The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Genome-wide analysis of disease progression in age-related macular degeneration
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Human genetics point to S2R as a promising therapeutic target for dry AMD, as several large-scale independent genome-wide association studies indicate that a single nucleotide polymorphism in the TMEM-VTN locus confers decreased risk for dry AMD.
“First, human genetics point to S2R as a promising therapeutic target, as indicated via several large-scale, independent genome-wide association studies. These studies indicate that a single nucleotide polymorphism in the TMEM-VTN locus confers decreased risk for dry AMD [168,169].”
From Sigma-2 Receptors—From Basic Biology to Therapeutic Target: A Focus on Age-Related Degenerative Diseases (2023) · cites this paper as [169]
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Cites
Maller, J., George, S., Purcell, S., Fagerness, J., Altshuler, D., Daly, M. J., & Seddon, J. M. (2006) · Nature Genetics · doi:10.1038/ng1873 · Cited by 599
Susceptibility genes for age-related maculopathy on chromosome 10q26
Jakobsdottir, J., Conley, Y. P., Weeks, D. E., Mah, T. S., Ferrell, R. E., & Gorin, M. B. (2005) · The American Journal of Human Genetics · doi:10.1086/444437 · Cited by 470
Self-citationLi, M., Atmaca-Sonmez, P., Othman, M., Branham, K. E. H., Khanna, R., Wade, M. S., Li, Y., Liang, L., Zareparsi, S., Swaroop, A., et al. (2006) · Nature Genetics · doi:10.1038/ng1871 · Cited by 354
Self-citationAssociation of CFH Y402H and LOC387715 A69S with progression of age-related macular degeneration
Seddon, J. M., Francis, P. J., George, S., Schultz, D. W., Rosner, B., & Klein, M. L. (2007) · JAMA · doi:10.1001/jama.297.16.1793 · Cited by 330
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Research works printed but not linked: 20
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- Fritsche, 2013, Seven new loci associated with age-related macular degeneration, Nat. Genet, 45, 433
- Fritsche, 2016, A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants, Nat. Genet, 48, 134
- Chen, 2010, Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration, Proc. Natl. Aacd Sci. U.S.A, 107, 7401
- Rivera, 2005, Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk, Hum. Mol. Genet, 14, 3227
- Seddon, 2011, Risk models for progression to advanced age-related macular degeneration using demographic, environmental, genetic, and ocular factors, Ophthalmology, 118, 2203
- Seddon, 2009, Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables, Invest. Ophthalmol. Vis. Sci, 50, 2044
- Farwick, 2010, Susceptibility genes and progression in age-related maculopathy: a study of single eyes, Invest. Ophthalmol. Vis. Sci, 51, 731
- Klein, 2011, Risk assessment model for development of advanced age-related macular degeneration, Arch. Ophthalmol, 129, 1543
- Ding, 2017, Bivariate analysis of age-related macular degeneration progression using genetic risk scores, Genetics, 206, 119
- Seddon, 2015, Risk prediction for progression of macular degeneration: 10 common and rare genetic variants, demographic, environmental, and macular covariates, Invest. Ophthalmol. Vis. Sci, 56, 2192
- Perlee, 2013, Inclusion of genotype with fundus phenotype improves accuracy of predicting choroidal neovascularization and geographic atrophy, Ophthalmology, 120, 1880
- Huang da, 2009, Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources, Nat. Protoc, 4, 44
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- Sardell, 2016, Progression rate from intermediate to advanced age-related macular degeneration is correlated with the number of risk alleles at the CFH locus, Invest. Ophthalmol. Vis. Sci, 57, 6107
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Cited by
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Lizama, B. N., Kahle, J., Catalano, S. M., Caggiano, A. O., Grundman, M., & Hamby, M. E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076251 · Cited by 54
Metadata
- Authors
- Yan, Q., Ding, Y., Liu, Y., Sun, T., Fritsche, L. G., Clemons, T., Ratnapriya, R., Klein, M. L., Cook, R. J., Liu, Y., Fan, R., Wei, L., Abecasis, G. R., Swaroop, A., Chew, E. Y., AREDS2 Research Group, Weeks, D. E., & Chen, W.
- Affiliations
- Division of Pulmonary Medicine, Allergy and Immunology, Department of Pediatrics, Children’s Hospital of Pittsburgh of UPMC University of Pittsburgh, Pittsburgh, PA 15224, USA,
- Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA
- Center for Statistical Genetics, Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA
- The Emmes Corporation, Rockville, MD 20850, USA
- Neurobiology Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA
- Casey Eye Institute, Oregon Health & Science University, Portland, OR 97239, USA
- Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, ON N2L 3G1, Canada
- State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong Province 510030, China
- Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, DC 20007, USA
- Division of Epidemiology and Clinical Applications, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA
- ORCID
- Chen, Wei
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2018-01-15
- Volume
- 27
- Issue
- 5
- Pages
- 929-940
- ISSN
- 0964-6906
- 1460-2083
- Cited by
- 98
- References
- 4
- Language
- en
- Funders
- National Institutes of Health (EY024226, EY022005, EY021532)
- National Eye Institute (EY000474, EY000546)
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