| GeneCards Version 3: the human gene integrator M Safran, I Dalah, J Alexander, N Rosen, T Iny Stein, M Shmoish, N Nativ, ... Database 2010, baq020, 2010 | 1708 | 2010 |
| The genome of a songbird WC Warren, DF Clayton, H Ellegren, AP Arnold, LDW Hillier, A Künstner, ... Nature 464 (7289), 757-762, 2010 | 964 | 2010 |
| A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families … H Lahat, E Pras, T Olender, N Avidan, E Ben-Asher, O Man, ... The American Journal of Human Genetics 69 (6), 1378-1384, 2001 | 798 | 2001 |
| Genome analysis of the platypus reveals unique signatures of evolution Nature 453 (7192), 175-183, 2008 | 773 | 2008 |
| 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 | 602 | 2001 |
| Widespread ectopic expression of olfactory receptor genes E Feldmesser, T Olender, M Khen, I Yanai, R Ophir, D Lancet BMC genomics 7, 1-18, 2006 | 284 | 2006 |
| Human gene-centric databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDE M Safran, V Chalifa-Caspi, O Shmueli, T Olender, M Lapidot, N Rosen, ... Nucleic acids research 31 (1), 142-146, 2003 | 241 | 2003 |
| GeneCards™ 2002: towards a complete, object-oriented, human gene compendium M Safran, I Solomon, O Shmueli, M Lapidot, S Shen-Orr, A Adato, ... Bioinformatics 18 (11), 1542-1543, 2002 | 240 | 2002 |
| In-silico human genomics with GeneCards G Stelzer, I Dalah, TI Stein, Y Satanower, N Rosen, N Nativ, D Oz-Levi, ... Human genomics 5, 1-9, 2011 | 239 | 2011 |
| The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation L Basel-Vanagaite, R Attia, M Yahav, RJ Ferland, L Anteki, CA Walsh, ... Journal of medical genetics 43 (3), 203-210, 2006 | 212 | 2006 |
| VarElect: the phenotype-based variation prioritizer of the GeneCards Suite G Stelzer, I Plaschkes, D Oz-Levi, A Alkelai, T Olender, S Zimmerman, ... BMC genomics 17, 195-206, 2016 | 205 | 2016 |
| Human olfaction: from genomic variation to phenotypic diversity Y Hasin-Brumshtein, D Lancet, T Olender Trends in Genetics 25 (4), 178-184, 2009 | 198 | 2009 |
| USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses A Adato, S Vreugde, T Joensuu, N Avidan, R Hamalainen, O Belenkiy, ... European Journal of Human Genetics 10 (6), 339-350, 2002 | 196 | 2002 |
| Spatiotemporal proteomic analysis of stress granule disassembly using APEX reveals regulation by SUMOylation and links to ALS pathogenesis H Marmor-Kollet, A Siany, N Kedersha, N Knafo, N Rivkin, YM Danino, ... Molecular cell 80 (5), 876-891. e6, 2020 | 185 | 2020 |
| Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy EK Ruzzo, JM Capo-Chichi, B Ben-Zeev, D Chitayat, H Mao, AL Pappas, ... Neuron 80 (2), 429-441, 2013 | 178 | 2013 |
| Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis D Oz-Levi, B Ben-Zeev, EK Ruzzo, Y Hitomi, A Gelman, K Pelak, ... The American Journal of Human Genetics 91 (6), 1065-1072, 2012 | 177 | 2012 |
| Genic insights from integrated human proteomics in GeneCards S Fishilevich, S Zimmerman, A Kohn, T Iny Stein, T Olender, E Kolker, ... Database 2016, baw030, 2016 | 162 | 2016 |
| The canine olfactory subgenome T Olender, T Fuchs, C Linhart, R Shamir, M Adams, F Kalush, M Khen, ... Genomics 83 (3), 361-372, 2004 | 156 | 2004 |
| Update on the olfactory receptor (OR) gene superfamily T Olender, D Lancet, DW Nebert Human genomics 3, 1-11, 2008 | 145 | 2008 |
| Why do young women smoke? I. Direct and interactive effects of environment, psychological characteristics and nicotinic cholinergic receptor genes L Greenbaum, K Kanyas, O Karni, Y Merbl, T Olender, A Horowitz, A Yakir, ... Molecular psychiatry 11 (3), 312-322, 2006 | 132 | 2006 |
