| The myoD Gene Family: Nodal Point During Specification of the Muscle Cell Lineage H Weintraub, R Davis, S Tapscott, M Thayer, M Krause, R Benezra, ... Science 251 (4995), 761-766, 1991 | 1952 | 1991 |
| Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD. H Weintraub, SJ Tapscott, RL Davis, MJ Thayer, MA Adam, AB Lassar, ... Proceedings of the National Academy of Sciences 86 (14), 5434-5438, 1989 | 1256 | 1989 |
| MyoD1: a nuclear phosphoprotein requiring a Myc homology region to convert fibroblasts to myoblasts SJ Tapscott, RL Davis, MJ Thayer, PF Cheng, H Weintraub, AB Lassar Science 242 (4877), 405-411, 1988 | 991 | 1988 |
| MyoD and the transcriptional control of myogenesis CA Berkes, SJ Tapscott Seminars in cell & developmental biology 16 (4-5), 585-595, 2005 | 965 | 2005 |
| The circuitry of a master switch: Myod and the regulation of skeletal muscle gene transcription SJ Tapscott Oxford University Press for The Company of Biologists Limited 132 (12), 2685 …, 2005 | 866 | 2005 |
| Decreased expression of striatal signaling genes in a mouse model of Huntington’s disease R Luthi-Carter, A Strand, NL Peters, SM Solano, ZR Hollingsworth, ... Human molecular genetics 9 (9), 1259-1271, 2000 | 850 | 2000 |
| A unifying genetic model for facioscapulohumeral muscular dystrophy RJLF Lemmers, PJ Van der Vliet, R Klooster, S Sacconi, P Camaño, ... Science 329 (5999), 1650-1653, 2010 | 762 | 2010 |
| Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 RJLF Lemmers, R Tawil, LM Petek, J Balog, GJ Block, GWE Santen, ... Nature genetics 44 (12), 1370-1374, 2012 | 653 | 2012 |
| Conserved roles of mouse DUX and human DUX4 in activating cleavage-stage genes and MERVL/HERVL retrotransposons PG Hendrickson, JA Doráis, EJ Grow, JL Whiddon, JW Lim, CL Wike, ... Nature genetics 49 (6), 925-934, 2017 | 645 | 2017 |
| Generation of neurons by transient expression of neural bHLH proteins in mammalian cells MH Farah, JM Olson, HB Sucic, RI Hume, SJ Tapscott, DL Turner Development 127 (4), 693-702, 2000 | 580 | 2000 |
| Positive autoregulation of the myogenic determination gene MyoD1 MJ Thayer, SJ Tapscott, RL Davis, WE Wright, AB Lassar, H Weintraub Cell 58 (2), 241-248, 1989 | 558 | 1989 |
| Genome-wide MyoD binding in skeletal muscle cells: a potential for broad cellular reprogramming Y Cao, Z Yao, D Sarkar, M Lawrence, GJ Sanchez, MH Parker, ... Developmental cell 18 (4), 662-674, 2010 | 526 | 2010 |
| Selective accumulation of MyoD and myogenin mRNAs in fast and slow adult skeletal muscle is controlled by innervation and hormones SM Hughes, JM Taylor, SJ Tapscott, CM Gurley, WJ Carter, CA Peterson Development 118 (4), 1137-1147, 1993 | 513 | 1993 |
| Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene L Snider, LN Geng, RJLF Lemmers, M Kyba, CB Ware, AM Nelson, ... PLoS genetics 6 (10), e1001181, 2010 | 504 | 2010 |
| Functional antagonism between c-Jun and MyoD proteins: a direct physical association E Bengal, L Ransone, R Scharfmann, VJ Dwarki, SJ Tapscott, ... Cell 68 (3), 507-519, 1992 | 500 | 1992 |
| DUX4 activates germline genes, retroelements, and immune mediators: implications for facioscapulohumeral dystrophy LN Geng, Z Yao, L Snider, AP Fong, JN Cech, JM Young, ... Developmental cell 22 (1), 38-51, 2012 | 471 | 2012 |
| Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain R Luthi-Carter, SA Hanson, AD Strand, DA Bergstrom, W Chun, NL Peters, ... Human molecular genetics 11 (17), 1911-1926, 2002 | 455 | 2002 |
| An efficient and robust statistical modeling approach to discover differentially expressed genes using genomic expression profiles JG Thomas, JM Olson, SJ Tapscott, LP Zhao Genome Research 11 (7), 1227-1236, 2001 | 434 | 2001 |
| Muscle-specific transcriptional activation by MyoD. H Weintraub, VJ Dwarki, I Verma, R Davis, S Hollenberg, L Snider, ... Genes & development 5 (8), 1377-1386, 1991 | 429 | 1991 |
| Loss of cell polarity causes severe brain dysplasia in Lgl1 knockout mice O Klezovitch, TE Fernandez, SJ Tapscott, V Vasioukhin Genes & development 18 (5), 559-571, 2004 | 408 | 2004 |
