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:
Mitochondria-Associated Membranes (MAMs): Overview and Its Role in Parkinson’s Disease
Mario Rodríguez‐Arribas, Sokhna M. S. Yakhine-Diop, José Manuel Bravo‐San Pedro, et al.
Molecular Neurobiology (2016) Vol. 54, Iss. 8, pp. 6287-6303
Closed Access | Times Cited: 74
Mario Rodríguez‐Arribas, Sokhna M. S. Yakhine-Diop, José Manuel Bravo‐San Pedro, et al.
Molecular Neurobiology (2016) Vol. 54, Iss. 8, pp. 6287-6303
Closed Access | Times Cited: 74
Showing 1-25 of 74 citing articles:
The regulation of autophagy by calcium signals: Do we have a consensus?
Martin D. Bootman, Tala Chehab, Geert Bultynck, et al.
Cell Calcium (2017) Vol. 70, pp. 32-46
Open Access | Times Cited: 222
Martin D. Bootman, Tala Chehab, Geert Bultynck, et al.
Cell Calcium (2017) Vol. 70, pp. 32-46
Open Access | Times Cited: 222
Sphingolipids and lipid rafts: Novel concepts and methods of analysis
Erhard Bieberich
Chemistry and Physics of Lipids (2018) Vol. 216, pp. 114-131
Open Access | Times Cited: 195
Erhard Bieberich
Chemistry and Physics of Lipids (2018) Vol. 216, pp. 114-131
Open Access | Times Cited: 195
Mitochondria-associated membranes in aging and senescence: structure, function, and dynamics
Justyna Janikiewicz, Jędrzej Szymański, Dominika Malińska, et al.
Cell Death and Disease (2018) Vol. 9, Iss. 3
Open Access | Times Cited: 194
Justyna Janikiewicz, Jędrzej Szymański, Dominika Malińska, et al.
Cell Death and Disease (2018) Vol. 9, Iss. 3
Open Access | Times Cited: 194
The redox language in neurodegenerative diseases: oxidative post-translational modifications by hydrogen peroxide
Yew Mun Lee, Weifeng He, Yih‐Cherng Liou
Cell Death and Disease (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 112
Yew Mun Lee, Weifeng He, Yih‐Cherng Liou
Cell Death and Disease (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 112
ER–mitochondria signaling in Parkinson’s disease
Patricia Gómez‐Suaga, José Manuel Bravo‐San Pedro, Rosa A. González‐Polo, et al.
Cell Death and Disease (2018) Vol. 9, Iss. 3
Open Access | Times Cited: 143
Patricia Gómez‐Suaga, José Manuel Bravo‐San Pedro, Rosa A. González‐Polo, et al.
Cell Death and Disease (2018) Vol. 9, Iss. 3
Open Access | Times Cited: 143
The Close Encounter Between Alpha-Synuclein and Mitochondria
Mattia Vicario, Domenico Cieri, Marisa Brini, et al.
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 111
Mattia Vicario, Domenico Cieri, Marisa Brini, et al.
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 111
Roles of sigma-1 receptors on mitochondrial functions relevant to neurodegenerative diseases
Tzu-Yu Weng, Shang‐Yi Tsai, Tsung‐Ping Su
Journal of Biomedical Science (2017) Vol. 24, Iss. 1
Open Access | Times Cited: 103
Tzu-Yu Weng, Shang‐Yi Tsai, Tsung‐Ping Su
Journal of Biomedical Science (2017) Vol. 24, Iss. 1
Open Access | Times Cited: 103
Role of mitochondrial dysfunction and dysregulation of Ca2+ homeostasis in the pathophysiology of insulin resistance and type 2 diabetes
Chih‐Hao Wang, Yau–Huei Wei
Journal of Biomedical Science (2017) Vol. 24, Iss. 1
Open Access | Times Cited: 101
Chih‐Hao Wang, Yau–Huei Wei
Journal of Biomedical Science (2017) Vol. 24, Iss. 1
Open Access | Times Cited: 101
Endoplasmic reticulum–mitochondria crosstalk: from junction to function across neurological disorders
Pabbala Veeresh, Harpreet Kaur, Deepaneeta Sarmah, et al.
Annals of the New York Academy of Sciences (2019) Vol. 1457, Iss. 1, pp. 41-60
Closed Access | Times Cited: 78
Pabbala Veeresh, Harpreet Kaur, Deepaneeta Sarmah, et al.
Annals of the New York Academy of Sciences (2019) Vol. 1457, Iss. 1, pp. 41-60
Closed Access | Times Cited: 78
FUNDC1-dependent mitochondria-associated endoplasmic reticulum membranes are involved in angiogenesis and neoangiogenesis
Cheng Wang, Xiaoyan Dai, Shengnan Wu, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 67
Cheng Wang, Xiaoyan Dai, Shengnan Wu, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 67
Reappraisal of metabolic dysfunction in neurodegeneration: Focus on mitochondrial function and calcium signaling
Pooja Jadiya, Joanne F. Garbincius, John W. Elrod
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 60
Pooja Jadiya, Joanne F. Garbincius, John W. Elrod
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 60
Valerie Perea, Christian M. Cole, Justine Lebeau, et al.
The EMBO Journal (2023) Vol. 42, Iss. 15
Open Access | Times Cited: 37
The Misfolding Mystery: α-syn and the Pathogenesis of Parkinson's Disease
Samir Negi, Navneet Khurana, Navneet Duggal
Neurochemistry International (2024) Vol. 177, pp. 105760-105760
Closed Access | Times Cited: 11
Samir Negi, Navneet Khurana, Navneet Duggal
Neurochemistry International (2024) Vol. 177, pp. 105760-105760
Closed Access | Times Cited: 11
Mitochondrial fission and fusion in neurodegenerative diseases:Ca2+ signalling
Xuan Liu, Tianjiao Li, Xiaoming Tu, et al.
Molecular and Cellular Neuroscience (2025), pp. 103992-103992
Closed Access | Times Cited: 1
Xuan Liu, Tianjiao Li, Xiaoming Tu, et al.
Molecular and Cellular Neuroscience (2025), pp. 103992-103992
Closed Access | Times Cited: 1
Recent development of mitochondrial metabolism and dysfunction in osteoarthritis
Pengchao Guo, Ahmad Alhaskawi, Safwat Adel Abdo Moqbel, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access | Times Cited: 1
Pengchao Guo, Ahmad Alhaskawi, Safwat Adel Abdo Moqbel, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access | Times Cited: 1
Interorganelle Communication between Mitochondria and the Endolysosomal System
Gonzalo Soto‐Heredero, Francesc Baixauli, Marı́a Mittelbrunn
Frontiers in Cell and Developmental Biology (2017) Vol. 5
Open Access | Times Cited: 86
Gonzalo Soto‐Heredero, Francesc Baixauli, Marı́a Mittelbrunn
Frontiers in Cell and Developmental Biology (2017) Vol. 5
Open Access | Times Cited: 86
Ascorbate peroxidase proximity labeling coupled with biochemical fractionation identifies promoters of endoplasmic reticulum–mitochondrial contacts
Il-Taeg Cho, Guillaume Adelmant, Youngshin Lim, et al.
Journal of Biological Chemistry (2017) Vol. 292, Iss. 39, pp. 16382-16392
Open Access | Times Cited: 82
Il-Taeg Cho, Guillaume Adelmant, Youngshin Lim, et al.
Journal of Biological Chemistry (2017) Vol. 292, Iss. 39, pp. 16382-16392
Open Access | Times Cited: 82
Mitochondria-Associated Membranes As Networking Platforms and Regulators of Cancer Cell Fate
Maria Livia Sassano, Alexander R. van Vliet, Patrizia Agostinis
Frontiers in Oncology (2017) Vol. 7
Open Access | Times Cited: 80
Maria Livia Sassano, Alexander R. van Vliet, Patrizia Agostinis
Frontiers in Oncology (2017) Vol. 7
Open Access | Times Cited: 80
Differential effects of TSPO ligands on mitochondrial function in mouse microglia cells
Stefanie M. Bader, Luisa Wolf, Vladimir M. Milenkovic, et al.
Psychoneuroendocrinology (2019) Vol. 106, pp. 65-76
Closed Access | Times Cited: 67
Stefanie M. Bader, Luisa Wolf, Vladimir M. Milenkovic, et al.
Psychoneuroendocrinology (2019) Vol. 106, pp. 65-76
Closed Access | Times Cited: 67
ER membranes associated with mitochondria: Possible therapeutic targets in heart-associated diseases
Alejandro Silva‐Palacios, Cecilia Zazueta, José Pedraza‐Chaverrí
Pharmacological Research (2020) Vol. 156, pp. 104758-104758
Closed Access | Times Cited: 60
Alejandro Silva‐Palacios, Cecilia Zazueta, José Pedraza‐Chaverrí
Pharmacological Research (2020) Vol. 156, pp. 104758-104758
Closed Access | Times Cited: 60
Is REDD1 a metabolic double agent? Lessons from physiology and pathology
Florian Britto, Karine Dumas, Sophie Giorgetti‐Peraldi, et al.
AJP Cell Physiology (2020) Vol. 319, Iss. 5, pp. C807-C824
Open Access | Times Cited: 54
Florian Britto, Karine Dumas, Sophie Giorgetti‐Peraldi, et al.
AJP Cell Physiology (2020) Vol. 319, Iss. 5, pp. C807-C824
Open Access | Times Cited: 54
The Parkinson’s disease-associated gene ITPKB protects against α-synuclein aggregation by regulating ER-to-mitochondria calcium release
Daniel J. Apicco, Evgeny Shlevkov, Catherine L. Nezich, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 118, Iss. 1
Open Access | Times Cited: 53
Daniel J. Apicco, Evgeny Shlevkov, Catherine L. Nezich, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 118, Iss. 1
Open Access | Times Cited: 53
Relevance of Autophagy and Mitophagy Dynamics and Markers in Neurodegenerative Diseases
Carlotta Giorgi, Esmaa Bouhamida, Alberto Danese, et al.
Biomedicines (2021) Vol. 9, Iss. 2, pp. 149-149
Open Access | Times Cited: 42
Carlotta Giorgi, Esmaa Bouhamida, Alberto Danese, et al.
Biomedicines (2021) Vol. 9, Iss. 2, pp. 149-149
Open Access | Times Cited: 42
Therapeutic Strategies Targeting Mitochondrial Calcium Signaling: A New Hope for Neurological Diseases?
Laura R. Rodríguez, Tamara Lapeña-Luzón, Noelia Benetó, et al.
Antioxidants (2022) Vol. 11, Iss. 1, pp. 165-165
Open Access | Times Cited: 29
Laura R. Rodríguez, Tamara Lapeña-Luzón, Noelia Benetó, et al.
Antioxidants (2022) Vol. 11, Iss. 1, pp. 165-165
Open Access | Times Cited: 29
Mitochondria‐associated endoplasmic reticulum membranes tethering protein VAPB‐PTPIP51 protects against ischemic stroke through inhibiting the activation of autophagy
Mingyang Li, Yonggang Zhang, Guixiang Yu, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 4
Open Access | Times Cited: 7
Mingyang Li, Yonggang Zhang, Guixiang Yu, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 4
Open Access | Times Cited: 7
