Detalhe da pesquisa
1.
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma.
Cell
; 187(2): 464-480.e10, 2024 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38242088
2.
Rare protective variants and glaucoma-relevant cell stressors modulate Angiopoietin-like 7 expression.
Hum Mol Genet
; 32(15): 2523-2531, 2023 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37220876
3.
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
4.
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
5.
Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature.
Circulation
; 145(2): 134-150, 2022 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34743558
6.
Long-term Alcohol Consumption and Risk of Exfoliation Glaucoma or Glaucoma Suspect Status among United States Health Professionals.
Ophthalmology
; 130(2): 187-197, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36041586
7.
Mitochondrial TXNRD2 and ME3 Genetic Risk Scores Are Associated with Specific Primary Open-Angle Glaucoma Phenotypes.
Ophthalmology
; 130(7): 756-763, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36813040
8.
The Association of Physical Activity with Glaucoma and Related Traits in the UK Biobank.
Ophthalmology
; 130(10): 1024-1036, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37331483
9.
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma.
Hum Mutat
; 43(2): 240-252, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34923728
10.
Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data.
Ophthalmology
; 129(6): 694-707, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35149155
11.
Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis.
Ophthalmology
; 129(6): 637-652, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35101531
12.
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
13.
The Association between Serum Lipids and Intraocular Pressure in 2 Large United Kingdom Cohorts.
Ophthalmology
; 129(9): 986-996, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35500606
14.
The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities-A review.
Clin Exp Ophthalmol
; 50(2): 143-162, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35037362
15.
Exome-based investigation of the genetic basis of human pigmentary glaucoma.
BMC Genomics
; 22(1): 477, 2021 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34174832
16.
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma.
Hum Mol Genet
; 28(8): 1298-1311, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30561643
17.
Characteristics of p.Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank.
Ophthalmology
; 128(9): 1300-1311, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713785
18.
Intraocular Pressure, Glaucoma, and Dietary Caffeine Consumption: A Gene-Diet Interaction Study from the UK Biobank.
Ophthalmology
; 128(6): 866-876, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33333105
19.
Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.
PLoS Genet
; 14(1): e1007145, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29370175
20.
Identification of Estrogen Signaling in a Prioritization Study of Intraocular Pressure-Associated Genes.
Int J Mol Sci
; 22(19)2021 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34638643