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OpenAlex Citation Counts

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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:

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
Magdalini Polymenidou, Clotilde Lagier‐Tourenne, Kasey R. Hutt, et al.
Nature Neuroscience (2011) Vol. 14, Iss. 4, pp. 459-468
Open Access | Times Cited: 1204

Showing 1-25 of 1204 citing articles:

Decoding ALS: from genes to mechanism
J. Paul Taylor, Robert H. Brown, Don W. Cleveland
Nature (2016) Vol. 539, Iss. 7628, pp. 197-206
Open Access | Times Cited: 1821
Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
Shuo‐Chien Ling, Magdalini Polymenidou, Don W. Cleveland
Neuron (2013) Vol. 79, Iss. 3, pp. 416-438
Open Access | Times Cited: 1603
Characterizing the RNA targets and position-dependent splicing regulation by TDP-43
James Tollervey, Tomaž Curk, Boris Rogelj, et al.
Nature Neuroscience (2011) Vol. 14, Iss. 4, pp. 452-458
Open Access | Times Cited: 1055
RNA mis-splicing in disease
Marina M. Scotti, Maurice S. Swanson
Nature Reviews Genetics (2015) Vol. 17, Iss. 1, pp. 19-32
Open Access | Times Cited: 1051
Overcoming cellular barriers for RNA therapeutics
Steven F. Dowdy
Nature Biotechnology (2017) Vol. 35, Iss. 3, pp. 222-229
Closed Access | Times Cited: 970
The changing scene of amyotrophic lateral sclerosis
Wim Robberecht, Thomas Philips
Nature reviews. Neuroscience (2013) Vol. 14, Iss. 4, pp. 248-264
Closed Access | Times Cited: 933
Stress granules as crucibles of ALS pathogenesis
Leslie A. Lange, Oliver D. King, James Shorter, et al.
The Journal of Cell Biology (2013) Vol. 201, Iss. 3, pp. 361-372
Open Access | Times Cited: 874
Long Noncoding RNA MALAT1 Controls Cell Cycle Progression by Regulating the Expression of Oncogenic Transcription Factor B-MYB
Vidisha Tripathi, Zhen Shen, Arindam Chakraborty, et al.
PLoS Genetics (2013) Vol. 9, Iss. 3, pp. e1003368-e1003368
Open Access | Times Cited: 709
MALAT1 — a paradigm for long noncoding RNA function in cancer
Tony Gutschner, Monika Hämmerle, Sven Diederichs
Journal of Molecular Medicine (2013) Vol. 91, Iss. 7, pp. 791-801
Closed Access | Times Cited: 685
Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs
Clotilde Lagier‐Tourenne, Magdalini Polymenidou, Kasey R. Hutt, et al.
Nature Neuroscience (2012) Vol. 15, Iss. 11, pp. 1488-1497
Open Access | Times Cited: 678
Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis
A. Aditya Prasad, Vidhya Bharathi, Vishwanath Sivalingam, et al.
Frontiers in Molecular Neuroscience (2019) Vol. 12
Open Access | Times Cited: 636
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
Edward B. Lee, Virginia M.‐Y. Lee, John Q. Trojanowski
Nature reviews. Neuroscience (2011) Vol. 13, Iss. 1, pp. 38-50
Open Access | Times Cited: 619
The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease
Oliver D. King, Aaron D. Gitler, James Shorter
Brain Research (2012) Vol. 1462, pp. 61-80
Open Access | Times Cited: 613
Axonal Transport of TDP-43 mRNA Granules Is Impaired by ALS-Causing Mutations
Nael H. Alami, Rebecca B. Smith, Mónica A. Carrasco, et al.
Neuron (2014) Vol. 81, Iss. 3, pp. 536-543
Open Access | Times Cited: 594
Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
Laura Ferraiuolo, Janine Kirby, Andrew J. Grierson, et al.
Nature Reviews Neurology (2011) Vol. 7, Iss. 11, pp. 616-630
Closed Access | Times Cited: 579
Disruption of DNA-methylation-dependent long gene repression in Rett syndrome
Harrison W. Gabel, Benyam Kinde, Hume Stroud, et al.
Nature (2015) Vol. 522, Iss. 7554, pp. 89-93
Open Access | Times Cited: 573
Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration
Clotilde Lagier‐Tourenne, Michael W. Baughn, Frank Rigo, et al.
Proceedings of the National Academy of Sciences (2013) Vol. 110, Iss. 47
Open Access | Times Cited: 534
TDP-43 repression of nonconserved cryptic exons is compromised in ALS-FTD
Jonathan P. Ling, Olga Pletniková, Juan C. Troncoso, et al.
Science (2015) Vol. 349, Iss. 6248, pp. 650-655
Open Access | Times Cited: 524
Drug Screening for ALS Using Patient-Specific Induced Pluripotent Stem Cells
Naohiro Egawa, Shiho Kitaoka, Kayoko Tsukita, et al.
Science Translational Medicine (2012) Vol. 4, Iss. 145
Closed Access | Times Cited: 520
Protein aggregation in amyotrophic lateral sclerosis
Anna M. Blokhuis, Ewout J. N. Groen, Max Koppers, et al.
Acta Neuropathologica (2013) Vol. 125, Iss. 6, pp. 777-794
Open Access | Times Cited: 519
Nuclear Long Noncoding RNAs: Key Regulators of Gene Expression
Qinyu Sun, Qinyu Hao, Kannanganattu V. Prasanth
Trends in Genetics (2017) Vol. 34, Iss. 2, pp. 142-157
Open Access | Times Cited: 509
ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair
Joseph R. Klim, Luis A. Williams, Francesco Limone, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 2, pp. 167-179
Open Access | Times Cited: 491
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration
Ze’ev Melamed, Jone López‐Erauskin, Michael W. Baughn, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 2, pp. 180-190
Open Access | Times Cited: 489
The role of mitochondria in amyotrophic lateral sclerosis
Emma F. Smith, Pamela J. Shaw, Kurt J. De Vos
Neuroscience Letters (2017) Vol. 710, pp. 132933-132933
Open Access | Times Cited: 476
Integrative Genome-wide Analysis Reveals Cooperative Regulation of Alternative Splicing by hnRNP Proteins
Stephanie C. Huelga, Anthony Q. Vu, Justin D. Arnold, et al.
Cell Reports (2012) Vol. 1, Iss. 2, pp. 167-178
Open Access | Times Cited: 449
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