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3.4.2 Gene studies (91)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies78047 Genetics of Exfoliation Syndrome
Aung T
Journal of Glaucoma 2018; 27: S12-S14
77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Choquet H
Nature communications 2018; 9: 2278
77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Wang X
Current Eye Research 2018; 43: 1334-1341
77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Horita S
BMC Medical Genetics 2018; 19: 103
77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Ou Z
Bioscience reports 2018; 38:
78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Macgregor S
Nature Genetics 2018; 50: 1067-1071
78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Pasquale LR
Journal of Glaucoma 2018; 27: S20-S23
78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Bashir R
Journal of the Pakistan Medical Association 2018; 68: 1205-1211
78197 Indistinguishable gene expression between healthy eyes and eyes with unilateral exfoliative glaucoma
Ayala M
Clinical Ophthalmology 2018; 12: 1155-1162
77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Gao XR
Human Molecular Genetics 2018; 27: 2205-2213
78026 Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
Swarup G
Frontiers in immunology 2018; 9: 1287
77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Syrimis A
Molecular medicine reports 2018; 18: 1623-1627
77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Tong L
Ocular Surface 2018; 16: 441-447
78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Ong JS
Nature Genetics 2018; 50: 1067-1071
78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Kang JH
Journal of Glaucoma 2018; 27: S20-S23
77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Liu G
Bioscience reports 2018; 38:
78197 Indistinguishable gene expression between healthy eyes and eyes with unilateral exfoliative glaucoma
Cuklev F
Clinical Ophthalmology 2018; 12: 1155-1162
78026 Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
Sayyad Z
Frontiers in immunology 2018; 9: 1287
78047 Genetics of Exfoliation Syndrome
Chan AS
Journal of Glaucoma 2018; 27: S12-S14
77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Hou AH
Ocular Surface 2018; 16: 441-447
77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Huang H
Human Molecular Genetics 2018; 27: 2205-2213
78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Yousaf K
Journal of the Pakistan Medical Association 2018; 68: 1205-1211
77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Paylakhi S
Nature communications 2018; 9: 2278
77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Nicolaou N
Molecular medicine reports 2018; 18: 1623-1627
77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Simsek E
BMC Medical Genetics 2018; 19: 103