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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:

Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report
Peter T. Nelson, Dennis W. Dickson, John Q. Trojanowski, et al.
Brain (2019) Vol. 142, Iss. 6, pp. 1503-1527
Open Access | Times Cited: 1157

Showing 1-25 of 1157 citing articles:

Dementia prevention, intervention, and care: 2020 report of the Lancet Commission
Gill Livingston, Jonathan Huntley, Andrew Sommerlad, et al.
The Lancet (2020) Vol. 396, Iss. 10248, pp. 413-446
Open Access | Times Cited: 7614
Biomarkers for neurodegenerative diseases
Oskar Hansson
Nature Medicine (2021) Vol. 27, Iss. 6, pp. 954-963
Open Access | Times Cited: 721
Clinical diagnosis of Alzheimer's disease: recommendations of the International Working Group
Bruno Dubois, Nicolas Villain, Giovanni B. Frisoni, et al.
The Lancet Neurology (2021) Vol. 20, Iss. 6, pp. 484-496
Open Access | Times Cited: 689
Alzheimer's disease
José Arguedas López, Hector M. González, Gabriel C. Léger
Handbook of clinical neurology (2019), pp. 231-255
Closed Access | Times Cited: 624
Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup
Clifford R. Jack, J. Scott Andrews, Thomas G. Beach, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 8, pp. 5143-5169
Open Access | Times Cited: 464
Phase Separation and Neurodegenerative Diseases: A Disturbance in the Force
Aurélie Zbinden, Manuela Pérez‐Berlanga, Pierre De Rossi, et al.
Developmental Cell (2020) Vol. 55, Iss. 1, pp. 45-68
Open Access | Times Cited: 372
Plasma phosphorylated tau 217 and phosphorylated tau 181 as biomarkers in Alzheimer's disease and frontotemporal lobar degeneration: a retrospective diagnostic performance study
Elisabeth H. Thijssen, Renaud La Joie, Amelia Strom, et al.
The Lancet Neurology (2021) Vol. 20, Iss. 9, pp. 739-752
Open Access | Times Cited: 372
TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A
X. Rosa, Mercedes Prudencio, Yuka Koike, et al.
Nature (2022) Vol. 603, Iss. 7899, pp. 124-130
Open Access | Times Cited: 332
The probabilistic model of Alzheimer disease: the amyloid hypothesis revised
Giovanni B. Frisoni, Daniele Altomare, Dietmar Rudolf Thal, et al.
Nature reviews. Neuroscience (2021) Vol. 23, Iss. 1, pp. 53-66
Open Access | Times Cited: 328
Biological subtypes of Alzheimer disease
Daniel Ferreira, Agneta Nordberg, Eric Westman
Neurology (2020) Vol. 94, Iss. 10, pp. 436-448
Open Access | Times Cited: 296
HSP70 chaperones RNA-free TDP-43 into anisotropic intranuclear liquid spherical shells
Haiyang Yu, Shan Lu, Kelsey Gasior, et al.
Science (2021) Vol. 371, Iss. 6529
Open Access | Times Cited: 290
Interpretation of risk loci from genome-wide association studies of Alzheimer's disease
Shea J. Andrews, Brian Fulton‐Howard, Alison Goate
The Lancet Neurology (2020) Vol. 19, Iss. 4, pp. 326-335
Open Access | Times Cited: 285
TDP-43 proteinopathies: a new wave of neurodegenerative diseases
Eva M. J. de Boer, Viyanti K Orie, Timothy L. Williams, et al.
Journal of Neurology Neurosurgery & Psychiatry (2020) Vol. 92, Iss. 1, pp. 86-95
Open Access | Times Cited: 269
Associations of Amyloid, Tau, and Neurodegeneration Biomarker Profiles With Rates of Memory Decline Among Individuals Without Dementia
Clifford R. Jack, Heather J. Wiste, Terry M. Therneau, et al.
JAMA (2019) Vol. 321, Iss. 23, pp. 2316-2316
Open Access | Times Cited: 254
The role of TDP-43 propagation in neurodegenerative diseases: integrating insights from clinical and experimental studies
Myungjin Jo, Shinrye Lee, Yu‐Mi Jeon, et al.
Experimental & Molecular Medicine (2020) Vol. 52, Iss. 10, pp. 1652-1662
Open Access | Times Cited: 254
The path forward in Alzheimer's disease therapeutics: Reevaluating the amyloid cascade hypothesis
Martin Tolar, Susan Abushakra, Marwan N. Sabbagh
Alzheimer s & Dementia (2019) Vol. 16, Iss. 11, pp. 1553-1560
Open Access | Times Cited: 233
Cryo-EM structures of four polymorphic TDP-43 amyloid cores
Qin Cao, David R. Boyer, M.R. Sawaya, et al.
Nature Structural & Molecular Biology (2019) Vol. 26, Iss. 7, pp. 619-627
Open Access | Times Cited: 228
FUS and TDP-43 Phases in Health and Disease
Bede Portz, Bo Lim Lee, James Shorter
Trends in Biochemical Sciences (2021) Vol. 46, Iss. 7, pp. 550-563
Open Access | Times Cited: 225
Neuropathology of Alzheimer's Disease
Jorge Trejo‐Lopez, Anthony T. Yachnis, Stefan Prokop
Neurotherapeutics (2021) Vol. 19, Iss. 1, pp. 173-185
Open Access | Times Cited: 219
Neuropathological consensus criteria for the evaluation of Lewy pathology in post-mortem brains: a multi-centre study
Johannes Attems, Jon B. Toledo, Lauren Walker, et al.
Acta Neuropathologica (2021) Vol. 141, Iss. 2, pp. 159-172
Open Access | Times Cited: 188
TDP-43 condensation properties specify its RNA-binding and regulatory repertoire
Martina Hallegger, Anob M. Chakrabarti, Flora Lee, et al.
Cell (2021) Vol. 184, Iss. 18, pp. 4680-4696.e22
Open Access | Times Cited: 188
Molecular pathology of neurodegenerative diseases: principles and practice
Gábor G. Kovács
Journal of Clinical Pathology (2019) Vol. 72, Iss. 11, pp. 725-735
Open Access | Times Cited: 186
TDP-43 Pathology in Alzheimer’s Disease
Axel Meneses, Shunsuke Koga, Justin O’Leary, et al.
Molecular Neurodegeneration (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 179
Comorbid neuropathological diagnoses in early versus late-onset Alzheimer’s disease
Salvatore Spina, Renaud La Joie, Cathrine Petersen, et al.
Brain (2021) Vol. 144, Iss. 7, pp. 2186-2198
Open Access | Times Cited: 173
Prevalence and Clinical Phenotype of Quadruple Misfolded Proteins in Older Adults
Shama Karanth, Peter T. Nelson, Yuriko Katsumata, et al.
JAMA Neurology (2020) Vol. 77, Iss. 10, pp. 1299-1299
Open Access | Times Cited: 162
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