Allikmets, Rando
Columbia University Irving Medical Center · Columbia University
19 papers on CoChatORCID 0000-0002-3344-4447
Most cited papers
- Verified
A common haplotype in the complement regulatory gene factor H ( HF1/CFH ) predisposes individuals to age-related macular degeneration
Hageman, G. S., Anderson, D. H., Johnson, L. V., Hancox, L. S., Taiber, A. J., Hardisty, L. I., Hageman, J. L., Stockman, H. A., Borchardt, J. D., Gehrs, K. M., et al. (2005) · Proceedings of the National Academy of Sciences
Retinal Diseases and TreatmentsComplement system in diseases
Cited by 1,961
- Verified
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Fritsche, L. G., Igl, W., Bailey, J. N. C., Grassmann, F., Sengupta, S., Bragg-Gresham, J. L., Burdon, K. P., Hebbring, S. J., Wen, C., Gorski, M., et al. (2016) · Nature Genetics
Retinal Diseases and TreatmentsGenetic Associations and Epidemiology
Cited by 1,544
- Verified
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy
Allikmets, R., Singh, N., Sun, H., Shroyer, N. F., Hutchinson, A., Chidambaram, A., Gerrard, B., Baird, L., Stauffer, D., Peiffer, A., et al. (1997) · Nature Genetics
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 1,435
- Verified
Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration
The AMD Genetics Clinical Study Group, Gold, B., Merriam, J. E., Zernant, J., Hancox, L. S., Taiber, A. J., Gehrs, K., Cramer, K., Neel, J., Bergeron, J., et al. (2006) · Nature Genetics
Retinal Diseases and TreatmentsComplement system in diseases
Cited by 1,075
- Verified
Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes
Stephens, J. C., Reich, D. E., Goldstein, D. B., Shin, H. D., Smith, M. W., Carrington, M., Winkler, C., Huttley, G. A., Allikmets, R., Schriml, L., et al. (1998) · The American Journal of Human Genetics
HIV Research and TreatmentForensic and Genetic Research
Cited by 520
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Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene ( LIPC )
Neale, B. M., Fagerness, J., Reynolds, R., Sobrin, L., Parker, M., Raychaudhuri, S., Tan, P. L., Oh, E. C., Merriam, J. E., Souied, E., et al. (2010) · Proceedings of the National Academy of Sciences
Retinal Diseases and TreatmentsGenetic Associations and Epidemiology
Cited by 442
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Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations
Cremers, F. P. M., Lee, W., Collin, R. W. J., & Allikmets, R. (2020) · Progress in Retinal and Eye Research
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 315
- Verified
Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration
Allikmets, R. (2000) · The American Journal of Human Genetics
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 303
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Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration
Yu, Y., Bhangale, T. R., Fagerness, J., Ripke, S., Thorleifsson, G., Tan, P. L., Souied, E. H., Richardson, A. J., Merriam, J. E., Buitendijk, G. H. S., et al. (2011) · Human Molecular Genetics
Retinal Diseases and TreatmentsGenetic Associations and Epidemiology
Cited by 254
- Verified
Isolation and characterization of a retinal pigment epithelial cell fluorophore: An all-trans -retinal dimer conjugate
Fishkin, N. E., Sparrow, J. R., Allikmets, R., & Nakanishi, K. (2005) · Proceedings of the National Academy of Sciences
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 146
- Verified
Simple and Complex ABCR: Genetic Predisposition to Retinal Disease
Allikmets, R. (2000) · The American Journal of Human Genetics
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 128
- Verified
Transduction of Photoreceptors With Equine Infectious Anemia Virus Lentiviral Vectors: Safety and Biodistribution of StarGen for Stargardt Disease
Binley, K., Widdowson, P., Loader, J., Kelleher, M., Iqball, S., Ferrige, G., de Belin, J., Carlucci, M., Angell-Manning, D., Hurst, F., et al. (2013) · Investigative Opthalmology & Visual Science
Retinal Development and DisordersVirus-based gene therapy research
Cited by 115
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A1120, a Nonretinoid RBP4 Antagonist, Inhibits Formation of Cytotoxic Bisretinoids in the Animal Model of Enhanced Retinal Lipofuscinogenesis
Dobri, N., Qin, Q., Kong, J., Yamamoto, K., Liu, Z., Moiseyev, G., Ma, J.-X., Allikmets, R., Sparrow, J. R., & Petrukhin, K. (2013) · Investigative Opthalmology & Visual Science
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 91
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Comprehensive Analysis of the Candidate Genes CCL2,CCR2, and TLR4 in Age-Related Macular Degeneration
Despriet, D. D. G., Bergen, A. A. B., Merriam, J. E., Zernant, J., Barile, G. R., Smith, R. T., Barbazetto, I. A., van Soest, S., Bakker, A., de Jong, P. T. V. M., et al. (2008) · Investigative Opthalmology & Visual Science
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 60
- Verified
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration
Strunz, T., Lauwen, S., Kiel, C., International AMD Genomics Consortium (IAMDGC), Fritsche, L. G., Igl, W., Bailey, J. N. C., Grassmann, F., Sengupta, S., Bragg-Gresham, J. L., et al. (2020) · Scientific Reports
Genetic Associations and EpidemiologyRetinal Diseases and Treatments
Cited by 60
- Verified
New syndrome with retinitis pigmentosa is caused by nonsense mutations in retinol dehydrogenase RDH11
Xie, Y. (., Lee, W., Cai, C., Gambin, T., Nõupuu, K., Sujirakul, T., Ayuso, C., Jhangiani, S., Muzny, D., Boerwinkle, E., et al. (2014) · Human Molecular Genetics
Retinal Development and DisordersRetinoids in leukemia and cellular processes
Cited by 40
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Molecular Genetics of Age-Related Macular Degeneration: Current Status
Allikmets, R. (1999) · European Journal of Ophthalmology
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 29
- Verified
Peripapillary sparing in RDH12-associated Leber congenital amaurosis
Garg, A., Lee, W., Sengillo, J. D., Allikmets, R., Garg, K., & Tsang, S. H. (2017) · Ophthalmic Genetics
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 27
- Verified
Bringing age-related macular degeneration into focus
Allikmets, R., & Dean, M. (2008) · Nature Genetics
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 26
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