| Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing Z Brownstein, A Abu-Rayyan, D Karfunkel-Doron, S Sirigu, B Davidov, ... European Journal of Human Genetics 22 (6), 768-775, 2014 | 48 | 2014 |
| Intranasal gonadotropin-releasing hormone agonist (GnRHa) for luteal-phase support following GnRHa triggering, a novel approach to avoid ovarian hyperstimulation syndrome in … I Bar-Hava, Y Mizrachi, D Karfunkel-Doron, Y Omer, L Sheena, N Carmon, ... Fertility and Sterility 106 (2), 330-333, 2016 | 47 | 2016 |
| The emergence and dissemination of CTX-M-producing Escherichia coli sequence type 131 causing community-onset bacteremia in Israel D Karfunkel, Y Carmeli, I Chmelnitsky, T Kotlovsky, S Navon-Venezia European journal of clinical microbiology & infectious diseases 32, 513-521, 2013 | 44 | 2013 |
| Cytoplasmic Mislocalization of POU 3 F 4 Due to Novel Mutations Leads to Deafness in Humans and Mice T Parzefall, S Shivatzki, DR Lenz, B Rathkolb, K Ushakov, D Karfunkel, ... Human mutation 34 (8), 1102-1110, 2013 | 24 | 2013 |
| Genomic medicine: principles and practice D Kumar, C Eng Oxford University Press, USA, 2015 | 8 | 2015 |
| Scopolamine treatment and adaptation to airsickness O Doron, O Samuel, D Karfunkel-Doron, D Tal Aerospace Medicine and Human Performance 91 (4), 313-317, 2020 | 4 | 2020 |
