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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:

C9orf72 expansion disrupts ATM-mediated chromosomal break repair
Callum Walker, Saúl Herranz-Martín, Evangelia Karyka, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 9, pp. 1225-1235
Open Access | Times Cited: 162

Showing 1-25 of 162 citing articles:

Amyotrophic lateral sclerosis
Orla Hardiman, Ammar Al‐Chalabi, Adriano Chiò, et al.
Nature Reviews Disease Primers (2017) Vol. 3, Iss. 1
Open Access | Times Cited: 1110
C9orf72-mediated ALS and FTD: multiple pathways to disease
Rubika Balendra, Adrian M. Isaacs
Nature Reviews Neurology (2018) Vol. 14, Iss. 9, pp. 544-558
Open Access | Times Cited: 616
Amyotrophic lateral sclerosis: a neurodegenerative disorder poised for successful therapeutic translation
Richard J. Mead, Ning Shan, H. Joseph Reiser, et al.
Nature Reviews Drug Discovery (2022) Vol. 22, Iss. 3, pp. 185-212
Open Access | Times Cited: 269
Sources, resolution and physiological relevance of R-loops and RNA–DNA hybrids
Eva Petermann, Li Lan, Lee Zou
Nature Reviews Molecular Cell Biology (2022) Vol. 23, Iss. 8, pp. 521-540
Closed Access | Times Cited: 237
Cellular functions of the protein kinase ATM and their relevance to human disease
Ji‐Hoon Lee, Tanya T. Paull
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 12, pp. 796-814
Closed Access | Times Cited: 191
Mutant FUS causes DNA ligation defects to inhibit oxidative damage repair in Amyotrophic Lateral Sclerosis
Haibo Wang, Wenting Guo, Joy Mitra, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 180
Early neuronal accumulation of DNA double strand breaks in Alzheimer’s disease
Niraj M. Shanbhag, Mark D. Evans, Wenjie Mao, et al.
Acta Neuropathologica Communications (2019) Vol. 7, Iss. 1
Open Access | Times Cited: 180
Motor Neuron Susceptibility in ALS/FTD
Audrey Ragagnin, Sina Shadfar, Marta Vidal, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 173
Human ALS/FTD brain organoid slice cultures display distinct early astrocyte and targetable neuronal pathology
Kornélia Szebényi, Léa M. D. Wenger, Yu Sun, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 11, pp. 1542-1554
Open Access | Times Cited: 122
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
Redox dysregulation as a driver for DNA damage and its relationship to neurodegenerative diseases
Sina Shadfar, Sonam Parakh, Md Shafi Jamali, et al.
Translational Neurodegeneration (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 69
DNA damage and its links to neuronal aging and degeneration
Ilse Delint‐Ramírez, Ram Madabhushi
Neuron (2025) Vol. 113, Iss. 1, pp. 7-28
Closed Access | Times Cited: 5
Dysregulated molecular pathways in amyotrophic lateral sclerosis–frontotemporal dementia spectrum disorder
Fen‐Biao Gao, Sandra Almeida, Rodrigo López‐González
The EMBO Journal (2017) Vol. 36, Iss. 20, pp. 2931-2950
Open Access | Times Cited: 166
Dual Processing of R-Loops and Topoisomerase I Induces Transcription-Dependent DNA Double-Strand Breaks
Agnese Cristini, Giulia Ricci, Sébastien Britton, et al.
Cell Reports (2019) Vol. 28, Iss. 12, pp. 3167-3181.e6
Open Access | Times Cited: 139
Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis
Alexander E. Volk, Jochen H. Weishaupt, Peter M. Andersen, et al.
Medizinische Genetik (2018) Vol. 30, Iss. 2, pp. 252-258
Open Access | Times Cited: 123
Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders
Manon Boivin, Véronique Pfister, Angéline Gaucherot, et al.
The EMBO Journal (2020) Vol. 39, Iss. 4
Open Access | Times Cited: 120
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia
Esther Nibbeling, Anna Duarri, Corien C. Verschuuren‐Bemelmans, et al.
Brain (2017) Vol. 140, Iss. 11, pp. 2860-2878
Open Access | Times Cited: 114
Epigenetics in amyotrophic lateral sclerosis: a role for histone post-translational modifications in neurodegenerative disease
Seth A. Bennett, Royena Tanaz, Samantha N. Cobos, et al.
Translational research (2018) Vol. 204, pp. 19-30
Open Access | Times Cited: 106
Disease-modifying therapies in amyotrophic lateral sclerosis
Adriano Chiò, Letizia Mazzini, Gabriele Mora
Neuropharmacology (2020) Vol. 167, pp. 107986-107986
Closed Access | Times Cited: 98
Repeat-associated non-ATG (RAN) translation
John D. Cleary, Amrutha Pattamatta, Laura P.W. Ranum
Journal of Biological Chemistry (2018) Vol. 293, Iss. 42, pp. 16127-16141
Open Access | Times Cited: 88
Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations
Anna Konopka, Donna R. Whelan, Md Shafi Jamali, et al.
Molecular Neurodegeneration (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 85
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin
Laura Mediani, Jordina Guillén‐Boixet, Jonathan Vinet, et al.
The EMBO Journal (2019) Vol. 38, Iss. 15
Open Access | Times Cited: 84
TEX264 coordinates p97- and SPRTN-mediated resolution of topoisomerase 1-DNA adducts
John Fielden, Katherine Wiseman, Ignacio Torrecilla, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 82
Dipeptide repeat proteins inhibit homology-directed DNA double strand break repair in C9ORF72 ALS/FTD
Nadja S. Andrade, Melina Ramic, Rustam Esanov, et al.
Molecular Neurodegeneration (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 76
DNA damage as a mechanism of neurodegeneration in ALS and a contributor to astrocyte toxicity
Jannigje Rachel Kok, Nelma M. Palminha, Cleide Dos Santos Souza, et al.
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 15, pp. 5707-5729
Open Access | Times Cited: 61
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