The 100 Most Frequently Cited Articles on Myopia

por Shemesh, Rachel, Dichter, Sarah, Mezer, Eedy, Wygnanski-Jaffe, Tamara
Publicado 2023

Childhood blindness incidence and aetiologies trends in Israel 2014–2020: what should we focus on?

por Israeli, Asaf, Peer, Hani, Gleitman, Ilana, Falick, Yishay, Mezer, Eedy
Publicado 2022

The Most-Cited Articles on Retinoblastoma: A Fifty-Year Perspective

por Shemesh, Rachel, Sandler, Hunter, Dichter, Sarah, Fabian, Ido Didi, Mezer, Eedy, Wygnanski-Jaffe, Tamara
Publicado 2023

Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1

por Rizel, Leah, Safieh, Christine, Shalev, Stavit A., Mezer, Eedy, Jabaly-Habib, Haneen, Ben-Neriah, Ziva, Chervinsky, Elena, Briscoe, Daniel, Ben-Yosef, Tamar
Publicado 2011

A novel intronic mutation of PDE6B is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews

por Tatour, Yasmin, Tamaiev, Jonathan, Shamaly, Shamaly, Colombo, Roberto, Bril, Ephrat, Rabinowitz, Tom, Yaakobi, Alona, Mezer, Eedy, Leibu, Rina, Tiosano, Beatrice, Shomron, Noam, Chowers, Itay, Banin, Eyal, Sharon, Dror, Ben-Yosef, Tamar
Publicado 2019

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

por Beryozkin, Avigail, Khateb, Samer, Idrobo-Robalino, Carlos Alberto, Khan, Muhammad Imran, Cremers, Frans P. M., Obolensky, Alexey, Hanany, Mor, Mezer, Eedy, Chowers, Itay, Newman, Hadas, Ben-Yosef, Tamar, Sharon, Dror, Banin, Eyal
Publicado 2020

The impact of the first peak of the COVID-19 pandemic on childhood myopia control practice patterns among ophthalmologists—an international pediatric ophthalmology and strabismus c...

por Kfir, Jonathan, Wygnanski-Jaffe, Tamara, Farzavandi, Sonal, Wei, Zhang, Yam, Jason C., de Faber, Jan Tjeerd, Orge, Faruk H., Aznauryan, Igor, Tsai, Chong-Bin, de Liano, Rosario Gomez, Natarajan, Sundaram, Dadeya, Subhash C., Agrawal, Siddharth, Sato, Miho, Shemesh, Rachel, Mezer, Eedy
Publicado 2022

Eight previously unidentified mutations found in the OA1 ocular albinism gene

por Mayeur, Hélène, Roche, Olivier, Vêtu, Christelle, Jaliffa, Carolina, Marchant, Dominique, Dollfus, Hélène, Bonneau, Dominique, Munier, Francis L, Schorderet, Daniel F, Levin, Alex V, Héon, Elise, Sutherland, Joanne, Lacombe, Didier, Said, Edith, Mezer, Eedy, Kaplan, Josseline, Dufier, Jean-Louis, Marsac, Cécile, Menasche, Maurice, Abitbol, Marc
Publicado 2006

Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry

por Ben Yosef, Tamar, Banin, Eyal, Chervinsky, Elana, Shalev, Stavit A., Leibu, Rina, Mezer, Eedy, Rotenstreich, Ygal, Goldenberg-Cohen, Nitza, Weiss, Shirel, Khan, Muhammad Imran, Panneman, Daan M., Hitti-Malin, Rebekkah J., Weiner, Chen, Roosing, Susanne, Cremers, Frans P. M., Pras, Eran, Zur, Dinah, Newman, Hadas, Deitch, Iris, Sharon, Dror, Ehrenberg, Miriam
Publicado 2023