| Direct evidence for epithelial-mesenchymal transitions in breast cancer AJ Trimboli, K Fukino, A De Bruin, G Wei, L Shen, SM Tanner, N Creasap, ... Cancer research 68 (3), 937-945, 2008 | 484 | 2008 |
| Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia A Raval, SM Tanner, JC Byrd, EB Angerman, JD Perko, SS Chen, ... Cell 129 (5), 879-890, 2007 | 455 | 2007 |
| The functional cobalamin (vitamin B12)–intrinsic factor receptor is a novel complex of cubilin and amnionless JC Fyfe, M Madsen, P Højrup, EI Christensen, SM Tanner, ... Blood 103 (5), 1573-1579, 2004 | 373 | 2004 |
| Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics K Virtaneva, FA Wright, SM Tanner, B Yuan, WJ Lemon, MA Caligiuri, ... Proceedings of the National Academy of Sciences 98 (3), 1124-1129, 2001 | 373 | 2001 |
| BAALC expression predicts clinical outcome of de novo acute myeloid leukemia patients with normal cytogenetics: a Cancer and Leukemia Group B Study CD Baldus, SM Tanner, AS Ruppert, SP Whitman, KJ Archer, G Marcucci, ... Blood 102 (5), 1613-1618, 2003 | 310 | 2003 |
| MTM1 mutations in X‐linked myotubular myopathy J Laporte, V Biancalana, SM Tanner, W Kress, V Schneider, ... Human mutation 15 (5), 393-409, 2000 | 240 | 2000 |
| Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes CD Baldus, S Liyanarachchi, K Mrózek, H Auer, SM Tanner, M Guimond, ... Proceedings of the National Academy of Sciences 101 (11), 3915-3920, 2004 | 219 | 2004 |
| BAALC, the human member of a novel mammalian neuroectoderm gene lineage, is implicated in hematopoiesis and acute leukemia SM Tanner, JL Austin, G Leone, LJ Rush, C Plass, K Heinonen, K Mrózek, ... Proceedings of the National Academy of Sciences 98 (24), 13901-13906, 2001 | 184 | 2001 |
| Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia SM Tanner, M Aminoff, FA Wright, S Liyanarachchi, M Kuronen, ... Nature genetics 33 (3), 426-429, 2003 | 172 | 2003 |
| Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal Cancer L Valle, T Serena-Acedo, S Liyanarachchi, H Hampel, I Comeras, Z Li, ... Science 321 (5894), 1361-1365, 2008 | 163 | 2008 |
| Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo Q He, M Madsen, A Kilkenney, B Gregory, EI Christensen, H Vorum, ... Blood 106 (4), 1447-1453, 2005 | 151 | 2005 |
| Mutations in the MTM1 gene implicated in X-linked myotubular myopathy J Laporte, C Guiraud-Chaumeil, MC Vincent, JL Mandel, SM Tanner, ... Human molecular genetics 6 (9), 1505-1511, 1997 | 148 | 1997 |
| Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene SM Tanner, Z Li, JD Perko, C Öner, M Çetin, Ç Altay, Z Yurtsever, ... Proceedings of the National Academy of Sciences 102 (11), 4130-4133, 2005 | 127 | 2005 |
| Aberrant promoter methylation of previously unidentified target genes is a common abnormality in medulloblastomas–Implications for tumor biology and potential clinical utility. MC Frühwald, MS O'Dorisio, Z Dai, SM Tanner, DA Balster, X Gao, ... Oncogene 20 (36), 2001 | 117 | 2001 |
| Aberrant promoter methylation of previously unidentified target genes is a common abnormality in medulloblastomas--implications for tumor biology and potential clinical utility. MC Frühwald, MS O'Dorisio, Z Dai, SM Tanner, DA Balster, X Gao, ... Oncogene 20 (36), 5033, 2001 | 117 | 2001 |
| BAALC, a novel marker of human hematopoietic progenitor cells CD Baldus, SM Tanner, DF Kusewitt, S Liyanarachchi, C Choi, ... Experimental hematology 31 (11), 1051-1056, 2003 | 103 | 2003 |
| RelA/p65 functions to maintain cellular senescence by regulating genomic stability and DNA repair J Wang, NK Jacob, KJ Ladner, A Beg, JD Perko, SM Tanner, ... EMBO reports 10 (11), 1272-1278, 2009 | 101 | 2009 |
| Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in … SM Tanner, Z Li, R Bisson, C Acar, C Öner, R Öner, M Çetin, MA Abdelaal, ... Human mutation 23 (4), 327-333, 2004 | 97 | 2004 |
| miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemia AK Eisfeld, G Marcucci, K Maharry, S Schwind, MD Radmacher, D Nicolet, ... Blood, The Journal of the American Society of Hematology 120 (2), 249-258, 2012 | 80 | 2012 |
| Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns SM Tanner, AC Sturm, EC Baack, S Liyanarachchi, A de la Chapelle Orphanet journal of rare diseases 7 (1), 1-15, 2012 | 63 | 2012 |
