| Year |
Citation |
Score |
| 2021 |
Perez BA, Shorrock HK, Banez-Coronel M, Zu T, Romano LE, Laboissonniere LA, Reid T, Ikeda Y, Reddy K, Gomez CM, Bird T, Ashizawa T, Schut LJ, Brusco A, Berglund JA, ... ... Ranum LP, et al. CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity. Embo Molecular Medicine. e14095. PMID 34632710 DOI: 10.15252/emmm.202114095 |
0.333 |
|
| 2018 |
Ayhan F, Perez BA, Shorrock HK, Zu T, Banez-Coronel M, Reid T, Furuya H, Clark HB, Troncoso JC, Ross CA, Subramony SH, Ashizawa T, Wang ET, Yachnis AT, Ranum LP. SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F. The Embo Journal. PMID 30206144 DOI: 10.15252/Embj.201899023 |
0.469 |
|
| 2018 |
Chen G, Carter RE, Cleary JD, Reid TS, Ranum LP, Swanson MS, Ebner TJ. Altered levels of the splicing factor muscleblind modifies cerebral cortical function in mouse models of myotonic dystrophy. Neurobiology of Disease. PMID 29331264 DOI: 10.1016/J.Nbd.2018.01.003 |
0.385 |
|
| 2017 |
Cleary JD, Ranum LP. New developments in RAN translation: insights from multiple diseases. Current Opinion in Genetics & Development. 44: 125-134. PMID 28365506 DOI: 10.1016/J.Gde.2017.03.006 |
0.51 |
|
| 2016 |
Liu Y, Pattamatta A, Zu T, Reid T, Bardhi O, Borchelt DR, Yachnis AT, Ranum LP. C9orf72 BAC Mouse Model with Motor Deficits and Neurodegenerative Features of ALS/FTD. Neuron. PMID 27112499 DOI: 10.1016/J.Neuron.2016.04.005 |
0.372 |
|
| 2015 |
Bañez-Coronel M, Ayhan F, Tarabochia AD, Zu T, Perez BA, Tusi SK, Pletnikova O, Borchelt DR, Ross CA, Margolis RL, Yachnis AT, Troncoso JC, Ranum LP. RAN Translation in Huntington Disease. Neuron. 88: 667-77. PMID 26590344 DOI: 10.1016/J.Neuron.2015.10.038 |
0.487 |
|
| 2015 |
Goodwin M, Mohan A, Batra R, Lee KY, Charizanis K, Gómez FJ, Eddarkaoui S, Sergeant N, Buée L, Kimura T, Clark HB, Dalton J, Takamura K, Weyn-Vanhentenryck SM, Zhang C, ... ... Ranum LP, et al. MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain. Cell Reports. PMID 26257173 DOI: 10.1016/J.Celrep.2015.07.029 |
0.403 |
|
| 2015 |
Xia G, Gao Y, Jin S, Subramony SH, Terada N, Ranum LP, Swanson MS, Ashizawa T. Genome modification leads to phenotype reversal in human myotonic dystrophy type 1 induced pluripotent stem cell-derived neural stem cells. Stem Cells (Dayton, Ohio). 33: 1829-38. PMID 25702800 DOI: 10.1002/Stem.1970 |
0.349 |
|
| 2014 |
Cleary JD, Ranum LP. Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders. Current Opinion in Genetics & Development. 26: 6-15. PMID 24852074 DOI: 10.1016/j.gde.2014.03.002 |
0.444 |
|
| 2013 |
Lee KY, Li M, Manchanda M, Batra R, Charizanis K, Mohan A, Warren SA, Chamberlain CM, Finn D, Hong H, Ashraf H, Kasahara H, Ranum LP, Swanson MS. Compound loss of muscleblind-like function in myotonic dystrophy. Embo Molecular Medicine. 5: 1887-900. PMID 24293317 DOI: 10.1002/Emmm.201303275 |
0.678 |
|
| 2013 |
Zu T, Liu Y, Bañez-Coronel M, Reid T, Pletnikova O, Lewis J, Miller TM, Harms MB, Falchook AE, Subramony SH, Ostrow LW, Rothstein JD, Troncoso JC, Ranum LP. RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia. Proceedings of the National Academy of Sciences of the United States of America. 110: E4968-77. PMID 24248382 DOI: 10.1073/Pnas.1315438110 |
0.449 |
|
| 2013 |
Cleary JD, Ranum LP. Repeat-associated non-ATG (RAN) translation in neurological disease. Human Molecular Genetics. 22: R45-51. PMID 23918658 DOI: 10.1093/hmg/ddt371 |
0.487 |
|
| 2013 |
Clippinger AK, D'Alton S, Lin WL, Gendron TF, Howard J, Borchelt DR, Cannon A, Carlomagno Y, Chakrabarty P, Cook C, Golde TE, Levites Y, Ranum L, Schultheis PJ, Xu G, et al. Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy. Acta Neuropathologica. 126: 39-50. PMID 23666556 DOI: 10.1007/S00401-013-1123-8 |
0.371 |
|
| 2012 |
Chamberlain CM, Ranum LP. Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise. Human Molecular Genetics. 21: 4645-54. PMID 22846424 DOI: 10.1093/Hmg/Dds306 |
0.673 |
|
| 2011 |
Zu T, Gibbens B, Doty NS, Gomes-Pereira M, Huguet A, Stone MD, Margolis J, Peterson M, Markowski TW, Ingram MA, Nan Z, Forster C, Low WC, Schoser B, Somia NV, ... ... Ranum LP, et al. Non-ATG-initiated translation directed by microsatellite expansions. Proceedings of the National Academy of Sciences of the United States of America. 108: 260-5. PMID 21173221 DOI: 10.1073/Pnas.1013343108 |
0.483 |
|
| 2010 |
Ranum LP, Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner T, Swanson MS. Double the trouble: bidirectional expression of the SCA8 CAG/CTG expansion mutation - evidence for RNA and protein gain of function effects. Rinshō Shinkeigaku = Clinical Neurology. 50: 982-3. PMID 21921535 DOI: JST.JSTAGE/clinicalneurol/50.982 |
0.386 |
|
| 2009 |
Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner TJ, Swanson MS, Ranum LP. RNA gain-of-function in spinocerebellar ataxia type 8. Plos Genetics. 5: e1000600. PMID 19680539 DOI: 10.1371/journal.pgen.1000600 |
0.476 |
|
| 2008 |
Slean MM, Panigrahi GB, Ranum LP, Pearson CE. Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability. Dna Repair. 7: 1135-54. PMID 18485833 DOI: 10.1016/J.Dnarep.2008.03.014 |
0.391 |
|
| 2008 |
Ikeda Y, Daughters RS, Ranum LP. Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes. Cerebellum (London, England). 7: 150-8. PMID 18418692 DOI: 10.1007/s12311-008-0010-7 |
0.429 |
|
| 2006 |
Dick KA, Margolis JM, Day JW, Ranum LP. Dominant non-coding repeat expansions in human disease. Genome Dynamics. 1: 67-83. PMID 18724054 DOI: 10.1159/000092501 |
0.442 |
|
| 2006 |
Moseley ML, Zu T, Ikeda Y, Gao W, Mosemiller AK, Daughters RS, Chen G, Weatherspoon MR, Clark HB, Ebner TJ, Day JW, Ranum LP. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8. Nature Genetics. 38: 758-69. PMID 16804541 DOI: 10.1038/Ng1827 |
0.47 |
|
| 2006 |
Ranum LP, Cooper TA. RNA-mediated neuromuscular disorders. Annual Review of Neuroscience. 29: 259-77. PMID 16776586 DOI: 10.1146/Annurev.Neuro.29.051605.113014 |
0.461 |
|
| 2006 |
Margolis JM, Schoser BG, Moseley ML, Day JW, Ranum LP. DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression. Human Molecular Genetics. 15: 1808-15. PMID 16624843 DOI: 10.1093/Hmg/Ddl103 |
0.507 |
|
| 2005 |
Day JW, Ranum LP. Genetics and molecular pathogenesis of the myotonic dystrophies. Current Neurology and Neuroscience Reports. 5: 55-9. PMID 15676109 DOI: 10.1007/S11910-005-0024-1 |
0.487 |
|
| 2005 |
Day JW, Ranum LP. RNA pathogenesis of the myotonic dystrophies. Neuromuscular Disorders : Nmd. 15: 5-16. PMID 15639115 DOI: 10.1016/J.Nmd.2004.09.012 |
0.409 |
|
| 2004 |
Ranum LP, Day JW. Pathogenic RNA repeats: an expanding role in genetic disease. Trends in Genetics : Tig. 20: 506-12. PMID 15363905 DOI: 10.1016/J.Tig.2004.08.004 |
0.442 |
|
| 2004 |
Savkur RS, Philips AV, Cooper TA, Dalton JC, Moseley ML, Ranum LP, Day JW. Insulin receptor splicing alteration in myotonic dystrophy type 2. American Journal of Human Genetics. 74: 1309-13. PMID 15114529 DOI: 10.1086/421528 |
0.409 |
|
| 2004 |
Ranum LP, Day JW. Myotonic dystrophy: RNA pathogenesis comes into focus. American Journal of Human Genetics. 74: 793-804. PMID 15065017 DOI: 10.1086/383590 |
0.481 |
|
| 2003 |
Udd B, Meola G, Krahe R, Thornton C, Ranum L, Day J, Bassez G, Ricker K. Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 13: 589-96. PMID 12921797 DOI: 10.1016/S0960-8966(03)00092-0 |
0.428 |
|
| 2002 |
Ranum LP, Day JW. Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2. Current Neurology and Neuroscience Reports. 2: 465-70. PMID 12169228 DOI: 10.1007/S11910-002-0074-6 |
0.441 |
|
| 2002 |
Ranum LP, Day JW. Dominantly inherited, non-coding microsatellite expansion disorders. Current Opinion in Genetics & Development. 12: 266-71. PMID 12076668 DOI: 10.1016/S0959-437X(02)00297-6 |
0.47 |
|
| 2001 |
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science (New York, N.Y.). 293: 864-7. PMID 11486088 DOI: 10.1126/Science.1062125 |
0.383 |
|
| 2001 |
Gaspar C, Lopes-Cendes I, Hayes S, Goto J, Arvidsson K, Dias A, Silveira I, Maciel P, Coutinho P, Lima M, Zhou YX, Soong BW, Watanabe M, Giunti P, Stevanin G, ... ... Ranum L, et al. Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study. American Journal of Human Genetics. 68: 523-8. PMID 11133357 DOI: 10.1086/318184 |
0.311 |
|
| 2000 |
Nemes JP, Benzow KA, Moseley ML, Ranum LP, Koob MD. The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1). Human Molecular Genetics. 9: 1543-51. PMID 10888605 DOI: 10.1093/Hmg/9.10.1543 |
0.411 |
|
| 1999 |
Kaytor MD, Duvick LA, Skinner PJ, Koob MD, Ranum LP, Orr HT. Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7. Human Molecular Genetics. 8: 1657-64. PMID 10441328 DOI: 10.1093/Hmg/8.9.1657 |
0.364 |
|
| 1998 |
Ranum LP, Rasmussen PF, Benzow KA, Koob MD, Day JW. Genetic mapping of a second myotonic dystrophy locus. Nature Genetics. 19: 196-8. PMID 9620781 DOI: 10.1038/570 |
0.324 |
|
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