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Jonathan Glass - Publications

Affiliations: 
Neurology Emory University, Atlanta, GA 
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24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.352
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  0.31
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  0.322
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  0.713
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  0.367
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  0.708
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  0.355
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  0.336
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  0.321
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