Research output per year
Research output per year
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Dive into the research topics where Hava Peretz is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Classical xanthinuria in nine israeli families and two isolated cases from germany: Molecular, biochemical and population genetics aspects
Peretz, H., Lagziel, A., Bittner, F., Kabha, M., Shtauber-Naamati, M., Zhuravel, V., Usher, S., Rump, S., Wollers, S., Bork, B., Mandel, H., Falik-Zaccai, T., Kalfon, L., Graessler, J., Zeharia, A., Heib, N., Shalev, H., Landau, D. & Levartovsky, D., Jul 2021, In: Biomedicines. 9, 7, 788.Research output: Contribution to journal › Article › peer-review
Open Access8 Scopus citations -
An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt
Peretz, H., Korostishevsky, M., Steinberg, D. M., Kabha, M., Usher, S., Krause, I., Shalev, H., Landau, D. & Levartovsky, D., Jan 2020, In: JIMD Reports. 51, 1, p. 45-52 8 p.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews
Peretz, H., Salomon, O., Mor-cohen, R., Usher, S., Zucker, M., Zivelin, A. & Seligsohn, U., Apr 2013, In: Journal of Thrombosis and Haemostasis. 11, 4, p. 724-730 7 p.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria
Peretz, H., Watson, D. G., Blackburn, G., Zhang, T., Lagziel, A., Shtauber-Naamati, M., Morad, T., Keren-Tardai, E., Greenshpun, V., Usher, S., Shalev, H., Landau, D. & Levartovsky, D., Oct 2012, In: Metabolomics. 8, 5, p. 951-959 9 p.Research output: Contribution to journal › Article › peer-review
22 Scopus citations -
Increased fibrosis progression rates in hepatitis C patients carrying the prothrombin G20210A mutation
Maharshak, N., Halfon, P., Deutsch, V., Peretz, H., Berliner, S., Fishman, S., Zelber-Sagi, S., Rozovski, U., Leshno, M. & Oren, R., 2011, In: World Journal of Gastroenterology. 17, 45, p. 5007-5013 7 p.Research output: Contribution to journal › Article › peer-review
Open Access25 Scopus citations