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YISHAY BEN MOSHE

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Shlomovitz O, Atias-Varon D, Yagel D, Barel O, Shasha-Lavsky H, Skorecki K, Eliyahu A, Bathish Y, Frajewicki V, Kushnir D, Zaid R, Paperna T, Ofir A, Tchirkov M, Hassan K, Kruzel E, Khazim K, Geron R, Weisman I, Hanut A, Nakhoul F, Kenig-Kozlovsky Y, Refael G, Antebi A, Storch S, Leiba M, Kagan M, Shukrun R, Rechavi G, Dekel B, Ben Moshe Y, Weiss K, Assady S, Vivante A. Genetic Markers Among the Israeli Druze Minority Population With End-Stage Kidney Disease. Am J Kidney Dis. 2024 02; 83(2):183-195. PMID: 37717846.
      Citations:    
    2. Kagan M, Semo-Oz R, Ben Moshe Y, Atias-Varon D, Tirosh I, Stern-Zimmer M, Eliyahu A, Raas-Rothschild A, Bivas M, Shlomovitz O, Chorin O, Rock R, Tzadok M, Ben-Zeev B, Heimer G, Bolkier Y, Gruber N, Dagan A, Bar Aluma BE, Pessach IM, Rechavi G, Barel O, Pode-Shakked B, Anikster Y, Vivante A. Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders. Front Genet. 2022; 13:1018062. PMID: 36699461; PMCID: PMC9868164.
      Citations:    
    3. Ben Moshe Y, Bekheirnia N, Smith RJH, Hicks J, Braun MC, Bekheirnia MR. Genetic diagnosis and renal biopsy findings in the setting of a renal genetics clinic. Am J Med Genet C Semin Med Genet. 2022 09; 190(3):302-308. PMID: 36239278.
      Citations: 1     Fields:    Translation:Humans
    4. Kagan M, Eliyahu A, Ben Moshe Y, Vivante A. [THE GENETIC BASIS OF CHRONIC KIDNEY DISEASE IN CHILDREN AND YOUNG ADULTS]. Harefuah. 2021 Dec; 160(12):839-846. PMID: 34957723.
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    5. Bolkier Y, Barel O, Marek-Yagel D, Atias-Varon D, Kagan M, Vardi A, Mishali D, Katz U, Salem Y, Tirosh-Wagner T, Jacobson JM, Raas-Rothschild A, Chorin O, Eliyahu A, Sarouf Y, Shlomovitz O, Veber A, Shalva N, Javasky E, Ben Moshe Y, Staretz-Chacham O, Rechavi G, Mane S, Anikster Y, Vivante A, Pode-Shakked B. Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects. J Med Genet. 2022 07; 59(7):691-696. PMID: 34215651.
      Citations:    
    6. Krausz M, Michaelson M, Israelit SH, Bahouth H, Lerner A, Hous N, Stahl S, Paled M, Hoffman A, Ben Moshe Y, Eldor L, Faber D, Barzely M, Netzer A, Zaaroor M, Miller B, Ziser A, Barlavie Y. [A seminar on the treatment of casualties of the Lebanon war 2006 at the Rambam Medical Center]. Harefuah. 2007 May; 146(5):322-4. PMID: 17674543.
      Citations:    
    7. Galinsky D, Fried V, Biderman A, Cwikel J, Ben Moshe Y. [Identifying the elderly at risk for falling and accompanying protocols]. Harefuah. 2000 Feb 01; 138(3):189-94, 271. PMID: 10883090.
      Citations:    Fields:    Translation:Humans
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