The combination of whole‐exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies von Abu Diab, Alaa, AlTalbishi, Ala'a, Rosin, Boris, Kanaan, Moien, Kamal, Lara, Swaroop, Anand, Chowers, Itay, Banin, Eyal, Sharon, Dror, Khateb, Samer

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Elschnig's Spots in the Acute and Remission Stages in Preeclampsia: Spectral-Domain Optical Coherence Tomographic Features von AlTalbishi, Ala'a, Khateb, Samer, Amer, Radgonde

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CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History von Daich Varela, Malena, Georgiou, Michalis, Alswaiti, Yahya, Kabbani, Jamil, Fujinami, Kaoru, Fujinami-Yokokawa, Yu, Khoda, Shaheeni, Mahroo, Omar A., Robson, Anthony G., Webster, Andrew R., AlTalbishi, Alaa, Michaelides, Michel

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Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD von Sangermano, Riccardo, Deitch, Iris, Peter, Virginie G., Ba-Abbad, Rola, Place, Emily M., Zampaglione, Erin, Wagner, Naomi E., Fulton, Anne B., Coutinho-Santos, Luisa, Rosin, Boris, Dunet, Vincent, AlTalbishi, Ala’a, Banin, Eyal, Sousa, Ana Berta, Neves, Mariana, Larson, Anna, Quinodoz, Mathieu, Michaelides, Michel, Ben-Yosef, Tamar, Pierce, Eric A., Rivolta, Carlo, Webster, Andrew R., Arno, Gavin, Sharon, Dror, Huckfeldt, Rachel M., Bujakowska, Kinga M.

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TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations von AlTalbishi, Alaa, Zelinger, Lina, Zeitz, Christina, Hendler, Karen, Namburi, Prasanthi, Audo, Isabelle, Sheffer, Ruth, Yahalom, Claudia, Khateb, Samer, Banin, Eyal, Sharon, Dror

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Swept-source optical coherence tomography changes and visual acuity among Palestinian retinitis Pigmentosa patients: a cross-sectional study von Shalabi, Orjowan, Nazzal, Zaher, Natsheh, Muath, Iriqat, Salam, Michaelides, Michel, Ghanem, Muyassar, Aslanian, Alice, Alswaiti, Yahya, AlTalbishi, Alaa

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Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis von Cornelis, Stéphanie S, IntHout, Joanna, Runhart, Esmee H, Grunewald, Olivier, Lin, Siying, Corradi, Zelia, Khan, Mubeen, Hitti-Malin, Rebekkah J, Whelan, Laura, Farrar, G Jane, Sharon, Dror, van den Born, L Ingeborgh, Arno, Gavin, Simcoe, Mark, Michaelides, Michel, Webster, Andrew R, Roosing, Susanne, Mahroo, Omar A, Dhaenens, Claire-Marie, Cremers, Frans P M

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Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher Syndrome von Daich Varela, Malena, Wong, Shiao Wei, Kiray, Gulunay, Schlottmann, Patricio G., Arno, Gavin, Shams, Amjaad N. Abu, Mahroo, Omar A., Webster, Andrew R., AlTalbishi, Alaa, Michaelides, Michel

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ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease von Corradi, Zelia, Salameh, Manar, Khan, Mubeen, Héon, Elise, Mishra, Ketan, Hitti-Malin, Rebekkah J, AlSwaiti, Yahya, Aslanian, Alice, Banin, Eyal, Brooks, Brian P, Zein, Wadih M, Hufnagel, Robert B, Roosing, Susanne, Dhaenens, Claire-Marie, Sharon, Dror, Cremers, Frans P M, AlTalbishi, Alaa

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Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss von Karali, Marianthi, García-García, Gema, Kaminska, Karolina, AlTalbishi, Alaa, Cancellieri, Francesca, Testa, Francesco, Barillari, Maria Rosaria, Panagiotou, Evangelia S, Psillas, George, Vaclavik, Veronika, Tran, Viet H, Janeschitz-Kriegl, Lucas, Scholl, Hendrik Pn, Salameh, Manar, Barberán-Martínez, Pilar, Rodríguez-Muñoz, Ana, Armengot, Miguel, Scarpato, Margherita, Zeuli, Roberta, Quinodoz, Mathieu, Simonelli, Francesca, Rivolta, Carlo, Banfi, Sandro, Millán, José M

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Towards uncovering the role of incomplete penetrance in maculopathies through sequencing of 105 disease-associated genes von Hitti-Malin, Rebekkah J, Panneman, Daan M, Corradi, Zelia, Boonen, Erica G. M, Astuti, Galuh, Dhaenens, Claire-Marie, Stoehr, Heidi, Weber, Bernhard H. F, Sharon, Dror, Banin, Eyal, Karali, Marianthi, Banfi, Sandro, Ben-Yosef, Tamar, Glavac, Damjan, Farrar, G. Jane, Ayuso, Carmen, Liskova, Petra, Dudakova, Lubica, Vajter, Marie, Oldak, Monika, Szaflik, Jacek P, Matynia, Anna, Gorin, Michael B, Kaempjaervi, Kati, Bauwens, Miriam, De Baere, Elfride, Hoyng, Carel B, Li, Catherina H. Z, Klaver, Caroline C. W, Inglehearn, Chris F, Fujinami, Kaoru, Rivolta, Carlo, Allikmets, Rando, Zernant, Jana, Lee, Winston, Podhajcer, Osvaldo L, Fakin, Ana, Sajovic, Jana, Altalbishi, Alaa, Valeina, Sandra, Taurina, Gita, Vincent, Andrea L, Roberts, Lisa, Ramesar, Raj, Sartor, Giovanna, Luppi, Elena, Downes, Susan M, van den Born, L. Ingeborgh, Mclaren, Terri L, De Roach, John N, Lamey, Tina M, Thompson, Jennifer A, Chen, Fred K, Tracewska, Anna M, Kamakari, Smaragda, Sallum, Juliana Maria Ferraz, Bolz, Hanno J, Kayserili, Huelya, Roosing, Susanne, Cremers, Frans P. M

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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics von Khan, Mubeen, Cornelis, Stephanie S, Del Pozo-Valero, Marta, Whelan, Laura, Runhart, Esmee H, Mishra, Ketan, Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F, van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian, Dudakova, Lubica, Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian, Glavac, Damjan, Gorin, Michael B, Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M, Hoischen, Alexander, Hoyng, Carel B, Hufendiek, Karsten, Jaegle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W, Kousal, Bohdan, Lamey, Tina M, MacDonald, Ian M, Matynia, Anna, McLaren, Terri L, Mena, Marcela D, Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika, Pieterse, Marc, Podhajcer, Osvaldo L, Puech, Bernard, Ramesar, Raj, Ruether, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P, Thompson, Jennifer A, Thuillier, Caroline, Tracewska, Anna M, van Zweeden, Martine, Vincent, Andrea L, Zanlonghi, Xavier, Liskova, Petra, Stoehr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa, Weber, Bernhard H. F, Dhaenens, Claire-Marie, Cremers, Frans P. M

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CRB1-associated Retinal Dystrophies: Genetics, Clinical Characteristics and Natural History von Varela, Malena Daich, Georgiou, Michalis, Alswaiti, Yahya, Kabbani, Jamil, Fujinami, Kaoru, Fujinami-Yokokawa, Yu, Khoda, Shaheeni, Mahroo, Omar A, Robson, Anthony G, Webster, Andrew R, AlTalbishi, Alaa, Michaelides, Michel

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