Detalhe da pesquisa
1.
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
; 17(10): e1009858, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662343
2.
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
; 17(5): e1009497, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33979322
3.
Genome-wide association study of corneal biomechanical properties identifies over 200 loci providing insight into the genetic etiology of ocular diseases.
Hum Mol Genet
; 29(18): 3154-3164, 2020 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32716492
4.
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Ophthalmology
; 129(6): 626-636, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35031440
5.
Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.
Hum Genet
; 137(10): 847-862, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30317457
6.
Smoking, Corneal Biomechanics, and Glaucoma: Results From Two Large Population-Based Cohorts.
Invest Ophthalmol Vis Sci
; 65(1): 11, 2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38170539
7.
Sex Distributions in Non-ABCA4 Autosomal Macular Dystrophies.
Invest Ophthalmol Vis Sci
; 65(5): 9, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38700873
8.
Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort.
Ophthalmol Retina
; 2024 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38219857
9.
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis.
JAMA Ophthalmol
; 142(5): 463-471, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38602673
10.
An Analysis of the Effect of ABCA4 p.Asn1868Ile Genotypes on Retinal Structure in 26,558 Participants in the UK Biobank.
Invest Ophthalmol Vis Sci
; 64(7): 31, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37342033
11.
Cascade screening for glaucoma in high-risk family members of African-Caribbean glaucoma patients in an urban population in London.
Br J Ophthalmol
; 106(3): 376-380, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33303425
12.
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color.
Sci Adv
; 7(11)2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33692100
13.
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.
Commun Biol
; 4(1): 266, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33649486
14.
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.
Nat Commun
; 12(1): 1258, 2021 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33627673
15.
Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes.
JAMA Ophthalmol
; 138(3): 294-299, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31999318
16.
The Role of Chromosome X in Intraocular Pressure Variation and Sex-Specific Effects.
Invest Ophthalmol Vis Sci
; 61(11): 20, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32926103
17.
Age-dependent regional retinal nerve fibre changes in SIX1/SIX6 polymorphism.
Sci Rep
; 10(1): 12485, 2020 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32719476
18.
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.
Nat Genet
; 52(4): 401-407, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32231278
19.
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Commun Biol
; 2: 435, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31798171
20.
Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma.
Nat Genet
; 50(6): 778-782, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29785010