David A Mackey

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321 articles

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Coautors

Alex HewittUniversity of TasmaniaCorreu electrònic verificat a utas.edu.au
Kathryn BurdonMenzies Institute for Medical Research, University of TasmaniaCorreu electrònic verificat a utas.edu.au
Stuart MacGregorProfessor, Statistical Genetics, QIMR Berghofer Medical Research Institute, Brisbane, AustraliaCorreu electrònic verificat a qimr.edu.au
Seyhan YazarGarvan Institute of Medical ResearchCorreu electrònic verificat a garvan.org.au
Paul SanfilippoBiostatistician and Data AnalystCorreu electrònic verificat a pgrad.unimelb.edu.au
Terri L YoungUniversity of WisconsinCorreu electrònic verificat a wisc.edu
Fred K ChenThe University of Western AustraliaCorreu electrònic verificat a lei.org.au
Nick MartinQIMR Berghofer Medical Research InstituteCorreu electrònic verificat a qimrberghofer.edu.au
Emmanuelle SouzeauCorreu electrònic verificat a flinders.edu.au
Edwin M. StoneUniversity of Iowa, Carver College of Medicine, Department of Ophthalmology and Visual SciencesCorreu electrònic verificat a uiowa.edu
Samantha Sze-Yee LeeLions Eye InstituteCorreu electrònic verificat a lei.org.au
John FingertProfessor of Ophthalmology, Carver College of Medicine, University of IowaCorreu electrònic verificat a uiowa.edu
sandra staffiericentre for eye research australiaCorreu electrònic verificat a unimelb.edu.au
Justin SherwinRoyal Victorian Eye and Ear Hospital MelbourneCorreu electrònic verificat a eyeandear.org.au
Chris InglehearnProfessor of Molecular Ophthalmology, University of LeedsCorreu electrònic verificat a leeds.ac.uk
Pirro HysiLondon, UKCorreu electrònic verificat a ucl.ac.uk
Val C. Sheffield, M.D., Ph.D.Investigator, Howard Hughes Medical Institute, Professor of Pediatrics, University of IowaCorreu electrònic verificat a uiowa.edu
Wallace AlwardProfessor of Ophthalmology, University of Iowa Carver College of MedicineCorreu electrònic verificat a uiowa.edu
Tim D SpectorGuys and St Thomas Hospital NHS Trust, Kings College LondonCorreu electrònic verificat a kcl.ac.uk
Grant MontgomeryProfessorial Research Fellow, Institute for Molecular Bioscience, The University of QueenslandCorreu electrònic verificat a uq.edu.au

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David A Mackey

Professor of Ophthalmology, University of Western Australia

Correu electrònic verificat a lei.org.au

Genetics of Eye Disease


Títol Ordena per cites Ordena per any Ordena per títol	Citada per Citada per	Any
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	1822	1997
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	1587	2016
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	718	1999
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	691	2017
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	688	2012
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	655	2010
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	563	1998
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	555	2022
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	554	2013
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	552	1999
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	482	2011
Retinal vascular caliber: systemic, environmental, and genetic associations C Sun, JJ Wang, DA Mackey, TY Wong Survey of ophthalmology 54 (1), 74-95, 2009	482	2009
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	481	1991
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	471	2010
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	441	1996
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	428	2004
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	369	2009
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	363	2013
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	357	2009
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	354	2002

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