DA, Is it not in my records doctor?, Clinical & experimental ophthalmology, 29 pp. 440-1. ISSN 1234-1234 (2001) [Refereed Article] 
McKie, AB and McHale, JC and Keen, TJ and Tarttelin, EE and Goliath, R and van Lith-Verhoeven, JJ and Greenberg, J and Ramesar, RS and Hoyng, CB and Cremers, FP and Mackey, DA and Bhattacharya, SS and Bird, AC and Markham, AF and Inglehearn, CF, Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13), Human molecular genetics, 10 pp. 1555-1562. ISSN 1234-1234 (2001) [Refereed Article] 
Baird, PN and Dickinson, JL and Craig, JE and Mackey, DA, The Taa1 Restriction Enzyme Provides a Simple Means to Identify the Q368STOP Mutation of the Myocilin Gene in Primary Open Angle Glaucoma, American Journal of Ophthalmology, 131, (4) pp. 510-511. ISSN 0002-9394 (2001) [Refereed Article] 
Mitchell, AE and Elder, JE and Mackey, DA and Waters, KD and Ashley, DM, Visual improvement despite radiologically stable disease after treatment with carboplatin in children with progressive low-grade optic/thalamic gliomas, Journal of pediatric hematology/oncology: official journal of the American Society of Pediatric Hematology/Oncology, 23 pp. 572-7. ISSN 1234-1234 (2001) [Refereed Article] 
McNaught, A and Allen, J and Healey, D and McCartney, P and Coote, M and Wong, T and Craig, JE and Green, C and Rait, J and Mackey, DA, Accuracy and implications of a reported family history of glaucoma, Archives of Ophthalmology, 118 pp. 900-904. ISSN 0003-9950 (2000) [Refereed Article] 
Stone, EM and Lotery, AJ and Munier, FL and Heon, E and Piguet, B and Guymer, RH and Vandenburgh, K and Cousin, P and Nishimura, D and Swiderski, RE and Silvestri, G and Mackey, DA and Hageman, GS and Bird, AC and Sheffield, VC and Schorderet, DF, A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy, Nature Genetics, 22, (1) pp. 199-202. ISSN 1061-4036 (1999) [Refereed Article] 
Fingert, JH and Heon, E and Liebmann, JM and Yamamoto, T and Craig, JE and Rait, J and Kawase, K and Hoh, ST and Buys, YM and Dickinson, JL and Hockey, RR and Williams-Lyn, D and Trope, G and Kitazawa, Y and Ritch, R and Mackey, DA and Alward, WLM and Sheffield, VC and Stone, EM, Analysis of myocilin mutations in 1703 glaucoma patients from five different populations, Human Molecular Genetics, 8, (5) pp. 899-905. ISSN 0964-6906 (1999) [Refereed Article] 
Simm, RM and Fingert, JH and Craig, JE and McNaught, AI and Mackey, DA, Normal range of hearing associated with myocilin THr377Met, Ophthalmic Genetics, 20, (3) pp. 205-207. ISSN 1381-6810 (1999) [Letter or Note in Journal] 
Alward, WLM and Fingert, JH and Coote, MA and Johnson, T and Lerner, SF and Junqua, D and Durcan, FJ and McCartney, PJ and Mackey, DA and Stone, EM and Sheffield, VC, Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A), The New England Journal of Medicine, 338 pp. 1022-1027. (1998) [Refereed Article] 
Howell, N and Mackey, DA, Low-Penetrance Branches in Matrilineal Pedigrees with Leber Hereditary Optic Neuropathy, American Journal of Human Genetics, 63 pp. 1220-1224. (1998) [Letter or Note in Journal] 
Howell, N and Bogolin, C and Jamieson, R and Marenda, DR and Mackey, DA, mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?, American Journal of Human Genetics, 62 pp. 196-202. (1998) [Letter or Note in Journal] 
Mackey, DA and Oostra, RJ and Rosenberg, T and Nikoskelainen, E and Poulton, J and Barratt, T and Bolhuis, P and Norby, S and Savontaus, ML and Chan, C and Howell, N, Reply to Hofmann et al, American Journal of Human Genetics, 62 pp. 492-495. (1998) [Letter or Note in Journal] 
Vickers, JC and Hof, PR and Schumer, RA and Wang, RT and Podos, SM and Morrison, JH, Magnocellular and parvocellular visual pathways are both affected in a macaque monkey model of glaucoma, Australian and New Zealand Journal of Opthalmology, 25, (3) pp. 239-243. (1997) [Refereed Article] 
Vickers, JC, The cellular mechanism underlying neuronal degeneration in glaucoma: Parallels with Alzheimer's disease, Australian and New Zealand Journal of Opthalmology, 25, (2) pp. 105-109. (1997) [Refereed Article] 

Conference Publication

Mackey, DA and Craig, JE, Glaucoma Inheritance Study in Tasmania: An International Collaboration, American Academy of Ophthalmology Basic Sciences Course Section 13 Internaltional Ophthalmology, Part 5. Collaborative Research, 2002, San Francisco, pp. 265-269. (2002) [Refereed Conference] 
Mackey, DA and Green, C and Sale, MM and Craig, JE and Dickinson, JL and Healey, D and Stanwix, SP and Wong, T and McNaught, A and McCartney, PJ, Familial aggregation of glaucoma: Experience with the glaucoma inheritance study in Tasmania (GIST), The Association for Research in Vision and Ophthalmology, April 30-May 5, 2000, Fort Lauderdale, Florida, pp. S527. (2000) [Conference Extract] 
Wirth, G and Sale, MM and Mackey, DA and Russell-Eggitt, I and Craig, JE and Charlesworth, JC and Elder, J, Inheritance of paediatric and congenital cataracts, The Association for Research in Vision and Ophthalmology, April 30-May 5,2000, Fort Lauderdale, Florida, pp. S2. (2000) [Conference Extract] 
Sale, MM and Craig, JE and Dickinson, JL and Love, J and Hanson, I and Matthews, S and Mackey, DA, Phenotypic variability in a large aniridia pedigree with a novel PAX6 1410delC, The Association for Research in Vision and Ophthalmology, April 30-May 5, 2000, Fort Lauderdale, Florida, pp. S822. (2000) [Conference Extract] 

Other Public Output

Mackey, DA, Glaucoma Inheritance Study, The Mercury, Tasmania, 15 January (1999) [Newspaper Article] 
Mackey, DA, Glaucoma Inheritance Study in Tasmania, 7ZR Radio, Hobart, 14 January (1999) [Media Interview] 
Mackey, DA, Grant for Glaucoma Research, 7ZR Radio, Tasmania, 11 August (1999) [Media Interview] 
Mackey, DA, Researchers have glaucoma treatment in sight, The Mercury, Tasmania, 12 August (1999) [Newspaper Article] 
Mackey, DA, Glaucoma testing, The Advocate, Tasmania, 15 Sept (1998) [Newspaper Article] 
Mackey, DA, Study based in Tasmania, The Examiner, Tasmania, 5 July (1998) [Newspaper Article] 
Mackey, DA, Glaucoma, Glaucoma, Mercury, Tasmania, 1 Feb (1997) [Newspaper Article] 
Mackey, DA, Glaucoma, Glaucoma, Mercury, Tasmania, 31 May (1997) [Newspaper Article] 
Mackey, DA, Glaucoma gene, Southern Cross TV News, Tasmania, 30/5/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene, ABC TV News, Tasmania, 30/5/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, 7ZR News, Tasmania, 31/1/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, 5AN Perth, Perth, 31/1/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, 4QR Brisbane News, Brisbane, 31/1/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, ABC TV News: Adelaide & Perth, Adelaide & Perth, 1/2/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, 5AN Adelaide News, Adelaide, 1/2/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, ABC TV News, Tasmania, 1/2/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, WIN TV News, Tasmania, 1/2/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, 7ZR News, Tasmania, 1/2/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma gene discovery, 7ZR Mornign Program, Tasmania, 25/2/97 (1997) [Media Interview] 
Mackey, DA, Glaucoma research, WIN TV News, Tasmania, 1/3/97 (1997) [Media Interview] 
This list was generated on Sat Nov 21 13:38:52 2009.
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