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DAVID C MACKEY

TitleProfessor
InstitutionMD Anderson
DepartmentAnesthesiology & PeriOperative Medicine
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Hysi PG, Valdes AM, Liu F, Furlotte NA, Evans DM, Bataille V, Visconti A, Hemani G, McMahon G, Ring SM, Smith GD, Duffy DL, Zhu G, Gordon SD, Medland SE, Lin BD, Willemsen G, Jan Hottenga J, Vuckovic D, Girotto G, Gandin I, Sala C, Concas MP, Brumat M, Gasparini P, Toniolo D, Cocca M, Robino A, Yazar S, Hewitt AW, Chen Y, Zeng C, Uitterlinden AG, Ikram MA, Hamer MA, van Duijn CM, Nijsten T, Mackey DA, Falchi M, Boomsma DI, Martin NG, Hinds DA, Kayser M, Spector TD. Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nat Genet. 2019 May 31. PMID: 31150021.
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    2. Spracklen CN, Karaderi T, Yaghootkar H, Schurmann C, Fine RS, Kutalik Z, Preuss MH, Lu Y, Wittemans LBL, Adair LS, Allison M, Amin N, Auer PL, Bartz TM, Blüher M, Boehnke M, Borja JB, Bork-Jensen J, Broer L, Chasman DI, Chen YI, Chirstofidou P, Demirkan A, van Duijn CM, Feitosa MF, Garcia ME, Graff M, Grallert H, Grarup N, Guo X, Haesser J, Hansen T, Harris TB, Highland HM, Hong J, Ikram MA, Ingelsson E, Jackson R, Jousilahti P, Kähönen M, Kizer JR, Kovacs P, Kriebel J, Laakso M, Lange LA, Lehtimäki T, Li J, Li-Gao R, Lind L, Luan J, Lyytikäinen LP, MacGregor S, Mackey DA, Mahajan A, Mangino M, Männistö S, McCarthy MI, McKnight B, Medina-Gomez C, Meigs JB, Molnos S, Mook-Kanamori D, Morris AP, de Mutsert R, Nalls MA, Nedeljkovic I, North KE, Pennell CE, Pradhan AD, Province MA, Raitakari OT, Raulerson CK, Reiner AP, Ridker PM, Ripatti S, Roberston N, Rotter JI, Salomaa V, Sandoval-Zárate AA, Sitlani CM, Spector TD, Strauch K, Stumvoll M, Taylor KD, Thuesen B, Tönjes A, Uitterlinden AG, Venturini C, Walker M, Wang CA, Wang S, Wareham NJ, Willems SM, Willems van Dijk K, Wilson JG, Wu Y, Yao J, Young KL, Langenberg C, Frayling TM, Kilpeläinen TO, Lindgren CM, Loos RJF, Mohlke KL. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. Am J Hum Genet. 2019 May 27. PMID: 31178129.
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    3. Laville V, Kang JH, Cousins CC, Iglesias AI, Nagy R, Cooke Bailey JN, Igo RP, Song YE, Chasman DI, Christen WG, Kraft P, Rosner BA, Hu F, Wilson JF, Gharahkhani P, Hewitt AW, Mackey DA, Hysi PG, Hammond CJ, vanDuijn CM, Haines JL, Vitart V, Fingert JH, Hauser MA, Aschard H, Wiggs JL, Khawaja AP, MacGregor S, Pasquale LR. Genetic correlations between diabetes and glaucoma: an analysis of continuous and dichotomous phenotypes. Am J Ophthalmol. 2019 May 20. PMID: 31121135.
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    4. Lee SSY, McArdle N, Sanfilippo PG, Yazar S, Eastwood PR, Hewitt AW, Li Q, Mackey DA. Associations between Optic Disc Measures and Obstructive Sleep Apnea in Young Adults. Ophthalmology. 2019 May 17. PMID: 31196726.
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    5. Toh SH, Coenen P, Howie EK, Mukherjee S, Mackey DA, Straker LM. Mobile touch screen device use and associations with musculoskeletal symptoms and visual health in a nationally representative sample of Singaporean adolescents. Ergonomics. 2019 Jun; 62(6):778-793. PMID: 30575442.
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    6. Hoskin AK, Mackey DA, Keay L, Agrawal R, Watson S. Eye Injuries across history and the evolution of eye protection. Acta Ophthalmol. 2019 Mar 25. PMID: 30907494.
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    7. Mountford JK, Davies WIL, Griffiths LR, Yazar S, Mackey DA, Hunt DM. Differential stability of variant OPN1LW gene transcripts in myopic patients. Mol Vis. 2019; 25:183-193. PMID: 30996587.
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    8. Gentzel I, Giese L, Zhao W, Alonso AP, Mackey D. A Simple Method for Measuring Apoplast Hydration and Collecting Apoplast Contents. Plant Physiol. 2019 04; 179(4):1265-1272. PMID: 30824565.
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    9. Tedja MS, Haarman AEG, Meester-Smoor MA, Kaprio J, Mackey DA, Guggenheim JA, Hammond CJ, Verhoeven VJM, Klaver CCW. IMI - Myopia Genetics Report. Invest Ophthalmol Vis Sci. 2019 Feb 28; 60(3):M89-M105. PMID: 30817828.
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    10. Richards MD, Barnes K, Yardley AE, Hanman K, Lam GC, Mackey DA. Traumatic hyphaema in children: a retrospective and prospective study of outcomes at an Australian paediatric centre. BMJ Open Ophthalmol. 2019; 4(1):e000215. PMID: 31179388.
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    11. Lingham G, Yazar S, Lucas RM, Walsh JP, Zhu K, Hunter M, Lim EM, Cooke BR, Mackey DA. Low 25-Hydroxyvitamin D Concentration Is Not Associated With Refractive Error in Middle-Aged and Older Western Australian Adults. Transl Vis Sci Technol. 2019 Jan; 8(1):13. PMID: 30697464.
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    12. Siggs OM, Souzeau E, Pasutto F, Dubowsky A, Smith JEH, Taranath D, Pater J, Rait JL, Narita A, Mauri L, Del Longo A, Reis A, Chappell A, Kearns LS, Staffieri SE, Elder JE, Ruddle JB, Hewitt AW, Burdon KP, Mackey DA, Craig JE. Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma. JAMA Ophthalmol. 2019 Jan 17. PMID: 30653210.
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    13. Duffy DL, Zhu G, Li X, Sanna M, Iles MM, Jacobs LC, Evans DM, Yazar S, Beesley J, Law MH, Kraft P, Visconti A, Taylor JC, Liu F, Wright MJ, Henders AK, Bowdler L, Glass D, Ikram MA, Uitterlinden AG, Madden PA, Heath AC, Nelson EC, Green AC, Chanock S, Barrett JH, Brown MA, Hayward NK, MacGregor S, Sturm RA, Hewitt AW, Kayser M, Hunter DJ, Newton Bishop JA, Spector TD, Montgomery GW, Mackey DA, Smith GD, Nijsten TE, Bishop DT, Bataille V, Falchi M, Han J, Martin NG. Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nat Commun. 2019 01 14; 10(1):299. PMID: 30643134.
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    14. Iglesias AI, Mishra A, Vitart V, Bykhovskaya Y, Höhn R, Springelkamp H, Cuellar-Partida G, Gharahkhani P, Bailey JNC, Willoughby CE, Li X, Yazar S, Nag A, Khawaja AP, Polašek O, Siscovick D, Mitchell P, Tham YC, Haines JL, Kearns LS, Hayward C, Shi Y, van Leeuwen EM, Taylor KD, Bonnemaijer P, Rotter JI, Martin NG, Zeller T, Mills RA, Souzeau E, Staffieri SE, Jonas JB, Schmidtmann I, Boutin T, Kang JH, Lucas SEM, Wong TY, Beutel ME, Wilson JF, Uitterlinden AG, Vithana EN, Foster PJ, Hysi PG, Hewitt AW, Khor CC, Pasquale LR, Montgomery GW, Klaver CCW, Aung T, Pfeiffer N, Mackey DA, Hammond CJ, Cheng CY, Craig JE, Rabinowitz YS, Wiggs JL, Burdon KP, van Duijn CM, MacGregor S. Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nat Commun. 2019 01 08; 10(1):155. PMID: 30622277.
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    15. Han X, Souzeau E, Ong JS, An J, Siggs OM, Burdon KP, Best S, Goldberg I, Healey PR, Graham SL, Ruddle JB, Mills RA, Landers J, Galanopoulos A, White AJR, Casson R, Mackey DA, Hewitt AW, Gharahkhani P, Craig JE, MacGregor S. Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based Studies. JAMA Ophthalmol. 2019 Jan 01; 137(1):28-35. PMID: 30267046.
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    16. Lee SSY, Yazar S, Pasquale LR, Sanfilippo PG, Hewitt AW, Hickey M, Skinner R, Mackey DA. The Relationship Between Optic Disc Parameters and Female Reproductive Factors in Young Women. Asia Pac J Ophthalmol (Phila). 2019 May-Jun; 8(3):224-228. PMID: 30596227.
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    17. McAllister IL, Smithies LA, Chen FK, Mackey DA, Sanfilippo PG. Two-Year Efficacy of Ranibizumab Plus Laser-Induced Chorioretinal Anastomosis vs Ranibizumab Monotherapy for Central Retinal Vein Occlusion: A Randomized Clinical Trial. JAMA Ophthalmol. 2018 Dec 01; 136(12):1391-1397. PMID: 30347030.
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    18. Mackey DA, Craig JE, Hewitt AW. Seeing the impact of the Glaucoma Inheritance Study in Tasmania after 25?years. Clin Exp Ophthalmol. 2018 Nov 22. PMID: 30467939.
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    19. Lingham G, Burton A, Brown HA, Huynh E, Yazar S, Coroneo MT, Mackey DA. Repurposing blue laser autofluorescence to measure ocular sun exposure. Clin Exp Ophthalmol. 2019 May; 47(4):445-452. PMID: 30345715.
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    20. Duffy DL, Zhu G, Li X, Sanna M, Iles MM, Jacobs LC, Evans DM, Yazar S, Beesley J, Law MH, Kraft P, Visconti A, Taylor JC, Liu F, Wright MJ, Henders AK, Bowdler L, Glass D, Ikram MA, Uitterlinden AG, Madden PA, Heath AC, Nelson EC, Green AC, Chanock S, Barrett JH, Brown MA, Hayward NK, MacGregor S, Sturm RA, Hewitt AW, Kayser M, Hunter DJ, Newton Bishop JA, Spector TD, Montgomery GW, Mackey DA, Smith GD, Nijsten TE, Bishop DT, Bataille V, Falchi M, Han J, Martin NG. Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nat Commun. 2018 11 14; 9(1):4774. PMID: 30429480.
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    21. Toruño TY, Shen M, Coaker G, Mackey D. Regulated Disorder: Posttranslational Modifications Control the RIN4 Plant Immune Signaling Hub. Mol Plant Microbe Interact. 2019 01; 32(1):56-64. PMID: 30418084.
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    22. Hogarty DT, Mackey DA, Hewitt AW. Current state and future prospects of artificial intelligence in ophthalmology: a review. Clin Exp Ophthalmol. 2019 Jan; 47(1):128-139. PMID: 30155978.
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    23. Sanfilippo P, Hewitt AW, Mackey DA. Plurality in multi-disciplinary research: multiple institutional affiliations are associated with increased citations. PeerJ. 2018; 6:e5664. PMID: 30280036.
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    24. Singh LN, Crowston JG, Lopez Sanchez MIG, Van Bergen NJ, Kearns LS, Hewitt AW, Yazar S, Mackey DA, Wallace DC, Trounce IA. Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma. Invest Ophthalmol Vis Sci. 2018 09 04; 59(11):4598-4602. PMID: 30242360.
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    25. Daniszewski M, Nguyen Q, Chy HS, Singh V, Crombie DE, Kulkarni T, Liang HH, Sivakumaran P, Lidgerwood GE, Hernández D, Conquest A, Rooney LA, Chevalier S, Andersen SB, Senabouth A, Vickers JC, Mackey DA, Craig JE, Laslett AL, Hewitt AW, Powell JE, Pébay A. Single-Cell Profiling Identifies Key Pathways Expressed by iPSCs Cultured in Different Commercial Media. iScience. 2018 Sep 28; 7:30-39. PMID: 30267684.
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    26. Shaaban S, MacKinnon S, Andrews C, Staffieri SE, Maconachie GDE, Chan WM, Whitman MC, Morton SU, Yazar S, MacGregor S, Elder JE, Traboulsi EI, Gottlob I, Hewitt AW, Hunter DG, Mackey DA, Engle EC. Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. Invest Ophthalmol Vis Sci. 2018 08 01; 59(10):4054-4064. PMID: 30098192.
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    27. MacGregor S, Ong JS, An J, Han X, Zhou T, Siggs OM, Law MH, Souzeau E, Sharma S, Lynn DJ, Beesley J, Sheldrick B, Mills RA, Landers J, Ruddle JB, Graham SL, Healey PR, White AJR, Casson RJ, Best S, Grigg JR, Goldberg I, Powell JE, Whiteman DC, Radford-Smith GL, Martin NG, Montgomery GW, Burdon KP, Mackey DA, Gharahkhani P, Craig JE, Hewitt AW. Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. Nat Genet. 2018 08; 50(8):1067-1071. PMID: 30054594.
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    28. De Smit E, Lukowski SW, Anderson L, Senabouth A, Dauyey K, Song S, Wyse B, Wheeler L, Chen CY, Cao K, Wong Ten Yuen A, Shuey N, Clarke L, Lopez Sanchez I, Hung SSC, Pébay A, Mackey DA, Brown MA, Hewitt AW, Powell JE. Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis. BMC Med Genomics. 2018 Jul 23; 11(1):61. PMID: 30037347.
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    29. Tang SM, Lau T, Rong SS, Yazar S, Chen LJ, Mackey DA, Lucas RM, Pang CP, Yam JC. Vitamin D and its pathway genes in myopia: systematic review and meta-analysis. Br J Ophthalmol. 2019 Jan; 103(1):8-17. PMID: 30018147.
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    30. Morgan VA, Clark M, Crewe J, Valuri G, Mackey DA, Badcock JC, Jablensky A. Congenital blindness is protective for schizophrenia and other psychotic illness. A whole-population study. Schizophr Res. 2018 Dec; 202:414-416. PMID: 30539775.
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    31. Warrington NM, Shevroja E, Hemani G, Hysi PG, Jiang Y, Auton A, Boer CG, Mangino M, Wang CA, Kemp JP, McMahon G, Medina-Gomez C, Hickey M, Trajanoska K, Wolke D, Ikram MA, Montgomery GW, Felix JF, Wright MJ, Mackey DA, Jaddoe VW, Martin NG, Tung JY, Davey Smith G, Pennell CE, Spector TD, van Meurs J, Rivadeneira F, Medland SE, Evans DM. Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Hum Mol Genet. 2018 06 01; 27(11):2025-2038. PMID: 29659830.
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    32. Tedja MS, Wojciechowski R, Hysi PG, Eriksson N, Furlotte NA, Verhoeven VJM, Iglesias AI, Meester-Smoor MA, Tompson SW, Fan Q, Khawaja AP, Cheng CY, Höhn R, Yamashiro K, Wenocur A, Grazal C, Haller T, Metspalu A, Wedenoja J, Jonas JB, Wang YX, Xie J, Mitchell P, Foster PJ, Klein BEK, Klein R, Paterson AD, Hosseini SM, Shah RL, Williams C, Teo YY, Tham YC, Gupta P, Zhao W, Shi Y, Saw WY, Tai ES, Sim XL, Huffman JE, Polašek O, Hayward C, Bencic G, Rudan I, Wilson JF, Joshi PK, Tsujikawa A, Matsuda F, Whisenhunt KN, Zeller T, van der Spek PJ, Haak R, Meijers-Heijboer H, van Leeuwen EM, Iyengar SK, Lass JH, Hofman A, Rivadeneira F, Uitterlinden AG, Vingerling JR, Lehtimäki T, Raitakari OT, Biino G, Concas MP, Schwantes-An TH, Igo RP, Cuellar-Partida G, Martin NG, Craig JE, Gharahkhani P, Williams KM, Nag A, Rahi JS, Cumberland PM, Delcourt C, Bellenguez C, Ried JS, Bergen AA, Meitinger T, Gieger C, Wong TY, Hewitt AW, Mackey DA, Simpson CL, Pfeiffer N, Pärssinen O, Baird PN, Vitart V, Amin N, van Duijn CM, Bailey-Wilson JE, Young TL, Saw SM, Stambolian D, MacGregor S, Guggenheim JA, Tung JY, Hammond CJ, Klaver CCW. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nat Genet. 2018 06; 50(6):834-848. PMID: 29808027.
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    33. Iglesias AI, Mishra A, Vitart V, Bykhovskaya Y, Höhn R, Springelkamp H, Cuellar-Partida G, Gharahkhani P, Bailey JNC, Willoughby CE, Li X, Yazar S, Nag A, Khawaja AP, Polašek O, Siscovick D, Mitchell P, Tham YC, Haines JL, Kearns LS, Hayward C, Shi Y, van Leeuwen EM, Taylor KD, Bonnemaijer P, Rotter JI, Martin NG, Zeller T, Mills RA, Souzeau E, Staffieri SE, Jonas JB, Schmidtmann I, Boutin T, Kang JH, Lucas SEM, Wong TY, Beutel ME, Wilson JF, Uitterlinden AG, Vithana EN, Foster PJ, Hysi PG, Hewitt AW, Khor CC, Pasquale LR, Montgomery GW, Klaver CCW, Aung T, Pfeiffer N, Mackey DA, Hammond CJ, Cheng CY, Craig JE, Rabinowitz YS, Wiggs JL, Burdon KP, van Duijn CM, MacGregor S. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nat Commun. 2018 05 14; 9(1):1864. PMID: 29760442.
      View in: PubMed
    34. Hysi PG, Valdes AM, Liu F, Furlotte NA, Evans DM, Bataille V, Visconti A, Hemani G, McMahon G, Ring SM, Smith GD, Duffy DL, Zhu G, Gordon SD, Medland SE, Lin BD, Willemsen G, Jan Hottenga J, Vuckovic D, Girotto G, Gandin I, Sala C, Concas MP, Brumat M, Gasparini P, Toniolo D, Cocca M, Robino A, Yazar S, Hewitt AW, Chen Y, Zeng C, Uitterlinden AG, Ikram MA, Hamer MA, van Duijn CM, Nijsten T, Mackey DA, Falchi M, Boomsma DI, Martin NG, Hinds DA, Kayser M, Spector TD. Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nat Genet. 2018 05; 50(5):652-656. PMID: 29662168.
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    35. Shiga Y, Akiyama M, Nishiguchi KM, Sato K, Shimozawa N, Takahashi A, Momozawa Y, Hirata M, Matsuda K, Yamaji T, Iwasaki M, Tsugane S, Oze I, Mikami H, Naito M, Wakai K, Yoshikawa M, Miyake M, Yamashiro K, Kashiwagi K, Iwata T, Mabuchi F, Takamoto M, Ozaki M, Kawase K, Aihara M, Araie M, Yamamoto T, Kiuchi Y, Nakamura M, Ikeda Y, Sonoda KH, Ishibashi T, Nitta K, Iwase A, Shirato S, Oka Y, Satoh M, Sasaki M, Fuse N, Suzuki Y, Cheng CY, Khor CC, Baskaran M, Perera S, Aung T, Vithana EN, Cooke Bailey JN, Kang JH, Pasquale LR, Haines JL, Wiggs JL, Burdon KP, Gharahkhani P, Hewitt AW, Mackey DA, MacGregor S, Craig JE, Allingham RR, Hauser M, Ashaye A, Budenz DL, Akafo S, Williams SEI, Kamatani Y, Nakazawa T, Kubo M. Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma. Hum Mol Genet. 2018 04 15; 27(8):1486-1496. PMID: 29452408.
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    36. Deb D, Mackey D, Opiyo SO, McDowell JM. Application of alignment-free bioinformatics methods to identify an oomycete protein with structural and functional similarity to the bacterial AvrE effector protein. PLoS One. 2018; 13(4):e0195559. PMID: 29641586.
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    37. Crewe JM, Brown H, Fyfe D, Mackey DA. Does including colour-blind men enhance search and rescue teams? Clin Exp Ophthalmol. 2018 09; 46(7):817-818. PMID: 29412483.
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    38. Gharahkhani P, Burdon KP, Cooke Bailey JN, Hewitt AW, Law MH, Pasquale LR, Kang JH, Haines JL, Souzeau E, Zhou T, Siggs OM, Landers J, Awadalla M, Sharma S, Mills RA, Ridge B, Lynn D, Casson R, Graham SL, Goldberg I, White A, Healey PR, Grigg J, Lawlor M, Mitchell P, Ruddle J, Coote M, Walland M, Best S, Vincent A, Gale J, RadfordSmith G, Whiteman DC, Montgomery GW, Martin NG, Mackey DA, Wiggs JL, MacGregor S, Craig JE. Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Sci Rep. 2018 Feb 15; 8(1):3124. PMID: 29449654.
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    39. Staffieri SE, Kearns LS, Sanfilippo PG, Craig JE, Mackey DA, Hewitt AW. Crowd-sourced Ontology for Photoleukocoria: Identifying Common Internet Search Terms for a Potentially Important Pediatric Ophthalmic Sign. Transl Vis Sci Technol. 2018 Feb; 7(1):18. PMID: 29464132.
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    40. Shah RL, Li Q, Zhao W, Tedja MS, Tideman JWL, Khawaja AP, Fan Q, Yazar S, Williams KM, Verhoeven VJM, Xie J, Wang YX, Hess M, Nickels S, Lackner KJ, Pärssinen O, Wedenoja J, Biino G, Concas MP, Uitterlinden A, Rivadeneira F, Jaddoe VWV, Hysi PG, Sim X, Tan N, Tham YC, Sensaki S, Hofman A, Vingerling JR, Jonas JB, Mitchell P, Hammond CJ, Höhn R, Baird PN, Wong TY, Cheng CY, Teo YY, Mackey DA, Williams C, Saw SM, Klaver CCW, Guggenheim JA, Bailey-Wilson JE. A genome-wide association study of corneal astigmatism: The CREAM Consortium. Mol Vis. 2018; 24:127-142. PMID: 29422769.
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    41. Bailey JNC, Gharahkhani P, Kang JH, Butkiewicz M, Sullivan DA, Weinreb RN, Aschard H, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, Budenz DL, Realini T, Gaasterland T, Scott WK, Singh K, Sit AJ, Igo RP, Song YE, Hark L, Ritch R, Rhee DJ, Vollrath D, Zack DJ, Medeiros F, Vajaranant TS, Chasman DI, Christen WG, Pericak-Vance MA, Liu Y, Kraft P, Richards JE, Rosner BA, Hauser MA, Craig JE, Burdon KP, Hewitt AW, Mackey DA, Haines JL, MacGregor S, Wiggs JL, Pasquale LR. Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets. Invest Ophthalmol Vis Sci. 2018 02 01; 59(2):629-636. PMID: 29392307.
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    42. Lingham G, Milne E, Cross D, English DR, Johnston RS, Lucas RM, Yazar S, Mackey DA. Investigating the long-term impact of a childhood sun-exposure intervention, with a focus on eye health: protocol for the Kidskin-Young Adult Myopia Study. BMJ Open. 2018 01 31; 8(1):e020868. PMID: 29391375.
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    43. Chen FK, Menghini M, Hansen A, Mackey DA, Constable IJ, Sampson DM. Intrasession Repeatability and Interocular Symmetry of Foveal Avascular Zone and Retinal Vessel Density in OCT Angiography. Transl Vis Sci Technol. 2018 Jan; 7(1):6. PMID: 29367891.
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    44. Lupton MK, Medland SE, Gordon SD, Goncalves T, MacGregor S, Mackey DA, Young TL, Duffy DL, Visscher PM, Wray NR, Nyholt DR, Bain L, Ferreira MA, Henders AK, Wallace L, Montgomery GW, Wright MJ, Martin NG. Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels. J Alzheimers Dis. 2018; 64(1):49-54. PMID: 29865051.
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    45. Wang M, Rui L, Yan H, Shi H, Zhao W, Lin JE, Zhang K, Blakeslee JJ, Mackey D, Tang D, Wei Z, Wang GL. The major leaf ferredoxin Fd2 regulates plant innate immunity in Arabidopsis. Mol Plant Pathol. 2018 06; 19(6):1377-1390. PMID: 28976113.
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    46. Wong EN, De Soyza JDA, Mackey DA, Constable IJ, Chen FK. Intersession Test-Retest Variability of Microperimetry in Type 2 Macular Telangiectasia. Transl Vis Sci Technol. 2017 Dec; 6(6):7. PMID: 29242756.
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    47. Cuellar-Partida G, Williams KM, Yazar S, Guggenheim JA, Hewitt AW, Williams C, Wang JJ, Kho PF, Saw SM, Cheng CY, Wong TY, Aung T, Young TL, Tideman JWL, Jonas JB, Mitchell P, Wojciechowski R, Stambolian D, Hysi P, Hammond CJ, Mackey DA, Lucas RM, MacGregor S. Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study. Int J Epidemiol. 2017 12 01; 46(6):1882-1890. PMID: 28586461.
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    48. Fang Kho P, Lea RA, Benton MC, Eccles D, Haupt LM, Hewitt AW, Sherwin JC, Mackey DA, Griffiths LR. Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size. J Hum Genet. 2018 Jan; 63(1):83-87. PMID: 29215094.
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    49. Thomson BR, Souma T, Tompson SW, Onay T, Kizhatil K, Siggs OM, Feng L, Whisenhunt KN, Yanovitch TL, Kalaydjieva L, Azmanov DN, Finzi S, Tanna CE, Hewitt AW, Mackey DA, Bradfield YS, Souzeau E, Javadiyan S, Wiggs JL, Pasutto F, Liu X, John SW, Craig JE, Jin J, Young TL, Quaggin SE. Angiopoietin-1 is required for Schlemm's canal development in mice and humans. J Clin Invest. 2017 12 01; 127(12):4421-4436. PMID: 29106382.
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    50. Souzeau E, Siggs OM, Zhou T, Galanopoulos A, Hodson T, Taranath D, Mills RA, Landers J, Pater J, Smith JE, Elder JE, Rait JL, Giles P, Phakey V, Staffieri SE, Kearns LS, Dubowsky A, Mackey DA, Hewitt AW, Ruddle JB, Burdon KP, Craig JE. Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants. Eur J Hum Genet. 2017 11; 25(11):1290. PMID: 29023440.
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    51. Javadiyan S, Craig JE, Souzeau E, Sharma S, Lower KM, Mackey DA, Staffieri SE, Elder JE, Taranath D, Straga T, Black J, Pater J, Casey T, Hewitt AW, Burdon KP. High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia. G3 (Bethesda). 2017 10 05; 7(10):3257-3268. PMID: 28839118.
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    52. Matovinovic E, Kho PF, Lea RA, Benton MC, Eccles DA, Haupt LM, Hewitt AW, Sherwin JC, Mackey DA, Griffiths LR. Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate. Mol Vis. 2017; 23:660-665. PMID: 28966548.
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    137. Andersson MX, Nilsson AK, Johansson ON, Boztas G, Adolfsson LE, Pinosa F, Petit CG, Aronsson H, Mackey D, Tör M, Hamberg M, Ellerström M. Involvement of the electrophilic isothiocyanate sulforaphane in Arabidopsis local defense responses. Plant Physiol. 2015 Jan; 167(1):251-61. PMID: 25371552.
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    138. Meier MH, Gillespie NA, Hansell NK, Hewitt AW, Hickie IB, Lu Y, MacGregor S, Medland SE, Sun C, Wong TY, Wright MJ, Zhu G, Martin NG, Mackey DA. Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults. Psychosom Med. 2014 Nov-Dec; 76(9):732-8. PMID: 25373892.
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    139. Yardley AM, Mackey DA, Tandon A. Running with scissors. J Pediatr. 2015 Jan; 166(1):205. PMID: 25304923.
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    140. Awadalla MS, Fingert JH, Roos BE, Chen S, Holmes R, Graham SL, Chehade M, Galanopolous A, Ridge B, Souzeau E, Zhou T, Siggs OM, Hewitt AW, Mackey DA, Burdon KP, Craig JE. Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma. Am J Ophthalmol. 2015 Jan; 159(1):124-30.e1. PMID: 25284765.
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    141. Sanfilippo PG, Wilkinson CH, Ruddle JB, Zhu G, Martin NG, Hewitt AW, Mackey DA. Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins. Clin Exp Optom. 2015 Mar; 98(2):172-6. PMID: 25251541.
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    142. Yazar S, Gooden GE, Mackey DA, Hewitt AW. Benchmarking undedicated cloud computing providers for analysis of genomic datasets. PLoS One. 2014; 9(9):e108490. PMID: 25247298.
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    143. Springelkamp H, Höhn R, Mishra A, Hysi PG, Khor CC, Loomis SJ, Bailey JN, Gibson J, Thorleifsson G, Janssen SF, Luo X, Ramdas WD, Vithana E, Nongpiur ME, Montgomery GW, Xu L, Mountain JE, Gharahkhani P, Lu Y, Amin N, Karssen LC, Sim KS, van Leeuwen EM, Iglesias AI, Verhoeven VJ, Hauser MA, Loon SC, Despriet DD, Nag A, Venturini C, Sanfilippo PG, Schillert A, Kang JH, Landers J, Jonasson F, Cree AJ, van Koolwijk LM, Rivadeneira F, Souzeau E, Jonsson V, Menon G, Weinreb RN, de Jong PT, Oostra BA, Uitterlinden AG, Hofman A, Ennis S, Thorsteinsdottir U, Burdon KP, Spector TD, Mirshahi A, Saw SM, Vingerling JR, Teo YY, Haines JL, Wolfs RC, Lemij HG, Tai ES, Jansonius NM, Jonas JB, Cheng CY, Aung T, Viswanathan AC, Klaver CC, Craig JE, Macgregor S, Mackey DA, Lotery AJ, Stefansson K, Bergen AA, Young TL, Wiggs JL, Pfeiffer N, Wong TY, Pasquale LR, Hewitt AW, van Duijn CM, Hammond CJ. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nat Commun. 2014 Sep 22; 5:4883. PMID: 25241763.
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    144. Franchina M, Yazar S, Booth L, Wan SL, Cox K, Kang MH, Hewitt AW, Mackey DA. Swimming goggle wear is not associated with an increased prevalence of glaucoma. Br J Ophthalmol. 2015 Feb; 99(2):255-7. PMID: 25204989.
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    145. Mackey DA, Hewitt AW. Genome-wide association study success in ophthalmology. Curr Opin Ophthalmol. 2014 Sep; 25(5):386-93. PMID: 25014751.
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    146. Gharahkhani P, Burdon KP, Fogarty R, Sharma S, Hewitt AW, Martin S, Law MH, Cremin K, Bailey JNC, Loomis SJ, Pasquale LR, Haines JL, Hauser MA, Viswanathan AC, McGuffin P, Topouzis F, Foster PJ, Graham SL, Casson RJ, Chehade M, White AJ, Zhou T, Souzeau E, Landers J, Fitzgerald JT, Klebe S, Ruddle JB, Goldberg I, Healey PR, Mills RA, Wang JJ, Montgomery GW, Martin NG, RadfordSmith G, Whiteman DC, Brown MA, Wiggs JL, Mackey DA, Mitchell P, MacGregor S, Craig JE. Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma. Nat Genet. 2014 Oct; 46(10):1120-1125. PMID: 25173105.
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    147. Hysi PG, Cheng CY, Springelkamp H, Macgregor S, Bailey JNC, Wojciechowski R, Vitart V, Nag A, Hewitt AW, Höhn R, Venturini C, Mirshahi A, Ramdas WD, Thorleifsson G, Vithana E, Khor CC, Stefansson AB, Liao J, Haines JL, Amin N, Wang YX, Wild PS, Ozel AB, Li JZ, Fleck BW, Zeller T, Staffieri SE, Teo YY, Cuellar-Partida G, Luo X, Allingham RR, Richards JE, Senft A, Karssen LC, Zheng Y, Bellenguez C, Xu L, Iglesias AI, Wilson JF, Kang JH, van Leeuwen EM, Jonsson V, Thorsteinsdottir U, Despriet DDG, Ennis S, Moroi SE, Martin NG, Jansonius NM, Yazar S, Tai ES, Amouyel P, Kirwan J, van Koolwijk LME, Hauser MA, Jonasson F, Leo P, Loomis SJ, Fogarty R, Rivadeneira F, Kearns L, Lackner KJ, de Jong PTVM, Simpson CL, Pennell CE, Oostra BA, Uitterlinden AG, Saw SM, Lotery AJ, Bailey-Wilson JE, Hofman A, Vingerling JR, Maubaret C, Pfeiffer N, Wolfs RCW, Lemij HG, Young TL, Pasquale LR, Delcourt C, Spector TD, Klaver CCW, Small KS, Burdon KP, Stefansson K, Wong TY, Viswanathan A, Mackey DA, Craig JE, Wiggs JL, van Duijn CM, Hammond CJ, Aung T. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nat Genet. 2014 Oct; 46(10):1126-1130. PMID: 25173106.
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    148. Geng X, Jin L, Shimada M, Kim MG, Mackey D. The phytotoxin coronatine is a multifunctional component of the virulence armament of Pseudomonas syringae. Planta. 2014 Dec; 240(6):1149-65. PMID: 25156488.
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    149. Yazar S, Mackey DA. Counting on caveolin for clues in glaucoma. Clin Exp Ophthalmol. 2014 Aug; 42(6):511-2. PMID: 25146306.
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    150. Forward H, Yazar S, Hewitt AW, Khan J, Mountain JA, Pesudovs K, McKnight CM, Tan AX, Pennell CE, Mackey DA, Newnham JP. Multiple prenatal ultrasound scans and ocular development: 20-year follow-up of a randomized controlled trial. Ultrasound Obstet Gynecol. 2014 Aug; 44(2):166-70. PMID: 24789332.
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    151. McKnight CM, Sherwin JC, Yazar S, Forward H, Tan AX, Hewitt AW, Pennell CE, McAllister IL, Young TL, Coroneo MT, Mackey DA. Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort study. Am J Ophthalmol. 2014 Nov; 158(5):1079-85. PMID: 25072831.
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    152. Hoskin AK, Mackey DA. Eye injuries and tasers. Med J Aust. 2014 Jul 21; 201(2):89-90. PMID: 25045981.
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    153. Yazar S, Hewitt AW, Black LJ, McKnight CM, Mountain JA, Sherwin JC, Oddy WH, Coroneo MT, Lucas RM, Mackey DA. Myopia is associated with lower vitamin D status in young adults. Invest Ophthalmol Vis Sci. 2014 Jun 26; 55(7):4552-9. PMID: 24970253.
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    154. Franchina M, Yazar S, Hunter M, Gajdatsy A, deSousa JL, Hewitt AW, Mackey DA. Myopia and skin cancer are inversely correlated: results of the Busselton Healthy Ageing Study. Med J Aust. 2014 May 19; 200(9):521-2. PMID: 24835711.
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    155. Breitenbach HH, Wenig M, Wittek F, Jordá L, Maldonado-Alconada AM, Sarioglu H, Colby T, Knappe C, Bichlmeier M, Pabst E, Mackey D, Parker JE, Vlot AC. Contrasting Roles of the Apoplastic Aspartyl Protease APOPLASTIC, ENHANCED DISEASE SUSCEPTIBILITY1-DEPENDENT1 and LEGUME LECTIN-LIKE PROTEIN1 in Arabidopsis Systemic Acquired Resistance. Plant Physiol. 2014 Jun; 165(2):791-809. PMID: 24755512.
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    156. Mackey DA, Crowston JG, McGhee CNj, McCluskey P. Publication output of senior academic ophthalmologists in Australia and New Zealand. Clin Exp Ophthalmol. 2014 Apr; 42(3):300-2. PMID: 23777318.
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    157. Sanfilippo PG, Chu BS, Bigault O, Kearns LS, Boon MY, Young TL, Hammond CJ, Hewitt AW, Mackey DA. What is the appropriate age cut-off for cycloplegia in refraction? Acta Ophthalmol. 2014 Sep; 92(6):e458-62. PMID: 24641244.
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    158. Nag A, Venturini C, Small KS, Young TL, Viswanathan AC, Mackey DA, Hysi PG, Hammond C. A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort. Hum Mol Genet. 2014 Jun 15; 23(12):3343-8. PMID: 24518671.
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    159. Yazar S, Hewitt AW, Forward H, McKnight CM, Tan A, Mountain JA, Mackey DA. Comparison of monochromatic aberrations in young adults with different visual acuity and refractive errors. J Cataract Refract Surg. 2014 Mar; 40(3):441-9. PMID: 24417894.
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    160. Hysi PG, Mahroo OA, Cumberland P, Wojciechowski R, Williams KM, Young TL, Mackey DA, Rahi JS, Hammond CJ. Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohorts. JAMA Ophthalmol. 2014 Jan; 132(1):50-6. PMID: 24264139.
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    161. Oliver VF, Franchina M, Jaffe AE, Branham KE, Othman M, Heckenlively JR, Swaroop A, Campochiaro B, Vote BJ, Craig JE, Saffery R, Mackey DA, Qian J, Zack DJ, Hewitt AW, Merbs SL. Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degeneration. Cell Rep. 2013 Dec 26; 5(6):1527-35. PMID: 24373284.
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    162. Gangadharan A, Sreerekha MV, Whitehill J, Ham JH, Mackey D. The Pseudomonas syringae pv. tomato type III effector HopM1 suppresses Arabidopsis defenses independent of suppressing salicylic acid signaling and of targeting AtMIN7. PLoS One. 2013; 8(12):e82032. PMID: 24324742.
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    163. Leal LG, Perez Á, Quintero A, Bayona Á, Ortiz JF, Gangadharan A, Mackey D, López C, López-Kleine L. Identification of immunity-related genes in Arabidopsis and cassava using genomic data. Genomics Proteomics Bioinformatics. 2013 Dec; 11(6):345-53. PMID: 24316329.
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    164. Poulter JA, Al-Araimi M, Conte I, van Genderen MM, Sheridan E, Carr IM, Parry DA, Shires M, Carrella S, Bradbury J, Khan K, Lakeman P, Sergouniotis PI, Webster AR, Moore AT, Pal B, Mohamed MD, Venkataramana A, Ramprasad V, Shetty R, Saktivel M, Kumaramanickavel G, Tan A, Mackey DA, Hewitt AW, Banfi S, Ali M, Inglehearn CF, Toomes C. Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism. Am J Hum Genet. 2013 Dec 05; 93(6):1143-50. PMID: 24290379.
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    165. Guggenheim JA, McMahon G, Northstone K, Mandel Y, Kaiserman I, Stone RA, Lin X, Saw SM, Forward H, Mackey DA, Yazar S, Young TL, Williams C. Birth order and myopia. Ophthalmic Epidemiol. 2013 Dec; 20(6):375-84. PMID: 24168726.
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    166. Hewitt AW, Mackey DA. Research: Keep PubMed running at all costs. Nature. 2013 Oct 17; 502(7471):303. PMID: 24132281.
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    167. James A, Hunter M, Straker L, Beilby J, Bucks R, Davis T, Eikelboom RH, Hillman D, Hui J, Hung J, Knuiman M, Mackey DA, Newton RU, Palmer LJ, Musk AB. Rationale, design and methods for a community-based study of clustering and cumulative effects of chronic disease processes and their effects on ageing: the Busselton healthy ageing study. BMC Public Health. 2013 Oct 08; 13:936. PMID: 24099269.
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    168. Dave A, Laurie K, Staffieri SE, Taranath D, Mackey DA, Mitchell P, Wang JJ, Craig JE, Burdon KP, Sharma S. Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia. PLoS One. 2013; 8(8):e72518. PMID: 24014202.
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    169. Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, Timpson NJ, Evans DM, Montgomery GW, Mishra A, Wang YX, Wang JJ, Rochtchina E, Polasek O, Wright AF, Amin N, van Leeuwen EM, Wilson JF, Pennell CE, van Duijn CM, de Jong PT, Vingerling JR, Zhou X, Chen P, Li R, Tay WT, Zheng Y, Chew M, Burdon KP, Craig JE, Iyengar SK, Igo RP, Lass JH, Chew EY, Haller T, Mihailov E, Metspalu A, Wedenoja J, Simpson CL, Wojciechowski R, Höhn R, Mirshahi A, Zeller T, Pfeiffer N, Lackner KJ, Bettecken T, Meitinger T, Oexle K, Pirastu M, Portas L, Nag A, Williams KM, Yonova-Doing E, Klein R, Klein BE, Hosseini SM, Paterson AD, Makela KM, Lehtimaki T, Kahonen M, Raitakari O, Yoshimura N, Matsuda F, Chen LJ, Pang CP, Yip SP, Yap MK, Meguro A, Mizuki N, Inoko H, Foster PJ, Zhao JH, Vithana E, Tai ES, Fan Q, Xu L, Campbell H, Fleck B, Rudan I, Aung T, Hofman A, Uitterlinden AG, Bencic G, Khor CC, Forward H, Pärssinen O, Mitchell P, Rivadeneira F, Hewitt AW, Williams C, Oostra BA, Teo YY, Hammond CJ, Stambolian D, Mackey DA, Klaver CC, Wong TY, Saw SM, Baird PN. Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am J Hum Genet. 2013 Aug 08; 93(2):264-77. PMID: 24144296.
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    170. Lim SH, St Germain E, Tran-Viet KN, Staffieri S, Marino M, Dollfus PH, Nading EB, Crowe S, Gole G, Perdomo-Trujillo Y, Haybittel M, Elder J, Pelletier V, Traboulsi E, Mackey D, Young TL. Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia. Ophthalmic Genet. 2014 Mar; 35(1):1-6. PMID: 23802135.
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    171. Sim X, Jensen RA, Ikram MK, Cotch MF, Li X, MacGregor S, Xie J, Smith AV, Boerwinkle E, Mitchell P, Klein R, Klein BE, Glazer NL, Lumley T, McKnight B, Psaty BM, de Jong PT, Hofman A, Rivadeneira F, Uitterlinden AG, van Duijn CM, Aspelund T, Eiriksdottir G, Harris TB, Jonasson F, Launer LJ, Attia J, Baird PN, Harrap S, Holliday EG, Inouye M, Rochtchina E, Scott RJ, Viswanathan A, Li G, Smith NL, Wiggins KL, Kuo JZ, Taylor KD, Hewitt AW, Martin NG, Montgomery GW, Sun C, Young TL, Mackey DA, van Zuydam NR, Doney AS, Palmer CN, Morris AD, Rotter JI, Tai ES, Gudnason V, Vingerling JR, Siscovick DS, Wang JJ, Wong TY. Genetic loci for retinal arteriolar microcirculation. PLoS One. 2013; 8(6):e65804. PMID: 23776548.
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    172. Yazar S, Mishra A, Ang W, Kearns LS, Mountain JA, Pennell C, Montgomery GW, Young TL, Hammond CJ, Macgregor S, Mackey DA, Hewitt AW. Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study. Mol Vis. 2013; 19:1238-46. PMID: 23761726.
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    173. Afzal AJ, Kim JH, Mackey D. The role of NOI-domain containing proteins in plant immune signaling. BMC Genomics. 2013 May 14; 14:327. PMID: 23672422.
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    174. Nag A, Venturini C, Hysi PG, Arno M, Aldecoa-Otalora Astarloa E, Macgregor S, Hewitt AW, Young TL, Mitchell P, Viswanathan AC, Mackey DA, Hammond CJ. Copy number variation at chromosome 5q21.2 is associated with intraocular pressure. Invest Ophthalmol Vis Sci. 2013 May 01; 54(5):3607-12. PMID: 23599335.
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    175. Hawthorne F, Feng S, Metlapally R, Li YJ, Tran-Viet KN, Guggenheim JA, Malecaze F, Calvas P, Rosenberg T, Mackey DA, Venturini C, Hysi PG, Hammond CJ, Young TL. Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2. Invest Ophthalmol Vis Sci. 2013 Mar 21; 54(3):2076-86. PMID: 23422819.
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    176. Ruddle JB, Staffieri SE, Crowston JG, Sherwin JC, Mackey DA. Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in Victoria, Australia. Clin Exp Ophthalmol. 2013 Sep-Oct; 41(7):653-61. PMID: 23332011.
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    177. Souzeau E, Burdon KP, Dubowsky A, Grist S, Usher B, Fitzgerald JT, Crawford A, Hewitt AW, Goldberg I, Mills RA, Ruddle JB, Landers J, Mackey DA, Craig JE. Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registry. Ophthalmology. 2013 Jun; 120(6):1135-43. PMID: 23453510.
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    178. Sanfilippo PG, Hewitt AW, Mountain JA, Mackey DA. A geometric morphometric assessment of hand shape and comparison to the 2D:4D digit ratio as a marker of sexual dimorphism. Twin Res Hum Genet. 2013 Apr; 16(2):590-600. PMID: 23442781.
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    179. Venkatakrishnan S, Mackey D, Meier I. Functional investigation of the plant-specific long coiled-coil proteins PAMP-INDUCED COILED-COIL (PICC) and PICC-LIKE (PICL) in Arabidopsis thaliana. PLoS One. 2013; 8(2):e57283. PMID: 23451199.
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    180. Verhoeven VJ, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GH, McMahon G, Kemp JP, Pourcain BS, Simpson CL, Mäkelä KM, Lehtimäki T, Kähönen M, Paterson AD, Hosseini SM, Wong HS, Xu L, Jonas JB, Pärssinen O, Wedenoja J, Yip SP, Ho DW, Pang CP, Chen LJ, Burdon KP, Craig JE, Klein BE, Klein R, Haller T, Metspalu A, Khor CC, Tai ES, Aung T, Vithana E, Tay WT, Barathi VA, Chen P, Li R, Liao J, Zheng Y, Ong RT, Döring A, Evans DM, Timpson NJ, Verkerk AJ, Meitinger T, Raitakari O, Hawthorne F, Spector TD, Karssen LC, Pirastu M, Murgia F, Ang W, Mishra A, Montgomery GW, Pennell CE, Cumberland PM, Cotlarciuc I, Mitchell P, Wang JJ, Schache M, Janmahasatian S, Janmahasathian S, Igo RP, Lass JH, Chew E, Iyengar SK, Gorgels TG, Rudan I, Hayward C, Wright AF, Polasek O, Vatavuk Z, Wilson JF, Fleck B, Zeller T, Mirshahi A, Müller C, Uitterlinden AG, Rivadeneira F, Vingerling JR, Hofman A, Oostra BA, Amin N, Bergen AA, Teo YY, Rahi JS, Vitart V, Williams C, Baird PN, Wong TY, Oexle K, Pfeiffer N, Mackey DA, Young TL, van Duijn CM, Saw SM, Bailey-Wilson JE, Stambolian D, Klaver CC, Hammond CJ. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet. 2013 Mar; 45(3):314-8. PMID: 23396134.
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    181. Lopes MC, Hysi PG, Verhoeven VJ, Macgregor S, Hewitt AW, Montgomery GW, Cumberland P, Vingerling JR, Young TL, van Duijn CM, Oostra B, Uitterlinden AG, Rahi JS, Mackey DA, Klaver CC, Andrew T, Hammond CJ. Identification of a candidate gene for astigmatism. Invest Ophthalmol Vis Sci. 2013 Feb 01; 54(2):1260-7. PMID: 23322567.
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    182. Yazar S, Forward H, McKnight CM, Tan A, Soloshenko A, Oates SK, Ang W, Sherwin JC, Wood D, Mountain JA, Pennell CE, Hewitt AW, Mackey DA. Raine eye health study: design, methodology and baseline prevalence of ophthalmic disease in a birth-cohort study of young adults. Ophthalmic Genet. 2013 Dec; 34(4):199-208. PMID: 23301674.
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    183. Lu Y, Vitart V, Burdon KP, Khor CC, Bykhovskaya Y, Mirshahi A, Hewitt AW, Koehn D, Hysi PG, Ramdas WD, Zeller T, Vithana EN, Cornes BK, Tay WT, Tai ES, Cheng CY, Liu J, Foo JN, Saw SM, Thorleifsson G, Stefansson K, Dimasi DP, Mills RA, Mountain J, Ang W, Hoehn R, Verhoeven VJ, Grus F, Wolfs R, Castagne R, Lackner KJ, Springelkamp H, Yang J, Jonasson F, Leung DY, Chen LJ, Tham CC, Rudan I, Vatavuk Z, Hayward C, Gibson J, Cree AJ, MacLeod A, Ennis S, Polasek O, Campbell H, Wilson JF, Viswanathan AC, Fleck B, Li X, Siscovick D, Taylor KD, Rotter JI, Yazar S, Ulmer M, Li J, Yaspan BL, Ozel AB, Richards JE, Moroi SE, Haines JL, Kang JH, Pasquale LR, Allingham RR, Ashley-Koch A, Mitchell P, Wang JJ, Wright AF, Pennell C, Spector TD, Young TL, Klaver CC, Martin NG, Montgomery GW, Anderson MG, Aung T, Willoughby CE, Wiggs JL, Pang CP, Thorsteinsdottir U, Lotery AJ, Hammond CJ, van Duijn CM, Hauser MA, Rabinowitz YS, Pfeiffer N, Mackey DA, Craig JE, Macgregor S, Wong TY. Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat Genet. 2013 Feb; 45(2):155-63. PMID: 23291589.
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    184. De Roach JN, McLaren TL, Paterson RL, O'Brien EC, Hoffmann L, Mackey DA, Hewitt AW, Lamey TM. Establishment and evolution of the Australian Inherited Retinal Disease Register and DNA Bank. Clin Exp Ophthalmol. 2013 Jul; 41(5):476-83. PMID: 23078154.
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    185. McKnight CM, Newnham JP, Stanley FJ, Mountain JA, Landau LI, Beilin LJ, Puddey IB, Pennell CE, Mackey DA. Birth of a cohort--the first 20 years of the Raine study. Med J Aust. 2012 Dec 10; 197(11):608-10. PMID: 23230915.
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    186. Geng X, Cheng J, Gangadharan A, Mackey D. The coronatine toxin of Pseudomonas syringae is a multifunctional suppressor of Arabidopsis defense. Plant Cell. 2012 Nov; 24(11):4763-74. PMID: 23204405.
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    187. Mishra A, Yazar S, Hewitt AW, Mountain JA, Ang W, Pennell CE, Martin NG, Montgomery GW, Hammond CJ, Young TL, Macgregor S, Mackey DA. Genetic variants near PDGFRA are associated with corneal curvature in Australians. Invest Ophthalmol Vis Sci. 2012 Oct 11; 53(11):7131-6. PMID: 22969067.
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    188. Wiggs JL, Hewitt AW, Fan BJ, Wang DY, Figueiredo Sena DR, O'Brien C, Realini A, Craig JE, Dimasi DP, Mackey DA, Haines JL, Pasquale LR. The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucoma. PLoS One. 2012; 7(9):e45613. PMID: 23049825.
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    189. Franchina M, Toniolo J, Mackey DA, Hewitt AW. Google-based search of common blinding diseases: a reflection of public concerns. Br J Ophthalmol. 2012 Nov; 96(11):1444-5. PMID: 22872671.
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    190. Souzeau E, Goldberg I, Healey PR, Mills RA, Landers J, Graham SL, Grigg JR, Usher B, Straga T, Crawford A, Casson RJ, Morgan WH, Ruddle JB, Coote MA, White A, Stewart J, Hewitt AW, Mackey DA, Burdon KP, Craig JE. Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment. Clin Exp Ophthalmol. 2012 Aug; 40(6):569-75. PMID: 22171965.
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    191. Mackey DC. Can we finally conquer the problem of medical quality? The systems-based opportunities of data registries and medical teamwork. Anesthesiology. 2012 Aug; 117(2):225-6. PMID: 22576143.
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    192. Dimasi DP, Burdon KP, Hewitt AW, Fitzgerald J, Wang JJ, Healey PR, Mitchell P, Mackey DA, Craig JE. Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucoma. Am J Ophthalmol. 2012 Nov; 154(5):833-842.e2. PMID: 22840486.
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    193. Sharma S, Burdon KP, Chidlow G, Klebe S, Crawford A, Dimasi DP, Dave A, Martin S, Javadiyan S, Wood JP, Casson R, Danoy P, Griggs K, Hewitt AW, Landers J, Mitchell P, Mackey DA, Craig JE. Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye. Invest Ophthalmol Vis Sci. 2012 Jul 24; 53(8):4917-25. PMID: 22714896.
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    194. Sherwin JC, Reacher MH, Keogh RH, Khawaja AP, Mackey DA, Foster PJ. The association between time spent outdoors and myopia in children and adolescents: a systematic review and meta-analysis. Ophthalmology. 2012 Oct; 119(10):2141-51. PMID: 22809757.
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    195. Sherwin JC, Hewitt AW, Coroneo MT, Kearns LS, Griffiths LR, Mackey DA. The association between time spent outdoors and myopia using a novel biomarker of outdoor light exposure. Invest Ophthalmol Vis Sci. 2012 Jul 01; 53(8):4363-70. PMID: 22669720.
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    196. Ma Y, Kawasaki R, Dobson LP, Ruddle JB, Kearns LS, Wong TY, Mackey DA. Quantitative analysis of retinal vessel attenuation in eyes with retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2012 Jun 28; 53(7):4306-14. PMID: 22661482.
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    197. Edwards TL, Burt BO, Black GC, Perveen R, Kearns LS, Staffieri SE, Toomes C, Buttery RG, Mackey DA. Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations. Clin Exp Ophthalmol. 2012 Jul; 40(5):476-83. PMID: 22574936.
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    198. Mackey DA. Your time starts now - translation time lines for major ophthalmic discoveries. Med J Aust. 2012 Jun 18; 196(11):672-4. PMID: 22708753.
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    199. Sanfilippo PG, Hammond CJ, Staffieri SE, Kearns LS, Melissa Liew SH, Barbour JM, Hewitt AW, Ge D, Snieder H, Mackinnon JR, Brown SA, Lorenz B, Spector TD, Martin NG, Wilmer JB, Mackey DA. Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error. Twin Res Hum Genet. 2012 Oct; 15(5):624-30. PMID: 22877876.
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    200. Verhoeven VJ, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, Cotch MF, Yamashiro K, Baird PN, Mackey DA, Wojciechowski R, Ikram MK, Hewitt AW, Duggal P, Janmahasatian S, Khor CC, Fan Q, Zhou X, Young TL, Tai ES, Goh LK, Li YJ, Aung T, Vithana E, Teo YY, Tay W, Sim X, Rudan I, Hayward C, Wright AF, Polasek O, Campbell H, Wilson JF, Fleck BW, Nakata I, Yoshimura N, Yamada R, Matsuda F, Ohno-Matsui K, Nag A, McMahon G, St Pourcain B, Lu Y, Rahi JS, Cumberland PM, Bhattacharya S, Simpson CL, Atwood LD, Li X, Raffel LJ, Murgia F, Portas L, Despriet DD, van Koolwijk LM, Wolfram C, Lackner KJ, Tönjes A, Mägi R, Lehtimäki T, Kähönen M, Esko T, Metspalu A, Rantanen T, Pärssinen O, Klein BE, Meitinger T, Spector TD, Oostra BA, Smith AV, de Jong PT, Hofman A, Amin N, Karssen LC, Rivadeneira F, Vingerling JR, Eiríksdóttir G, Gudnason V, Döring A, Bettecken T, Uitterlinden AG, Williams C, Zeller T, Castagné R, Oexle K, van Duijn CM, Iyengar SK, Mitchell P, Wang JJ, Höhn R, Pfeiffer N, Bailey-Wilson JE, Stambolian D, Wong TY, Hammond CJ, Klaver CC. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum Genet. 2012 Sep; 131(9):1467-80. PMID: 22665138.
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    201. van Koolwijk LM, Ramdas WD, Ikram MK, Jansonius NM, Pasutto F, Hysi PG, Macgregor S, Janssen SF, Hewitt AW, Viswanathan AC, ten Brink JB, Hosseini SM, Amin N, Despriet DD, Willemse-Assink JJ, Kramer R, Rivadeneira F, Struchalin M, Aulchenko YS, Weisschuh N, Zenkel M, Mardin CY, Gramer E, Welge-Lüssen U, Montgomery GW, Carbonaro F, Young TL, Bellenguez C, McGuffin P, Foster PJ, Topouzis F, Mitchell P, Wang JJ, Wong TY, Czudowska MA, Hofman A, Uitterlinden AG, Wolfs RC, de Jong PT, Oostra BA, Paterson AD, Mackey DA, Bergen AA, Reis A, Hammond CJ, Vingerling JR, Lemij HG, Klaver CC, van Duijn CM. Common genetic determinants of intraocular pressure and primary open-angle glaucoma. PLoS Genet. 2012; 8(5):e1002611. PMID: 22570627.
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    202. Burdon KP, Crawford A, Casson RJ, Hewitt AW, Landers J, Danoy P, Mackey DA, Mitchell P, Healey PR, Craig JE. Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucoma. Ophthalmology. 2012 Aug; 119(8):1539-45. PMID: 22521085.
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    203. Abbott D, Li YJ, Guggenheim JA, Metlapally R, Malecaze F, Calvas P, Rosenberg T, Paget S, Zayats T, Mackey DA, Feng S, Young TL. An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error. Mol Vis. 2012; 18:720-9. PMID: 22509102.
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    204. Sherwin JC, McKnight CM, Hewitt AW, Griffiths LR, Coroneo MT, Mackey DA. Reliability and validity of conjunctival ultraviolet autofluorescence measurement. Br J Ophthalmol. 2012 Jun; 96(6):801-5. PMID: 22408236.
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    205. Ng WY, Pasutto F, Bardakjian TM, Wilson MJ, Watson G, Schneider A, Mackey DA, Grigg JR, Zenker M, Jamieson RV. A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family. Clin Genet. 2013 Feb; 83(2):162-8. PMID: 22283518.
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    206. Mackey DA, Warrington NM, Hewitt AW, Oates SK, Yazar S, Soloshenko A, Crawford GJ, Mountain JA, Pennell CE. Role of the TCF4 gene intronic variant in normal variation of corneal endothelium. Cornea. 2012 Feb; 31(2):162-6. PMID: 22146553.
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    207. Webb TR, Matarin M, Gardner JC, Kelberman D, Hassan H, Ang W, Michaelides M, Ruddle JB, Pennell CE, Yazar S, Khor CC, Aung T, Yogarajah M, Robson AG, Holder GE, Cheetham ME, Traboulsi EI, Moore AT, Sowden JC, Sisodiya SM, Mackey DA, Tuft SJ, Hardcastle AJ. X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development. Am J Hum Genet. 2012 Feb 10; 90(2):247-59. PMID: 22284829.
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    208. Mackey DA. Genetic eye research in Tasmania: a historical overview. Clin Exp Ophthalmol. 2012 Mar; 40(2):205-10. PMID: 22044574.
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    209. Sherwin JC, Hewitt AW, Kearns LS, Griffiths LR, Mackey DA, Coroneo MT. The association between pterygium and conjunctival ultraviolet autofluorescence: the Norfolk Island Eye Study. Acta Ophthalmol. 2013 Jun; 91(4):363-70. PMID: 22176664.
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    210. Pratap DS, Lim LL, Wang JJ, Mackey DA, Kearns LS, Stawell RJ, Burdon KP, Mitchell P, Craig JE, Hall AJ, Hewitt AW. The role of toll-like receptor variants in acute anterior uveitis. Mol Vis. 2011; 17:2970-7. PMID: 22128242.
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    211. Afzal AJ, da Cunha L, Mackey D. Separable fragments and membrane tethering of Arabidopsis RIN4 regulate its suppression of PAMP-triggered immunity. Plant Cell. 2011 Oct; 23(10):3798-811. PMID: 21984695.
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    212. Ali M, Hocking PM, McKibbin M, Finnegan S, Shires M, Poulter JA, Prescott K, Booth A, Raashid Y, Jafri H, Ruddle JB, Mackey DA, Jacobson SG, Toomes C, Lester DH, Burt DW, Curry WJ, Inglehearn CF. Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2011 Sep 27; 52(10):7432-40. PMID: 21862650.
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    213. Mackey DA, Sanfilippo P, Godfrey A, Zambotti E. Fail-to-attend rates in a private ophthalmology clinic by age group. Clin Exp Ophthalmol. 2012 Mar; 40(2):221-3. PMID: 21718419.
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    214. Rance G, Kearns LS, Tan J, Gravina A, Rosenfeld L, Henley L, Carew P, Graydon K, O'Hare F, Mackey DA. Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees. J Neurol. 2012 Mar; 259(3):542-50. PMID: 21887510.
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    215. Forward H, Hewitt AW, Mackey DA. Missing X and Y: a review of participant ages in population-based eye studies. Clin Exp Ophthalmol. 2012 Apr; 40(3):305-19. PMID: 21668774.
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    216. Larsson M, Duffy DL, Zhu G, Liu JZ, Macgregor S, McRae AF, Wright MJ, Sturm RA, Mackey DA, Montgomery GW, Martin NG, Medland SE. GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. Am J Hum Genet. 2011 Aug 12; 89(2):334-43. PMID: 21835309.
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    217. Mackey DA, Hewitt AW, Ruddle JB, Vote B, Buttery RG, Toomes C, Metlapally R, Li YJ, Tran-Viet KN, Malecaze F, Calvas P, Rosenberg T, Guggenheim JA, Young TL. Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family. Mol Vis. 2011; 17:2118-28. PMID: 21850187.
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    218. Sanfilippo PG, Medland SE, Hewitt AW, Kearns LS, Ruddle JB, Sun C, Hammond CJ, Young TL, Martin NG, Mackey DA. Ophthalmic phenotypes and the representativeness of twin data for the general population. Invest Ophthalmol Vis Sci. 2011 Jul 29; 52(8):5565-72. PMID: 21498610.
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    219. Van Bergen NJ, Crowston JG, Kearns LS, Staffieri SE, Hewitt AW, Cohn AC, Mackey DA, Trounce IA. Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy. PLoS One. 2011; 6(6):e21347. PMID: 21731710.
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    220. Sherwin JC, Kelly J, Hewitt AW, Kearns LS, Griffiths LR, Mackey DA. Prevalence and predictors of refractive error in a genetically isolated population: the Norfolk Island Eye Study. Clin Exp Ophthalmol. 2011 Nov; 39(8):734-42. PMID: 21631679.
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    221. Burdon KP, Macgregor S, Hewitt AW, Sharma S, Chidlow G, Mills RA, Danoy P, Casson R, Viswanathan AC, Liu JZ, Landers J, Henders AK, Wood J, Souzeau E, Crawford A, Leo P, Wang JJ, Rochtchina E, Nyholt DR, Martin NG, Montgomery GW, Mitchell P, Brown MA, Mackey DA, Craig JE. Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nat Genet. 2011 Jun; 43(6):574-8. PMID: 21532571.
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    222. Staffieri SE, Ruddle JB, Kearns LS, Barbour JM, Edwards TL, Paul P, Mackey DA. Telemedicine model to prevent blindness from familial glaucoma. Clin Exp Ophthalmol. 2011 Nov; 39(8):760-5. PMID: 21749595.
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    223. Sherwin JC, Hewitt AW, Kearns LS, Coroneo MT, Griffiths LR, Mackey DA. Distribution of conjunctival ultraviolet autofluorescence in a population-based study: the Norfolk Island Eye Study. Eye (Lond). 2011 Jul; 25(7):893-900. PMID: 21494284.
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    224. Sherwin JC, Kearns LS, Hewitt AW, Ma Y, Kelly J, Griffiths LR, Mackey DA. Prevalence of chronic ocular diseases in a genetic isolate: the Norfolk Island Eye Study (NIES). Ophthalmic Epidemiol. 2011 Apr; 18(2):61-71. PMID: 21401413.
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    225. Mackey DA, Wilkinson CH, Kearns LS, Hewitt AW. Classification of iris colour: review and refinement of a classification schema. Clin Exp Ophthalmol. 2011 Jul; 39(5):462-71. PMID: 21176045.
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    226. Kinnick TR, Mullins RF, Dev S, Leys M, Mackey DA, Kay CN, Lam BL, Fishman GA, Traboulsi E, Iezzi R, Stone EM. Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patients. Retina. 2011 Mar; 31(3):581-95. PMID: 21273940.
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    227. Fahy SJ, Sun C, Zhu G, Healey PR, Spector TD, Martin NG, Mitchell P, Wong TY, Mackey DA, Hammond CJ, Andrew T. The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease. Invest Ophthalmol Vis Sci. 2011 Feb; 52(2):975-81. PMID: 20926817.
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    228. Chung EH, da Cunha L, Wu AJ, Gao Z, Cherkis K, Afzal AJ, Mackey D, Dangl JL. Specific threonine phosphorylation of a host target by two unrelated type III effectors activates a host innate immune receptor in plants. Cell Host Microbe. 2011 Feb 17; 9(2):125-36. PMID: 21320695.
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    229. Mackey DA, Sherwin JC, Kearns LS, Ma Y, Kelly J, Chu BS, Macmillan R, Barbour JM, Wilkinson CH, Matovinovic E, Cox HC, Bellis C, Lea RA, Quinlan S, Griffiths LR, Hewitt AW. The Norfolk Island Eye Study (NIES): rationale, methodology and distribution of ocular biometry (biometry of the bounty). Twin Res Hum Genet. 2011 Feb; 14(1):42-52. PMID: 21314255.
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    230. Geng X, Mackey D. Dose-response to and systemic movement of dexamethasone in the GVG-inducible transgene system in Arabidopsis. Methods Mol Biol. 2011; 712:59-68. PMID: 21359800.
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    231. O'Neill EC, Danesh-Meyer HV, Kong GX, Hewitt AW, Coote MA, Mackey DA, Crowston JG. Optic disc evaluation in optic neuropathies: the optic disc assessment project. Ophthalmology. 2011 May; 118(5):964-70. PMID: 21126771.
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    232. Sun C, Ponsonby AL, Brown SA, Kearns LS, Mackinnon JR, Barbour JM, Ruddle JB, Hewitt AW, Wright MJ, Martin NG, Dwyer T, Mackey DA. Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: the Australian Twins Eye Study. Am J Ophthalmol. 2010 Dec; 150(6):909-16. PMID: 20970773.
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    233. Cohn AC, Turnbull C, Ruddle JB, Guymer RH, Kearns LS, Staffieri S, Daggett HT, Hewitt AW, Mackey DA. Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations. Eye (Lond). 2011 Feb; 25(2):208-17. PMID: 21109774.
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    234. Azmanov DN, Dimitrova S, Florez L, Cherninkova S, Draganov D, Morar B, Saat R, Juan M, Arostegui JI, Ganguly S, Soodyall H, Chakrabarti S, Padh H, López-Nevot MA, Chernodrinska V, Anguelov B, Majumder P, Angelova L, Kaneva R, Mackey DA, Tournev I, Kalaydjieva L. LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population. Eur J Hum Genet. 2011 Mar; 19(3):326-33. PMID: 21081970.
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    235. Burdon KP, Hewitt AW, Mackey DA, Mitchell P, Craig JE. Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. Mol Vis. 2010 Nov 04; 16:2286-93. PMID: 21139974.
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    236. Ikram MK, Sim X, Xueling S, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BE, Breteler MM, Cheung N, Liew G, Mitchell P, Uitterlinden AG, Rivadeneira F, Hofman A, de Jong PT, van Duijn CM, Kao L, Cheng CY, Smith AV, Glazer NL, Lumley T, McKnight B, Psaty BM, Jonasson F, Eiriksdottir G, Aspelund T, Harris TB, Launer LJ, Taylor KD, Li X, Iyengar SK, Xi Q, Sivakumaran TA, Mackey DA, Macgregor S, Martin NG, Young TL, Bis JC, Wiggins KL, Heckbert SR, Hammond CJ, Andrew T, Fahy S, Attia J, Holliday EG, Scott RJ, Islam FM, Rotter JI, McAuley AK, Boerwinkle E, Tai ES, Gudnason V, Siscovick DS, Vingerling JR, Wong TY. Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet. 2010 Oct 28; 6(10):e1001184. PMID: 21060863.
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    237. Mackey DA, Kanaris A. Missing the cue: recognising parents with English as second language. J Paediatr Child Health. 2010 Oct; 46(10):611. PMID: 20958823.
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    238. Sanfilippo PG, Hewitt AW, Hammond CJ, Mackey DA. The heritability of ocular traits. Surv Ophthalmol. 2010 Nov-Dec; 55(6):561-83. PMID: 20851442.
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    239. Thorleifsson G, Walters GB, Hewitt AW, Masson G, Helgason A, DeWan A, Sigurdsson A, Jonasdottir A, Gudjonsson SA, Magnusson KP, Stefansson H, Lam DS, Tam PO, Gudmundsdottir GJ, Southgate L, Burdon KP, Gottfredsdottir MS, Aldred MA, Mitchell P, St Clair D, Collier DA, Tang N, Sveinsson O, Macgregor S, Martin NG, Cree AJ, Gibson J, Macleod A, Jacob A, Ennis S, Young TL, Chan JC, Karwatowski WS, Hammond CJ, Thordarson K, Zhang M, Wadelius C, Lotery AJ, Trembath RC, Pang CP, Hoh J, Craig JE, Kong A, Mackey DA, Jonasson F, Thorsteinsdottir U, Stefansson K. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet. 2010 Oct; 42(10):906-9. PMID: 20835238.
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    240. Solouki AM, Verhoeven VJ, van Duijn CM, Verkerk AJ, Ikram MK, Hysi PG, Despriet DD, van Koolwijk LM, Ho L, Ramdas WD, Czudowska M, Kuijpers RW, Amin N, Struchalin M, Aulchenko YS, van Rij G, Riemslag FC, Young TL, Mackey DA, Spector TD, Gorgels TG, Willemse-Assink JJ, Isaacs A, Kramer R, Swagemakers SM, Bergen AA, van Oosterhout AA, Oostra BA, Rivadeneira F, Uitterlinden AG, Hofman A, de Jong PT, Hammond CJ, Vingerling JR, Klaver CC. A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. Nat Genet. 2010 Oct; 42(10):897-901. PMID: 20835239.
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    241. Hysi PG, Young TL, Mackey DA, Andrew T, Fernández-Medarde A, Solouki AM, Hewitt AW, Macgregor S, Vingerling JR, Li YJ, Ikram MK, Fai LY, Sham PC, Manyes L, Porteros A, Lopes MC, Carbonaro F, Fahy SJ, Martin NG, van Duijn CM, Spector TD, Rahi JS, Santos E, Klaver CC, Hammond CJ. A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nat Genet. 2010 Oct; 42(10):902-5. PMID: 20835236.
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    242. Mackey DA, Trounce I. Genetics: Optic nerve genetics--more than meets the eye. Nat Rev Neurol. 2010 Jul; 6(7):357-8. PMID: 20639910.
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    243. Ruddle JB, Mackey DA. Pseudoexfoliation syndrome: more than meets the eye. Clin Exp Ophthalmol. 2010 Jul; 38(5):437-8. PMID: 20649612.
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    244. Sanfilippo PG, Cardini A, Sigal IA, Ruddle JB, Chua BE, Hewitt AW, Mackey DA. A geometric morphometric assessment of the optic cup in glaucoma. Exp Eye Res. 2010 Sep; 91(3):405-14. PMID: 20599965.
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    245. Tang L, Scheetz TE, Mackey DA, Hewitt AW, Fingert JH, Kwon YH, Quellec G, Reinhardt JM, Abràmoff MD. Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape. Invest Ophthalmol Vis Sci. 2010 Nov; 51(11):5870-7. PMID: 20505201.
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    246. Xu J, Ishikawa H, Wollstein G, Bilonick RA, Kagemann L, Craig JE, Mackey DA, Hewitt AW, Schuman JS. Automated volumetric evaluation of stereoscopic disc photography. Opt Express. 2010 May 24; 18(11):11347-59. PMID: 20588996.
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    247. Lu Y, Dimasi DP, Hysi PG, Hewitt AW, Burdon KP, Toh T, Ruddle JB, Li YJ, Mitchell P, Healey PR, Montgomery GW, Hansell N, Spector TD, Martin NG, Young TL, Hammond CJ, Macgregor S, Craig JE, Mackey DA. Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genet. 2010 May 13; 6(5):e1000947. PMID: 20485516.
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    248. Liu F, Wollstein A, Hysi PG, Ankra-Badu GA, Spector TD, Park D, Zhu G, Larsson M, Duffy DL, Montgomery GW, Mackey DA, Walsh S, Lao O, Hofman A, Rivadeneira F, Vingerling JR, Uitterlinden AG, Martin NG, Hammond CJ, Kayser M. Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genet. 2010 May 06; 6(5):e1000934. PMID: 20463881.
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    249. Towns KV, Kipioti A, Long V, McKibbin M, Maubaret C, Vaclavik V, Ehsani P, Springell K, Kamal M, Ramesar RS, Mackey DA, Moore AT, Mukhopadhyay R, Webster AR, Black GC, O'Sullivan J, Bhattacharya SS, Pierce EA, Beggs JD, Inglehearn CF. Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes. Hum Mutat. 2010 May; 31(5):E1361-76. PMID: 20232351.
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    250. Metlapally R, Ki CS, Li YJ, Tran-Viet KN, Abbott D, Malecaze F, Calvas P, Mackey DA, Rosenberg T, Paget S, Guggenheim JA, Young TL. Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort. Invest Ophthalmol Vis Sci. 2010 Sep; 51(9):4476-9. PMID: 20435602.
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    251. Macgregor S, Hewitt AW, Hysi PG, Ruddle JB, Medland SE, Henders AK, Gordon SD, Andrew T, McEvoy B, Sanfilippo PG, Carbonaro F, Tah V, Li YJ, Bennett SL, Craig JE, Montgomery GW, Tran-Viet KN, Brown NL, Spector TD, Martin NG, Young TL, Hammond CJ, Mackey DA. Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Hum Mol Genet. 2010 Jul 01; 19(13):2716-24. PMID: 20395239.
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    252. Staffieri SE, Ruddle JB, Mackey DA. Rock, paper and scissors? Traumatic paediatric cataract in Victoria 1992-2006. Clin Exp Ophthalmol. 2010 Apr; 38(3):237-41. PMID: 20447118.
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    253. Dimasi DP, Burdon KP, Hewitt AW, Savarirayan R, Healey PR, Mitchell P, Mackey DA, Craig JE. Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness. Mol Vis. 2010 Mar 31; 16:562-9. PMID: 20360993.
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    254. Kitsos G, Petrou Z, Grigoriadou M, Samples JR, Hewitt AW, Kokotas H, Giannoulia-Karantana A, Mackey DA, Wirtz MK, Moschou M, Ioannidis JP, Petersen MB. Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece. Clin Ophthalmol. 2010 Mar 24; 4:171-8. PMID: 20390039.
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    255. Charlesworth J, Kramer PL, Dyer T, Diego V, Samples JR, Craig JE, Mackey DA, Hewitt AW, Blangero J, Wirtz MK. The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness. Invest Ophthalmol Vis Sci. 2010 Jul; 51(7):3509-14. PMID: 20237253.
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    256. O'Neill EC, Danesh-Meyer HV, Connell PP, Trounce IA, Coote MA, Mackey DA, Crowston JG. The optic nerve head in acquired optic neuropathies. Nat Rev Neurol. 2010 Apr; 6(4):221-36. PMID: 20212512.
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    257. Kearns LS, Forrest M, Cohn AC, Churchill AJ, Mackey DA. Does acute loss of vision in autosomal dominant optic atrophy occur early in childhood? Ophthalmic Genet. 2010 Mar; 31(1):44-6. PMID: 20141358.
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    258. Carbonaro F, Andrew T, Mackey DA, Spector TD, Hammond CJ. Comparison of three methods of intraocular pressure measurement and their relation to central corneal thickness. Eye (Lond). 2010 Jul; 24(7):1165-70. PMID: 20150923.
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    259. Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, Hayashi K, Mackey DA, Kearns LS, Ruddle JB, Craig JE, Pierce EA, Downey LM, Mohamed MD, Markham AF, Inglehearn CF, Toomes C. Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy. Am J Hum Genet. 2010 02 12; 86(2):248-53. PMID: 20159112.
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    260. Tischfield MA, Baris HN, Wu C, Rudolph G, Van Maldergem L, He W, Chan WM, Andrews C, Demer JL, Robertson RL, Mackey DA, Ruddle JB, Bird TD, Gottlob I, Pieh C, Traboulsi EI, Pomeroy SL, Hunter DG, Soul JS, Newlin A, Sabol LJ, Doherty EJ, de Uzcátegui CE, de Uzcátegui N, Collins ML, Sener EC, Wabbels B, Hellebrand H, Meitinger T, de Berardinis T, Magli A, Schiavi C, Pastore-Trossello M, Koc F, Wong AM, Levin AV, Geraghty MT, Descartes M, Flaherty M, Jamieson RV, Møller HU, Meuthen I, Callen DF, Kerwin J, Lindsay S, Meindl A, Gupta ML, Pellman D, Engle EC. Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell. 2010 Jan 08; 140(1):74-87. PMID: 20074521.
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    261. Rowe BH, Villa-Roel C, Abu-Laban RB, Stenstrom R, Mackey D, Stiell IG, Campbell S, Young B. Admissions to Canadian hospitals for acute asthma: a prospective, multicentre study. Can Respir J. 2010 Jan-Feb; 17(1):25-30. PMID: 20186368.
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    262. Hewitt AW, Wu J, Green CM, Lai T, Kearns LS, Craig JE, Mackey DA. Systemic disease associations of familial and sporadic glaucoma: the Glaucoma Inheritance Study in Tasmania. Acta Ophthalmol. 2010 Feb; 88(1):70-4. PMID: 19958295.
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    263. Mackey DA, Mackinnon JR, Brown SA, Kearns LS, Ruddle JB, Sanfilippo PG, Sun C, Hammond CJ, Young TL, Martin NG, Hewitt AW. Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twins. Twin Res Hum Genet. 2009 Oct; 12(5):441-54. PMID: 19803772.
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    264. Dimasi DP, Chen JY, Hewitt AW, Klebe S, Davey R, Stirling J, Thompson E, Forbes R, Tan TY, Savarirayan R, Mackey DA, Healey PR, Mitchell P, Burdon KP, Craig JE. Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes. Hum Genet. 2010 Jan; 127(1):33-44. PMID: 19714363.
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    265. Sun C, Zhu G, Wong TY, Hewitt AW, Ruddle JB, Hodgson L, Montgomery GW, Young TL, Hammond CJ, Craig JE, Martin NG, He M, Mackey DA. Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye Study. Hypertension. 2009 Oct; 54(4):788-95. PMID: 19687348.
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    266. Downie AC, Mackey DA, Vote BJ. Isolated corneal opacification and microphthalmia: a suspected warfarin embryopathy. Clin Exp Ophthalmol. 2009 Aug; 37(6):624-5. PMID: 19702715.
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    267. Zayats T, Young TL, Mackey DA, Malecaze F, Calvas P, Guggenheim JA. Quality of DNA extracted from mouthwashes. PLoS One. 2009 Jul 07; 4(7):e6165. PMID: 19582144.
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    268. Mackey DA. The 'I' in personalized genetics: 2008 Ian Constable lecture. Clin Exp Ophthalmol. 2009 Jul; 37(5):434-43. PMID: 19624338.
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    269. Sanfilippo PG, Cardini A, Hewitt AW, Crowston JG, Mackey DA. Optic disc morphology--rethinking shape. Prog Retin Eye Res. 2009 Jul; 28(4):227-48. PMID: 19520180.
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    270. Ham JH, Majerczak DR, Nomura K, Mecey C, Uribe F, He SY, Mackey D, Coplin DL. Multiple activities of the plant pathogen type III effector proteins WtsE and AvrE require WxxxE motifs. Mol Plant Microbe Interact. 2009 Jun; 22(6):703-12. PMID: 19445595.
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    271. Ruddle JB, Ebenezer ND, Kearns LS, Mulhall LE, Mackey DA, Hardcastle AJ. RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population. Br J Ophthalmol. 2009 Sep; 93(9):1151-4. PMID: 19429592.
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    272. Carbonaro F, Andrew T, Mackey DA, Young TL, Spector TD, Hammond CJ. Repeated measures of intraocular pressure result in higher heritability and greater power in genetic linkage studies. Invest Ophthalmol Vis Sci. 2009 Nov; 50(11):5115-9. PMID: 19420339.
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    273. Landers JA, Hewitt AW, Dimasi DP, Charlesworth JC, Straga T, Mills RA, Savarirayan R, Mackey DA, Burdon KP, Craig JE. Heritability of central corneal thickness in nuclear families. Invest Ophthalmol Vis Sci. 2009 Sep; 50(9):4087-90. PMID: 19420341.
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    274. O'Neill EC, Mackey DA, Connell PP, Hewitt AW, Danesh-Meyer HV, Crowston JG. The optic nerve head in hereditary optic neuropathies. Nat Rev Neurol. 2009 May; 5(5):277-87. PMID: 19488085.
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    275. Zhang T, Hua R, Xiao W, Burdon KP, Bhattacharya SS, Craig JE, Shang D, Zhao X, Mackey DA, Moore AT, Luo Y, Zhang J, Zhang X. Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract. Hum Mutat. 2009 May; 30(5):E603-11. PMID: 19306328.
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    276. Metlapally R, Li YJ, Tran-Viet KN, Abbott D, Czaja GR, Malecaze F, Calvas P, Mackey D, Rosenberg T, Paget S, Zayats T, Owen MJ, Guggenheim JA, Young TL. COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Invest Ophthalmol Vis Sci. 2009 Sep; 50(9):4080-6. PMID: 19387081.
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    277. Ali M, McKibbin M, Booth A, Parry DA, Jain P, Riazuddin SA, Hejtmancik JF, Khan SN, Firasat S, Shires M, Gilmour DF, Towns K, Murphy AL, Azmanov D, Tournev I, Cherninkova S, Jafri H, Raashid Y, Toomes C, Craig J, Mackey DA, Kalaydjieva L, Riazuddin S, Inglehearn CF. Null mutations in LTBP2 cause primary congenital glaucoma. Am J Hum Genet. 2009 May; 84(5):664-71. PMID: 19361779.
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    278. Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, Young TL. An international collaborative family-based whole-genome linkage scan for high-grade myopia. Invest Ophthalmol Vis Sci. 2009 Jul; 50(7):3116-27. PMID: 19324860.
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    279. Hewitt AW, Sanfilippo P, Ring MA, Craig JE, Mackey DA. Mortality in primary open-angle glaucoma: 'two cupped discs and a funeral'. Eye (Lond). 2010 Jan; 24(1):59-63. PMID: 19247389.
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    280. Sherwin JC, Hewitt AW, Bennett SL, Baird PN, Craig JE, Mackey DA. Primary open angle glaucoma in subjects harbouring the predicted GLC1L haplotype reveals a normotensive phenotype. Clin Exp Ophthalmol. 2009 Mar; 37(2):201-7. PMID: 19723129.
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    281. Sun C, Ponsonby AL, Wong TY, Brown SA, Kearns LS, Cochrane J, MacKinnon JR, Ruddle JB, Hewitt AW, Liew G, Dwyer T, Scurrah K, Mackey DA. Effect of birth parameters on retinal vascular caliber: the Twins Eye Study in Tasmania. Hypertension. 2009 Mar; 53(3):487-93. PMID: 19139377.
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    282. Sun C, Wang JJ, Mackey DA, Wong TY. Retinal vascular caliber: systemic, environmental, and genetic associations. Surv Ophthalmol. 2009 Jan-Feb; 54(1):74-95. PMID: 19171211.
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    283. Widjaja I, Naumann K, Roth U, Wolf N, Mackey D, Dangl JL, Scheel D, Lee J. Combining subproteome enrichment and Rubisco depletion enables identification of low abundance proteins differentially regulated during plant defense. Proteomics. 2009 Jan; 9(1):138-47. PMID: 19053141.
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    284. Ivings L, Towns KV, Matin MA, Taylor C, Ponchel F, Grainger RJ, Ramesar RS, Mackey DA, Inglehearn CF. Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa. Mol Vis. 2008; 14:2357-66. PMID: 19096719.
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    285. Devaney N, Dalimier E, Farrell T, Coburn D, Mackey R, Mackey D, Laurent F, Daly E, Dainty C. Correction of ocular and atmospheric wavefronts: a comparison of the performance of various deformable mirrors. Appl Opt. 2008 Dec 10; 47(35):6550-62. PMID: 19079464.
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    286. Sherwin JC, Hewitt AW, Ruddle JB, Mackey DA. Genetic isolates in ophthalmic diseases. Ophthalmic Genet. 2008 Dec; 29(4):149-61. PMID: 19005985.
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    287. Kim MG, Geng X, Lee SY, Mackey D. The Pseudomonas syringae type III effector AvrRpm1 induces significant defenses by activating the Arabidopsis nucleotide-binding leucine-rich repeat protein RPS2. Plant J. 2009 Feb; 57(4):645-53. PMID: 18980653.
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    288. FitzGerald LM, Patterson B, Thomson R, Polanowski A, Quinn S, Brohede J, Thornton T, Challis D, Mackey DA, Dwyer T, Foote S, Hannan GN, Stankovich J, McKay JD, Dickinson JL. Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease. Eur J Hum Genet. 2009 Mar; 17(3):368-77. PMID: 18830231.
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    289. Burdon KP, Hattersley K, Lachke SA, Laurie KJ, Maas RL, Mackey DA, Craig JE. Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract. Mol Vis. 2008; 14:1799-804. PMID: 18843385.
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    290. Burdon KP, Sharma S, Hewitt AW, McMellon AE, Wang JJ, Mackey DA, Mitchell P, Craig JE. Genetic analysis of the clusterin gene in pseudoexfoliation syndrome. Mol Vis. 2008 Sep 22; 14:1727-36. PMID: 18806885.
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    291. Medland SE, Duffy DL, Wright MJ, Geffen GM, Hay DA, Levy F, van-Beijsterveldt CE, Willemsen G, Townsend GC, White V, Hewitt AW, Mackey DA, Bailey JM, Slutske WS, Nyholt DR, Treloar SA, Martin NG, Boomsma DI. Genetic influences on handedness: data from 25,732 Australian and Dutch twin families. Neuropsychologia. 2009 Jan; 47(2):330-7. PMID: 18824185.
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    292. Ham JH, Majerczak D, Ewert S, Sreerekha MV, Mackey D, Coplin D. WtsE, an AvrE-family type III effector protein of Pantoea stewartii subsp. stewartii, causes cell death in non-host plants. Mol Plant Pathol. 2008 Sep; 9(5):633-43. PMID: 19018993.
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    293. Carbonaro F, Andrew T, Mackey DA, Spector TD, Hammond CJ. Heritability of intraocular pressure: a classical twin study. Br J Ophthalmol. 2008 Aug; 92(8):1125-8. PMID: 18653607.
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    294. Cohn AC, Toomes C, Hewitt AW, Kearns LS, Inglehearn CF, Craig JE, Mackey DA. The natural history of OPA1-related autosomal dominant optic atrophy. Br J Ophthalmol. 2008 Oct; 92(10):1333-6. PMID: 18653586.
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    295. Mackey DA. Gillies lecture: dissecting glaucoma: understanding the molecular risk factors. Clin Exp Ophthalmol. 2008 Jul; 36(5):403-9. PMID: 18925913.
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    296. Kim MG, Kim SY, Kim WY, Mackey D, Lee SY. Responses of Arabidopsis thaliana to challenge by Pseudomonas syringae. Mol Cells. 2008 May 31; 25(3):323-31. PMID: 18483469.
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    297. Carbonaro F, Andrew T, Mackey DA, Spector TD, Hammond CJ. The heritability of corneal hysteresis and ocular pulse amplitude: a twin study. Ophthalmology. 2008 Sep; 115(9):1545-9. PMID: 18439682.
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    298. Craig JE, Friend KL, Gecz J, Rattray KM, Troski M, Mackey DA, Burdon KP. A novel locus for X-linked congenital cataract on Xq24. Mol Vis. 2008 Apr 18; 14:721-6. PMID: 18431456.
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    299. He M, Ge J, Wang D, Zhang J, Hewitt AW, Hur YM, Mackey DA, Foster PJ. Heritability of the iridotrabecular angle width measured by optical coherence tomography in Chinese children: the Guangzhou twin eye study. Invest Ophthalmol Vis Sci. 2008 Apr; 49(4):1356-61. PMID: 18385050.
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    300. Hewitt AW, Mackey DA, Craig JE. Myocilin allele-specific glaucoma phenotype database. Hum Mutat. 2008 Feb; 29(2):207-11. PMID: 17966125.
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    301. Kim MG, Mackey D. Measuring cell-wall-based defenses and their effect on bacterial growth in Arabidopsis. Methods Mol Biol. 2008; 415:443-52. PMID: 18370170.
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    302. He M, Wang D, Zheng Y, Zhang J, Yin Q, Huang W, Mackey DA, Foster PJ. Heritability of anterior chamber depth as an intermediate phenotype of angle-closure in Chinese: the Guangzhou Twin Eye Study. Invest Ophthalmol Vis Sci. 2008 Jan; 49(1):81-6. PMID: 18172078.
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    303. Green CM, Kearns LS, Wu J, Barbour JM, Wilkinson RM, Ring MA, Craig JE, Wong TL, Hewitt AW, Mackey DA. How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania. Clin Exp Ophthalmol. 2007 Dec; 35(9):793-9. PMID: 18173405.
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    304. Hewitt AW, Sharma S, Burdon KP, Wang JJ, Baird PN, Dimasi DP, Mackey DA, Mitchell P, Craig JE. Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people. Hum Mol Genet. 2008 Mar 01; 17(5):710-6. PMID: 18037624.
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    305. Ponsonby AL, Brown SA, Kearns LS, MacKinnon JR, Scotter LW, Cochrane JA, Mackey DA. The association between maternal smoking in pregnancy, other early life characteristics and childhood vision: the Twins Eye Study in Tasmania. Ophthalmic Epidemiol. 2007 Nov-Dec; 14(6):351-9. PMID: 18161608.
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    306. Mackey DA. Central corneal thickness and glaucoma in the Australian Aboriginal population. Clin Exp Ophthalmol. 2007 Nov; 35(8):691-2. PMID: 17997768.
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    307. Zhu G, Hewitt AW, Ruddle JB, Kearns LS, Brown SA, Mackinnon JR, Chen CY, Hammond CJ, Craig JE, Montgomery GW, Martin NG, Mackey DA. Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q. Ophthalmology. 2008 Jun; 115(6):1053-1057.e2. PMID: 17964656.
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    308. Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, Craig JE. Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma. Clin Genet. 2007 Sep; 72(3):255-60. PMID: 17718864.
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    309. Hewitt AW, Kearns LS, Jamieson RV, Williamson KA, van Heyningen V, Mackey DA. PAX6 mutations may be associated with high myopia. Ophthalmic Genet. 2007 Sep; 28(3):179-82. PMID: 17896318.
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    310. Balaratnasingam C, Morgan WH, Nelson J, Mackey DA, Dimasi DP, Lam G. Abnormal iris processes may be a marker of glaucoma gene carrier status in some cases of primary infantile glaucoma. Ophthalmic Genet. 2007 Sep; 28(3):157-62. PMID: 17896314.
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    311. da Cunha L, Sreerekha MV, Mackey D. Defense suppression by virulence effectors of bacterial phytopathogens. Curr Opin Plant Biol. 2007 Aug; 10(4):349-57. PMID: 17625953.
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    312. Burdon KP, Sharma S, Chen CS, Dimasi DP, Mackey DA, Craig JE. A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. Hum Mutat. 2007 Jul; 28(7):742. PMID: 17579362.
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    313. Ham JH, Kim MG, Lee SY, Mackey D. Layered basal defenses underlie non-host resistance of Arabidopsis to Pseudomonas syringae pv. phaseolicola. Plant J. 2007 Aug; 51(4):604-16. PMID: 17573803.
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    314. Hewitt AW, Poulsen JP, Alward WL, Bennett SL, Budde WM, Cooper RL, Craig JE, Fingert JH, Foster PJ, Garway-Heath DF, Green CM, Hammond CJ, Hayreh SS, Jonas JB, Kaufman PL, Miller NR, Morgan WH, Newman NJ, Quigley HA, Samples JR, Spaeth GL, Pesudovs K, Mackey DA. Heritable features of the optic disc: a novel twin method for determining genetic significance. Invest Ophthalmol Vis Sci. 2007 Jun; 48(6):2469-75. PMID: 17525172.
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    315. Hewitt AW, Samples JR, Allingham RR, Järvelä I, Kitsos G, Krishnadas SR, Richards JE, Lichter PR, Petersen MB, Sundaresan P, Wiggs JL, Mackey DA, Wirtz MK. Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds. Mol Vis. 2007 Mar 28; 13:487-92. PMID: 17417609.
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    316. Symons RC, Turakulov R, Foote SJ, Craig JE, McCartney PJ, Mackey DA. No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma. Ophthalmic Genet. 2007 Mar; 28(1):39-41. PMID: 17454746.
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    317. Fingert JH, Alward WL, Kwon YH, Shankar SP, Andorf JL, Mackey DA, Sheffield VC, Stone EM. No association between variations in the WDR36 gene and primary open-angle glaucoma. Arch Ophthalmol. 2007 Mar; 125(3):434-6. PMID: 17353431.
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    318. Cohn AC, Toomes C, Potter C, Towns KV, Hewitt AW, Inglehearn CF, Craig JE, Mackey DA. Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations. Am J Ophthalmol. 2007 Apr; 143(4):656-62. PMID: 17306754.
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    319. Bent AF, Mackey D. Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions. Annu Rev Phytopathol. 2007; 45:399-436. PMID: 17506648.
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    320. Hewitt AW, Bennett SL, Fingert JH, Cooper RL, Stone EM, Craig JE, Mackey DA. The optic nerve head in myocilin glaucoma. Invest Ophthalmol Vis Sci. 2007 Jan; 48(1):238-43. PMID: 17197538.
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    321. Hewitt AW, Bennett SL, Richards JE, Dimasi DP, Booth AP, Inglehearn C, Anwar R, Yamamoto T, Fingert JH, Héon E, Craig JE, Mackey DA. Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals. Arch Ophthalmol. 2007 Jan; 125(1):98-104. PMID: 17210859.
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    322. Bennett SL, Hewitt AW, Poulsen JL, Kearns LS, Morgan JE, Craig JE, Mackey DA. Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees. Arch Ophthalmol. 2007 Jan; 125(1):112-6. PMID: 17210861.
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    323. Mackey DA. Training peer reviewers. Nature. 2006 Oct 19; 443(7113):880. PMID: 17106961.
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    324. Self JE, Ennis S, Collins A, Shawkat F, Harris CM, Mackey DA, Hodgkins PR, Temple IK, Chen X, Lotery AJ. Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3. Mol Vis. 2006 Oct 18; 12:1211-6. PMID: 17102799.
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    325. Hewitt AW, MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA. Familial transmission risk of infantile glaucoma in Australia. Ophthalmic Genet. 2006 Sep; 27(3):93-7. PMID: 17050285.
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    326. Dickinson JL, Sale MM, Passmore A, FitzGerald LM, Wheatley CM, Burdon KP, Craig JE, Tengtrisorn S, Carden SM, Maclean H, Mackey DA. Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. Clin Exp Ophthalmol. 2006 Sep-Oct; 34(7):682-8. PMID: 16970763.
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    327. Andersson MX, Kourtchenko O, Dangl JL, Mackey D, Ellerström M. Phospholipase-dependent signalling during the AvrRpm1- and AvrRpt2-induced disease resistance responses in Arabidopsis thaliana. Plant J. 2006 Sep; 47(6):947-59. PMID: 16925603.
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    328. Mackey D, McFall AJ. MAMPs and MIMPs: proposed classifications for inducers of innate immunity. Mol Microbiol. 2006 Sep; 61(6):1365-71. PMID: 16899081.
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    329. Craig JE, Hewitt AW, Dimasi DP, Howell N, Toomes C, Cohn AC, Mackey DA. The role of the Met98Lys optineurin variant in inherited optic nerve diseases. Br J Ophthalmol. 2006 Nov; 90(11):1420-4. PMID: 16885188.
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    330. Hewitt AW, Dimasi DP, Mackey DA, Craig JE. A Glaucoma Case-control Study of the WDR36 Gene D658G sequence variant. Am J Ophthalmol. 2006 Aug; 142(2):324-5. PMID: 16876519.
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    331. Mimiwati Z, Mackey DA, Craig JE, Mackinnon JR, Rait JL, Liebelt JE, Ayala-Lugo R, Vollrath D, Richards JE. Nail-patella syndrome and its association with glaucoma: a review of eight families. Br J Ophthalmol. 2006 Dec; 90(12):1505-9. PMID: 16825280.
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    332. Wu J, Hewitt AW, Green CM, Ring MA, McCartney PJ, Craig JE, Mackey DA. Disease severity of familial glaucoma compared with sporadic glaucoma. Arch Ophthalmol. 2006 Jul; 124(7):950-4. PMID: 16832017.
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    333. Hewitt AW, Craig JE, Mackey DA. Complex genetics of complex traits: the case of primary open-angle glaucoma. Clin Exp Ophthalmol. 2006 Jul; 34(5):472-84. PMID: 16872346.
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    334. Sharma S, Ang SL, Shaw M, Mackey DA, Gécz J, McAvoy JW, Craig JE. Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions. Hum Mol Genet. 2006 Jun 15; 15(12):1972-83. PMID: 16675532.
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    335. Burdon KP, McKay JD, Wirth MG, Russell-Eggit IM, Bhatti S, Ruddle JB, Dimasi D, Mackey DA, Craig JE. The PITX3 gene in posterior polar congenital cataract in Australia. Mol Vis. 2006 Apr 18; 12:367-71. PMID: 16636655.
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    336. Mackey DA. 2005 Gregg Lecture: Congenital cataract--from rubella to genetics. Clin Exp Ophthalmol. 2006 Apr; 34(3):199-207. PMID: 16671898.
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    337. Hewitt AW, Traill A, Cooper RL, Morgan JE, Mackey DA. Tools for cup:disc ratio measurement. Clin Exp Ophthalmol. 2006 Apr; 34(3):288-9; author reply 289. PMID: 16671916.
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    338. da Cunha L, McFall AJ, Mackey D. Innate immunity in plants: a continuum of layered defenses. Microbes Infect. 2006 Apr; 8(5):1372-81. PMID: 16697674.
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    339. Hewitt AW, Bennett SL, Dimasi DP, Craig JE, Mackey DA. A myocilin Gln368STOP homozygote does not exhibit a more severe glaucoma phenotype than heterozygous cases. Am J Ophthalmol. 2006 Feb; 141(2):402-3. PMID: 16458712.
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    340. Petersen MB, Kitsos G, Samples JR, Gaudette ND, Economou-Petersen E, Sykes R, Rust K, Grigoriadou M, Aperis G, Choi D, Psilas K, Craig JE, Kramer PL, Mackey DA, Wirtz MK. A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability. Invest Ophthalmol Vis Sci. 2006 Feb; 47(2):620-5. PMID: 16431959.
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    341. Charlesworth JC, Stankovich JM, Mackey DA, Craig JE, Haybittel M, Westmore RN, Sale MM. Confirmation of the adult-onset primary open angle glaucoma locus GLC1B at 2cen-q13 in an Australian family. Ophthalmologica. 2006; 220(1):23-30. PMID: 16374045.
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    342. Charlesworth JC, Dyer TD, Stankovich JM, Blangero J, Mackey DA, Craig JE, Green CM, Foote SJ, Baird PN, 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. Invest Ophthalmol Vis Sci. 2005 Oct; 46(10):3723-9. PMID: 16186355.
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    343. Baird PN, Richardson AJ, Mackey DA, Craig JE, Faucher M, Raymond V. A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families. Am J Ophthalmol. 2005 Oct; 140(4):760-2. PMID: 16226543.
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    344. Toh T, Liew SH, MacKinnon JR, Hewitt AW, Poulsen JL, Spector TD, Gilbert CE, Craig JE, Hammond CJ, Mackey DA. Central corneal thickness is highly heritable: the twin eye studies. Invest Ophthalmol Vis Sci. 2005 Oct; 46(10):3718-22. PMID: 16186354.
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    345. Krafchak CM, Pawar H, Moroi SE, Sugar A, Lichter PR, Mackey DA, Mian S, Nairus T, Elner V, Schteingart MT, Downs CA, Kijek TG, Johnson JM, Trager EH, Rozsa FW, Mandal MN, Epstein MP, Vollrath D, Ayyagari R, Boehnke M, Richards JE. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells. Am J Hum Genet. 2005 Nov; 77(5):694-708. PMID: 16252232.
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    346. Dimasi DP, Hewitt AW, Green CM, Mackey DA, Craig JE. Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma. J Med Genet. 2005 Sep; 42(9):e55. PMID: 16140998.
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    347. McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes. Br J Ophthalmol. 2005 Jul; 89(7):831-4. PMID: 15965161.
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    348. Kim MG, da Cunha L, McFall AJ, Belkhadir Y, DebRoy S, Dangl JL, Mackey D. Two Pseudomonas syringae type III effectors inhibit RIN4-regulated basal defense in Arabidopsis. Cell. 2005 Jun 03; 121(5):749-59. PMID: 15935761.
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    349. Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA. Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia. Clin Exp Ophthalmol. 2005 Jun; 33(3):233-9. PMID: 15932525.
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    350. Baird PN, Richardson AJ, Craig JE, Rochtchina E, Mackey DA, Mitchell P. The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye Study. Am J Ophthalmol. 2005 Jun; 139(6):1125-6. PMID: 15953455.
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    351. Toh T, Kearns LS, Scotter LW, Mackey DA. Post-cycloplegia myopic shift in an older population. Ophthalmic Epidemiol. 2005 Jun; 12(3):215-9. PMID: 16036481.
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    352. Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Evidence for a novel glaucoma locus at chromosome 3p21-22. Hum Genet. 2005 Jul; 117(2-3):249-57. PMID: 15906098.
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    353. Smallcombe KA, Kearns LS, Mackey DA. Introducing a new retinitis pigmentosa patient information website. Clin Exp Ophthalmol. 2005 Apr; 33(2):227. PMID: 15807840.
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    354. Cohn AC, Kearns LS, Savarirayan R, Ryan J, Craig JE, Mackey DA. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter. Ophthalmic Genet. 2005 Mar; 26(1):45-53. PMID: 15823925.
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    355. Baird PN, Richardson AJ, Craig JE, Mackey DA, Rochtchina E, Mitchell P. Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye Study. Clin Exp Ophthalmol. 2004 Oct; 32(5):518-22. PMID: 15498064.
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    356. Belkhadir Y, Nimchuk Z, Hubert DA, Mackey D, Dangl JL. Arabidopsis RIN4 negatively regulates disease resistance mediated by RPS2 and RPM1 downstream or independent of the NDR1 signal modulator and is not required for the virulence functions of bacterial type III effectors AvrRpt2 or AvrRpm1. Plant Cell. 2004 Oct; 16(10):2822-35. PMID: 15361584.
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    357. Connell BJ, Wilkinson RM, Barbour JM, Scotter LW, Poulsen JL, Wirth MG, Essex RW, Savarirayan R, Mackey DA. Are Duane syndrome and infantile esotropia allelic? Ophthalmic Genet. 2004 Sep; 25(3):189-98. PMID: 15512995.
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    358. Healey DL, Craig JE, Wilkinson CH, Stone EM, Mackey DA. Attitudes to predictive DNA testing for myocilin glaucoma: experience with a large Australian family. J Glaucoma. 2004 Aug; 13(4):304-11. PMID: 15226659.
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    359. Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance. J Med Genet. 2004 Aug; 41(8):e106. PMID: 15286166.
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    360. Toomes C, Bottomley HM, Scott S, Mackey DA, Craig JE, Appukuttan B, Stout JT, Flaxel CJ, Zhang K, Black GC, Fryer A, Downey LM, Inglehearn CF. Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy. Invest Ophthalmol Vis Sci. 2004 Jul; 45(7):2083-90. PMID: 15223780.
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    361. Yamada K, Chan WM, Andrews C, Bosley TM, Sener EC, Zwaan JT, Mullaney PB, Oztürk BT, Akarsu AN, Sabol LJ, Demer JL, Sullivan TJ, Gottlob I, Roggenkäemper P, Mackey DA, De Uzcategui CE, Uzcategui N, Ben-Zeev B, Traboulsi EI, Magli A, de Berardinis T, Gagliardi V, Awasthi-Patney S, Vogel MC, Rizzo JF, Engle EC. Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). Invest Ophthalmol Vis Sci. 2004 Jul; 45(7):2218-23. PMID: 15223798.
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    362. Morgan L, Pearson M, de Iongh R, Mackey D, van der Wall H, Peters M, Rutland J. Scintigraphic measurement of tracheal mucus velocity in vivo. Eur Respir J. 2004 Apr; 23(4):518-22. PMID: 15083747.
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    363. Yu-Wai-Man P, Howell N, Mackey DA, Nørby S, Rosenberg T, Turnbull DM, Chinnery PF. Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees. J Med Genet. 2004 04; 41(4):e41. PMID: 15060117.
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    364. Toomes C, Bottomley HM, Jackson RM, Towns KV, Scott S, Mackey DA, Craig JE, Jiang L, Yang Z, Trembath R, Woodruff G, Gregory-Evans CY, Gregory-Evans K, Parker MJ, Black GC, Downey LM, Zhang K, Inglehearn CF. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. Am J Hum Genet. 2004 Apr; 74(4):721-30. PMID: 15024691.
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    365. MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA. Primary infantile glaucoma in an Australian population. Clin Exp Ophthalmol. 2004 Feb; 32(1):14-8. PMID: 14746584.
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    366. Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Investigation of crystallin genes in familial cataract, and report of two disease associated mutations. Br J Ophthalmol. 2004 Jan; 88(1):79-83. PMID: 14693780.
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    367. Burdon KP, Wilkinson RM, Barbour JM, Dickinson JL, Stankovich JM, Mackey DA, Sale MM. Investigation of albinism genes in congenital esotropia. Mol Vis. 2003 Dec 16; 9:710-4. PMID: 14685142.
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    368. Mackey DA, Craig JE. Predictive DNA testing for glaucoma: reality in 2003. Ophthalmol Clin North Am. 2003 Dec; 16(4):639-45. PMID: 14741004.
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    369. Craig JE, Clark JB, McLeod JL, Kirkland MA, Grant G, Elder JE, Toohey MG, Kowal L, Savoia HF, Chen C, Roberts S, Wirth MG, Mackey DA. Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations. Arch Ophthalmol. 2003 Dec; 121(12):1753-61. PMID: 14662596.
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    370. Alward WL, Kwon YH, Kawase K, Craig JE, Hayreh SS, Johnson AT, Khanna CL, Yamamoto T, Mackey DA, Roos BR, Affatigato LM, Sheffield VC, Stone EM. Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma. Am J Ophthalmol. 2003 Nov; 136(5):904-10. PMID: 14597044.
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    371. Burdon KP, McKay JD, Sale MM, Russell-Eggitt IM, Mackey DA, Wirth MG, Elder JE, Nicoll A, Clarke MP, FitzGerald LM, Stankovich JM, Shaw MA, Sharma S, Gajovic S, Gruss P, Ross S, Thomas P, Voss AK, Thomas T, Gécz J, 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. Am J Hum Genet. 2003 Nov; 73(5):1120-30. PMID: 14564667.
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    372. Ruddle JB, Mackey DA, Downie NA. Clinical progression of keratoconus following a Vth nerve palsy. Clin Exp Ophthalmol. 2003 Aug; 31(4):363-5. PMID: 12880466.
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    373. Mackey DA, Healey DL, Fingert JH, Coote MA, Wong TL, Wilkinson CH, McCartney PJ, Rait JL, de Graaf AP, Stone EM, Craig JE. Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation. Arch Ophthalmol. 2003 Aug; 121(8):1172-80. PMID: 12912696.
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    374. Wilkinson CH, van der Straaten D, Craig JE, Coote MA, McCartney PJ, Stankovich J, Stone EM, Mackey DA. Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriers. J Glaucoma. 2003 Jun; 12(3):237-42. PMID: 12782842.
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    375. Howell N, Herrnstadt C, Shults C, Mackey DA. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background. Am J Med Genet A. 2003 Jun 01; 119A(2):147-51. PMID: 12749053.
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    376. Howell N, Oostra RJ, Bolhuis PA, Spruijt L, Clarke LA, Mackey DA, Preston G, Herrnstadt C. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy. Am J Hum Genet. 2003 Jun; 72(6):1460-9. PMID: 12736867.
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    377. Mackey DA, Héon E, Webster AR. Predictive DNA testing in ophthalmology. Br J Ophthalmol. 2003 May; 87(5):633. PMID: 12714411.
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    378. Mackey DA. Overview. Predictive DNA testing in ophthalmology. Br J Ophthalmol. 2003 May; 87(5):637-8. PMID: 12714413.
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    379. Ng WT, Toohey MG, Mulhall L, Mackey DA. Pigmentary retinopathy, macular oedema, and abnormal ERG with mitotane treatment. Br J Ophthalmol. 2003 Apr; 87(4):500-1. PMID: 12642318.
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    380. Mackey DA, Fingert JH, Luzhansky JZ, McCluskey PJ, Howell N, Hall AJ, Pierce AB, Hoy JF. Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus. Eye (Lond). 2003 Apr; 17(3):312-7. PMID: 12724691.
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    381. Mackey D, Belkhadir Y, Alonso JM, Ecker JR, Dangl JL. Arabidopsis RIN4 is a target of the type III virulence effector AvrRpt2 and modulates RPS2-mediated resistance. Cell. 2003 Feb 07; 112(3):379-89. PMID: 12581527.
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    382. Howell N, Smejkal CB, Mackey DA, Chinnery PF, Turnbull DM, Herrnstadt C. The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates. Am J Hum Genet. 2003 Mar; 72(3):659-70. PMID: 12571803.
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    383. Howell N, Miller NR, Mackey DA, Arnold A, Herrnstadt C, Williams IM, Kubacka I. Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations. J Neuroophthalmol. 2002 Dec; 22(4):262-9. PMID: 12464729.
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    384. Steinberg RB, Liu SS, Wu CL, Mackey DC, Grass JA, Ahlén K, Jeppsson L. Comparison of ropivacaine-fentanyl patient-controlled epidural analgesia with morphine intravenous patient-controlled analgesia for perioperative analgesia and recovery after open colon surgery. J Clin Anesth. 2002 Dec; 14(8):571-7. PMID: 12565114.
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    385. Baird PN, Craig JE, Richardson AJ, Ring MA, Sim P, Stanwix S, Foote SJ, Mackey DA. Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilin. Hum Genet. 2003 Feb; 112(2):110-6. PMID: 12522550.
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    386. Vickers JC, Craig JE, Stankovich J, McCormack GH, West AK, Dickinson JL, McCartney PJ, Coote MA, Healey DL, Mackey DA. The apolipoprotein epsilon4 gene is associated with elevated risk of normal tension glaucoma. Mol Vis. 2002 Oct 14; 8:389-93. PMID: 12379839.
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    387. Sale MM, Craig JE, Charlesworth JC, FitzGerald LM, Hanson IM, Dickinson JL, Matthews SJ, Heyningen Vv Vv, Fingert JH, Mackey DA. Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene. Hum Mutat. 2002 Oct; 20(4):322. PMID: 12325030.
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    388. Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Retinopathy of prematurity: recent advances in our understanding. Arch Dis Child Fetal Neonatal Ed. 2002 Sep; 87(2):F78-82. PMID: 12193510.
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    389. Marchbank NJ, Craig JE, Leek JP, Toohey M, Churchill AJ, Markham AF, Mackey DA, Toomes C, Inglehearn CF. Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease. J Med Genet. 2002 Aug; 39(8):e47. PMID: 12161614.
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    390. Wirth MG, Russell-Eggitt IM, Craig JE, Elder JE, Mackey DA. Aetiology of congenital and paediatric cataract in an Australian population. Br J Ophthalmol. 2002 Jul; 86(7):782-6. PMID: 12084750.
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    391. Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Retinopathy of prematurity: recent advances in our understanding. Br J Ophthalmol. 2002 Jun; 86(6):696-700. PMID: 12034695.
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    392. Keen TJ, Hims MM, McKie AB, Moore AT, Doran RM, Mackey DA, Mansfield DC, Mueller RF, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF. Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa. Eur J Hum Genet. 2002 Apr; 10(4):245-9. PMID: 12032732.
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    393. Fullerton J, Paprocki P, Foote S, Mackey DA, Williamson R, Forrest S. Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia. Hum Genet. 2002 May; 110(5):462-70. PMID: 12073017.
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    394. Mackey DA, Chan WM, Chan C, Gillies WE, Brooks AM, O'Day J, Engle EC. Congenital fibrosis of the vertically acting extraocular muscles maps to the FEOM3 locus. Hum Genet. 2002 May; 110(5):510-2. PMID: 12073023.
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    395. Mackey D, Holt BF, Wiig A, Dangl JL. RIN4 interacts with Pseudomonas syringae type III effector molecules and is required for RPM1-mediated resistance in Arabidopsis. Cell. 2002 Mar 22; 108(6):743-54. PMID: 11955429.
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    396. McLean IM, Mueller E, Buttery RG, Mackey DA. Visual field assessment and the Austroads driving standard. Clin Exp Ophthalmol. 2002 Feb; 30(1):3-7. PMID: 11885792.
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    397. Mitchell AE, Elder JE, Mackey DA, Waters KD, Ashley DM. Visual improvement despite radiologically stable disease after treatment with carboplatin in children with progressive low-grade optic/thalamic gliomas. J Pediatr Hematol Oncol. 2001 Dec; 23(9):572-7. PMID: 11902299.
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    398. MacKinnon JR, Challis DR, Mackey DA. Is it not in my records, doctor? Clin Exp Ophthalmol. 2001 Dec; 29(6):440-1. PMID: 11778820.
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    399. Craig JE, Baird PN, Healey DL, McNaught AI, McCartney PJ, Rait JL, Dickinson JL, Roe L, Fingert JH, Stone EM, Mackey DA. Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier. Ophthalmology. 2001 Sep; 108(9):1607-20. PMID: 11535458.
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    400. Howell N, Herrnstadt C, Mackey DA. Different patterns of expansion/contraction during the evolution of an mtDNA simple repeat. Mol Biol Evol. 2001 Aug; 18(8):1593-6. PMID: 11470851.
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    401. McKie AB, McHale JC, Keen TJ, Tarttelin EE, Goliath R, van Lith-Verhoeven JJ, Greenberg J, Ramesar RS, Hoyng CB, Cremers FP, Mackey DA, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF. Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13). Hum Mol Genet. 2001 Jul 15; 10(15):1555-62. PMID: 11468273.
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    402. Toomes C, Marchbank NJ, Mackey DA, Craig JE, Newbury-Ecob RA, Bennett CP, Vize CJ, Desai SP, Black GC, Patel N, Teimory M, Markham AF, Inglehearn CF, Churchill AJ. Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy. Hum Mol Genet. 2001 Jun 15; 10(13):1369-78. PMID: 11440989.
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    403. Baird PN, Dickinson J, Craig JE, Mackey DA. The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucoma. Am J Ophthalmol. 2001 Apr; 131(4):510-1. PMID: 11292420.
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    404. Dickinson JL, Sale MM, Craig JE, Mackey DA. Laboratory methods in ophthalmic genetics: obtaining DNA from patients. Ophthalmic Genet. 2001 Mar; 22(1):49-60. PMID: 11262650.
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    405. Nishimura DY, Searby CC, Alward WL, Walton D, Craig JE, Mackey DA, Kawase K, Kanis AB, Patil SR, Stone EM, Sheffield VC. A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye. Am J Hum Genet. 2001 Feb; 68(2):364-72. PMID: 11170889.
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    406. Fingert JH, Clark AF, Craig JE, Alward WL, Snibson GR, McLaughlin M, Tuttle L, Mackey DA, Sheffield VC, Stone EM. Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension. Invest Ophthalmol Vis Sci. 2001 Jan; 42(1):145-52. PMID: 11133859.
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    407. Ott MC, Meschia JF, Mackey DC, Brodersen MP, Burger C, Echols JD, Fenton DS. Cerebral embolization presenting as delayed, severe obtundation in the postanesthesia care unit after total hip arthroplasty. Mayo Clin Proc. 2000 Nov; 75(11):1209-13. PMID: 11075754.
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    408. McNaught AI, Allen JG, Healey DL, McCartney PJ, Coote MA, Wong TL, Craig JE, Green CM, Rait JL, Mackey DA. Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in Tasmania. Arch Ophthalmol. 2000 Jul; 118(7):900-4. PMID: 10900101.
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    409. Russell-Eggitt IM, Mackey DA, Taylor DS, Timms C, Walker JW. Vigabatrin-associated visual field defects in children. Eye (Lond). 2000 Jun; 14 ( Pt 3A):334-9. PMID: 11026995.
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    410. Holt BF, Mackey D, Dangl JL. Recognition of pathogens by plants. Curr Biol. 2000 Jan 13; 10(1):R5-7. PMID: 10660284.
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    411. Mitchell P, Cumming RG, Mackey DA. Inhaled corticosteroids, family history, and risk of glaucoma. Ophthalmology. 1999 Dec; 106(12):2301-6. PMID: 10599661.
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    412. Simm RM, Fingert JH, Craig JE, McNaught AI, Mackey DA. Normal range of hearing associated with myocilin Thr377Met. Ophthalmic Genet. 1999 Sep; 20(3):205-7. PMID: 10610189.
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    413. Stone EM, Lotery AJ, Munier FL, Héon E, Piguet B, Guymer RH, Vandenburgh K, Cousin P, Nishimura D, Swiderski RE, Silvestri G, Mackey DA, Hageman GS, Bird AC, Sheffield VC, Schorderet DF. A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Nat Genet. 1999 Jun; 22(2):199-202. PMID: 10369267.
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    414. Fingert JH, Héon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey DA, Alward WL, Sheffield VC, Stone EM. Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Hum Mol Genet. 1999 May; 8(5):899-905. PMID: 10196380.
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    415. Craig JE, Mackey DA. Glaucoma genetics: where are we? Where will we go? Curr Opin Ophthalmol. 1999 Apr; 10(2):126-34. PMID: 10537763.
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    416. Mackey D, Sugden B. Applications of oriP plasmids and their mode of replication. Methods Enzymol. 1999; 306:308-28. PMID: 10432462.
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    417. Carden SM, Colville DJ, Davidson AJ, McKenzie IM, Mackey DA, McKenzie J, Elder JE. Adjunctive intra-operative local anaesthesia in paediatric strabismus surgery: a randomized controlled trial. Aust N Z J Ophthalmol. 1998 Nov; 26(4):289-97. PMID: 9843256.
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    418. Howell N, Mackey DA. Low-penetrance branches in matrilineal pedigrees with Leber hereditary optic neuropathy. Am J Hum Genet. 1998 Oct; 63(4):1220-4. PMID: 9867707.
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    419. Alward WL, Fingert JH, Coote MA, Johnson AT, Lerner SF, Junqua D, Durcan FJ, McCartney PJ, Mackey DA, Sheffield VC, Stone EM. Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A) N Engl J Med. 1998 Apr 09; 338(15):1022-7. PMID: 9535666.
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    420. Mackey D, Oostra RJ, Rosenberg T, Nikoskelainen E, Poulton J, Barratt T, Bolhuis P, Norby S, Savontaus ML, Chan C, Howell N. Reply to Hofmann et al. Am J Hum Genet. 1998 Feb; 62(2):492-5. PMID: 9463338.
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    421. Howell N, Bogolin C, Jamieson R, Marenda DR, Mackey DA. mtDNA mutations that cause optic neuropathy: how do we know? Am J Hum Genet. 1998 Jan; 62(1):196-202. PMID: 9443868.
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    422. Mulroy MF, Neal JM, Mackey DC, Harrington BE. 2-Chloroprocaine and bupivacaine are unreliable indicators of intravascular injection in the premedicated patient. Reg Anesth Pain Med. 1998 Jan-Feb; 23(1):9-13. PMID: 9552772.
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    423. Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Identification of a gene that causes primary open angle glaucoma. Science. 1997 Jan 31; 275(5300):668-70. PMID: 9005853.
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    424. Coote MA, McCartney PJ, Wilkinson RM, Mackey DA. The 'GIST' score: ranking glaucoma for genetic studies. Glaucoma Inheritance Study of Tasmania. Ophthalmic Genet. 1996 Dec; 17(4):199-208. PMID: 9010871.
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    425. Sack J, Healey DL, de Graaf AP, Wilkinson RM, Wilkinson CH, Barbour JM, Coote MA, McCartney PJ, Rait JL, Cooper RL, Ring MA, Mackey DA. The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (GIST). Ophthalmic Genet. 1996 Dec; 17(4):209-14. PMID: 9010872.
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    426. Mackey DC, Grossman AR. Narcotic prescription for pain management in Florida: the physician and the law. J Fla Med Assoc. 1996 Dec; 83(10):673-4. PMID: 9019055.
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    427. Howell N, Kubacka I, Mackey DA. How rapidly does the human mitochondrial genome evolve? Am J Hum Genet. 1996 Sep; 59(3):501-9. PMID: 8751850.
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    428. Mackey DA, Oostra RJ, Rosenberg T, Nikoskelainen E, Bronte-Stewart J, Poulton J, Harding AE, Govan G, Bolhuis PA, Norby S. Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy. Am J Hum Genet. 1996 Aug; 59(2):481-5. PMID: 8755941.
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    429. Chan C, Mackey DA, Byrne E. Sporadic Leber hereditary optic neuropathy in Australia and New Zealand. Aust N Z J Ophthalmol. 1996 Feb; 24(1):7-14. PMID: 8742999.
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    430. Waun JE. Payment for routine postoperative patient-controlled analgesia. Anesthesiology. 1996 Jan; 84(1):237-8. PMID: 8572344.
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    431. Mackey DA. Recent advances in hereditary disease and neuro-ophthalmology. Curr Opin Ophthalmol. 1995 Dec; 6(6):48-53. PMID: 10160419.
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    432. Mackey D, Middleton T, Sugden B. Multiple regions within EBNA1 can link DNAs. J Virol. 1995 Oct; 69(10):6199-208. PMID: 7666521.
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    433. Liu SS, Carpenter RL, Mackey DC, Thirlby RC, Rupp SM, Shine TS, Feinglass NG, Metzger PP, Fulmer JT, Smith SL. Effects of perioperative analgesic technique on rate of recovery after colon surgery. Anesthesiology. 1995 Oct; 83(4):757-65. PMID: 7574055.
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    434. Mackey DC, Ebener MK, Howe BL. Patient-controlled analgesia and the acute pain service in the United States: Health-Care Financing Administration policy is impeding optimal patient-controlled analgesia management. Anesthesiology. 1995 Aug; 83(2):433-4. PMID: 7631973.
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    435. Thompson RC, Mackey DC, Lane GE, Blackshear JL, Shine TS, Ebener MK, Safford RE. Improved detection of silent cardiac ischemia with a 12-lead portable microprocessor-driven real-time electrocardiographic monitor. Mayo Clin Proc. 1995 May; 70(5):434-42. PMID: 7731252.
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    436. Howell N, Kubacka I, Halvorson S, Howell B, McCullough DA, Mackey D. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees. Genetics. 1995 May; 140(1):285-302. PMID: 7635294.
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    437. Sokolove PE, Mackey D, Wiles J, Lewis RJ. Exposure of emergency department personnel to tuberculosis: PPD testing during an epidemic in the community. Ann Emerg Med. 1994 Sep; 24(3):418-21. PMID: 8080139.
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    438. Mackey D. Misconceptions about Leber hereditary optic neuropathy. Med J Aust. 1994 Jun 20; 160(12):763-6. PMID: 8208192.
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    439. Mackey D, Howell N. Tobacco amblyopia. Am J Ophthalmol. 1994 Jun 15; 117(6):817-9. PMID: 8198176.
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    440. Mackey DA. Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy. Eye (Lond). 1994; 8 ( Pt 4):431-6. PMID: 7821467.
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    441. Mackey DA. Leber's hereditary optic neuropathy. Is it a disease of northern Europe and Asia? Ophthalmic Paediatr Genet. 1993 Sep; 14(3):105-7. PMID: 8115116.
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    442. Brown DL, Mackey DC. Management of postoperative pain: influence of anesthetic and analgesic choice. Mayo Clin Proc. 1993 Aug; 68(8):768-77. PMID: 8392654.
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    443. Mackey D, Nasioulas S, Forrest S. Finger prick blood testing in Leber hereditary optic neuropathy. Br J Ophthalmol. 1993 May; 77(5):311-2. PMID: 8318469.
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    444. Mackey D. Blindness in offspring of women blinded by Leber's hereditary optic neuropathy. Lancet. 1993 Apr 17; 341(8851):1020-1. PMID: 8096896.
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    445. Howell N, Kubacka I, Halvorson S, Mackey D. Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene. Genetics. 1993 Jan; 133(1):133-6. PMID: 8417984.
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    446. Mackey D, Howell N. A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology. Am J Hum Genet. 1992 Dec; 51(6):1218-28. PMID: 1463007.
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    447. Mackey DA, Buttery RG. Leber hereditary optic neuropathy in Australia. Aust N Z J Ophthalmol. 1992 Aug; 20(3):177-84. PMID: 1449769.
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    448. Bower SP, Hawley I, Mackey DA. Cardiac arrhythmia and Leber's hereditary optic neuropathy. Lancet. 1992 Jun 06; 339(8806):1427-8. PMID: 1350847.
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    449. Howell N, McCullough DA, Kubacka I, Halvorson S, Mackey D. The sequence of human mtDNA: the question of errors versus polymorphisms. Am J Hum Genet. 1992 Jun; 50(6):1333-40. PMID: 1598914.
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    450. Howell N, Bindoff LA, McCullough DA, Kubacka I, Poulton J, Mackey D, Taylor L, Turnbull DM. Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees. Am J Hum Genet. 1991 Nov; 49(5):939-50. PMID: 1928099.
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    451. Orr MB, Mackey D, McNally K. A pilot study of the effects of mechanical shortening of ewes' incisors (bite correction) on body weight and the development of periodontal disease. N Z Vet J. 1991 Sep; 39(3):108-10. PMID: 16031632.
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    452. Mackey DA, Buttery RG, Wise GM, Denton MJ. Description of X-linked megalocornea with identification of the gene locus. Arch Ophthalmol. 1991 Jun; 109(6):829-33. PMID: 2043071.
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    453. Holland MS, Gammill BG, Mackey DC. AANA Journal course: new technologies in anesthesia: update for nurse anesthetists--alternatives for postoperative pain management. AANA J. 1990 Jun; 58(3):201-11. PMID: 2378236.
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    454. Chen JD, Mackey D, Fuller H, Serravalle S, Olsson J, Denton MJ. X-linked megalocornea: close linkage to DXS87 and DXS94. Hum Genet. 1989 Oct; 83(3):292-4. PMID: 2571565.
      View in: PubMed
    455. Kopacz DJ, Carpenter RL, Mackey DC. Effect of ropivacaine on cutaneous capillary blood flow in pigs. Anesthesiology. 1989 Jul; 71(1):69-74. PMID: 2751142.
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    456. Mackey DC, Carpenter RL, Thompson GE, Brown DL, Bodily MN. Bradycardia and asystole during spinal anesthesia: a report of three cases without morbidity. Anesthesiology. 1989 May; 70(5):866-8. PMID: 2655502.
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    457. Carpenter RL, Kopacz DJ, Mackey DC. Accuracy of laser Doppler capillary flow measurements for predicting blood loss from skin incisions in pigs. Anesth Analg. 1989 Mar; 68(3):308-11. PMID: 2645809.
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    458. Bendl BJ, Mackey D, Al-Saati F, Sheth KV, Ofole SN, Bailey TM. Mycetoma in Saudi Arabia. J Trop Med Hyg. 1987 Apr; 90(2):51-9. PMID: 3550122.
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    459. Kingston ME, Mackey D. Skin clues in the diagnosis of life-threatening infections. Rev Infect Dis. 1986 Jan-Feb; 8(1):1-11. PMID: 3513282.
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    460. Mackey D, Dowling F, Sheehan J. An evaluation of the prophylactic value of rotary beds on the incidence of deep vein thrombosis following total hip replacement. Ir Med J. 1983 Jul; 76(7):305-7. PMID: 6885325.
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    461. Mackey D. A private health centre for young people. Aust Fam Physician. 1980 Dec; 9(12):869-73. PMID: 7213226.
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    462. Glycopyrrolate does not prevent bradycardia during spinal anesthesia. Regional Anesthesia. 14:95.
    463. Sacroiliac block of therapeutic but non diagnostic value. Regional Anesthesia. 20:16.
    464. Erratum. Anesthesiology. 84:756.
    465. Incidence of bradycardia during spinal anesthesia. Regional Anesthesia. 14:8.
    466. 2-chloroprocaine and bupivacaine as indicators of intravascular injection. Regional Anesthesia. 13:4-5.
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