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Rapid molecular epidemiology investigations into two recent measles outbreaks in Israel detected from October 2023 to January 2024.
Bucris E, Indenbaum V, Levin T, Kanaaneh Y, Friedman K, Kushnir T, Sheffer R, Savion M, Salama M, Di-Castro N, Labay K, Butera M, Shihada B, Mor Z, Lustig Y, Zuckerman NS. Bucris E, et al. Among authors: sheffer r. Euro Surveill. 2024 Apr;29(16):2400202. doi: 10.2807/1560-7917.ES.2024.29.16.2400202. Euro Surveill. 2024. PMID: 38639095 Free PMC article.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, Kerkhof J, McConkey H, Chen CA, Batzir NA, Wang X, Palomares M, Carels M; ZFHX3 consortium; Dermaut B, Sadikovic B, Menten B, Yuan B, Vergult S, Callewaert B. Pérez Baca MDR, et al. Am J Hum Genet. 2024 Mar 7;111(3):509-528. doi: 10.1016/j.ajhg.2024.01.013. Epub 2024 Feb 26. Am J Hum Genet. 2024. PMID: 38412861
Hepatitis C Virus Elimination Program among Prison Inmates, Israel.
Eisen L, Mor Z, Madar M, Rabinovitch R, Dadon Y, Sheffer R, Kaliner E, Goldstein L. Eisen L, et al. Among authors: sheffer r. Emerg Infect Dis. 2023 Nov;29(11):2358-2361. doi: 10.3201/eid2911.230728. Emerg Infect Dis. 2023. PMID: 37877627 Free PMC article.
Hepatitis A virus transmission in a dental clinic setting.
Vinograd A, Ben-David D, Gozlan Y, Mor O, Mor Z, Sheffer R, Savion M. Vinograd A, et al. Among authors: sheffer r. Infect Control Hosp Epidemiol. 2023 Apr;44(4):692-693. doi: 10.1017/ice.2023.16. Epub 2023 Feb 15. Infect Control Hosp Epidemiol. 2023. PMID: 36789643 No abstract available.
Monkeypox outbreak in the Tel Aviv District, Israel, 2022.
Sheffer R, Savion M, Nuss N, Amitai Z, Salama M. Sheffer R, et al. Int J Infect Dis. 2023 Mar;128:88-90. doi: 10.1016/j.ijid.2022.12.023. Epub 2022 Dec 22. Int J Infect Dis. 2023. PMID: 36566775 Free PMC article.
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder.
Küry S, Ebstein F, Mollé A, Besnard T, Lee MK, Vignard V, Hery T, Nizon M, Mancini GMS, Giltay JC, Cogné B, McWalter K, Deb W, Mor-Shaked H, Li H, Schnur RE, Wentzensen IM, Denommé-Pichon AS, Fourgeux C, Verheijen FW, Faurie E, Schot R, Stevens CA, Smits DJ, Barr E, Sheffer R, Bernstein JA, Stimach CL, Kovitch E, Shashi V, Schoch K, Smith W, van Jaarsveld RH, Hurst ACE, Smith K, Baugh EH, Bohm SG, Vyhnálková E, Ryba L, Delnatte C, Neira J, Bonneau D, Toutain A, Rosenfeld JA; Undiagnosed Diseases Network; Audebert-Bellanger S, Gilbert-Dussardier B, Odent S, Laumonnier F, Berger SI, Smith ACM, Bourdeaut F, Stern MH, Redon R, Krüger E, Margueron R, Bézieau S, Poschmann J, Isidor B. Küry S, et al. Among authors: sheffer r. Am J Hum Genet. 2022 Feb 3;109(2):361-372. doi: 10.1016/j.ajhg.2021.12.011. Epub 2022 Jan 19. Am J Hum Genet. 2022. PMID: 35051358 Free PMC article.
99 results