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Dive into the research topics where Ruth Schreiber is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure
Chowers, G., Ben-Ruby, D., Atias-Varon, D., Shlomovitz, O., Slabodnik-Kaner, K., Kagan, M., Avayou, S., Romanjuk, E., Rogachev, B., Haviv, Y. S., Birk, O. S., Hadar, N., Bathish, Y., Barshack, I., Volkov, A., Avivi, C., Pavlovsky, A., Haskin, O., Simon, A. J. & Glick-Saar, E. & 10 others, , 1 Apr 2025, In: Kidney International Reports. 10, 4, p. 1274-1278 5 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula Ancestry
Agam, N., Wormser, O., Biller, A., Hadar, N., Dolgin, V., Freund, O., Jean, M. M., Safran, A., Poleg, T., Kanengisser-Pines, B., Kebesch-Assi, R., Mazor-Oring, M., Cohen-Zontag, O., Zmudjak-Olevson, M., Ben-Menachem, S., Ben-Ruby, D., Shlomovitz, O., Vivante, A., Dekel, B. & Birk, O. S. & 1 others, , 1 Dec 2025, In: American Journal of Kidney Diseases. 86, 6, p. 730-739.e1Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure
Ben-Moshe, Y., Shlomovitz, O., Atias-Varon, D., Haskin, O., Ben-Shalom, E., Shasha Lavsky, H., Volovelsky, O., Mane, S., Ben-Ruby, D., Chowers, G., Skorecki, K., Borovitz, Y., Kagan, M., Mor, N., Khavkin, Y., Tzvi-Behr, S., Pollack, S., Toder, M. P., Geylis, M. & Schnapp, A. & 8 others, , 1 Oct 2023, In: Kidney International Reports. 8, 10, p. 2126-2135 10 p.Research output: Contribution to journal › Article › peer-review
Open Access11 Scopus citations -
RAAS-deficient organoids indicate delayed angiogenesis as a possible cause for autosomal recessive renal tubular dysgenesis
Pode-Shakked, N., Slack, M., Sundaram, N., Schreiber, R., McCracken, K. W., Dekel, B., Helmrath, M. & Kopan, R., 1 Dec 2023, In: Nature Communications. 14, 1, 8159.Research output: Contribution to journal › Article › peer-review
Open Access17 Scopus citations -
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome
Hadar, N., Schreiber, R., Eskin-Schwartz, M., Kristal, E., Shubinsky, G., Ling, G., Cohen, I., Geylis, M., Nahum, A., Yogev, Y. & Birk, O. S., 1 Oct 2023, In: European Journal of Human Genetics. 31, 10, p. 1101-1107 7 p.Research output: Contribution to journal › Article › peer-review
Open Access7 Scopus citations -
Hypoparathyroidism-retardation-dysmorphism syndrome—Clinical insights from a large longitudinal cohort in a single medical center
David, O., Agur, R., Novoa, R., Shaki, D., Walker, D., Carmon, L., Eskin-Schwartz, M., Birk, O. S., Ling, G., Schreiber, R., Loewenthal, N., Haim, A. & Hershkovitz, E., 22 Jul 2022, In: Frontiers in Pediatrics. 10, 916679.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Glomerular involvement in children with H syndrome
David, O., Geylis, M., Kristal, E., Ling, G. & Schreiber, R., 1 Mar 2021, In: Pediatric Nephrology. 36, 3, p. 721-724 4 p.Research output: Contribution to journal › Article › peer-review
5 Scopus citations -
דיסגנזיס של אבובית הכליה (Renal tubular dysgenesis) משנית למוטציות בגן המהפך אנגיוטנסין: [מתוך המדור: מאמרים]
Translated title of the contribution :Renal tubular dysgenesis secondary to mutations in genes encoding the renin-angiotensis system Research output: Contribution to journal › Article › peer-review
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Listeria meningitis in an immunocompetent adolescent
Hassin, O., Danino, D., Schreiber, R., Leibovitz, E. & Amit, N., 1 Mar 2020, In: Israel Medical Association Journal. 22, 3, p. 195-196 2 p.Research output: Contribution to journal › Comment/debate
4 Scopus citations -
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I
Halperin, D., Dolgin, V., Geylis, M., Drabkin, M., Yogev, Y., Wormser, O., Schreiber, R., Shalev, H., Landau, D. & Birk, O. S., 1 Jan 2019, In: Annals of Human Genetics. 83, 5, p. 361-366 6 p.Research output: Contribution to journal › Article › peer-review
5 Scopus citations