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3.4.2 Gene studies (105)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Criscione J
Cold Spring Harbor molecular case studies 2019; 5:
85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Stiemke AB
Frontiers in genetics 2020; 11: 31
85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Yousefian A
Journal of ophthalmic & vision research 2020; 15: 45-52
85057 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes
Simcoe MJ
JAMA ophthalmology 2020; 0:
84521 Role of matrix metalloproteinase-9 gene polymorphisms in glaucoma: A hospital-based study in Chinese patients
Zhao F
Journal of Clinical Laboratory Analysis 2020; 34: e23105
84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kim YW
Scientific reports 2020; 10: 221
84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Kondkar AA
PLoS ONE 2020; 15: e0227417
85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Siggs OM
Ophthalmology 2020; 127: 758-766
84752 Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Gauthier AC
Experimental Eye Research 2020; 190: 107893
84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Liu H
Journal of Gene Medicine 2020; 22: e3139
85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Rauf B
Molecular Vision 2020; 26: 14-25
84918 Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
AlSaad R
American Journal of Case Reports 2020; 21: e918128
84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Nandeesh BN
Neuropathology 2020; 40: 93-98
85034 Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree
Quist TS
American Journal of Ophthalmology 2020; 214: 52-62
84848 Update in Genetics and Surgical Management of Primary Congenital Glaucoma
Mocan MC
Turkish journal of ophthalmology 2019; 49: 347-355
85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Bashir R
Journal of the Pakistan Medical Association 2020; 70: 208-212
84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Bindu PS
Neuropathology 2020; 40: 93-98
84848 Update in Genetics and Surgical Management of Primary Congenital Glaucoma
Mehta AA
Turkish journal of ophthalmology 2019; 49: 347-355
84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Qi S
Journal of Gene Medicine 2020; 22: e3139
84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kim YJ
Scientific reports 2020; 10: 221
85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Souzeau E
Ophthalmology 2020; 127: 758-766
85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Irfan B
Journal of the Pakistan Medical Association 2020; 70: 208-212
84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Ji W
Cold Spring Harbor molecular case studies 2019; 5:
84918 Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
ElMansoury J
American Journal of Case Reports 2020; 21: e918128
85034 Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree
Johnson CA
American Journal of Ophthalmology 2020; 214: 52-62