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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 expansions in frontotemporal dementia and amyotrophic lateral sclerosis
Jonathan D. Rohrer, Adrian M. Isaacs, Sarah Mizielinska, et al.
The Lancet Neurology (2015) Vol. 14, Iss. 3, pp. 291-301
Closed Access | Times Cited: 224

Showing 1-25 of 224 citing articles:

Hallmarks of neurodegenerative diseases
David M. Wilson, Mark Cookson, Ludo Van Den Bosch, et al.
Cell (2023) Vol. 186, Iss. 4, pp. 693-714
Open Access | Times Cited: 846
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
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference
Alexandra L. Young, Răzvan V. Marinescu, Neil P. Oxtoby, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 412
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
The ALS/FTLD associated protein C9orf72 associates with SMCR8 and WDR41 to regulate the autophagy-lysosome pathway
Peter M. Sullivan, Xiaolai Zhou, Adam M. Robins, et al.
Acta Neuropathologica Communications (2016) Vol. 4, Iss. 1
Open Access | Times Cited: 270
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
Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders
Simon Ducharme, Annemiek Dols, Robert Laforce, et al.
Brain (2020) Vol. 143, Iss. 6, pp. 1632-1650
Open Access | Times Cited: 240
The role of TREX in gene expression and disease
Catherine G. Heath, Nicolas Viphakone, Stuart A. Wilson
Biochemical Journal (2016) Vol. 473, Iss. 19, pp. 2911-2935
Open Access | Times Cited: 197
Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations
Tammaryn Lashley, Jonathan D. Rohrer, Simon Mead, et al.
Neuropathology and Applied Neurobiology (2015) Vol. 41, Iss. 7, pp. 858-881
Closed Access | Times Cited: 190
Dendritic Spine Pathology in Neurodegenerative Diseases
Jochen Herms, Mario M. Dorostkar
Annual Review of Pathology Mechanisms of Disease (2016) Vol. 11, Iss. 1, pp. 221-250
Closed Access | Times Cited: 180
C9orf72 Poly(PR) Dipeptide Repeats Disturb Biomolecular Phase Separation and Disrupt Nucleolar Function
Michael R. White, Diana M. Mitrea, Peipei Zhang, et al.
Molecular Cell (2019) Vol. 74, Iss. 4, pp. 713-728.e6
Open Access | Times Cited: 174
Frontotemporal lobar degeneration
Murray Grossman, William W. Seeley, Adam L. Boxer, et al.
Nature Reviews Disease Primers (2023) Vol. 9, Iss. 1
Closed Access | Times Cited: 69
Familial Amyotrophic Lateral Sclerosis
Khrista Boylan
Neurologic Clinics (2015) Vol. 33, Iss. 4, pp. 807-830
Open Access | Times Cited: 166
Neurotransmitter deficits from frontotemporal lobar degeneration
Alexander G. Murley, James B. Rowe
Brain (2017) Vol. 141, Iss. 5, pp. 1263-1285
Open Access | Times Cited: 162
Frontotemporal dementia: latest evidence and clinical implications
Juan Young, Mallika Lavakumar, Deena J. Tampi, et al.
Therapeutic Advances in Psychopharmacology (2017) Vol. 8, Iss. 1, pp. 33-48
Open Access | Times Cited: 160
Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts
Elisa Onesto, Claudia Colombrita, Valentina Gumina, et al.
Acta Neuropathologica Communications (2016) Vol. 4, Iss. 1
Open Access | Times Cited: 158
Pathogenesis of amyotrophic lateral sclerosis
Sarah Morgan, Richard W. Orrell
British Medical Bulletin (2016) Vol. 119, Iss. 1, pp. 87-98
Open Access | Times Cited: 153
Genetics of FTLD: overview and what else we can expect from genetic studies
Cyril Pottier, Thomas A. Ravenscroft, Mónica Sánchez-Contreras, et al.
Journal of Neurochemistry (2016) Vol. 138, Iss. S1, pp. 32-53
Open Access | Times Cited: 138
The clinical spectrum of sporadic and familial forms of frontotemporal dementia
Ione Woollacott, Jonathan D. Rohrer
Journal of Neurochemistry (2016) Vol. 138, Iss. S1, pp. 6-31
Open Access | Times Cited: 130
SRSF1-dependent nuclear export inhibition of C9ORF72 repeat transcripts prevents neurodegeneration and associated motor deficits
Guillaume M. Hautbergue, Lydia M. Castelli, Laura Ferraiuolo, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 130
Progranulin: a new avenue towards the understanding and treatment of neurodegenerative disease
Babykumari P. Chitramuthu, H.P.J. Bennett, Andrew Bateman
Brain (2017) Vol. 140, Iss. 12, pp. 3081-3104
Open Access | Times Cited: 122
Genetics of Frontotemporal Dementia
Diana A. Olszewska, Róisín Lonergan, Emer Fallon, et al.
Current Neurology and Neuroscience Reports (2016) Vol. 16, Iss. 12
Closed Access | Times Cited: 121
Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia
Alberto Benussi, Alessandro Padovani, Barbara Borroni
Frontiers in Aging Neuroscience (2015) Vol. 7
Open Access | Times Cited: 104
Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers
Tania F. Gendron, Marka van Blitterswijk, Kevin F. Bieniek, et al.
Acta Neuropathologica (2015) Vol. 130, Iss. 4, pp. 559-573
Open Access | Times Cited: 99
Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic risk
Ricarda Menke, Malcolm J. Proudfoot, Joanne Wuu, et al.
Journal of Neurology Neurosurgery & Psychiatry (2016) Vol. 87, Iss. 6, pp. 580-588
Open Access | Times Cited: 91
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