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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:

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie, Alan E. Renton, Kin Y. Mok, et al.
The Lancet Neurology (2012) Vol. 11, Iss. 4, pp. 323-330
Open Access | Times Cited: 1145

Showing 26-50 of 1145 citing articles:

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population
Jon Beck, Mark Poulter, Davina J. Hensman Moss, et al.
The American Journal of Human Genetics (2013) Vol. 92, Iss. 3, pp. 345-353
Open Access | Times Cited: 333
Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress
Yong‐Jie Zhang, Karen Jansen‐West, Ya-Fei Xu, et al.
Acta Neuropathologica (2014) Vol. 128, Iss. 4, pp. 505-524
Open Access | Times Cited: 319
C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
Sarah Mizielinska, Tammaryn Lashley, Frances E. Norona, et al.
Acta Neuropathologica (2013) Vol. 126, Iss. 6, pp. 845-857
Open Access | Times Cited: 315
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis
Sorana Ciura, Serena Lattante, Isabelle Le Ber, et al.
Annals of Neurology (2013) Vol. 74, Iss. 2, pp. 180-187
Closed Access | Times Cited: 314
Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons
Sandra Almeida, Eduardo Gascon, Hélène Tran, et al.
Acta Neuropathologica (2013) Vol. 126, Iss. 3, pp. 385-399
Open Access | Times Cited: 311
TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets
Emma L. Scotter, Han-Jou Chen, Christopher E. Shaw
Neurotherapeutics (2015) Vol. 12, Iss. 2, pp. 352-363
Open Access | Times Cited: 308
Genetics of dementia
Clement T. Loy, Peter R. Schofield, Anne Turner, et al.
The Lancet (2013) Vol. 383, Iss. 9919, pp. 828-840
Closed Access | Times Cited: 306
The role of TDP-43 mislocalization in amyotrophic lateral sclerosis
Terry R. Suk, Maxime W.C. Rousseaux
Molecular Neurodegeneration (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 304
Drosophila as an In Vivo Model for Human Neurodegenerative Disease
Leeanne McGurk, Amit Berson, Nancy M. Bonini
Genetics (2015) Vol. 201, Iss. 2, pp. 377-402
Open Access | Times Cited: 302
A Small Molecule Screen in Stem-Cell-Derived Motor Neurons Identifies a Kinase Inhibitor as a Candidate Therapeutic for ALS
Yin Yang, Shailesh Gupta, Kevin J. Kim, et al.
Cell stem cell (2013) Vol. 12, Iss. 6, pp. 713-726
Open Access | Times Cited: 294
Immune dysregulation in amyotrophic lateral sclerosis: mechanisms and emerging therapies
David R. Beers, Stanley H. Appel
The Lancet Neurology (2019) Vol. 18, Iss. 2, pp. 211-220
Closed Access | Times Cited: 293
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Cyril Pottier, Kevin F. Bieniek, Ni Cole A. Finch, et al.
Acta Neuropathologica (2015) Vol. 130, Iss. 1, pp. 77-92
Open Access | Times Cited: 288
Antisense Oligonucleotide Therapies for Neurodegenerative Diseases
C. Frank Bennett, Adrian R. Krainer, Don W. Cleveland
Annual Review of Neuroscience (2019) Vol. 42, Iss. 1, pp. 385-406
Open Access | Times Cited: 280
ALS Genes in the Genomic Era and their Implications for FTD
Hung Phuoc Nguyen, Christine Van Broeckhoven, Julie van der Zee
Trends in Genetics (2018) Vol. 34, Iss. 6, pp. 404-423
Open Access | Times Cited: 271
The genetics and neuropathology of frontotemporal lobar degeneration
Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Acta Neuropathologica (2012) Vol. 124, Iss. 3, pp. 353-372
Open Access | Times Cited: 268
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion
Adrian J. Waite, Dirk Bäumer, Simon Z. East, et al.
Neurobiology of Aging (2014) Vol. 35, Iss. 7, pp. 1779.e5-1779.e13
Open Access | Times Cited: 263
A Pan‐European Study of theC9orf72Repeat Associated withFTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
Julie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Human Mutation (2012) Vol. 34, Iss. 2, pp. 363-373
Open Access | Times Cited: 260
Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases
Jian Sheng Loh, Wen Qi Mak, Li Tan, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 255
Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia
Oliver H. Tam, Nikolay V. Rozhkov, Regina Shaw, et al.
Cell Reports (2019) Vol. 29, Iss. 5, pp. 1164-1177.e5
Open Access | Times Cited: 247
Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine
David J. Irwin, Nigel J. Cairns, Murray Grossman, et al.
Acta Neuropathologica (2014) Vol. 129, Iss. 4, pp. 469-491
Open Access | Times Cited: 245
Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice
Owen M. Peters, Gabriela Toro Cabrera, Hélène Tran, et al.
Neuron (2015) Vol. 88, Iss. 5, pp. 902-909
Open Access | Times Cited: 244
The Role of Dipeptide Repeats in C9ORF72-Related ALS-FTD
Brian D. Freibaum, J. Paul Taylor
Frontiers in Molecular Neuroscience (2017) Vol. 10
Open Access | Times Cited: 244
Antisense Oligonucleotides: Translation from Mouse Models to Human Neurodegenerative Diseases
Kathleen M. Schoch, Timothy M. Miller
Neuron (2017) Vol. 94, Iss. 6, pp. 1056-1070
Open Access | Times Cited: 244
TARDBPandFUSMutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update
Serena Lattante, Guy A. Rouleau, Edor Kabashi
Human Mutation (2013) Vol. 34, Iss. 6, pp. 812-826
Closed Access | Times Cited: 241
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits
Max Koppers, Anna M. Blokhuis, Henk‐Jan Westeneng, et al.
Annals of Neurology (2015) Vol. 78, Iss. 3, pp. 426-438
Open Access | Times Cited: 239

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