The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
The Heritability of Ocular Traits
Open accessAbstract
Heritability is the proportion of phenotypic variation in a population that is attributable to genetic variation among individuals. Many ophthalmic disorders and biometric traits are known to have a genetic basis and consequently much work has been published in the literature estimating the heritability of various ocular parameters. We collated and summarized the findings of heritability studies conducted in the field of ophthalmology. We grouped the various studies broadly by phenotype as follows: refraction, primary open-angle glaucoma, age-related macular degeneration (AMD), cataract, diabetic retinopathy, and others. A total of 82 articles were retrieved from the literature relating to estimation of heritability for an ocular disease or biometric trait; of these, 37 papers were concerned with glaucoma, 28 with refraction, 4 with AMD, 5 with diabetic retinopathy, and 4 with cataract. The highest reported heritability for an ophthalmic trait is 0.99 for the phenotype ≥ 20 small hard drusen, indicating that observed variation in this parameter is largely governed by genetic factors. Over 60% of the studies employed a twin study design and a similar percentage utilized variance components methods and structural equation modeling (SEM) to derive their heritability values. Using modern SEM techniques, heritability estimates derived from twin subjects were generally higher than those from family data. Many of the estimates are in the moderate to high range, but to date the majority of genetic variants accounting for these findings have not been uncovered, hence much work remains to be undertaken to elucidate fully their molecular etiology.
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Cites
Finding the missing heritability of complex diseases
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) · Nature · doi:10.1038/nature08494 · Cited by 8,336
Complement factor H polymorphism in age-related macular degeneration
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Data and Theory Point to Mainly Additive Genetic Variance for Complex Traits
Hill, W. G., Goddard, M. E., & Visscher, P. M. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000008 · Cited by 1,039
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Seddon, J. M. (2005) · Archives of Ophthalmology · doi:10.1001/archopht.123.3.321 · Cited by 446
Familial aggregation of age-related maculopathy
SEDDON, J. M., AJANI, U. A., & MITCHELL, B. D. (1997) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)71036-0 · Cited by 350
Genetic influence on early age-related maculopathy
Hammond, C. J., Webster, A. R., Snieder, H., Bird, A. C., Gilbert, C. E., & Spector, T. D. (2002) · Ophthalmology · doi:10.1016/s0161-6420(01)01049-1 · Cited by 237
Self-citationDeleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome
Abu, A., Frydman, M., Marek, D., Pras, E., Nir, U., Reznik-Wolf, H., & Pras, E. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2008.04.001 · Cited by 139
Cited by
UK Biobank Eye and Vision Consortium, Khawaja, A. P., NEIGHBORHOOD Consortium, Cooke Bailey, J. N., Wareham, N. J., Scott, R. A., Simcoe, M., Igo, R. P., Song, Y. E., Wojciechowski, R., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0126-8 · Cited by 346
Self-citationTedja, M. S., Haarman, A. E. G., Meester-Smoor, M. A., Kaprio, J., Mackey, D. A., Guggenheim, J. A., Hammond, C. J., Verhoeven, V. J. M., Klaver, C. C. W., & for the CREAM Consortium (2019) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.18-25965 · Cited by 304
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Metadata
- Authors
- Sanfilippo, P. G., Hewitt, A. W., Hammond, C. J., & Mackey, D. A.
- Venue
- Survey of Ophthalmology
- Publisher
- Elsevier BV
- Published
- 2010-11
- Volume
- 55
- Issue
- 6
- Pages
- 561-583
- ISSN
- 0039-6257 (ISSN-L)
- OpenAlex
- W1995110743
- Cited by
- 173
- References
- 8
- FWCI
- 8.90
- Type
- journal article
- Language
- en
- Open access
- green
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