
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
ALS/FTD-Linked Mutation in FUS Suppresses Intra-axonal Protein Synthesis and Drives Disease Without Nuclear Loss-of-Function of FUS
Jone López‐Erauskin, Takahiro Tadokoro, Michael W. Baughn, et al.
Neuron (2018) Vol. 100, Iss. 4, pp. 816-830.e7
Open Access | Times Cited: 203
Jone López‐Erauskin, Takahiro Tadokoro, Michael W. Baughn, et al.
Neuron (2018) Vol. 100, Iss. 4, pp. 816-830.e7
Open Access | Times Cited: 203
Showing 1-25 of 203 citing articles:
ALS Genetics: Gains, Losses, and Implications for Future Therapies
Garam Kım, Olivia Gautier, Eduardo Tassoni-Tsuchida, et al.
Neuron (2020) Vol. 108, Iss. 5, pp. 822-842
Open Access | Times Cited: 301
Garam Kım, Olivia Gautier, Eduardo Tassoni-Tsuchida, et al.
Neuron (2020) Vol. 108, Iss. 5, pp. 822-842
Open Access | Times Cited: 301
Disruption of RNA Metabolism in Neurological Diseases and Emerging Therapeutic Interventions
Julia K. Nussbacher, Ricardos Tabet, G Yeo, et al.
Neuron (2019) Vol. 102, Iss. 2, pp. 294-320
Open Access | Times Cited: 230
Julia K. Nussbacher, Ricardos Tabet, G Yeo, et al.
Neuron (2019) Vol. 102, Iss. 2, pp. 294-320
Open Access | Times Cited: 230
Bridging biophysics and neurology: aberrant phase transitions in neurodegenerative disease
Natalia B. Nedelsky, J. Paul Taylor
Nature Reviews Neurology (2019) Vol. 15, Iss. 5, pp. 272-286
Closed Access | Times Cited: 187
Natalia B. Nedelsky, J. Paul Taylor
Nature Reviews Neurology (2019) Vol. 15, Iss. 5, pp. 272-286
Closed Access | Times Cited: 187
Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis
Giulia E. Tyzack, Raphaëlle Luisier, Doaa M. Taha, et al.
Brain (2019) Vol. 142, Iss. 9, pp. 2572-2580
Open Access | Times Cited: 153
Giulia E. Tyzack, Raphaëlle Luisier, Doaa M. Taha, et al.
Brain (2019) Vol. 142, Iss. 9, pp. 2572-2580
Open Access | Times Cited: 153
RNA transport and local translation in neurodevelopmental and neurodegenerative disease
Michael S. Fernandopulle, Jennifer Lippincott‐Schwartz, Michael E. Ward
Nature Neuroscience (2021) Vol. 24, Iss. 5, pp. 622-632
Open Access | Times Cited: 140
Michael S. Fernandopulle, Jennifer Lippincott‐Schwartz, Michael E. Ward
Nature Neuroscience (2021) Vol. 24, Iss. 5, pp. 622-632
Open Access | Times Cited: 140
Axonal TDP-43 condensates drive neuromuscular junction disruption through inhibition of local synthesis of nuclear encoded mitochondrial proteins
Topaz Altman, Ariel Ionescu, Amjad Ibraheem, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 109
Topaz Altman, Ariel Ionescu, Amjad Ibraheem, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 109
Liquid-Liquid Phase Separation of TDP-43 and FUS in Physiology and Pathology of Neurodegenerative Diseases
Jenny L. Carey, Lin Guo
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 102
Jenny L. Carey, Lin Guo
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 102
Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
Naoki Suzuki, Ayumi Nishiyama, Hitoshi Warita, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 131-152
Open Access | Times Cited: 93
Naoki Suzuki, Ayumi Nishiyama, Hitoshi Warita, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 131-152
Open Access | Times Cited: 93
Neuromuscular Junction Dysfunction in Amyotrophic Lateral Sclerosis
Sagar Verma, Shiffali Khurana, Kavita Vats, et al.
Molecular Neurobiology (2022) Vol. 59, Iss. 3, pp. 1502-1527
Closed Access | Times Cited: 73
Sagar Verma, Shiffali Khurana, Kavita Vats, et al.
Molecular Neurobiology (2022) Vol. 59, Iss. 3, pp. 1502-1527
Closed Access | Times Cited: 73
Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implications
Thomas G. Moens, Sandrine Da Cruz, Manuela Neumann, et al.
The Lancet Neurology (2025) Vol. 24, Iss. 2, pp. 166-178
Closed Access | Times Cited: 4
Thomas G. Moens, Sandrine Da Cruz, Manuela Neumann, et al.
The Lancet Neurology (2025) Vol. 24, Iss. 2, pp. 166-178
Closed Access | Times Cited: 4
RNA dysregulation in neurodegenerative diseases
Yini Li, Shuying Sun
The EMBO Journal (2025) Vol. 44, Iss. 3, pp. 613-638
Open Access | Times Cited: 3
Yini Li, Shuying Sun
The EMBO Journal (2025) Vol. 44, Iss. 3, pp. 613-638
Open Access | Times Cited: 3
ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay
Marisa Kamelgarn, Jing Chen, Lisha Kuang, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 51
Open Access | Times Cited: 161
Marisa Kamelgarn, Jing Chen, Lisha Kuang, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 51
Open Access | Times Cited: 161
ALS-linked FUS mutations confer loss and gain of function in the nucleus by promoting excessive formation of dysfunctional paraspeckles
Haiyan An, Lucy Skelt, Antonietta Notaro, et al.
Acta Neuropathologica Communications (2019) Vol. 7, Iss. 1
Open Access | Times Cited: 122
Haiyan An, Lucy Skelt, Antonietta Notaro, et al.
Acta Neuropathologica Communications (2019) Vol. 7, Iss. 1
Open Access | Times Cited: 122
Local translation in neuronal processes
Anne Biever, Paul G. Donlin‐Asp, Erin M. Schuman
Current Opinion in Neurobiology (2019) Vol. 57, pp. 141-148
Closed Access | Times Cited: 114
Anne Biever, Paul G. Donlin‐Asp, Erin M. Schuman
Current Opinion in Neurobiology (2019) Vol. 57, pp. 141-148
Closed Access | Times Cited: 114
Cytoplasmic functions of TDP-43 and FUS and their role in ALS
Nicol Birsa, Matthew P. Bentham, Pietro Fratta
Seminars in Cell and Developmental Biology (2019) Vol. 99, pp. 193-201
Open Access | Times Cited: 106
Nicol Birsa, Matthew P. Bentham, Pietro Fratta
Seminars in Cell and Developmental Biology (2019) Vol. 99, pp. 193-201
Open Access | Times Cited: 106
FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagy
Lara Marrone, Hannes C. A. Drexler, Jie Wang, et al.
Acta Neuropathologica (2019) Vol. 138, Iss. 1, pp. 67-84
Open Access | Times Cited: 105
Lara Marrone, Hannes C. A. Drexler, Jie Wang, et al.
Acta Neuropathologica (2019) Vol. 138, Iss. 1, pp. 67-84
Open Access | Times Cited: 105
Human sensorimotor organoids derived from healthy and amyotrophic lateral sclerosis stem cells form neuromuscular junctions
João D. Pereira, D Dubreuil, Anna‐Claire Devlin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 101
João D. Pereira, D Dubreuil, Anna‐Claire Devlin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 101
The Role of RNA Binding Proteins for Local mRNA Translation: Implications in Neurological Disorders
Maximilian Paul Thelen, Min Jeong Kye
Frontiers in Molecular Biosciences (2020) Vol. 6
Open Access | Times Cited: 95
Maximilian Paul Thelen, Min Jeong Kye
Frontiers in Molecular Biosciences (2020) Vol. 6
Open Access | Times Cited: 95
RNA-binding proteins in neurological development and disease
Shavanie Prashad, Pallavi P. Gopal
RNA Biology (2020) Vol. 18, Iss. 7, pp. 972-987
Open Access | Times Cited: 94
Shavanie Prashad, Pallavi P. Gopal
RNA Biology (2020) Vol. 18, Iss. 7, pp. 972-987
Open Access | Times Cited: 94
Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
Mehdi Eshraghi, Pabalu P. Karunadharma, Juliana Blin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 90
Mehdi Eshraghi, Pabalu P. Karunadharma, Juliana Blin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 90
Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis
Francesca De Giorgio, Cheryl Maduro, Elizabeth Fisher, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 86
Francesca De Giorgio, Cheryl Maduro, Elizabeth Fisher, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 86
Overriding FUS autoregulation in mice triggers gain-of-toxic dysfunctions in RNA metabolism and autophagy-lysosome axis
Shuo‐Chien Ling, Somasish Ghosh Dastidar, Seiya Tokunaga, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 80
Shuo‐Chien Ling, Somasish Ghosh Dastidar, Seiya Tokunaga, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 80
ALS/FTLD-Linked Mutations in FUS Glycine Residues Cause Accelerated Gelation and Reduced Interactions with Wild-Type FUS
Kevin Rhine, Monika A. Makurath, James Liu, et al.
Molecular Cell (2020) Vol. 80, Iss. 4, pp. 666-681.e8
Open Access | Times Cited: 77
Kevin Rhine, Monika A. Makurath, James Liu, et al.
Molecular Cell (2020) Vol. 80, Iss. 4, pp. 666-681.e8
Open Access | Times Cited: 77
Dysregulation of RNA-Binding Proteins in Amyotrophic Lateral Sclerosis
Yuan Chao Xue, Chen Seng Ng, Pinhao Xiang, et al.
Frontiers in Molecular Neuroscience (2020) Vol. 13
Open Access | Times Cited: 74
Yuan Chao Xue, Chen Seng Ng, Pinhao Xiang, et al.
Frontiers in Molecular Neuroscience (2020) Vol. 13
Open Access | Times Cited: 74
ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs
Yueh-Lin Tsai, Tristan H. Coady, Lei Lü, et al.
Genes & Development (2020) Vol. 34, Iss. 11-12, pp. 785-805
Open Access | Times Cited: 71
Yueh-Lin Tsai, Tristan H. Coady, Lei Lü, et al.
Genes & Development (2020) Vol. 34, Iss. 11-12, pp. 785-805
Open Access | Times Cited: 71