Dryja, Thaddeus P.

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

Friend, S. H., Bernards, R., Rogelj, S., Weinberg, R. A., Rapaport, J. M., Albert, D. M., & Dryja, T. P. (1986) · Nature

Ocular Oncology and TreatmentsCancer-related Molecular Pathways

Cited by 2,948

Retinitis pigmentosa

Hartong, D. T., Berson, E. L., & Dryja, T. P. (2006) · The Lancet

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 2,924

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Dryja, T. P., McGee, T. L., Reichel, E., Hahn, L. B., Cowley, G. S., Yandell, D. W., Sandberg, M. A., & Berson, E. L. (1990) · Nature

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 1,072

Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis

Hueber, W., Patel, D. D., Dryja, T., Wright, A. M., Koroleva, I., Bruin, G., Antoni, C., Draelos, Z., Gold, M. H., the Psoriasis Study Group, et al. (2010) · Science Translational Medicine

Psoriasis: Treatment and PathogenesisRheumatoid Arthritis Research and Therapies

Cited by 860

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis

Morimura, H., Fishman, G. A., Grover, S. A., Fulton, A. B., Berson, E. L., & Dryja, T. P. (1998) · Proceedings of the National Academy of Sciences

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 481

Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa

Olsson, J. E., Gordon, J. W., Pawlyk, B. S., Roof, D., Hayes, A., Molday, R. S., Mukai, S., Cowley, G. S., Berson, E. L., & Dryja, T. P. (1992) · Neuron

Retinal Development and DisordersPhotoreceptor and optogenetics research

Cited by 455

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Rosenfeld, P. J., Cowley, G. S., McGee, T. L., Sandberg, M. A., Berson, E. L., & Dryja, T. P. (1992) · Nature Genetics

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 422

Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus

Yamamoto, H., Simon, A., Eriksson, U., Harris, E., Berson, E. L., & Dryja, T. P. (1999) · Nature Genetics

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 298

Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture

Dryja, T. P. (2000) · American Journal of Ophthalmology

Retinal Development and DisordersPhotoreceptor and optogenetics research

Cited by 191

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa

Morimura, H., Saindelle-Ribeaudeau, F., Berson, E. L., & Dryja, T. P. (1999) · Nature Genetics

Retinal Development and DisordersPhotoreceptor and optogenetics research

Cited by 143

A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

den Hollander, A. I., McGee, T. L., Ziviello, C., Banfi, S., Dryja, T. P., Gonzalez-Fernandez, F., Ghosh, D., & Berson, E. L. (2009) · Investigative Opthalmology & Visual Science

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 109

Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration

DeAngelis, M. M., Ji, F., Adams, S., Morrison, M. A., Harring, A. J., Sweeney, M. O., Capone, A., Miller, J. W., Dryja, T. P., Ott, J., et al. (2008) · Ophthalmology

Retinal Diseases and TreatmentsRetinal Imaging and Analysis

Cited by 104

AAV-mediated RLBP1 gene therapy improves the rate of dark adaptation in Rlbp1 knockout mice

Choi, V. W., Bigelow, C. E., McGee, T. L., Gujar, A. N., Li, H., Hanks, S. M., Vrouvlianis, J., Maker, M., Leehy, B., Zhang, Y., et al. (2015) · Molecular Therapy - Methods & Clinical Development

Retinal Development and DisordersVirus-based gene therapy research

Cited by 35

Complement factor B is critical for sub-RPE deposit accumulation in a model of Doyne honeycomb retinal dystrophy with features of age-related macular degeneration

Crowley, M. A., Garland, D. L., Sellner, H., Banks, A., Fan, L., Rejtar, T., Buchanan, N., Delgado, O., Xu, Y. Y., Jose, S., et al. (2023) · Human Molecular Genetics

Retinal Diseases and TreatmentsRetinal Development and Disorders

Cited by 20