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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Projects
- 1 Finished
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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 -
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 -
Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases
Qian, X., Wang, J., Wang, M., Igelman, A. D., Jones, K. D., Li, Y., Wang, K., Goetz, K. E., Birch, D. G., Yang, P., Pennesi, M. E. & Chen, R., Mar 2 2021, In: Frontiers in Genetics. 12, 647400.Research output: Contribution to journal › Article › peer-review
Open Access -
KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course—KCNV2 Study Group Report 1
Georgiou, M., Robson, A. G., Fujinami, K., Leo, S. M., Vincent, A., Nasser, F., Cabral De Guimarães, T. A., Khateb, S., Pontikos, N., Fujinami-Yokokawa, Y., Liu, X., Tsunoda, K., Hayashi, T., Vargas, M. E., Thiadens, A. A. H. J., de Carvalho, E. R., Nguyen, X. T. A., Arno, G., Mahroo, O. A., Martin-Merida, M. I. & 16 others, , May 2021, In: American journal of ophthalmology. 225, p. 95-107 13 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Noncoding mutation in rpgrip1 contributes to inherited retinal degenerations
Zou, G., Zhang, T., Cheng, X., Igelman, A. D., Wang, J., Qian, X., Fu, S., Wang, K., Koenekoop, R. K., Fishman, G. A., Yang, P., Li, Y., Pennesi, M. E. & Chen, R., 2021, In: Molecular vision. 27, p. 95-106 12 p.Research output: Contribution to journal › Article › peer-review