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WGC-2021

3.4.2 Gene studies (156)

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78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Wubben TJ
Ophthalmic Genetics 2018; 39: 615-618
78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Lin Y
Molecular medicine reports 2018; 18: 4439-4445
79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Tan Y
Chinese Journal of Medical Genetics 2018; 35: 737-740
78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Qashqai M
Journal of ophthalmic & vision research 2018; 13: 403-410
78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Takitani GEDS
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439
79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetics research international 2018; 2018: 2148056
78902
Stamenkovic M
International Journal of Ophthalmology 2018; 11: 1514-1520
79084 Transcriptional profiling analysis predicts potential biomarkers for glaucoma: HGF, AKR1B10 and AKR1C3
Nie Q
Experimental and therapeutic medicine 2018; 16: 5103-5111
78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Restrepo NA
BMC Medical Genomics 2018; 11: 70
78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Pandav SS
European Journal of Ophthalmology 2018; 0: 1120672118795405
79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Shihadeh W
International Journal of Ophthalmology 2018; 11: 1583-1587
79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Wang S
BMC Ophthalmology 2018; 18: 271
78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yaz Y
Turkish journal of ophthalmology 2018; 48: 215-220
78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Afzal R
Congenital anomalies 2018; 0:
78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Yu-Wai-Man C
European Journal of Human Genetics 2018; 26: 1713-1718
79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Saeedi O
Genes 2018; 9:
78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Singh LN
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602
78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Khawaja AP
Journal of Glaucoma 2018; 27: 743-749
79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Kondkar AA
BMC research notes 2018; 11: 733
78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Abu-Amero KK
Clinical Ophthalmology 2018; 12: 1413-1416
78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Oliveira MB
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091
78902
Stamenkovic M
International Journal of Ophthalmology 2018; 11: 1514-1520
79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen Y
Frontiers in genetics 2018; 9: 488
78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Azevedo AGB
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439
79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Sultan T
BMC research notes 2018; 11: 733

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