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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:

A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies
Celeste M. Karch, Aimee W. Kao, Anna Karydas, et al.
Stem Cell Reports (2019) Vol. 13, Iss. 5, pp. 939-955
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

Regenerative Stem Cell Therapy for Neurodegenerative Diseases: An Overview
Farzane Sivandzade, Luca Cucullo
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 4, pp. 2153-2153
Open Access | Times Cited: 148
Human brain organoids assemble functionally integrated bilateral optic vesicles
Elke Gabriel, Walid Albanna, Giovanni Pasquini, et al.
Cell stem cell (2021) Vol. 28, Iss. 10, pp. 1740-1757.e8
Open Access | Times Cited: 146
ELAVL4, splicing, and glutamatergic dysfunction precede neuron loss in MAPT mutation cerebral organoids
Kathryn R. Bowles, M. Catarina Silva, Kristen Whitney, et al.
Cell (2021) Vol. 184, Iss. 17, pp. 4547-4563.e17
Open Access | Times Cited: 120
Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines
Emily G. Baxi, Terri G. Thompson, Jonathan Li, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 2, pp. 226-237
Open Access | Times Cited: 112
Cellular and pathological functions of tau
C Bravo, Sarah Naguib, Li Gan
Nature Reviews Molecular Cell Biology (2024) Vol. 25, Iss. 11, pp. 845-864
Closed Access | Times Cited: 39
Human iPSC 4R tauopathy model uncovers modifiers of tau propagation
C Bravo, Alice Maria Giani, Jesus Madero-Perez, et al.
Cell (2024) Vol. 187, Iss. 10, pp. 2446-2464.e22
Open Access | Times Cited: 26
Modeling Sporadic Progressive Supranuclear Palsy in 3D Midbrain Organoids: Recapitulating Disease Features for In Vitro Diagnosis and Drug Discovery
Elvira Immacolata Parrotta, Valeria Lucchino, Clara Zannino, et al.
Annals of Neurology (2025)
Open Access | Times Cited: 2
TFEB regulates lysosomal exocytosis of tau and its loss of function exacerbates tau pathology and spreading
Yin Xu, Shuqi Du, Jacob Marsh, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 10, pp. 5925-5939
Open Access | Times Cited: 104
Alzheimer's-associated PU.1 expression levels regulate microglial inflammatory response
Anna A. Pimenova, Manon Herbinet, Ishaan Gupta, et al.
Neurobiology of Disease (2020) Vol. 148, pp. 105217-105217
Open Access | Times Cited: 78
Tackling neurodegenerative diseases with genomic engineering: A new stem cell initiative from the NIH
Daniel M. Ramos, William C. Skarnes, Andrew Singleton, et al.
Neuron (2021) Vol. 109, Iss. 7, pp. 1080-1083
Open Access | Times Cited: 72
Current directions in tau research: Highlights from Tau 2020
Claire E. Sexton, Heather M. Snyder, Dirk Beher, et al.
Alzheimer s & Dementia (2021) Vol. 18, Iss. 5, pp. 988-1007
Open Access | Times Cited: 61
Genetically Encoded, pH-Sensitive mTFP1 Biosensor for Probing Lysosomal pH
Marcus Y. Chin, Anand Patwardhan, Kean-Hooi Ang, et al.
ACS Sensors (2021) Vol. 6, Iss. 6, pp. 2168-2180
Open Access | Times Cited: 59
Recapitulation of endogenous 4R tau expression and formation of insoluble tau in directly reprogrammed human neurons
Lucia S Capano, Chihiro Sato, Elena Ficulle, et al.
Cell stem cell (2022) Vol. 29, Iss. 6, pp. 918-932.e8
Open Access | Times Cited: 41
Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation
Fabia Filipello, Shih‐Feng You, Farzaneh S. Mirfakhar, et al.
Acta Neuropathologica (2023) Vol. 145, Iss. 6, pp. 749-772
Open Access | Times Cited: 33
Neurodegeneration cell per cell
Sriram Balusu, Roman Praschberger, Elsa Lauwers, et al.
Neuron (2023) Vol. 111, Iss. 6, pp. 767-786
Open Access | Times Cited: 31
ER‐mitochondria contacts and cholesterol metabolism are disrupted by disease‐associated tau protein
Leonora Szabo, Nadia Cummins, Paolo Paganetti, et al.
EMBO Reports (2023) Vol. 24, Iss. 8
Open Access | Times Cited: 25
Comparative characterization of human accelerated regions in neurons
Xiekui Cui, Han Yang, Charles Q. Cai, et al.
Nature (2025)
Closed Access | Times Cited: 1
17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes
Kathryn R. Bowles, Derian A. Pugh, Yiyuan Liu, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 35
Person‐specific differences in ubiquitin‐proteasome mediated proteostasis in human neurons
Yi‐Chen Hsieh, Zachary M. Augur, Mason Arbery, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 4, pp. 2952-2967
Open Access | Times Cited: 7
A framework for translating tauopathy therapeutics: Drug discovery to clinical trials
Howard Feldman, Jeffrey L. Cummings, Adam L. Boxer, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 11, pp. 8129-8152
Open Access | Times Cited: 7
Somatic mutations in neurodegeneration: An update
Christos Proukakis
Neurobiology of Disease (2020) Vol. 144, pp. 105021-105021
Open Access | Times Cited: 42
TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy
Carolina Alquézar, Kathleen M. Schoch, Ethan G. Geier, et al.
Science Advances (2021) Vol. 7, Iss. 45
Open Access | Times Cited: 38
Human tau mutations in cerebral organoids induce a progressive dyshomeostasis of cholesterol
Stella M.K. Glasauer, Susan K. Goderie, Jennifer N. Rauch, et al.
Stem Cell Reports (2022) Vol. 17, Iss. 9, pp. 2127-2140
Open Access | Times Cited: 27
Conserved gene signatures shared among MAPT mutations reveal defects in calcium signaling
Miguel Minaya, Sidhartha Mahali, Abhirami K. Iyer, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 16
Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
Chiara Pedicone, Sarah A. Weitzman, Alan E. Renton, et al.
Molecular Neurodegeneration (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 5
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