| Year |
Citation |
Score |
| 2022 |
Pant DC, Parameswaran J, Rao L, Loss I, Chilukuri G, Parlato R, Shi L, Glass JD, Bassell GJ, Koch P, Yilmaz R, Weishaupt JH, Gennerich A, Jiang J. ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain-of-function. Embo Reports. e54234. PMID 35735139 DOI: 10.15252/embr.202154234 |
0.364 |
|
| 2020 |
Glass JD. Stathmin-2: adding another piece to the puzzle of TDP-43 proteinopathies and neurodegeneration. The Journal of Clinical Investigation. PMID 33074248 DOI: 10.1172/JCI142854 |
0.306 |
|
| 2020 |
Miller T, Cudkowicz M, Shaw PJ, Andersen PM, Atassi N, Bucelli RC, Genge A, Glass J, Ladha S, Ludolph AL, Maragakis NJ, McDermott CJ, Pestronk A, Ravits J, Salachas F, et al. Phase 1-2 Trial of Antisense Oligonucleotide Tofersen for ALS. The New England Journal of Medicine. 383: 109-119. PMID 32640130 DOI: 10.1056/Nejmoa2003715 |
0.351 |
|
| 2018 |
Wright ML, Fournier C, Houser MC, Tansey M, Glass J, Hertzberg VS. Potential Role of the Gut Microbiome in ALS: A Systematic Review. Biological Research For Nursing. 1099800418784202. PMID 29925252 DOI: 10.1177/1099800418784202 |
0.309 |
|
| 2017 |
Smith BN, Topp SD, Fallini C, Shibata H, Chen HJ, Troakes C, King A, Ticozzi N, Kenna KP, Soragia-Gkazi A, Miller JW, Sato A, Dias DM, Jeon M, Vance C, ... ... Glass JD, et al. Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis. Science Translational Medicine. 9. PMID 28469040 DOI: 10.1126/Scitranslmed.Aad9157 |
0.323 |
|
| 2016 |
Ayers JI, Diamond J, Sari A, Fromholt S, Galaleldeen A, Ostrow LW, Glass JD, Hart PJ, Borchelt DR. Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS. Acta Neuropathologica. PMID 27704280 DOI: 10.1007/S00401-016-1623-4 |
0.301 |
|
| 2013 |
Fischer-Hayes LR, Brotherton T, Glass JD. Axonal degeneration in the peripheral nervous system: implications for the pathogenesis of amyotrophic lateral sclerosis. Experimental Neurology. 246: 6-13. PMID 23664960 DOI: 10.1016/J.Expneurol.2013.05.001 |
0.712 |
|
| 2013 |
Lee SM, Sha D, Mohammed AA, Asress S, Glass JD, Chin LS, Li L. Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot-Marie-Tooth disease type 1C. Human Molecular Genetics. 22: 1755-70. PMID 23359569 DOI: 10.1093/Hmg/Ddt022 |
0.368 |
|
| 2013 |
Brotherton TE, Li Y, Glass JD. Cellular toxicity of mutant SOD1 protein is linked to an easily soluble, non-aggregated form in vitro. Neurobiology of Disease. 49: 49-56. PMID 22926189 DOI: 10.1016/J.Nbd.2012.08.010 |
0.707 |
|
| 2012 |
Wu CH, Fallini C, Ticozzi N, Keagle PJ, Sapp PC, Piotrowska K, Lowe P, Koppers M, McKenna-Yasek D, Baron DM, Kost JE, Gonzalez-Perez P, Fox AD, Adams J, Taroni F, ... ... Glass JD, et al. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis. Nature. 488: 499-503. PMID 22801503 DOI: 10.1038/Nature11280 |
0.339 |
|
| 2012 |
Brotherton TE, Li Y, Cooper D, Gearing M, Julien JP, Rothstein JD, Boylan K, Glass JD. Localization of a toxic form of superoxide dismutase 1 protein to pathologically affected tissues in familial ALS. Proceedings of the National Academy of Sciences of the United States of America. 109: 5505-10. PMID 22431618 DOI: 10.1073/Pnas.1115009109 |
0.731 |
|
| 2012 |
Fischer LR, Li Y, Asress SA, Jones DP, Glass JD. Absence of SOD1 leads to oxidative stress in peripheral nerve and causes a progressive distal motor axonopathy. Experimental Neurology. 233: 163-71. PMID 21963651 DOI: 10.1016/J.Expneurol.2011.09.020 |
0.688 |
|
| 2011 |
Igoudjil A, Magrané J, Fischer LR, Kim HJ, Hervias I, Dumont M, Cortez C, Glass JD, Starkov AA, Manfredi G. In vivo pathogenic role of mutant SOD1 localized in the mitochondrial intermembrane space. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 15826-37. PMID 22049426 DOI: 10.1523/Jneurosci.1965-11.2011 |
0.688 |
|
| 2011 |
Fischer LR, Igoudjil A, Magrané J, Li Y, Hansen JM, Manfredi G, Glass JD. SOD1 targeted to the mitochondrial intermembrane space prevents motor neuropathy in the Sod1 knockout mouse. Brain : a Journal of Neurology. 134: 196-209. PMID 21078595 DOI: 10.1093/Brain/Awq314 |
0.695 |
|
| 2011 |
Brotherton T, Polak M, Kelly C, Birve A, Andersen P, Marklund SL, Glass JD. A novel ALS SOD1 C6S mutation with implications for aggregation related toxicity and genetic counseling. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 12: 215-9. PMID 21073275 DOI: 10.3109/17482968.2010.531279 |
0.704 |
|
| 2010 |
Fischer LR, Glass JD. Oxidative stress induced by loss of Cu,Zn-superoxide dismutase (SOD1) or superoxide-generating herbicides causes axonal degeneration in mouse DRG cultures. Acta Neuropathologica. 119: 249-59. PMID 20039174 DOI: 10.1007/S00401-009-0631-Z |
0.686 |
|
| 2009 |
Esmon CT, Glass JD. The APCs of neuroprotection. The Journal of Clinical Investigation. 119: 3205-7. PMID 19841538 DOI: 10.1172/JCI40682 |
0.324 |
|
| 2007 |
Hammad M, Silva A, Glass J, Sladky JT, Benatar M. Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS. Neurology. 69: 2236-2242. PMID 18071143 DOI: 10.1212/01.Wnl.0000286948.99150.16 |
0.386 |
|
| 2007 |
Fischer LR, Glass JD. Axonal degeneration in motor neuron disease. Neuro-Degenerative Diseases. 4: 431-42. PMID 17934327 DOI: 10.1159/000107704 |
0.713 |
|
| 2005 |
Fischer LR, Culver DG, Davis AA, Tennant P, Wang M, Coleman M, Asress S, Adalbert R, Alexander GM, Glass JD. The WldS gene modestly prolongs survival in the SOD1G93A fALS mouse. Neurobiology of Disease. 19: 293-300. PMID 15837585 DOI: 10.1016/J.Nbd.2005.01.008 |
0.684 |
|
| 2004 |
Fischer LR, Culver DG, Tennant P, Davis AA, Wang M, Castellano-Sanchez A, Khan J, Polak MA, Glass JD. Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Experimental Neurology. 185: 232-40. PMID 14736504 DOI: 10.1016/J.Expneurol.2003.10.004 |
0.711 |
|
| 2001 |
Wang MS, Fang G, Culver DG, Davis AA, Rich MM, Glass JD. The WldS protein protects against axonal degeneration: a model of gene therapy for peripheral neuropathy. Annals of Neurology. 50: 773-9. PMID 11761475 DOI: 10.1002/Ana.10039 |
0.356 |
|
| 2001 |
Wang M, Wu Y, Culver DG, Glass JD. The gene for slow Wallerian degeneration (Wld(s)) is also protective against vincristine neuropathy. Neurobiology of Disease. 8: 155-61. PMID 11162249 DOI: 10.1006/nbdi.2000.0334 |
0.337 |
|
| 1995 |
Boylan KB, Cornblath DR, Glass JD, Alderson K, Kuncl RW, Kleyn PW, Gilliam TC. Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 45: 699-704. PMID 7723957 DOI: 10.1212/WNL.45.4.699 |
0.322 |
|
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