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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:

Plastic mitochondria-endoplasmic reticulum (ER) contacts use chaperones and tethers to mould their structure and signaling
Thomas Simmen, Maria Sol Herrera-Cruz
Current Opinion in Cell Biology (2018) Vol. 53, pp. 61-69
Closed Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

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: 562
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles
Ren-qi Yao, Chao Ren, Zhaofan Xia, et al.
Autophagy (2020) Vol. 17, Iss. 2, pp. 385-401
Open Access | Times Cited: 313
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: 264
Motion of VAPB molecules reveals ER–mitochondria contact site subdomains
Christopher J. Obara, Jonathon Nixon‐Abell, Andrew S. Moore, et al.
Nature (2024) Vol. 626, Iss. 7997, pp. 169-176
Open Access | Times Cited: 42
Ferritinophagy: A novel insight into the double‐edged sword in ferritinophagy–ferroptosis axis and human diseases
Jing‐Yan Li, Yan‐Hua Feng, Yuxuan Li, et al.
Cell Proliferation (2024) Vol. 57, Iss. 7
Open Access | Times Cited: 20
Mutual interaction between endoplasmic reticulum and mitochondria in nonalcoholic fatty liver disease
Jin Wang, Wanping He, Ping-Ju Tsai, et al.
Lipids in Health and Disease (2020) Vol. 19, Iss. 1
Open Access | Times Cited: 115
Mitochondrial function in development and disease
Marlies P. Rossmann, Sonia M. Dubois, Suneet Agarwal, et al.
Disease Models & Mechanisms (2021) Vol. 14, Iss. 6
Open Access | Times Cited: 104
ER-mitochondria interactions: Both strength and weakness within cancer cells
Mabrouka Doghman, Enzo Lalli
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2019) Vol. 1866, Iss. 4, pp. 650-662
Open Access | Times Cited: 79
Organizing principles of astrocytic nanoarchitecture in the mouse cerebral cortex
Christopher Salmon, Tabish A. Syed, J. Benjamin Kacerovsky, et al.
Current Biology (2023) Vol. 33, Iss. 5, pp. 957-972.e5
Open Access | Times Cited: 37
Novel tumor therapy strategies targeting endoplasmic reticulum-mitochondria signal pathways
Hongzheng Wu, Wanxin Chen, Zhenni Chen, et al.
Ageing Research Reviews (2023) Vol. 88, pp. 101951-101951
Open Access | Times Cited: 24
VAP spatially stabilizes dendritic mitochondria to locally support synaptic plasticity
Ojasee Bapat, Tejas Purimetla, Sarah Kruessel, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 16
Mitochondria-associated endoplasmic reticulum membrane (MAM): a dark horse for diabetic cardiomyopathy treatment
Yong Liu, Jin-Ling Huo, Kaidi Ren, et al.
Cell Death Discovery (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 13
Protein-rich foods, sea foods, and gut microbiota amplify immune responses in chronic diseases and cancers – Targeting PERK as a novel therapeutic strategy for chronic inflammatory diseases, neurodegenerative disorders, and cancer
Fatma Saaoud, Yifan Lu, Keman Xu, et al.
Pharmacology & Therapeutics (2024) Vol. 255, pp. 108604-108604
Open Access | Times Cited: 9
Crosstalk Between Autophagy and Oxidative Stress in Hematological Malignancies: Mechanisms, Implications, and Therapeutic Potential
Antonio José Cabrera-Serrano, José Manuel Sánchez‐Maldonado, Carmen González‐Olmedo, et al.
Antioxidants (2025) Vol. 14, Iss. 3, pp. 264-264
Open Access | Times Cited: 1
Cell organelles as targets of mammalian cadmium toxicity
Wing‐Kee Lee, Frank Thévenod
Archives of Toxicology (2020) Vol. 94, Iss. 4, pp. 1017-1049
Closed Access | Times Cited: 66
ER membranes associated with mitochondria: Possible therapeutic targets in heart-associated diseases
Alejandro Silva‐Palacios, Cecilia Zazueta, José Pedraza-Chaverrı́
Pharmacological Research (2020) Vol. 156, pp. 104758-104758
Closed Access | Times Cited: 60
Amyotrophic Lateral Sclerosis (ALS): Stressed by Dysfunctional Mitochondria-Endoplasmic Reticulum Contacts (MERCs)
Junsheng Chen, Arthur Bassot, Fabrizio Giuliani, et al.
Cells (2021) Vol. 10, Iss. 7, pp. 1789-1789
Open Access | Times Cited: 44
ER-mitochondria communication is involved in NLRP3 inflammasome activation under stress conditions in the innate immune system
Ana Catarina Pereira, Jessica De Pascale, Rosa Resende, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 4
Closed Access | Times Cited: 38
Mitochondria‐associated endoplasmic reticulum membrane: Overview and inextricable link with cancer
Xi Yang, Zhuang Jing, Weilong Song, et al.
Journal of Cellular and Molecular Medicine (2023) Vol. 27, Iss. 7, pp. 906-919
Open Access | Times Cited: 23
Mitochondrial mechanisms in the pathogenesis of chronic inflammatory musculoskeletal disorders
Kailun Wu, Ju-sheng Shieh, Ling Qin, et al.
Cell & Bioscience (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 8
Mapping the lipidome in mitochondria‐associated membranes (MAMs) in an in vitro model of Alzheimer's disease
Tânia Fernandes, Tânia Melo, Tiago Conde, et al.
Journal of Neurochemistry (2024) Vol. 168, Iss. 7, pp. 1237-1253
Open Access | Times Cited: 7
Structural and Functional Alterations in Mitochondria-Associated Membranes (MAMs) and in Mitochondria Activate Stress Response Mechanisms in an In Vitro Model of Alzheimer’s Disease
Tânia Fernandes, Rosa Resende, Diana F. Silva, et al.
Biomedicines (2021) Vol. 9, Iss. 8, pp. 881-881
Open Access | Times Cited: 37
PERK, Beyond an Unfolded Protein Response Sensor in Estrogen-Induced Apoptosis in Endocrine-Resistant Breast Cancer
Ping Fan, V. Craig Jordan
Molecular Cancer Research (2021) Vol. 20, Iss. 2, pp. 193-201
Open Access | Times Cited: 34
A Perspective on the Link between Mitochondria-Associated Membranes (MAMs) and Lipid Droplets Metabolism in Neurodegenerative Diseases
Tânia Fernandes, M. Rosário M. Domingues, Paula I. Moreira, et al.
Biology (2023) Vol. 12, Iss. 3, pp. 414-414
Open Access | Times Cited: 14
Balancing life and death: BCL‐2 family members at diverse ER–mitochondrial contact sites
Robert E. Means, Samuel G. Katz
FEBS Journal (2021) Vol. 289, Iss. 22, pp. 7075-7112
Open Access | Times Cited: 31
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