| Distinctive patterns of microRNA expression in primary muscular disorders I Eisenberg, A Eran, I Nishino, M Moggio, C Lamperti, AA Amato, ... Proceedings of the National Academy of Sciences 104 (43), 17016-17021, 2007 | 603 | 2007 |
| The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy I Eisenberg, N Avidan, T Potikha, H Hochner, M Chen, T Olender, ... Nature genetics 29 (1), 83-87, 2001 | 592 | 2001 |
| Trained memory of human uterine NK cells enhances their function in subsequent pregnancies M Gamliel, D Goldman-Wohl, B Isaacson, C Gur, N Stein, R Yamin, ... Immunity 48 (5), 951-962. e5, 2018 | 269 | 2018 |
| MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation MS Alexander, G Kawahara, N Motohashi, JC Casar, I Eisenberg, ... Cell Death & Differentiation 20 (9), 1194-1208, 2013 | 154 | 2013 |
| Regulatory role of microRNAs in ovarian function T Imbar, I Eisenberg Fertility and sterility 101 (6), 1524-1530, 2014 | 149 | 2014 |
| miRNAS in normal and diseased skeletal muscle I Eisenberg, MS Alexander, LM Kunkel Journal of cellular and molecular medicine 13 (1), 2-11, 2009 | 148 | 2009 |
| MicroRNA-486–dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy–associated symptoms MS Alexander, JC Casar, N Motohashi, NM Vieira, I Eisenberg, ... The Journal of clinical investigation 124 (6), 2651-2667, 2014 | 141 | 2014 |
| Hereditary inclusion body myopathy: the Middle Eastern genetic cluster Z Argov, I Eisenberg, G Grabov–Nardini, M Sadeh, I Wirguin, D Soffer, ... Neurology 60 (9), 1519-1523, 2003 | 130 | 2003 |
| Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps I Eisenberg, G Grabov‐Nardini, H Hochner, M Korner, M Sadeh, ... Human mutation 21 (1), 99-99, 2003 | 128 | 2003 |
| Muscular dystrophy due to dysferlin deficiency in Libyan Jews: clinical and genetic features Z Argov, M Sadeh, K Mazor, D Soffer, E Kahana, I Eisenberg, ... Brain 123 (6), 1229-1237, 2000 | 127 | 2000 |
| Zika Virus Infects Early-and Midgestation Human Maternal Decidual Tissues, Inducing Distinct Innate Tissue Responses in the Maternal-Fetal Interface (vol 91, e01905-16, 2017) Y Weisblum, E Oiknine-Djian, OM Vorontsov, R Haimov-Kochman, ... JOURNAL OF VIROLOGY 93 (22), 2019 | 111* | 2019 |
| Zika virus infects early-and midgestation human maternal decidual tissues, inducing distinct innate tissue responses in the maternal-fetal interface Y Weisblum, E Oiknine-Djian, OM Vorontsov, R Haimov-Kochman, ... Journal of virology 91 (4), e01905-16, 2017 | 111 | 2017 |
| No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation I Salama, S Hinderlich, Z Shlomai, I Eisenberg, S Krause, K Yarema, ... Biochemical and biophysical research communications 328 (1), 221-226, 2005 | 106 | 2005 |
| Regulation of DMD pathology by an ankyrin-encoded miRNA MS Alexander, JC Casar, N Motohashi, JA Myers, I Eisenberg, ... Skeletal muscle 1 (1), 1-17, 2011 | 99 | 2011 |
| The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular … S Hinderlich, I Salama, I Eisenberg, T Potikha, LR Mantey, KJ Yarema, ... FEBS letters 566 (1-3), 105-109, 2004 | 93 | 2004 |
| Various types of herediary inclusion body myopathies map to chromosome 9p1‐q1 Z Argov, E Tirman, I Eisenberg, M Sadeh, CE Siedman, JG Siedman, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 79 | 1997 |
| Multimarker RT–PCR assay for the detection of minimal residual disease in sentinel lymph nodes of breast cancer patients A Nissan, D Jager, M Roystacher, D Prus, T Peretz, I Eisenberg, ... British journal of cancer 94 (5), 681-685, 2006 | 78 | 2006 |
| Multimarker RT-PCR assay for the detection of minimal residual disease in sentinel lymph nodes of breast cancer patients. A Nissan, D Jager, T Peretz, M Roycetacher, D Prus, I Eisenberg, ... Cancer Research 64 (7 Supplement), 759-759, 2004 | 78 | 2004 |
| Attention deficit hyperactivity disorder in obese melanocortin‐4‐receptor (MC4R) deficient subjects: A newly described expression of MC4R deficiency A Agranat‐Meged, Y Ghanadri, I Eisenberg, Z Ben Neriah, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 62 | 2008 |
| Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers P Arashiro, I Eisenberg, AT Kho, AMP Cerqueira, M Canovas, HCA Silva, ... Proceedings of the National Academy of Sciences 106 (15), 6220-6225, 2009 | 60 | 2009 |
