| Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 HT Orr, M Chung, S Banfi, TJ Kwiatkowski, A Servadio, AL Beaudet, ... Nature genetics 4 (3), 221-226, 1993 | 1995 | 1993 |
| Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9 CL Liquori, K Ricker, ML Moseley, JF Jacobsen, W Kress, SL Naylor, ... Science 293 (5531), 864-867, 2001 | 1514 | 2001 |
| Non-ATG–initiated translation directed by microsatellite expansions T Zu, B Gibbens, NS Doty, M Gomes-Pereira, A Huguet, MD Stone, ... Proceedings of the National Academy of Sciences 108 (1), 260-265, 2011 | 956 | 2011 |
| RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia T Zu, Y Liu, M Bañez-Coronel, T Reid, O Pletnikova, J Lewis, TM Miller, ... Proceedings of the National Academy of Sciences 110 (51), E4968-E4977, 2013 | 839 | 2013 |
| An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) MD Koob, ML Moseley, LJ Schut, KA Benzow, TD Bird, JW Day, ... Nature genetics 21 (4), 379-384, 1999 | 705 | 1999 |
| Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I M Chung, LPW Ranum, LA Duvick, A Servadio, HY Zoghbi, HT Orr Nature genetics 5 (3), 254-258, 1993 | 590 | 1993 |
| RNA-mediated neuromuscular disorders LPW Ranum, TA Cooper Annu. Rev. Neurosci. 29, 259-277, 2006 | 577 | 2006 |
| Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum JW Day, K Ricker, JF Jacobsen, LJ Rasmussen, KA Dick, W Kress, ... Neurology 60 (4), 657-664, 2003 | 546 | 2003 |
| Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8 ML Moseley, T Zu, Y Ikeda, W Gao, AK Mosemiller, RS Daughters, ... Nature genetics 38 (7), 758-769, 2006 | 469 | 2006 |
| Spectrin mutations cause spinocerebellar ataxia type 5 Y Ikeda, KA Dick, MR Weatherspoon, D Gincel, KR Armbrust, JC Dalton, ... Nature genetics 38 (2), 184-190, 2006 | 427 | 2006 |
| C9orf72 BAC mouse model with motor deficits and neurodegenerative features of ALS/FTD Y Liu, A Pattamatta, T Zu, T Reid, O Bardhi, DR Borchelt, AT Yachnis, ... Neuron 90 (3), 521-534, 2016 | 381 | 2016 |
| Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11 LPW Ranum, LJ Schut, JK Lundgren, HT Orr, DM Livingston Nature genetics 8 (3), 280-284, 1994 | 380 | 1994 |
| Genetic mapping of a second myotonic dystrophy locus LPW Ranum, PF Rasmussen, KA Benzow, MD Koob, JW Day Nature genetics 19 (2), 196-198, 1998 | 357 | 1998 |
| RAN translation in Huntington disease M Bañez-Coronel, F Ayhan, AD Tarabochia, T Zu, BA Perez, SK Tusi, ... Neuron 88 (4), 667-677, 2015 | 356 | 2015 |
| Mutant huntingtin disrupts the nuclear pore complex JC Grima, JG Daigle, N Arbez, KC Cunningham, K Zhang, J Ochaba, ... Neuron 94 (1), 93-107. e6, 2017 | 317 | 2017 |
| RNA gain-of-function in spinocerebellar ataxia type 8 RS Daughters, DL Tuttle, W Gao, Y Ikeda, ML Moseley, TJ Ebner, ... PLoS genetics 5 (8), e1000600, 2009 | 311 | 2009 |
| Myotonic dystrophy: RNA pathogenesis comes into focus LPW Ranum, JW Day The American Journal of Human Genetics 74 (5), 793-804, 2004 | 299 | 2004 |
| Correlating phenotype and genotype in the periodic paralyses TM Miller, MRD Da Silva, HA Miller, H Kwiecinski, JR Mendell, R Tawil, ... Neurology 63 (9), 1647-1655, 2004 | 290 | 2004 |
| Isolation and characterization of the nitrate reductase structural gene of Chlamydomonas reinhardtii E Fernández, R Schnell, LP Ranum, SC Hussey, CD Silflow, PA Lefebvre Proceedings of the National Academy of Sciences 86 (17), 6449-6453, 1989 | 282 | 1989 |
| Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families ML Moseley, KA Benzow, LJ Schut, TD Bird, CM Gomez, PE Barkhaus, ... Neurology 51 (6), 1666-1671, 1998 | 272 | 1998 |
