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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:

ER-mitochondria tethering by PDZD8 regulates Ca 2+ dynamics in mammalian neurons
Yusuke Hirabayashi, Seok‐Kyu Kwon, Hunki Paek, et al.
Science (2017) Vol. 358, Iss. 6363, pp. 623-630
Open Access | Times Cited: 399

Showing 1-25 of 399 citing articles:

The machineries, regulation and cellular functions of mitochondrial calcium
Carlotta Giorgi, Saverio Marchi, Paolo Pinton
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 11, pp. 713-730
Closed Access | Times Cited: 699
Here, there, and everywhere: The importance of ER membrane contact sites
Haoxi Wu, Pedro Carvalho, Gia K. Voeltz
Science (2018) Vol. 361, Iss. 6401
Open Access | Times Cited: 602
Coming together to define membrane contact sites
Luca Scorrano, Maria Antonietta De Matteis, Scott D. Emr, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 591
Visualizing Intracellular Organelle and Cytoskeletal Interactions at Nanoscale Resolution on Millisecond Timescales
Yuting Guo, Di Li, Siwei Zhang, et al.
Cell (2018) Vol. 175, Iss. 5, pp. 1430-1442.e17
Open Access | Times Cited: 570
The functional universe of membrane contact sites
William A. Prinz, Alexandre Toulmay, Tamás Balla
Nature Reviews Molecular Cell Biology (2019) Vol. 21, Iss. 1, pp. 7-24
Open Access | Times Cited: 547
Distinct fission signatures predict mitochondrial degradation or biogenesis
Tatjana Kleele, Timo Rey, Julius Winter, et al.
Nature (2021) Vol. 593, Iss. 7859, pp. 435-439
Open Access | Times Cited: 530
VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites
Nikit Kumar, Marianna Leonzino, William Hancock‐Cerutti, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 10, pp. 3625-3639
Open Access | Times Cited: 509
Endoplasmic Reticulum–Mitochondrial Contactology: Structure and Signaling Functions
György Csordás, David Weaver, György Hajnóczky
Trends in Cell Biology (2018) Vol. 28, Iss. 7, pp. 523-540
Open Access | Times Cited: 495
Lipid transfer proteins: the lipid commute via shuttles, bridges and tubes
Louise H. Wong, Alberto T. Gatta, Tim P. Levine
Nature Reviews Molecular Cell Biology (2018) Vol. 20, Iss. 2, pp. 85-101
Closed Access | Times Cited: 415
Interacting organelles
Sarah Cohen, Alex M. Valm, Jennifer Lippincott‐Schwartz
Current Opinion in Cell Biology (2018) Vol. 53, pp. 84-91
Open Access | Times Cited: 282
Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson’s Disease
Maria Nguyen, Yvette C. Wong, Daniel Ysselstein, et al.
Trends in Neurosciences (2018) Vol. 42, Iss. 2, pp. 140-149
Open Access | Times Cited: 267
Impaired mitochondrial calcium efflux contributes to disease progression in models of Alzheimer’s disease
Pooja Jadiya, Devin W. Kolmetzky, Dhanendra Tomar, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 265
Mitochondria in health, disease, and aging
John S. Harrington, Stefan W. Ryter, Maria Plataki, et al.
Physiological Reviews (2023) Vol. 103, Iss. 4, pp. 2349-2422
Open Access | Times Cited: 261
Regulation and Function of Mitochondria–Lysosome Membrane Contact Sites in Cellular Homeostasis
Yvette C. Wong, Soojin Kim, Wesley Peng, et al.
Trends in Cell Biology (2019) Vol. 29, Iss. 6, pp. 500-513
Open Access | Times Cited: 259
Split-TurboID enables contact-dependent proximity labeling in cells
Kelvin F. Cho, Tess C. Branon, Sanjana Rajeev, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 22, pp. 12143-12154
Open Access | Times Cited: 246
Mitochondrial calcium exchange in physiology and disease
Joanne F. Garbincius, John W. Elrod
Physiological Reviews (2021) Vol. 102, Iss. 2, pp. 893-992
Open Access | Times Cited: 233
Mitochondria-lysosome contacts regulate mitochondrial Ca 2+ dynamics via lysosomal TRPML1
Wesley Peng, Yvette C. Wong, Dimitri Krainc
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 32, pp. 19266-19275
Open Access | Times Cited: 231
Regulation of Mitochondrial ATP Production: Ca2+ Signaling and Quality Control
Liron Boyman, Mariusz Karbowski, W. Jonathan Lederer
Trends in Molecular Medicine (2019) Vol. 26, Iss. 1, pp. 21-39
Open Access | Times Cited: 212
Mitochondrial dysfunction: mechanisms and advances in therapy
Zong Yao, Hao Li, Peng Liao, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 195
Pleiotropic Mitochondria: The Influence of Mitochondria on Neuronal Development and Disease
Vidhya Rangaraju, Tommy L. Lewis, Yusuke Hirabayashi, et al.
Journal of Neuroscience (2019) Vol. 39, Iss. 42, pp. 8200-8208
Open Access | Times Cited: 190
Molecular Tuning of the Axonal Mitochondrial Ca2+ Uniporter Ensures Metabolic Flexibility of Neurotransmission
Ghazaleh Ashrafi, Jaime de Juan‐Sanz, Ryan Farrell, et al.
Neuron (2019) Vol. 105, Iss. 4, pp. 678-687.e5
Open Access | Times Cited: 187
Mitochondrial proteostasis in the context of cellular and organismal health and aging
Erica A. Moehle, Koning Shen, Andrew Dillin
Journal of Biological Chemistry (2018) Vol. 294, Iss. 14, pp. 5396-5407
Open Access | Times Cited: 162
Regulation of the ER stress response by a mitochondrial microprotein
Qian Chu, Thomas F. Martínez, Sammy Weiser Novak, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 152
Dysregulation of mitochondria-lysosome contacts by GBA1 dysfunction in dopaminergic neuronal models of Parkinson’s disease
Soojin Kim, Yvette C. Wong, Fanding Gao, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 140
Organelle-level precision with next-generation targeting technologies
Anand Saminathan, Matthew Zajac, Palapuravan Anees, et al.
Nature Reviews Materials (2021) Vol. 7, Iss. 5, pp. 355-371
Closed Access | Times Cited: 118
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