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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:

Interaction of tau with the RNA-Binding Protein TIA1 Regulates tau Pathophysiology and Toxicity
Tara Vanderweyde, Daniel J. Apicco, Katherine Youmans-Kidder, et al.
Cell Reports (2016) Vol. 15, Iss. 7, pp. 1455-1466
Open Access | Times Cited: 290

Showing 1-25 of 290 citing articles:

Protein Phase Separation: A New Phase in Cell Biology
Steven Boeynaems, Simon Alberti, Nicolas L. Fawzi, et al.
Trends in Cell Biology (2018) Vol. 28, Iss. 6, pp. 420-435
Open Access | Times Cited: 1836
Tau protein liquid–liquid phase separation can initiate tau aggregation
Susanne Wegmann, Bahareh Eftekharzadeh, Katharina Tepper, et al.
The EMBO Journal (2018) Vol. 37, Iss. 7
Open Access | Times Cited: 929
Roles of tau protein in health and disease
Tong Guo, Wendy Noble, Diane P. Hanger
Acta Neuropathologica (2017) Vol. 133, Iss. 5, pp. 665-704
Open Access | Times Cited: 821
Liquid–Liquid Phase Separation in Disease
Simon Alberti, Dorothee Dormann
Annual Review of Genetics (2019) Vol. 53, Iss. 1, pp. 171-194
Open Access | Times Cited: 772
Liquid–liquid phase separation of the microtubule-binding repeats of the Alzheimer-related protein Tau
Susmitha Ambadipudi, Jacek Biernat, Dietmar Riedel, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 708
Stress granules and neurodegeneration
Benjamin Wolozin, Pavel Ivanov
Nature reviews. Neuroscience (2019) Vol. 20, Iss. 11, pp. 649-666
Open Access | Times Cited: 599
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
Ian R. Mackenzie, Alexandra M. Nicholson, Mohona Sarkar, et al.
Neuron (2017) Vol. 95, Iss. 4, pp. 808-816.e9
Open Access | Times Cited: 570
Tau and tauopathies
Thomas Arendt, Jens Stieler, Max Holzer
Brain Research Bulletin (2016) Vol. 126, pp. 238-292
Closed Access | Times Cited: 520
Converging pathways in neurodegeneration, from genetics to mechanisms
Li Gan, Mark Cookson, Leonard Petrucelli, et al.
Nature Neuroscience (2018) Vol. 21, Iss. 10, pp. 1300-1309
Open Access | Times Cited: 415
Tau Protein Disrupts Nucleocytoplasmic Transport in Alzheimer’s Disease
Bahareh Eftekharzadeh, J. Gavin Daigle, Larisa E. Kapinos, et al.
Neuron (2018) Vol. 99, Iss. 5, pp. 925-940.e7
Open Access | Times Cited: 377
Gut Microbiota and Dysbiosis in Alzheimer’s Disease: Implications for Pathogenesis and Treatment
Shan Liu, Jiguo Gao, Mingqin Zhu, et al.
Molecular Neurobiology (2020) Vol. 57, Iss. 12, pp. 5026-5043
Open Access | Times Cited: 344
Friend or foe—Post-translational modifications as regulators of phase separation and RNP granule dynamics
Mario Hofweber, Dorothee Dormann
Journal of Biological Chemistry (2018) Vol. 294, Iss. 18, pp. 7137-7150
Open Access | Times Cited: 338
Liquid-liquid phase separation induces pathogenic tau conformations in vitro
Nicholas M. Kanaan, Chelsey Hamel, Tessa Grabinski, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 301
Cytoplasmic stress granules: Dynamic modulators of cell signaling and disease
Hicham Mahboubi, Ursula Stochaj
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2017) Vol. 1863, Iss. 4, pp. 884-895
Closed Access | Times Cited: 259
Mechanisms of secretion and spreading of pathological tau protein
Cecilia A. Brunello, Maria Merezhko, Riikka‐Liisa Uronen, et al.
Cellular and Molecular Life Sciences (2019) Vol. 77, Iss. 9, pp. 1721-1744
Open Access | Times Cited: 253
Reducing the RNA binding protein TIA1 protects against tau-mediated neurodegeneration in vivo
Daniel J. Apicco, Peter E.A. Ash, Brandon F. Maziuk, et al.
Nature Neuroscience (2017) Vol. 21, Iss. 1, pp. 72-80
Open Access | Times Cited: 233
Disruption of RNA Metabolism in Neurological Diseases and Emerging Therapeutic Interventions
Julia K. Nussbacher, Ricardos Tabet, G Yeo, et al.
Neuron (2019) Vol. 102, Iss. 2, pp. 294-320
Open Access | Times Cited: 230
Lysine/RNA-interactions drive and regulate biomolecular condensation
Tina Ukmar, Saskia Hutten, Matthew P. Grieshop, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 221
Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration
Tara E. Tracy, Jesús Madero‐Pérez, Danielle L. Swaney, et al.
Cell (2022) Vol. 185, Iss. 4, pp. 712-728.e14
Open Access | Times Cited: 212
Impaired ribosome biogenesis: mechanisms and relevance to cancer and aging
Zsofia Turi, Matthew Lacey, Martin Mistrík, et al.
Aging (2019) Vol. 11, Iss. 8, pp. 2512-2540
Open Access | Times Cited: 190
Atypical, non-standard functions of the microtubule associated Tau protein
Ioannis Sotiropoulos, Marie‐Christine Galas, Joana Silva, et al.
Acta Neuropathologica Communications (2017) Vol. 5, Iss. 1
Open Access | Times Cited: 175
Tau aggregates are RNA-protein assemblies that mislocalize multiple nuclear speckle components
Evan Lester, Felicia K. Ooi, Nadine Bakkar, et al.
Neuron (2021) Vol. 109, Iss. 10, pp. 1675-1691.e9
Open Access | Times Cited: 167
Tau-Mediated Disruption of the Spliceosome Triggers Cryptic RNA Splicing and Neurodegeneration in Alzheimer’s Disease
Yi‐Chen Hsieh, Caiwei Guo, Hari Krishna Yalamanchili, et al.
Cell Reports (2019) Vol. 29, Iss. 2, pp. 301-316.e10
Open Access | Times Cited: 154
Interaction of tau with HNRNPA2B1 and N6-methyladenosine RNA mediates the progression of tauopathy
Lulu Jiang, Weiwei Lin, Cheng Zhang, et al.
Molecular Cell (2021) Vol. 81, Iss. 20, pp. 4209-4227.e12
Open Access | Times Cited: 132
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
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