Reuven Sharony

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70 Article
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2 Review article
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Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1–8 does not cause Beals syndrome
Maya, I., Kahana, S., Agmon-Fishman, I., Klein, C., Matar, R., Berger, R., Shohat, M., Basel-Salmon, L., Sharony, R. & Sagi-Dain, L., Oct 2020, In: European Journal of Medical Genetics. 63, 10, 104008.
Research output: Contribution to journal › Article › peer-review
3 Scopus citations
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1
Brownstein, Z., Gulsuner, S., Walsh, T., Martins, F. T. A., Taiber, S., Isakov, O., Lee, M. K., Bordeynik-Cohen, M., Birkan, M., Chang, W., Casadei, S., Danial-Farran, N., Abu-Rayyan, A., Carlson, R., Kamal, L., Arnthórsson, A., Sokolov, M., Gilony, D., Lipschitz, N. & Frydman, M. & 30 others, Davidov, B., Macarov, M., Sagi, M., Vinkler, C., Poran, H., Sharony, R., Samra, N., Zvi, N., Baris-Feldman, H., Singer, A., Handzel, O., Hertzano, R., Ali-Naffaa, D., Ruhrman-Shahar, N., Madgar, O., Sofrin-Drucker, E., Peleg, A., Khayat, M., Shohat, M., Basel-Salmon, L., Pras, E., Lev, D., Wolf, M., Steingrimsson, E., Shomron, N., Kelley, M. W., Kanaan, M. N., Allon-Shalev, S., King, M. C. & Avraham, K. B., 1 Oct 2020, In: Clinical Genetics. 98, 4, p. 353-364 12 p.
Research output: Contribution to journal › Article › peer-review

Open Access
22 Scopus citations
Chromosomal microarray findings in pregnancies with an isolated pelvic kidney
Sagi-Dain, L., Singer, A., Frumkin, A., Shalata, A., Koifman, A., Segel, R., Benyamini, L., Rienstein, S., Kahyat, M., Sharony, R., Maya, I. & Shachar, S. B., 1 Jan 2019, In: Journal of Perinatal Medicine. 47, 1, p. 30-34 5 p.
Research output: Contribution to journal › Article › peer-review
9 Scopus citations
Non-visualization of fetal gallbladder in microarray era–a retrospective cohort study and review of the literature
Sagi-Dain, L., Singer, A., Hadid, Y., Sharony, R., Vinkler, C., Bar-Shira, A., Segel, R., Ben Shachar, S. & Maya, I., 18 Aug 2019, In: Journal of Maternal-Fetal and Neonatal Medicine. 32, 16, p. 2643-2648 6 p.
Research output: Contribution to journal › Article › peer-review
10 Scopus citations
The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally ^†
Sukenik-Halevy, R., Katz, A., Regev, R. H., Markovitch, O., Sharony, R., Ganor Paz, Y. & Biron-Shental, T., 4 Mar 2019, In: Journal of Maternal-Fetal and Neonatal Medicine. 32, 5, p. 753-759 7 p.
Research output: Contribution to journal › Article › peer-review
2 Scopus citations

Reuven Sharony

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Research output

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1–8 does not cause Beals syndrome

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney

Non-visualization of fetal gallbladder in microarray era–a retrospective cohort study and review of the literature

The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally †

The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally ^†