| Citral is a new inducer of caspase-3 in tumor cell lines N Dudai, Y Weinstein, M Krup, T Rabinski, R Ofir Planta medica 71 (05), 484-488, 2005 | 290 | 2005 |
| Negative and positive regulation by transcription factor cAMP response element-binding protein is modulated by phosphorylation. WW Lamph, VJ Dwarki, R Ofir, M Montminy, IM Verma Proceedings of the National Academy of Sciences 87 (11), 4320-4324, 1990 | 283 | 1990 |
| Phosphorylation of the C terminus of Fos protein is required for transcriptional transrepression of the c-fos promoter R Ofir, VJ Dwarki, D Rashid, IM Verma Nature 348 (6296), 80-82, 1990 | 234 | 1990 |
| Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9 O Barel, SA Shalev, R Ofir, A Cohen, J Zlotogora, Z Shorer, G Mazor, ... The American Journal of Human Genetics 83 (2), 193-199, 2008 | 229 | 2008 |
| PLA2G6 mutation underlies infantile neuroaxonal dystrophy S Khateeb, H Flusser, R Ofir, I Shelef, G Narkis, G Vardi, Z Shorer, R Levy, ... The American Journal of Human Genetics 79 (5), 942-948, 2006 | 215 | 2006 |
| β‐Caryophyllene, a Compound Isolated from the Biblical Balm of Gilead (Commiphora gileadensis), Is a Selective Apoptosis Inducer for Tumor Cell Lines E Amiel, R Ofir, N Dudai, E Soloway, T Rabinsky, S Rachmilevitch Evidence‐Based Complementary and Alternative Medicine 2012 (1), 872394, 2012 | 189 | 2012 |
| Taxol-induced apoptosis in human SKOV3 ovarian and MCF7 breast carcinoma cells is caspase-3 and caspase-9 independent R Ofir, R Seidman, T Rabinski, M Krup, V Yavelsky, Y Weinstein, ... Cell Death & Differentiation 9 (6), 636-642, 2002 | 179 | 2002 |
| Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy O Agamy, BB Zeev, D Lev, B Marcus, D Fine, D Su, G Narkis, R Ofir, ... The American Journal of Human Genetics 87 (4), 538-544, 2010 | 170 | 2010 |
| Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ O Barel, Z Shorer, H Flusser, R Ofir, G Narkis, G Finer, H Shalev, ... The American Journal of Human Genetics 82 (5), 1211-1216, 2008 | 160 | 2008 |
| Anticancer potential of aloes: antioxidant, antiproliferative, and immunostimulatory attributes E Harlev, E Nevo, EP Lansky, R Ofir, A Bishayee Planta medica 78 (09), 843-852, 2012 | 152 | 2012 |
| Gene expression microarray profiles of cumulus cells in lean and overweight-obese polycystic ovary syndrome patients S Kenigsberg, Y Bentov, V Chalifa-Caspi, G Potashnik, R Ofir, OS Birk Molecular human reproduction 15 (2), 89-103, 2009 | 144 | 2009 |
| Screening of desert plants for use against bacterial pathogens in fish S Abutbul, A Golan-Goldhirsh, O Barazani, R Ofir, D Zilberg Israeli Journal of Aquaculture/Bamidgeh 57 (2), 71-80, 2005 | 129 | 2005 |
| High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2 S Mordechai, L Gradstein, A Pasanen, R Ofir, K El Amour, J Levy, ... The American Journal of Human Genetics 89 (3), 438-445, 2011 | 128 | 2011 |
| Inhibition of serotonin re-uptake by licorice constituents R Ofir, S Tamir, S Khatib, J Vaya Journal of molecular neuroscience 20, 135-140, 2003 | 123 | 2003 |
| Lethal contractural syndrome type 3 (LCCS3) is caused by a mutation in PIP5K1C, which encodes PIPKIγ of the phophatidylinsitol pathway G Narkis, R Ofir, D Landau, E Manor, M Volokita, R Hershkowitz, ... The American Journal of Human Genetics 81 (3), 530-539, 2007 | 121 | 2007 |
| CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds U Bar-Yosef, I Abuelaish, T Harel, N Hendler, R Ofir, OS Birk Human genetics 115, 302-309, 2004 | 111 | 2004 |
| Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2C H Romi, I Cohen, D Landau, S Alkrinawi, B Yerushalmi, R Hershkovitz, ... The American Journal of Human Genetics 90 (5), 893-899, 2012 | 96 | 2012 |
| Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein RY Birnbaum, A Zvulunov, D Hallel-Halevy, E Cagnano, G Finer, R Ofir, ... Nature genetics 38 (7), 749-751, 2006 | 96 | 2006 |
| Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract D Cohen, U Bar-Yosef, J Levy, L Gradstein, N Belfair, R Ofir, S Joshua, ... Investigative ophthalmology & visual science 48 (5), 2208-2213, 2007 | 82 | 2007 |
| Alteration of a cyclic AMP-dependent protein kinase phosphorylation site in the c-Fos protein augments its transforming potential I Tratner, R Ofir, IM Verma Molecular and cellular biology 12 (3), 998-1006, 1992 | 82 | 1992 |
