David A. Mackey

发表

Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations

D. Mackey, R. Guymer, A. Hewitt, 2011, Eye.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

H. Stefánsson, A. Sigurdsson, A. Jonasdottir, 2010, Nature Genetics.

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

Adriana I. Iglesias, A. Hofman, A. Uitterlinden, 2017, Human molecular genetics.

Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family

D. Mackey, T. Rosenberg, P. Calvas, 2011, Molecular vision.

Genome-wide risk prediction of primary open-angle glaucoma across multiple ancestries

A. Hewitt, J. Wiggs, A. Khawaja, 2023, medRxiv.

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Tin Aung, Paul Mitchell, Ching-Yu Cheng, 2013, Nature Genetics.

A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family

D. Mackey, M. Zenker, T. Bardakjian, 2013, Clinical genetics.

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

Claire L. Simpson, A. Hofman, A. Uitterlinden, 2012, Human Genetics.

Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo

Hofman, A. Uitterlinden, T. Lumley, 2010, PLoS genetics.

mtDNA mutations that cause optic neuropathy: how do we know?

D. Mackey, N. Howell, D. Marenda, 1998, American journal of human genetics.

Meta-analysis of 542,934 subjects of European ancestry identifies 336 1 novel genes and mechanisms predisposing to refractive error and 2 myopia 3

V. Vitart, A. Hewitt, V. Verhoeven, 2022 .