eCite Digital Repository

Author: Craig, JE (Mr Jamie Craig)

Number of items: 32

Journal Article
Mackey, DA and Green, CM and Craig, JE and Hewitt, A, The pathogenesis of the glaucoma: nature versus nurture, Clinical and Experimental Ophthalmology pp. 297. ISSN 1442-6404 (2008) [Letter or Note in Journal] 
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] 
Bennett, SL and Hewitt, A 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 pedigrees, Archives of Ophthalmology, 125, (1) pp. 112-116. ISSN 0003-9950 (2007) [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, (1) pp. 23-30. ISSN 0030-3755 (2006) [Refereed Article] 
McKay, JD and Patterson, B and Craig, JE and Russell-Eggitt, E and Wirth, MG and Burdon, KP and Hewitt, A 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, MG and Mackey, DA and Russell-Eggitt, IM and Craig, JE and Elder, JE 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, (8) pp. e106-109. ISSN 0022-2593 (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, (5) 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, 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] 
Baird, PN and Craig, JE and Richardson, AJ and Ring, MA and Sim, P and Stanwix, SP and Foote, SJ and Mackey, DA, Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilin, Human genetics, 112, (2) pp. 110-116. ISSN 0340-6717 (2003) [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 patients with open-angle glaucoma, American Journal of Ophthalmology, 136, (5) pp. 904-910. ISSN 0002-9394 (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, (8) pp. 1172-1180. ISSN 0003-9950 (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, (12) pp. 1753-1761. ISSN 0003-9950 (2003) [Refereed Article] 
Burdon, KP and McKay, JD and Sale, MM and Russell-Eggitt, IM and Mackey, DA and Wirth, MG and Elder, JE and Nicoll, A and Clarke, MP and Fitzgerald, LM and Stankovich, J and Shaw, MA and Sarma, S and Gajovic, S and Gruss, P and Ross, S and Thomas, P and Voss, AK and Thomas, T and Gecz, J and Craig, JE, Mutations in a Novel Gene, NHS, Cause the Pleiotropic Effects of Nance-Horan Syndrome, Including Severe Congenital Cataract, Dental Anomalies, and Mental Retardation, American Journal of Human Genetics, 73, (5) pp. 1120-1130. ISSN 0002-9297 (2003) [Refereed Article] 
Mackey, DA and Craig, JE, Predictive DNA testing for glaucoma: Reality in 2003, Ophthalmology clinics of North America, 16, (4) pp. 639-645. ISSN 0896-1549 (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, (3) pp. 237-242. ISSN 1057-0829 (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, (7) pp. 782-786. ISSN 0007-1161 (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 1098-1004 (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, (8) pp. e47. ISSN 1468-6244 (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] 
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] 
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 epsilon 4 gene is associated with elevated risk of normal tension glaucoma, Molecular Vision, 8, (40) pp. 389-393. ISSN 1090-0535 (2002) [Refereed Article] 
Nishimura, D and Searby, C and Alward, W and Walton, D and Craig, JE and Mackey, DA and Kawase, K and Kanis, A and Patil, S and Stone, E and Sheffield, V, A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye, Americal Journal of Human Genetics, 68, (2) pp. 364-372. ISSN 0002-9297 (2001) [Refereed Article] 
Fingert, JH and Clark, AF and Craig, JE and Alward, WLM and Snibson, GR and McLaughlin, M and Tuttle, L and Mackey, DA and Sheffield, VC and Stone, EM, Evaluation of the Myocilin (MYOC) Glaucoma Gene in Monkey and Human Steroid-Induced Ocular Hypertension, Investigative Ophthalmology & Visual Science, 42, (1) pp. 145-152. ISSN 0146-0404 (2001) [Refereed Article] 
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] 
Dickinson, JL and Sale, MM and Craig, JE and Mackey, DA, Laboratory methods in ophthalmic genetics: obtaining DNA from patients, Ophthalmic Genetics, 22, (1) pp. 49-60. ISSN 1381-6810 (2001) [Professional, Non 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 - Experience from the glaucoma inheritance study in Tasmania, Archives of Ophthalmology, 118, (7) pp. 900-904. ISSN 0003-9950 (2000) [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 Paper] 
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] 

This list was generated on Sat Nov 25 03:46:46 2017.