Projects per year
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Dive into the research topics where Mark Pennesi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Serotonin Receptor Modulation of Neurotrophic Factors in the Retina
Project: Research project
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Serotonin Receptor Modulation of Neurotrophic Factors in the Retina
2/1/11 → 1/31/16
Project: Research project
Research output
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Adaptive optics ophthalmoscopy, multifocal ERG and OCTA in unique case of suspected torpedo maculopathy presenting with vitelliform lesion
Lambert, N. G., Grigorian, F., Vasconcelos, H., Watzke, R. C. & Pennesi, M. E., Mar 2021, In: American Journal of Ophthalmology Case Reports. 21, 100996.Research output: Contribution to journal › Article › peer-review
Open Access -
Characterization of the spectrum of ophthalmic changes in patients with alagille syndrome
da Palma, M. M., Igelman, A. D., Ku, C., Burr, A., You, J. Y., Place, E. M., Wang, N. K., Oh, J. K., Branham, K. E., Zhang, X., Ahn, J., Gorin, M. B., Lam, B. L., Ronquillo, C. C., Bernstein, P. S., Nagiel, A., Huckfeldt, R., Cabrera, M. T., Kelly, J. P., Bakall, B. & 8 others, , Jun 2021, In: Investigative Ophthalmology and Visual Science. 62, 7, 27.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
DNA- And RNA-based Gene Therapies in Ophthalmology
Ciulla, T., Pennesi, M. E., Kiss, S. & Cunningham, E. T., Jun 1 2021, In: International ophthalmology clinics. 61, 3, p. 3-16 14 p.Research output: Contribution to journal › Article › peer-review
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Examining whether aoslo-based foveal cone metrics in achromatopsia and albinism are representative of foveal cone structure
Litts, K. M., Woertz, E. N., Wynne, N., Brooks, B. P., Chacon, A., Connor, T. B., Costakos, D., Dumitrescu, A., Drack, A. V., Fishman, G. A., Hauswirth, W. W., Kay, C. N., Lam, B. L., Michaelides, M., Pennesi, M. E., Stepien, K. E., Strul, S., Summers, C. G. & Carroll, J., 2021, In: Translational Vision Science and Technology. 10, 6, 22.Research output: Contribution to journal › Article › peer-review
Open Access -
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome
Igelman, A. D., Ku, C., da Palma, M. M., Georgiou, M., Schiff, E. R., Lam, B. L., Sankila, E. M., Ahn, J., Pyers, L., Vincent, A., Ferraz Sallum, J. M., Zein, W. M., Oh, J. K., Maldonado, R. S., Ryu, J., Tsang, S. H., Gorin, M. B., Webster, A. R., Michaelides, M., Yang, P. & 1 others, , 2021, In: Ophthalmic Genetics. 42, 6, p. 664-673 10 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations