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:

Mitochondria-Endoplasmic Reticulum Contacts in Reactive Astrocytes Promote Vascular Remodeling
Jana Göbel, Esther Engelhardt, Patric Pelzer, et al.
Cell Metabolism (2020) Vol. 31, Iss. 4, pp. 791-808.e8
Open Access | Times Cited: 112

Showing 1-25 of 112 citing articles:

Inflammation, epigenetics, and metabolism converge to cell senescence and ageing: the regulation and intervention
Xudong Zhu, Zhiyang Chen, Weiyan Shen, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 229

Reactive astrocytes facilitate vascular repair and remodeling after stroke
Michael R. Williamson, Cathleen Joy A. Fuertes, Andrew K. Dunn, et al.
Cell Reports (2021) Vol. 35, Iss. 4, pp. 109048-109048
Open Access | Times Cited: 122

Astrocyte Endfeet in Brain Function and Pathology: Open Questions
Blanca Díaz‐Castro, Stefanie Robel, Anusha Mishra
Annual Review of Neuroscience (2023) Vol. 46, Iss. 1, pp. 101-121
Open Access | Times Cited: 93

Mitochondrial signalling and homeostasis: from cell biology to neurological disease
Jack J. Collier, Monika Oláhová, Thomas G. McWilliams, et al.
Trends in Neurosciences (2023) Vol. 46, Iss. 2, pp. 137-152
Open Access | Times Cited: 75

Astrocytic cannabinoid receptor 1 promotes resilience by dampening stress-induced blood–brain barrier alterations
Katarzyna Dudek, Sam E.J. Paton, Luisa Bandeira Binder, et al.
Nature Neuroscience (2025)
Open Access | Times Cited: 4

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

Mitochondrial biogenesis in developing astrocytes regulates astrocyte maturation and synapse formation
Tamara Zehnder, Francesco Petrelli, Jennifer Romanos, et al.
Cell Reports (2021) Vol. 35, Iss. 2, pp. 108952-108952
Open Access | Times Cited: 88

Ca2+ handling at the mitochondria-ER contact sites in neurodegeneration
Dmitry Lim, Giulia Dematteis, Laura Tapella, et al.
Cell Calcium (2021) Vol. 98, pp. 102453-102453
Closed Access | Times Cited: 79

Astrocytes in the regulation of cerebrovascular functions
Martine Cohen‐Salmon, Leila Slaoui, Noémie Mazaré, et al.
Glia (2020) Vol. 69, Iss. 4, pp. 817-841
Closed Access | Times Cited: 72

Mitochondrial Dysfunction in Astrocytes: A Role in Parkinson’s Disease?
Collin M. Bantle, Warren D. Hirst, Andreas Weihofen, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 8
Open Access | Times Cited: 65

Mitochondrial Dynamics: A Potential Therapeutic Target for Ischemic Stroke
Xiangyue Zhou, Han‐Min Chen, Ling Wang, et al.
Frontiers in Aging Neuroscience (2021) Vol. 13
Open Access | Times Cited: 59

Mitochondrial Fission and Fusion in Tumor Progression to Metastasis
Dillon P. Boulton, M. Cecilia Caino
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 58

Endocannabinoid signaling in astrocytes
Abel Eraso‐Pichot, Sandrine Pouvreau, Alexandre Oliveira-Pinto, et al.
Glia (2022) Vol. 71, Iss. 1, pp. 44-59
Open Access | Times Cited: 54

Maraviroc promotes recovery from traumatic brain injury in mice by suppression of neuroinflammation and activation of neurotoxic reactive astrocytes
Yuan Zhou, Shu Zhang, Jianning Zhang, et al.
Neural Regeneration Research (2022) Vol. 18, Iss. 1, pp. 141-141
Open Access | Times Cited: 51

Dysregulation of organelle membrane contact sites in neurological diseases
Soojin Kim, Robert Coukos, Fanding Gao, et al.
Neuron (2022) Vol. 110, Iss. 15, pp. 2386-2408
Open Access | Times Cited: 47

Metabolic control of adult neural stem cell self-renewal by the mitochondrial protease YME1L
Gulzar A. Wani, Hans‐Georg Sprenger, Kristiano Ndoci, et al.
Cell Reports (2022) Vol. 38, Iss. 7, pp. 110370-110370
Open Access | Times Cited: 40

NAD+ rescues aging-induced blood-brain barrier damage via the CX43-PARP1 axis
Rui Zhan, Xia Meng, Dongping Tian, et al.
Neuron (2023) Vol. 111, Iss. 22, pp. 3634-3649.e7
Closed Access | Times Cited: 40

Mitochondria in endothelial cells angiogenesis and function: current understanding and future perspectives
Zhen Luo, Jianbo Yao, Zhe Wang, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 31

Call to action to properly utilize electron microscopy to measure organelles to monitor disease
Kit Neikirk, Edgar-Garza Lopez, Andrea G. Marshall, et al.
European Journal of Cell Biology (2023) Vol. 102, Iss. 4, pp. 151365-151365
Open Access | Times Cited: 30

Mitochondria associated ER membranes and cerebral ischemia: Molecular mechanisms and therapeutic strategies
Ruiqi Jiang, Qiqi Li, Rui Sheng
Pharmacological Research (2023) Vol. 191, pp. 106761-106761
Open Access | Times Cited: 25

Enhanced mitochondrial fusion during a critical period of synaptic plasticity in adult-born neurons
Sandra M.V. Kochan, Meret Cepero Malo, Milica Jevtic, et al.
Neuron (2024) Vol. 112, Iss. 12, pp. 1997-2014.e6
Open Access | Times Cited: 16

Shared inflammatory glial cell signature after stab wound injury, revealed by spatial, temporal, and cell-type-specific profiling of the murine cerebral cortex
Christina Koupourtidou, Veronika Schwarz, Hananeh Aliee, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 15

Regulation of blood-brain barrier integrity by Dmp1 -expressing astrocytes through mitochondrial transfer
Delin Liu, Peng Liao, Hao Li, et al.
Science Advances (2024) Vol. 10, Iss. 26
Open Access | Times Cited: 14

Direct neuronal reprogramming of NDUFS4 patient cells identifies the unfolded protein response as a novel general reprogramming hurdle
Giovanna Sonsalla, Ana Belén Malpartida, Therese Riedemann, et al.
Neuron (2024) Vol. 112, Iss. 7, pp. 1117-1132.e9
Open Access | Times Cited: 9

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