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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:

Insights into VPS13 properties and function reveal a new mechanism of eukaryotic lipid transport
Marianna Leonzino, Karin M. Reinisch, Pietro De Camilli
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids (2021) Vol. 1866, Iss. 10, pp. 159003-159003
Open Access | Times Cited: 92

Showing 1-25 of 92 citing articles:

Mitochondria at the crossroads of health and disease
Anu Suomalainen, Jodi Nunnari
Cell (2024) Vol. 187, Iss. 11, pp. 2601-2627
Open Access | Times Cited: 100
ER-lysosome lipid transfer protein VPS13C/PARK23 prevents aberrant mtDNA-dependent STING signaling
William Hancock‐Cerutti, Zheng Wu, Peng Xu, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 7
Open Access | Times Cited: 70
ATG9 vesicles comprise the seed membrane of mammalian autophagosomes
Taryn J. Olivas, Yumei Wu, Shenliang Yu, et al.
The Journal of Cell Biology (2023) Vol. 222, Iss. 7
Open Access | Times Cited: 60
RBG Motif Bridge-Like Lipid Transport Proteins: Structure, Functions, and Open Questions
Michael G. Hanna, Andrés Guillén-Samander, Pietro De Camilli
Annual Review of Cell and Developmental Biology (2023) Vol. 39, Iss. 1, pp. 409-434
Open Access | Times Cited: 48
In situ architecture of the lipid transport protein VPS13C at ER–lysosome membrane contacts
Shujun Cai, Yumei Wu, Andrés Guillén-Samander, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 29
Open Access | Times Cited: 62
Structural and biochemical insights into lipid transport by VPS13 proteins
Jyoti Adlakha, Zhouping Hong, Peiqi Li, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 5
Open Access | Times Cited: 52
A partnership between the lipid scramblase XK and the lipid transfer protein VPS13A at the plasma membrane
Andrés Guillén-Samander, Yumei Wu, S. Sebastian Pineda, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 35
Open Access | Times Cited: 52
A possible role for VPS13-family proteins in bulk lipid transfer, membrane expansion and organelle biogenesis
Thomas J. Melia, Karin M. Reinisch
Journal of Cell Science (2022) Vol. 135, Iss. 5
Open Access | Times Cited: 50
Vps13-like proteins provide phosphatidylethanolamine for GPI anchor synthesis in the ER
Alexandre Toulmay, Fawn B. Whittle, Jerry Yang, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 3
Open Access | Times Cited: 46
VAP-A intrinsically disordered regions enable versatile tethering at membrane contact sites
Mélody Subra, Manuela Dezi, Joëlle Bigay, et al.
Developmental Cell (2023) Vol. 58, Iss. 2, pp. 121-138.e9
Open Access | Times Cited: 25
Lysosome damage triggers acute formation of ER to lysosomes membrane tethers mediated by the bridge-like lipid transport protein VPS13C
Xinbo Wang, Peng Xu, Amanda Bentley‐DeSousa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 13
Mitochondrial membrane lipids in the regulation of bioenergetic flux
Stephen Thomas Decker, Katsuhiko Funai
Cell Metabolism (2024) Vol. 36, Iss. 9, pp. 1963-1978
Open Access | Times Cited: 11
Requirement of Xk and Vps13a for the P2X7-mediated phospholipid scrambling and cell lysis in mouse T cells
Yuta Ryoden, Katsumori Segawa, Shigekazu Nagata
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 7
Open Access | Times Cited: 36
Sequence Analysis and Structural Predictions of Lipid Transfer Bridges in the Repeating Beta Groove (RBG) Superfamily Reveal Past and Present Domain Variations Affecting Form, Function and Interactions of VPS13, ATG2, SHIP164, Hobbit and Tweek
Tim P. Levine
Contact (2022) Vol. 5, pp. 251525642211343-251525642211343
Open Access | Times Cited: 33
Interaction between VPS13A and the XK scramblase is important for VPS13A function in humans
Jae-Sook Park, Yiying Hu, Nancy M. Hollingsworth, et al.
Journal of Cell Science (2022) Vol. 135, Iss. 17
Open Access | Times Cited: 29
Bacterial AsmA-Like Proteins: Bridging the Gap in Intermembrane Phospholipid Transport
Sujeet Kumar, Natividad Ruiz
Contact (2023) Vol. 6
Open Access | Times Cited: 17
Endoplasmic Reticulum Membrane Contact Sites, Lipid Transport, and Neurodegeneration
Andrés Guillén-Samander, Pietro De Camilli
Cold Spring Harbor Perspectives in Biology (2022) Vol. 15, Iss. 4, pp. a041257-a041257
Closed Access | Times Cited: 27
Inter-organellar Communication in Parkinson's and Alzheimer's Disease: Looking Beyond Endoplasmic Reticulum-Mitochondria Contact Sites
Stephanie Vrijsen, Céline Vrancx, Mara Del Vecchio, et al.
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 26
SHIP164 is a chorein motif lipid transfer protein that controls endosome–Golgi membrane traffic
Michael G. Hanna, Patreece Suen, Yumei Wu, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 6
Open Access | Times Cited: 23
Neuroacanthocytosis Syndromes: The Clinical Perspective
Ruth H. Walker, Kevin Peikert, Hans H. Jung, et al.
Contact (2023) Vol. 6
Open Access | Times Cited: 14
Common genetic risk for Parkinson's disease and dysfunction of the endo-lysosomal system
Noopur Bhore, Erin C. Bogacki, Benjamin O’Callaghan, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2024) Vol. 379, Iss. 1899
Open Access | Times Cited: 5
A conserved megaprotein-based molecular bridge critical for lipid trafficking and cold resilience
Changnan Wang, Bingying Wang, Taruna Pandey, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 20
The Endoplasmic Reticulum and Its Contacts: Emerging Roles in Axon Development, Neurotransmission, and Degeneration
Marijn Kuijpers, Phuong The Nguyen, Volker Haucke
The Neuroscientist (2023) Vol. 30, Iss. 5, pp. 545-559
Open Access | Times Cited: 12
Role of Macroautophagy in Mammalian Male Reproductive Physiology
Doaa Kirat, Ahmed Mohamed Alahwany, Ahmed Hamed Arisha, et al.
Cells (2023) Vol. 12, Iss. 9, pp. 1322-1322
Open Access | Times Cited: 12
Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea‐Acanthocytosis
Gábriel Miltenberger-Miltényi, Attila Jones, Amber M. Tetlow, et al.
Movement Disorders (2023) Vol. 38, Iss. 8, pp. 1535-1541
Closed Access | Times Cited: 11
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