A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)
Sharon, Dror, Ben‐Yosef, Tamar, Goldenberg‐Cohen, Nitza, Pras, Eran, Gradstein, Libe, Soudry, Shiri, Mezer, Eedy, Zur, Dinah, Abbasi, Anan H., Zeitz, Christina, Cremers, Frans P. M., Khan, Muhammad I., Levy, Jaime, Rotenstreich, Ygal, Birk, Ohad S., Ehrenberg, Miriam, Leibu, Rina, Newman, Hadas, Shomron, Noam, Banin, Eyal, Perlman, Ido
Published in Human mutation (01.01.2020)
Published in Human mutation (01.01.2020)
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Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa
Collin, Rob W.J., Safieh, Christine, Littink, Karin W., Shalev, Stavit A., Garzozi, Hanna J., Rizel, Leah, Abbasi, Anan H., Cremers, Frans P.M., den Hollander, Anneke I., Klevering, B. Jeroen, Ben-Yosef, Tamar
Published in American journal of human genetics (14.05.2010)
Published in American journal of human genetics (14.05.2010)
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Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: The pitfalls of homozygosity mapping
Benayoun, Liat, Spiegel, Ronen, Auslender, Noa, Abbasi, Anan H, Rizel, Leah, Hujeirat, Yasir, Salama, Ihsan, Garzozi, Hanna J., Allon-Shalev, Stavit, Ben-Yosef, Tamar
Published in American journal of medical genetics. Part A (01.04.2009)
Published in American journal of medical genetics. Part A (01.04.2009)
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A Common Founder Mutation of CERKL Underlies Autosomal Recessive Retinal Degeneration with Early Macular Involvement among Yemenite Jews
Auslender, Noa, Sharon, Dror, Abbasi, Anan H, Garzozi, Hanna J, Banin, Eyal, Ben-Yosef, Tamar
Published in Investigative ophthalmology & visual science (01.12.2007)
Published in Investigative ophthalmology & visual science (01.12.2007)
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Kidney-ear axis
Abbasi, Anan H, Ramadan, Rawi, Hoffman, Aaron, Abassi, Zaid
Published in The Israel Medical Association journal (01.11.2007)
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Published in The Israel Medical Association journal (01.11.2007)
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