Detalhe da pesquisa
1.
GWAS on retinal vasculometry phenotypes.
PLoS Genet
; 19(2): e1010583, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36757925
2.
Combined genome-wide association study of 136 quantitative ear morphology traits in multiple populations reveal 8 novel loci.
PLoS Genet
; 19(7): e1010786, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37459304
3.
Education interacts with genetic variants near GJD2, RBFOX1, LAMA2, KCNQ5 and LRRC4C to confer susceptibility to myopia.
PLoS Genet
; 18(11): e1010478, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36395078
4.
Electrical responses from human retinal cone pathways associate with a common genetic polymorphism implicated in myopia.
Proc Natl Acad Sci U S A
; 119(21): e2119675119, 2022 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35594404
5.
A genome-wide analysis of 340 318 participants identifies four novel loci associated with the age of first spectacle wear.
Hum Mol Genet
; 31(17): 3012-3019, 2022 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35220419
6.
Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.
Hum Mol Genet
; 31(11): 1909-1919, 2022 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35022715
7.
Circulating metabolites modulated by diet are associated with depression.
Mol Psychiatry
; 28(9): 3874-3887, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37495887
8.
Cone-driven strong flash electroretinograms in healthy adults: Prevalence of negative waveforms.
Doc Ophthalmol
; 148(1): 25-36, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37924416
9.
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
10.
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
11.
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
12.
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology.
Hum Mol Genet
; 28(21): 3680-3690, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31809533
13.
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair.
Hum Mol Genet
; 27(3): 559-575, 2018 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29220522
14.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Hum Mol Genet
; 27(11): 2025-2038, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29659830
15.
Comparison of Associations with Different Macular Inner Retinal Thickness Parameters in a Large Cohort: The UK Biobank.
Ophthalmology
; 127(1): 62-71, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31585827
16.
A commonly occurring genetic variant within the NPLOC4-TSPAN10-PDE6G gene cluster is associated with the risk of strabismus.
Hum Genet
; 138(7): 723-737, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31073882
17.
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
18.
A genome-wide association study of corneal astigmatism: The CREAM Consortium.
Mol Vis
; 24: 127-142, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29422769
19.
APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans.
PLoS Genet
; 11(8): e1005432, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26313004
20.
Haplotype reference consortium panel: Practical implications of imputations with large reference panels.
Hum Mutat
; 38(8): 1025-1032, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28493391