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1991 …2026

Research activity per year

Personal profile

Expertise related to UN Sustainable Development Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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Collaborations and top research areas from the last five years

Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
  • De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

    Quinodoz, M., Rodenburg, K., Cvackova, Z., Kaminska, K., de Bruijn, S. E., Iglesias-Romero, A. B., Boonen, E. G. M., Ullah, M., Zomer, N., Folcher, M., Bijon, J., Holtes, L. K., Tsang, S. H., Corradi, Z., Freund, K. B., Shliaga, S., Panneman, D. M., Hitti-Malin, R. J., Ali, M. & AlTalbishi, A. & 168 others, Andréasson, S., Ansari, G., Arno, G., Astuti, G. D. N., Ayuso, C., Ayyagari, R., Banfi, S., Banin, E., Barakat, T. S., Barboni, M. T. S., Bauwens, M., Ben-Yosef, T., Bernard, V., Birch, D. G., Biswas, P., Blanco-Kelly, F., Bocquet, B., Boon, C. J. F., Branham, K., Bremond-Gignac, D., Britten-Jones, A. C., Bujakowska, K. M., Burin des Roziers, C., Cadena, E. L., Calzetti, G., Cancellieri, F., Cattaneo, L., Chadderton, N., Charbel Issa, P., Coutinho-Santos, L., Daiger, S. P., De Baere, E., De Bruyne, M., de la Cerda, B., De Roach, J. N., De Zaeytijd, J., Derks, R., Dhaenens, C. M., Dudakova, L., Duncan, J. L., Farrar, G. J., Feltgen, N., Fenner, B. J., Fernández-Caballero, L., Ferraz Sallum, J. M., Gana, S., Garanto, A., Gardner, J. C., Gilissen, C., Gonzàlez-Duarte, R., Goto, K., Griffiths-Jones, S., Haack, T. B., Haer-Wigman, L., Hardcastle, A. J., Hayashi, T., Héon, E., Hoefsloot, L. H., Hoischen, A., Holtan, J. P., Hoyng, C. B., Ibanez, M. B. B., Inglehearn, C. F., Iwata, T., Jensson, B. O., Jones, K., Kalatzis, V., Kamakari, S., Karali, M., Kellner, U., Klaver, C. C. W., Knézy, K., Koenekoop, R. K., Kohl, S., Kominami, T., Kühlewein, L., Lamey, T. M., Leibu, R., Leroy, B. P., Liskova, P., Lopez, I., López-Rodríguez, V. R. D. J., Mahieu, Q., Mahroo, O. A., Manes, G., Mansard, L., Martín-Gutiérrez, M. P., Martins, N., Mauring, L., McKibbin, M., McLaren, T. L., Meunier, I., Michaelides, M., Millán, J. M., Mizobuchi, K., Mukherjee, R., Nagy, Z. Z., Neveling, K., Ołdak, M., Oorsprong, M., Pan, Y., Papachristou, A., Percesepe, A., Pfau, M., Pierce, E. A., Place, E., Ramesar, R., Ramond, F., Rasquin, F. A., Rice, G. I., Roberts, L., Rodríguez-Hidalgo, M., Ruiz-Ederra, J., Sabir, A. H., Sajiki, A. F., Sánchez-Barbero, A. I., Sarma, A. S., Sangermano, R., Santos, C. M., Scarpato, M., Scholl, H. P. N., Sharon, D., Signorini, S. G., Simonelli, F., Sousa, A. B., Stefaniotou, M., Stefansson, K., Stingl, K., Suga, A., Sulem, P., Sullivan, L. S., Szabó, V., Szaflik, J. P., Taurina, G., Thiadens, A. A. H. J., Toomes, C., Tran, V. H., Tsilimbaris, M. K., Tsoka, P., Vaclavik, V., Vajter, M., Valeina, S., Valente, E. M., Valentine, C., Valero, R., Valleix, S., van Aerschot, J., van den Born, L. I., Van Heetvelde, M., Verhoeven, V. J. M., Vincent, A. L., Webster, A. R., Whelan, L., Wissinger, B., Yioti, G. G., Yoshitake, K., Zenteno, J. C., Zeuli, R., Zuleger, T., Landau, C., Jacob, A. I., Lin, S., Cremers, F. P. M., Lee, W., Ellingford, J. M., Stanek, D., Roosing, S. & Rivolta, C., Jan 2026, In: Nature Genetics. 58, 1, p. 169-179 11 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    4 Scopus citations
  • RNA editing of pathogenic variants causing inherited retinal diseases using endogenous ADAR-current and future perspectives

    Salameh, M., Schneider, N., Valensi, J., Sarma, A. S., Levanon, E. Y., Ben-Aroya, S. & Sharon, D., Jun 2026, In: Molecular Aspects of Medicine. 109, 101475.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population

    Shalom, S., Gradstein, L., Pras, E., Valensi, J., Birk, O. S., Blumenfeld, A., Eilat, A., Macarov, M., Poleg, T., Cremers, F. P. M., Roosing, S., Panneman, D. M., Hollander, N., Goldenberg-Cohen, N., Yahalom, C., Banin, E., Ben-Yosef, T. & Sharon, D., Apr 2026, In: Investigative Ophthalmology and Visual Science. 67, 4, 24.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • The potential use of anti-codon engineered tRNAs (ACE-tRNAs) to treat nonsense variants causing inherited retinal diseases

    Sarma, A. S. & Sharon, D., Feb 2026, In: Molecular Aspects of Medicine. 107, 101443.

    Research output: Contribution to journalArticlepeer-review

  • Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy

    Ehrenberg, M., Avraham, M., Asodu, S. S., Moye, A. R., Sangermano, R., Rizel, L., Ali-Nasser, T., Sher, I., Gurwitz, D., Chao, K. R., Rivera, A., Webster, A. R., Rivolta, C., Newman, H., Pras, E., Rotenstreich, Y., Banin, E., Pierce, E. A., Zur, D. & Arno, G. & 4 others, Bujakowska, K. M., Lin, S., Sharon, D. & Ben-Yosef, T., Jun 2025, In: Genetics in Medicine. 27, 6, 101401.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    3 Scopus citations