Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping
Beryozkin, Avigail, Zelinger, Lina, Bandah-Rozenfeld, Dikla, Shevach, Elia, Harel, Anat, Storm, Tim, Sagi, Michal, Eli, Dalia, Merin, Saul, Banin, Eyal, Sharon, Dror
Published in Investigative ophthalmology & visual science (24.02.2014)
Published in Investigative ophthalmology & visual science (24.02.2014)
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Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in Israel
Banin, Eyal, Bandah-Rozenfeld, Dikla, Obolensky, Alexey, Cideciyan, Artur V, Aleman, Tomas S, Marks-Ohana, Devora, Sela, Malka, Boye, Sanford, Sumaroka, Alexander, Roman, Alejandro J, Schwartz, Sharon B, Hauswirth, William W, Jacobson, Samuel G, Hemo, Itzhak, Sharon, Dror
Published in Human gene therapy (01.12.2010)
Published in Human gene therapy (01.12.2010)
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The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients
Bandah, Dikla, Merin, Saul, Ashhab, Munther, Banin, Eyal, Sharon, Dror
Published in Archives of ophthalmology (1960) (01.03.2009)
Published in Archives of ophthalmology (1960) (01.03.2009)
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Journal Article
A Complex Expression Pattern of Pax6 in the Pigeon Retina
Bandah, Dikla, Swissa, Tomer, Ben-Shlomo, Gil, Banin, Eyal, Ofri, Ron, Sharon, Dror
Published in Investigative ophthalmology & visual science (01.06.2007)
Published in Investigative ophthalmology & visual science (01.06.2007)
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Journal Article
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia
Bandah, Dikla, Rosenmann, Ada, Blumenfeld, Anat, Averbukh, Edward, Banin, Eyal, Sharon, Dror
Published in Molecular vision (28.01.2008)
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Published in Molecular vision (28.01.2008)
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A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews
Zelinger, Lina, Banin, Eyal, Obolensky, Alexey, Mizrahi-Meissonnier, Liliana, Beryozkin, Avigail, Bandah-Rozenfeld, Dikla, Frenkel, Shahar, Ben-Yosef, Tamar, Merin, Saul, Schwartz, Sharon B., Cideciyan, Artur V., Jacobson, Samuel G., Sharon, Dror
Published in American journal of human genetics (11.02.2011)
Published in American journal of human genetics (11.02.2011)
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Journal Article
Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa
Bandah-Rozenfeld, Dikla, Mizrahi-Meissonnier, Liliana, Farhy, Chen, Obolensky, Alexey, Chowers, Itay, Pe'er, Jacob, Merin, Saul, Ben-Yosef, Tamar, Ashery-Padan, Ruth, Banin, Eyal, Sharon, Dror
Published in American journal of human genetics (10.09.2010)
Published in American journal of human genetics (10.09.2010)
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Journal Article
Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews
Auslender, Noa, Bandah, Dikla, Rizel, Leah, Behar, Doron M, Shohat, Mordechai, Banin, Eyal, Allon-Shalev, Stavit, Sharony, Reuven, Sharon, Dror, Ben-Yosef, Tamar
Published in Genetic testing (01.06.2008)
Published in Genetic testing (01.06.2008)
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FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies
DI GIOIA, Silvio Alessandro, LETTEBOER, Stef J. F, KOSTIC, Corinne, BANDAH-ROZENFELD, Dikla, HETTERSCHIJT, Lisette, SHARON, Dror, ARSENIJEVIC, Yvan, ROEPMAN, Ronald, RIVOLTA, Carlo
Published in Human molecular genetics (01.12.2012)
Published in Human molecular genetics (01.12.2012)
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Journal Article
Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations
Beryozkin, Avigail, Zelinger, Lina, Bandah-Rozenfeld, Dikla, Harel, Anat, Strom, Tim A, Merin, Saul, Chowers, Itay, Banin, Eyal, Sharon, Dror
Published in Investigative ophthalmology & visual science (01.03.2013)
Published in Investigative ophthalmology & visual science (01.03.2013)
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Journal Article
Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa
Bandah-Rozenfeld, Dikla, Collin, Rob W.J., Banin, Eyal, Ingeborgh van den Born, L., Coene, Karlien L.M., Siemiatkowska, Anna M., Zelinger, Lina, Khan, Muhammad I., Lefeber, Dirk J., Erdinest, Inbar, Testa, Francesco, Simonelli, Francesca, Voesenek, Krysta, Blokland, Ellen A.W., Strom, Tim M., Klaver, Caroline C.W., Qamar, Raheel, Banfi, Sandro, Cremers, Frans P.M., Sharon, Dror, den Hollander, Anneke I.
Published in American journal of human genetics (13.08.2010)
Published in American journal of human genetics (13.08.2010)
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Journal Article
Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population
Bandah-Rozenfeld, Dikla, Littink, Karin W, Ben-Yosef, Tamar, Strom, Tim M, Chowers, Itay, Collin, Rob W J, den Hollander, Anneke I, van den Born, L Ingeborgh, Zonneveld, Marijke N, Merin, Saul, Banin, Eyal, Cremers, Frans P M, Sharon, Dror
Published in Investigative ophthalmology & visual science (01.09.2010)
Published in Investigative ophthalmology & visual science (01.09.2010)
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Journal Article
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa
Van Schil, Kristof, Klevering, B Jeroen, Leroy, Bart P, Pott, Jan Willem R, Bandah-Rozenfeld, Dikla, Zonneveld-Vrieling, Marijke N, Sharon, Dror, den Hollander, Anneke I, Cremers, Frans P M, De Baere, Elfride, Collin, Rob W J, van den Born, L Ingeborgh
Published in Investigative ophthalmology & visual science (01.11.2015)
Published in Investigative ophthalmology & visual science (01.11.2015)
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Enhanced S-cone function with preserved rod function: a new clinical phenotype
Kinori, Michael, Pras, Eran, Kolker, Andrew, Ferman-Attar, Gili, Moroz, Iris, Moisseiev, Joseph, Bandah-Rozenfeld, Dikla, Mizrahi-Meissonnier, Liliana, Sharon, Dror, Rotenstreich, Ygal
Published in Molecular vision (2011)
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Published in Molecular vision (2011)
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