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Wiggs JL 44
Showing records 1 to 25 | Display all abstracts from Wiggs JL98548 The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities-A review
Aboobakar IF
Clinical and Experimental Ophthalmology 2022; 50: 143-162
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Stuart KV
Ophthalmology 2022; 129: 637-652
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Collantes ERA
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Simcoe MJ
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Delfin MS
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Shah A
Ophthalmology 2022; 129: 626-636
98548 The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities-A review
Wiggs JL
Clinical and Experimental Ophthalmology 2022; 50: 143-162
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Madjedi K
Ophthalmology 2022; 129: 637-652
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Fan B
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Fan B
Ophthalmology 2022; 129: 626-636
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Luben RN
Ophthalmology 2022; 129: 637-652
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Choquet H
Ophthalmology 2022; 129: 626-636
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Chua SYL
Ophthalmology 2022; 129: 637-652
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Torregosa JMR
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Weisschuh N
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Siguan-Bell C
Human Mutation 2022; 43: 240-252
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Warwick AN; Chia M
Ophthalmology 2022; 129: 637-652
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Waseem NH
Ophthalmology 2022; 129: 626-636
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Florcruz NVG
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Jiang C
Ophthalmology 2022; 129: 626-636
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Pasquale LR
Ophthalmology 2022; 129: 637-652
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Martinez JMD; Masna-Hidalgo BJ
Human Mutation 2022; 43: 240-252
98535 Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Melles RB
Ophthalmology 2022; 129: 626-636
98707 Alcohol, Intraocular Pressure, and Open-Angle Glaucoma: A Systematic Review and Meta-analysis
Wiggs JL
Ophthalmology 2022; 129: 637-652
98388 EFEMP1 rare variants cause familial juvenile-onset open-angle glaucoma
Guzman VPT
Human Mutation 2022; 43: 240-252
