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Papers authored by Mackey DA

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Repeated measures of intraocular pressure result in higher heritability and greater power in genetic linkage studies.

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Carbonaro F, Andrew T, Mackey DA, Young TL, Spector TD, and Hammond CJ

Investigative ophthalmology & visual science 50(11):5115-9, 2009 Nov - Who cited this? | PubMed ID: 19420339 | Fulltext

Quantitative genetic analysis of the retinal vascular caliber: the Australian twins eye study.

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Sun C, Zhu G, Wong TY, Hewitt AW, Ruddle JB, Hodgson L, Montgomery GW, Young TL, Hammond CJ, Craig JE, Martin NG, He M, and Mackey DA

Hypertension 54(4):788-95, 2009 Oct - Who cited this? | PubMed ID: 19687348 | Fulltext

Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins.

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Mackey DA, Mackinnon JR, Brown SA, Kearns LS, Ruddle JB, Sanfilippo PG, Sun C, Hammond CJ, Young TL, Martin NG, and Hewitt AW

Twin research and human genetics : the official journal of the International Society for Twin Studies 12(5):441-54, 2009 Oct - Who cited this? | PubMed ID: 19803772 | Fulltext

RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population.

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Ruddle JB, Ebenezer ND, Kearns LS, Mulhall LE, Mackey DA, and Hardcastle AJ

The British journal of ophthalmology 93(9):1151-4, 2009 Sep - Who cited this? | PubMed ID: 19429592 | Fulltext

Heritability of central corneal thickness in nuclear families.

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Landers JA, Hewitt AW, Dimasi DP, Charlesworth JC, Straga T, Mills RA, Savarirayan R, Mackey DA, Burdon KP, and Craig JE

Investigative ophthalmology & visual science 50(9):4087-90, 2009 Sep - Who cited this? | PubMed ID: 19420341 | Fulltext

Isolated corneal opacification and microphthalmia: a suspected warfarin embryopathy.

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Downie AC, Mackey DA, and Vote BJ

Clinical & experimental ophthalmology 37(6):624-5, 2009 Aug - Who cited this? | PubMed ID: 19702715 | Fulltext

An international collaborative family-based whole-genome linkage scan for high-grade myopia.

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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, and Young TL

Investigative ophthalmology & visual science 50(7):3116-27, 2009 Jul - Who cited this? | PubMed ID: 19324860 | Fulltext

Optic disc morphology--rethinking shape.

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Sanfilippo PG, Cardini A, Hewitt AW, Crowston JG, and Mackey DA

Progress in retinal and eye research 28(4):227-48, 2009 Jul - Who cited this? | PubMed ID: 19520180 | Fulltext

The 'I' in personalized genetics: 2008 Ian Constable lecture.

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Mackey DA

Clinical & experimental ophthalmology 37(5):434-43, 2009 Jul - Who cited this? | PubMed ID: 19624338 | Fulltext

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract.

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Zhang T, Hua R, Xiao W, Burdon KP, Bhattacharya SS, Craig JE, Shang D, Zhao X, Mackey DA, Moore AT, Luo Y, Zhang J, and Zhang X

Human mutation 30(5):E603-11, 2009 May - Who cited this? | PubMed ID: 19306328 | Fulltext

Null mutations in LTBP2 cause primary congenital glaucoma.

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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,

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American journal of human genetics 84(5):664-71, 2009 May - Who cited this? | PubMed ID: 19361779 | Fulltext

The optic nerve head in hereditary optic neuropathies.

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O'Neill EC, Mackey DA, Connell PP, Hewitt AW, Danesh-Meyer HV, and Crowston JG

Nature reviews. Neurology 5(5):277-87, 2009 May - Who cited this? | PubMed ID: 19488085 | Fulltext

Effect of birth parameters on retinal vascular caliber: the twins eye study in tasmania.

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Sun C, Ponsonby AL, Wong TY, Brown SA, Kearns LS, Cochrane J, Mackinnon JR, Ruddle JB, Hewitt AW, Liew G, Dwyer T, Scurrah K, and Mackey DA

Hypertension 53(3):487-93, 2009 Mar - Who cited this? | PubMed ID: 19139377 | Fulltext

Primary open angle glaucoma in subjects harbouring the predicted GLC1L haplotype reveals a normotensive phenotype.

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Sherwin JC, Hewitt AW, Bennett SL, Baird PN, Craig JE, and Mackey DA

Clinical & experimental ophthalmology 37(2):201-7, 2009 Mar - Who cited this? | PubMed ID: 19723129 | Fulltext

Retinal vascular caliber: systemic, environmental, and genetic associations.

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Sun C, Wang JJ, Mackey DA, and Wong TY

Survey of ophthalmology 54(1):74-95, 2009 - Who cited this? | PubMed ID: 19171211 | Fulltext

Quality of DNA extracted from mouthwashes.

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Zayats T, Young TL, Mackey DA, Malecaze F, Calvas P, and Guggenheim JA

PLoS ONE 4(7):e6165, 2009 - Who cited this? | PubMed ID: 19582144 | Fulltext

Genetic isolates in ophthalmic diseases.

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Sherwin JC, Hewitt AW, Ruddle JB, and Mackey DA

Ophthalmic genetics 29(4):149-61, 2008 Dec - Who cited this? | PubMed ID: 19005985 | Fulltext

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease.

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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, and Dickinson JL

European journal of human genetics : EJHG, 2008 Oct 1 - Who cited this? | PubMed ID: 18830231 | Fulltext

The natural history of OPA1-related autosomal dominant optic atrophy.

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Cohn AC, Toomes C, Hewitt AW, Kearns LS, Inglehearn CF, Craig JE, and Mackey DA

The British journal of ophthalmology 92(10):1333-6, 2008 Oct - Who cited this? | PubMed ID: 18653586 | Fulltext

Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families.

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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,

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Neuropsychologia, 2008 Sep 9 - Who cited this? | PubMed ID: 18824185 | Fulltext

The heritability of corneal hysteresis and ocular pulse amplitude a twin study.

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Carbonaro F, Andrew T, Mackey DA, Spector TD, and Hammond CJ

Ophthalmology 115(9):1545-9, 2008 Sep - Who cited this? | PubMed ID: 18439682 | Fulltext

Heritability of intraocular pressure: a classical twin study.

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Carbonaro F, Andrew T, Mackey DA, Spector TD, and Hammond CJ

The British journal of ophthalmology 92(8):1125-8, 2008 Aug - Who cited this? | PubMed ID: 18653607 | Fulltext

Gillies Lecture: Dissecting glaucoma: understanding the molecular risk factors.

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Mackey DA

Clinical & experimental ophthalmology 36(5):403-9, 2008 Jul - Who cited this? | PubMed ID: 18925913 | Fulltext

Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q.

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Zhu G, Hewitt AW, Ruddle JB, Kearns LS, Brown SA, Mackinnon JR, Chen CY, Hammond CJ, Craig JE, Montgomery GW, Martin NG, and Mackey DA

Ophthalmology 115(6):1053-1057.e2, 2008 Jun - Who cited this? | PubMed ID: 17964656 | Fulltext

Heritability of the iridotrabecular angle width measured by optical coherence tomography in chinese children: the guangzhou twin eye study.

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He M, Ge J, Wang D, Zhang J, Hewitt AW, Hur YM, Mackey DA, and Foster PJ

Investigative ophthalmology & visual science 49(4):1356-61, 2008 Apr - Who cited this? | PubMed ID: 18385050 | Fulltext

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.

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Hewitt AW, Sharma S, Burdon KP, Wang JJ, Baird PN, Dimasi DP, Mackey DA, Mitchell P, and Craig JE

Human molecular genetics 17(5):710-6, 2008 Mar 1 - Who cited this? | PubMed ID: 18037624 | Fulltext

Myocilin allele-specific glaucoma phenotype database.

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Hewitt AW, Mackey DA, and Craig JE

Human mutation 29(2):207, 2008 Feb - Who cited this? | PubMed ID: 17966125 | Fulltext

Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.

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Burdon KP, Sharma S, Hewitt AW, McMellon AE, Wang JJ, Mackey DA, Mitchell P, and Craig JE

Molecular vision 14:1727, 2008 - Who cited this? | PubMed ID: 18806885 | Fulltext

Heritability of anterior chamber depth as an intermediate phenotype of angle-closure in chinese: the guangzhou twin eye study.

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He M, Wang D, Zheng Y, Zhang J, Yin Q, Huang W, Mackey DA, and Foster PJ

Investigative ophthalmology & visual science 49(1):81-6, 2008 Jan - Who cited this? | PubMed ID: 18172078 | Fulltext

A novel locus for X-linked congenital cataract on Xq24.

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Craig JE, Friend KL, Gecz J, Rattray KM, Troski M, Mackey DA, and Burdon KP

Molecular vision 14:721-6, 2008 - Who cited this? | PubMed ID: 18431456 | Fulltext

Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.

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Burdon KP, Hattersley K, Lachke SA, Laurie KJ, Maas RL, Mackey DA, and Craig JE

Molecular vision 14:1799-804, 2008 - Who cited this? | PubMed ID: 18843385 | Fulltext

Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa.

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Ivings L, Towns KV, Matin MA, Taylor C, Ponchel F, Grainger RJ, Ramesar RS, Mackey DA, and Inglehearn CF

Molecular vision 14:2357-66, 2008 - Who cited this? | PubMed ID: 19096719 | Fulltext

How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania.

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Green CM, Kearns LS, Wu J, Barbour JM, Wilkinson RM, Ring MA, Craig JE, Wong TL, Hewitt AW, and Mackey DA

Clinical & experimental ophthalmology 35(9):793-9, 2007 Dec - Who cited this? | PubMed ID: 18173405 | Fulltext

Central corneal thickness and glaucoma in the Australian Aboriginal population.

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Mackey DA

Clinical & experimental ophthalmology 35(8):691-2, 2007 Nov - Who cited this? | PubMed ID: 17997768 | Fulltext

Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma.

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Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, and Craig JE

Clinical genetics 72(3):255-60, 2007 Sep - Who cited this? | PubMed ID: 17718864 | Fulltext

Abnormal iris processes may be a marker of glaucoma gene carrier status in some cases of primary infantile glaucoma.

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Balaratnasingam C, Morgan WH, Nelson J, Mackey DA, Dimasi DP, and Lam G

Ophthalmic genetics 28(3):157-62, 2007 Sep - Who cited this? | PubMed ID: 17896314 | Fulltext

PAX6 mutations may be associated with high myopia.

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Hewitt AW, Kearns LS, Jamieson RV, Williamson KA, van Heyningen V, and Mackey DA

Ophthalmic genetics 28(3):179-82, 2007 Sep - Who cited this? | PubMed ID: 17896318 | Fulltext

A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.

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Burdon KP, Sharma S, Chen CS, Dimasi DP, Mackey DA, and Craig JE

Human mutation 28(7):742, 2007 Jul - Who cited this? | PubMed ID: 17579362 | Fulltext

Heritable features of the optic disc: a novel twin method for determining genetic significance.

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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,

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Investigative ophthalmology & visual science 48(6):2469-75, 2007 Jun - Who cited this? | PubMed ID: 17525172 | Fulltext

Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations.

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Cohn AC, Toomes C, Potter C, Towns KV, Hewitt AW, Inglehearn CF, Craig JE, and Mackey DA

American journal of ophthalmology 143(4):656-62, 2007 Apr - Who cited this? | PubMed ID: 17306754 | Fulltext

No association between variations in the WDR36 gene and primary open-angle glaucoma.

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Fingert JH, Alward WL, Kwon YH, Shankar SP, Andorf JL, Mackey DA, Sheffield VC, and Stone EM

Archives of ophthalmology 125(3):434-6, 2007 Mar - Who cited this? | PubMed ID: 17353431 | Fulltext

No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma.

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Symons RC, Turakulov R, Foote SJ, Craig JE, McCartney PJ, and Mackey DA

Ophthalmic genetics 28(1):39-41, 2007 Mar - Who cited this? | PubMed ID: 17454746 | Fulltext

Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees.

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Bennett SL, Hewitt AW, Poulsen JL, Kearns LS, Morgan JE, Craig JE, and Mackey DA

Archives of ophthalmology 125(1):112, 2007 Jan - Who cited this? | PubMed ID: 17210861 | Fulltext

The optic nerve head in myocilin glaucoma.

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Hewitt AW, Bennett SL, Fingert JH, Cooper RL, Stone EM, Craig JE, and Mackey DA

Investigative ophthalmology & visual science 48(1):238-43, 2007 Jan - Who cited this? | PubMed ID: 17197538 | Fulltext

Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.

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Hewitt AW, Bennett SL, Richards JE, Dimasi DP, Booth AP, Inglehearn C, Anwar R, Yamamoto T, Fingert JH, Héon E, Craig JE, and Mackey DA

Archives of ophthalmology 125(1):98-104, 2007 Jan - Who cited this? | PubMed ID: 17210859 | Fulltext

Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds.

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Hewitt AW, Samples JR, Allingham RR, Järvelä I, Kitsos G, Krishnadas SR, Richards JE, Lichter PR, Petersen MB, Sundaresan P, Wiggs JL, Mackey DA, and Wirtz MK

Molecular vision 13:487-92, 2007 - Who cited this? | PubMed ID: 17417609 | Fulltext

The association between maternal smoking in pregnancy, other early life characteristics and childhood vision: the twins eye study in tasmania.

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Ponsonby AL, Brown SA, Kearns LS, Mackinnon JR, Scotter LW, Cochrane JA, and Mackey DA

Ophthalmic epidemiology 14(6):351-9, 2007 - Who cited this? | PubMed ID: 18161608 | Fulltext

Nail-patella syndrome and its association with glaucoma: a review of eight families.

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Mimiwati Z, Mackey DA, Craig JE, Mackinnon JR, Rait JL, Liebelt JE, Ayala-Lugo R, Vollrath D, and Richards JE

The British journal of ophthalmology 90(12):1505-9, 2006 Dec - Who cited this? | PubMed ID: 16825280 | Fulltext

The role of the Met98Lys optineurin variant in inherited optic nerve diseases.

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Craig JE, Hewitt AW, Dimasi DP, Howell N, Toomes C, Cohn AC, and Mackey DA

The British journal of ophthalmology 90(11):1420-4, 2006 Nov - Who cited this? | PubMed ID: 16885188 | Fulltext

Training peer reviewers.

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Mackey DA

Nature 443(7113):880, 2006 Oct 19 - Who cited this? | PubMed ID: 17106961 | Fulltext

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