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David A Mackey
David A Mackey
Professor of Ophthalmology, University of Western Australia
Verified email at lei.org.au
Title
Cited by
Cited by
Year
Identification of a gene that causes primary open angle glaucoma
EM Stone, JH Fingert, WLM Alward, TD Nguyen, JR Polansky, ...
Science 275 (5300), 668-670, 1997
17811997
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
14392016
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
JH Fingert, E Héon, JM Liebmann, T Yamamoto, JE Craig, J Rait, ...
Human molecular genetics 8 (5), 899-905, 1999
6981999
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
6422017
The association between time spent outdoors and myopia in children and adolescents: a systematic review and meta-analysis
JC Sherwin, MH Reacher, RH Keogh, AP Khawaja, DA Mackey, PJ Foster
Ophthalmology 119 (10), 2141-2151, 2012
6282012
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance
MA Tischfield, HN Baris, C Wu, G Rudolph, L Van Maldergem, W He, ...
Cell 140 (1), 74-87, 2010
6212010
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)
WLM Alward, JH Fingert, MA Coote, AT Johnson, SF Lerner, D Junqua, ...
New England Journal of Medicine 338 (15), 1022-1027, 1998
5511998
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy
EM Stone, AJ Lotery, FL Munier, E Héon, B Piguet, RH Guymer, ...
Nature genetics 22 (2), 199-202, 1999
5311999
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
VJM Verhoeven, PG Hysi, R Wojciechowski, Q Fan, JA Guggenheim, ...
Nature genetics 45 (3), 314-318, 2013
5292013
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
N Howell, LA Bindoff, DA McCullough, I Kubacka, J Poulton, D Mackey, ...
American journal of human genetics 49 (5), 939, 1991
4761991
Retinal vascular caliber: systemic, environmental, and genetic associations
C Sun, JJ Wang, DA Mackey, TY Wong
Survey of ophthalmology 54 (1), 74-95, 2009
4732009
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
KP Burdon, S Macgregor, AW Hewitt, S Sharma, G Chidlow, RA Mills, ...
Nature genetics 43 (6), 574-578, 2011
4672011
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ...
Nature genetics 42 (10), 906-909, 2010
4542010
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
DA Mackey, RJ Oostra, T Rosenberg, E Nikoskelainen, J Bronte-Stewart, ...
American journal of human genetics 59 (2), 481, 1996
4311996
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q
C Toomes, HM Bottomley, RM Jackson, KV Towns, S Scott, DA Mackey, ...
The American Journal of Human Genetics 74 (4), 721-730, 2004
4212004
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155-163, 2013
3562013
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
3462022
Genetic influences on handedness: data from 25,732 Australian and Dutch twin families
SE Medland, DL Duffy, MJ Wright, GM Geffen, DA Hay, F Levy, ...
Neuropsychologia 47 (2), 330-337, 2009
3462009
Retinopathy of prematurity: recent advances in our understanding
CM Wheatley, JL Dickinson, DA Mackey, JE Craig, MM Sale
British Journal of Ophthalmology 86 (6), 696-700, 2002
3442002
Null mutations in LTBP2 cause primary congenital glaucoma
M Ali, M McKibbin, A Booth, DA Parry, P Jain, SA Riazuddin, ...
The American Journal of Human Genetics 84 (5), 664-671, 2009
3432009
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