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Primary open-angle glaucoma genes.
scientific article published on May 2011
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scholarly article
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Europe PubMed Central
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3171270
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21562585%20AND%20SRC:MED&resulttype=core&format=json
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31 January 2020
review article
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Europe PubMed Central
title
Primary open-angle glaucoma genes
(English)
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Europe PubMed Central
PMCID
3171270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21562585%20AND%20SRC:MED&resulttype=core&format=json
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31 January 2020
main subject
open-angle glaucoma
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inferred from title
author
John H. Fingert
series ordinal
1
1 reference
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Europe PubMed Central
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3171270
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21562585%20AND%20SRC:MED&resulttype=core&format=json
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31 January 2020
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J H Fingert
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1
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3171270
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24 August 2017
publication date
1 May 2011
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31 January 2020
published in
Eye
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3171270
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31 January 2020
volume
25
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PMCID
3171270
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31 January 2020
page(s)
587-595
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Europe PubMed Central
PMCID
3171270
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31 January 2020
issue
5
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Europe PubMed Central
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3171270
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31 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/eye.2011.97
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Different WDR36 mutation pattern in Chinese patients with primary open-angle glaucoma
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Transgenic mice expressing the Tyr437His mutant of human myocilin protein develop glaucoma
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Enhanced binding of TBK1 by an optineurin mutant that causes a familial form of primary open angle glaucoma
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Identification of mutations in the myocilin (MYOC) gene in Taiwanese patients with juvenile-onset open-angle glaucoma.
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Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
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The role of the WDR36 gene on chromosome 5q22.1 in a large family with primary open-angle glaucoma mapped to this region
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Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1.
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Genetic dissection of myocilin glaucoma
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Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
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6 September 2017
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing
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Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma
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A case-control comparison of the clinical characteristics of glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutation
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6 September 2017
Adult-onset primary open-angle glaucoma caused by mutations in optineurin
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6 September 2017
Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region
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6 September 2017
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6 September 2017
Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q.
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6 September 2017
Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq
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6 September 2017
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6 September 2017
Reversal of mutant myocilin non-secretion and cell killing: implications for glaucoma
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Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort
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Elevated amounts of myocilin in the aqueous humor of transgenic mice cause significant changes in ocular gene expression
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23 June 2018
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice
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Age-dependent prevalence of mutations at the GLC1A locus in primary open-angle glaucoma
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23 June 2018
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucoma
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23 June 2018
Primary open-angle glaucoma in 2 monozygotic twin pairs
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Glaucoma in the beagle
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Lack of association between optineurin gene variants T34T, E50K, M98K, 691_692insAG and R545Q and primary open angle glaucoma in Brazilian patients.
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1 September 2018
Expression of mutated mouse myocilin induces open-angle glaucoma in transgenic mice.
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1 September 2018
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma.
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Central corneal thickness is highly heritable: the twin eye studies.
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1 September 2018
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
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1 September 2018
Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients.
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1 September 2018
Molecular genetic analysis of optineurin gene for primary open-angle and normal tension glaucoma in the Japanese population
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1 September 2018
Mutations in the optineurin gene in Japanese patients with primary open-angle glaucoma and normal tension glaucoma.
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1 September 2018
Heritability of risk factors for primary open-angle glaucoma: the Beaver Dam Eye Study.
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1 September 2018
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier.
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1 September 2018
Risk of multisystem disease in isolated ocular angioma (haemangioblastoma)
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1 September 2018
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3171270
retrieved
1 September 2018
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3171270
retrieved
1 September 2018
No Association Between Variations in the WDR36 Gene and Primary Open-Angle Glaucoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEYE.2011.97
retrieved
21 January 2018
Collagen-related genes influence the glaucoma risk factor, central corneal thickness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEYE.2011.97
retrieved
21 January 2018
Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEYE.2011.97
retrieved
21 January 2018
Primary open-angle glaucoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEYE.2011.97
retrieved
21 January 2018
The genetic determination of ocular pressure in the normal eye
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21562585
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21562585
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Intracellular sequestration of hetero-oligomers formed by wild-type and glaucoma-causing myocilin mutants
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21562585
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetic determination of cup/disc ratio of the optic nerve
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21562585
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Heritability of ocular pressure in normal and suspect ranges
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21562585
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Corneal thickness. II. Environmental and genetic factors
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21562585
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/EYE.2011.97
1 reference
stated in
Europe PubMed Central
PMCID
3171270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21562585%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
PMCID
3171270
1 reference
stated in
Europe PubMed Central
PMCID
3171270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21562585%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
PubMed ID
21562585
1 reference
stated in
Europe PubMed Central
PMCID
3171270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21562585%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
ResearchGate publication ID
51117489
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