| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1001/ARCHOPHT.125.1.30 |
| P698 | PubMed publication ID | 17210849 |
| P2093 | author name string | Janey L Wiggs | |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 30-37 | |
| P577 | publication date | 2007-01-01 | |
| P1433 | published in | JAMA Ophthalmology | Q4787301 |
| P1476 | title | Genetic etiologies of glaucoma | |
| P478 | volume | 125 |
| Q36572668 | A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16 |
| Q36055920 | A role for epigenetic changes in the development of retinal neurodegenerative conditions |
| Q43057762 | ASK1 deficiency attenuates neural cell death in GLAST-deficient mice, a model of normal tension glaucoma |
| Q42456498 | An eye for discovery |
| Q33621903 | Angiopoietin-like 7 secretion is induced by glaucoma stimuli and its concentration is elevated in glaucomatous aqueous humor |
| Q34936970 | Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b |
| Q42414496 | Anticipation, anti-glaucoma drug treatment response and phenotype of a Chinese family with glaucoma caused by the Pro370Leu myocilin mutation |
| Q33515435 | Aqueous humor level of sCD44 in patients with degenerative myopia and primary open-angle glaucoma |
| Q33767167 | Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders |
| Q35065411 | Association between p53 codon 72 (Arg72Pro) polymorphism and primary open-angle glaucoma in Iranian patients. |
| Q92112426 | Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies |
| Q33854304 | Association of SIX1/SIX6 locus polymorphisms with regional circumpapillary retinal nerve fibre layer thickness: The Nagahama study. |
| Q33586390 | Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts |
| Q42375294 | Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma |
| Q34559060 | Association of glutathione S transferases polymorphisms with glaucoma: a meta-analysis |
| Q37257704 | Association of microsatellite polymorphisms of the GPDS1 locus with normal tension glaucoma in the Japanese population |
| Q37087161 | Association study of genetic variants on chromosome 7q31 with susceptibility to normal tension glaucoma in a Japanese population. |
| Q42600591 | Astrocytes in glaucomatous optic neuropathy |
| Q34325988 | CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies |
| Q36905164 | Cellular and molecular biology of optineurin |
| Q38151211 | Chromosome 9p21 primary open-angle glaucoma susceptibility locus: a review. |
| Q42129535 | Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma model |
| Q44201576 | Corticosteroid-induced intraocular pressure elevation in keratoconus is common following uncomplicated penetrating keratoplasty. |
| Q52655385 | Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing. |
| Q35166639 | Development of spontaneous neuropathy in NF-κBp50-deficient mice by calcineurin-signal involving impaired NF-κB activation |
| Q24329037 | Differential effects of myocilin and optineurin, two glaucoma genes, on neurite outgrowth |
| Q90310445 | Do epigenetic changes caused by commensal microbiota contribute to development of ocular disease? A review of evidence |
| Q35007225 | Effect of PITX2 knockdown on transcriptome of primary human trabecular meshwork cell cultures |
| Q38383050 | Effect of epigallocatechin-gallate on inner retinal function in ocular hypertension and glaucoma: a short-term study by pattern electroretinogram |
| Q39140153 | Epigenetics and Signaling Pathways in Glaucoma |
| Q24336657 | Evidence for RPGRIP1 gene as risk factor for primary open angle glaucoma |
| Q30406706 | Exome Sequencing Identifies a Missense Variant in EFEMP1 Co-Segregating in a Family with Autosomal Dominant Primary Open-Angle Glaucoma |
| Q37724017 | Family-based analysis identified CD2 as a susceptibility gene for primary open angle glaucoma in Chinese Han population |
| Q36784718 | Fine mapping of the GLC1K juvenile primary open-angle glaucoma locus and exclusion of candidate genes |
| Q41411098 | Gene and protein expression pilot profiling and biomarkers in an experimental mouse model of hypertensive glaucoma |
| Q41210821 | Gene therapy in glaucoma-part 2: Genetic etiology and gene mapping |
| Q35220900 | Genetic dissection of the Gpnmb network in the eye |
| Q35005896 | Genetic variants associated with optic nerve vertical cup-to-disc ratio are risk factors for primary open angle glaucoma in a US Caucasian population |
| Q56880536 | Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area |
| Q34200382 | Genome-wide association studies: applications and insights gained in Ophthalmology |
| Q55002650 | Genomic Locus Modulating IOP in the BXD RI Mouse Strains. |
| Q48166078 | Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma. |
| Q33652045 | Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE). |
| Q83757307 | Glaucoma |
| Q34090204 | Glaucoma: genes, phenotypes, and new directions for therapy |
| Q36499373 | Glutathione S-transferase M1 and T1 polymorphisms in Arab glaucoma patients. |
| Q52371448 | Heritability of glaucoma and glaucoma-related endophenotypes: systematic review and meta-analysis protocol. |
| Q24657994 | Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma |
| Q33634013 | Impairment of protein trafficking upon overexpression and mutation of optineurin |
| Q30400845 | In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma |
| Q37098009 | Inherited mitochondrial optic neuropathies |
| Q64097447 | Investigating a downstream gene of using the systems genetics method |
| Q34848918 | Investigation of the association between SLC1A3 gene polymorphisms and normal tension glaucoma |
| Q37257670 | Investigation of the association between the GLC3A locus and normal tension glaucoma in Japanese patients by microsatellite analysis |
| Q35089333 | Is the GSTM1 null polymorphism a risk factor in primary open angle glaucoma? |
| Q37163570 | Lack of Association between LOXL1 Variants and Primary Open- Angle Glaucoma in Three Different Populations |
| Q41040992 | Lack of association between lysyl oxidase-like 1 polymorphisms and primary open angle glaucoma: a meta-analysis |
| Q36145925 | Lack of association of SNP rs4236601 near CAV1 and CAV2 with POAG in a Saudi cohort |
| Q34152110 | Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies |
| Q37190995 | Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients |
| Q34664035 | Mouse models of retinal ganglion cell death and glaucoma |
| Q36051019 | Myocilin mutations are not a major cause of primary congenital glaucoma in Iranian patients. |
| Q34431440 | Myocilin polymorphisms and primary open-angle glaucoma: a systematic review and meta-analysis. |
| Q35736309 | Non-housekeeping genes expressed in human trabecular meshwork cell cultures |
| Q40061826 | OPA1 increases the risk of normal but not high tension glaucoma |
| Q36951789 | Open-angle glaucoma -- an epidemiologic overview |
| Q38018840 | Ophthalmic drug discovery: novel targets and mechanisms for retinal diseases and glaucoma |
| Q37019290 | Optineurin coding variants in Ghanaian patients with primary open-angle glaucoma |
| Q40641339 | Polymorphism of CYP46A1 and PPARγ2 Genes in Risk Prediction of Primary Open Angle Glaucoma Among North Indian Population |
| Q27334656 | Posttranslational modifications, localization, and protein interactions of optineurin, the product of a glaucoma gene |
| Q33562386 | Preliminary quantitative proteomic characterization of glaucomatous rat retinal ganglion cells. |
| Q45398387 | Prevalence of chronic ocular diseases in a genetic isolate: the Norfolk Island Eye Study (NIES). |
| Q57728691 | Primary open-angle glaucoma |
| Q28570083 | Processing of optineurin in neuronal cells |
| Q37058798 | Progress toward personalized medicine for glaucoma |
| Q35523559 | Quantitative proteomics: TGFβ₂ signaling in trabecular meshwork cells |
| Q34545233 | Quantitative trait loci associated with murine central corneal thickness |
| Q33356801 | Rgcs1, a dominant QTL that affects retinal ganglion cell death after optic nerve crush in mice |
| Q35060902 | Role of the APOE ε2/ε3/ε4 polymorphism in the development of primary open-angle glaucoma: evidence from a comprehensive meta-analysis |
| Q59280895 | STOP Glaucoma in Sub Saharan Africa: enhancing awareness, detection, management, and capacity for glaucoma care |
| Q28506021 | Spink2 modulates apoptotic susceptibility and is a candidate gene in the Rgcs1 QTL that affects retinal ganglion cell death after optic nerve damage |
| Q47151549 | Targeted Delivery of Mitochondrial Calcium Channel Regulators: The Future of Glaucoma Treatment? |
| Q48535186 | The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma |
| Q22305862 | The current research status of normal tension glaucoma |
| Q38580900 | The effect of flavonoids on visual function in patients with glaucoma or ocular hypertension: a systematic review and meta-analysis. |
| Q34077810 | The evaluation of the oxidative stress parameters in patients with primary angle-closure glaucoma |
| Q37343118 | The genetics of primary open-angle glaucoma: a review |
| Q37362502 | The novel Y371D myocilin mutation causes an aggressive form of juvenile open-angle glaucoma in a Caucasian family from the Middle-East |
| Q42748164 | The potential role of glutamate transporters in the pathogenesis of normal tension glaucoma |
| Q36499603 | The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucoma. |
| Q35209212 | Toll-like receptor 4 gene polymorphisms do not associate with normal tension glaucoma in a Korean population |
| Q42009875 | Toward a Genetic Understanding of Glaucoma-Breakthroughs and Challenges from Studies of Exfoliation Glaucoma |
| Q90379308 | Using BXD mouse strains in vision research: A systems genetics approach |
| Q58728158 | and genotypes as risk determinants of primary open angle glaucoma among smokers |
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