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:

CRISPR screens for lipid regulators reveal a role for ER-bound SNX13 in lysosomal cholesterol export
Albert Lu, F. Hsieh, Bikal R. Sharma, et al.
The Journal of Cell Biology (2021) Vol. 221, Iss. 2
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndrome
Michael D. Healy, Kerrie E. McNally, Rebeka Butkovič, et al.
Cell (2023) Vol. 186, Iss. 10, pp. 2219-2237.e29
Open Access | Times Cited: 54

Organelle-selective click labeling coupled with flow cytometry allows pooled CRISPR screening of genes involved in phosphatidylcholine metabolism
Masaki Tsuchiya, Nobuhiko Tachibana, Kohjiro Nagao, et al.
Cell Metabolism (2023) Vol. 35, Iss. 6, pp. 1072-1083.e9
Open Access | Times Cited: 35

Cholesterol Metabolism in Aging and Age-Related Disorders
Gesine Saher
Annual Review of Neuroscience (2023) Vol. 46, Iss. 1, pp. 59-78
Open Access | Times Cited: 30

Parallel CRISPR-Cas9 screens identify mechanisms of PLIN2 and lipid droplet regulation
Melissa A. Roberts, Kirandeep K. Deol, Alyssa J. Mathiowetz, et al.
Developmental Cell (2023) Vol. 58, Iss. 18, pp. 1782-1800.e10
Open Access | Times Cited: 28

Altered lipid homeostasis is associated with cerebellar neurodegeneration in SNX14 deficiency
Yijing Zhou, Vanessa Sánchez, Peining Xu, et al.
JCI Insight (2024) Vol. 9, Iss. 10
Open Access | Times Cited: 8

GCAF(TMEM251) regulates lysosome biogenesis by activating the mannose-6-phosphate pathway
Weichao Zhang, Xi Yang, Yingxiang Li, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 28

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

The multiple facets of Rab proteins modulating the cellular distribution of cholesterol from the late endosomal compartment
Mai Khanh Linh Nguyen, C. Pinkenburg, Jianfeng Du, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2025) Vol. 1872, Iss. 3, pp. 119896-119896
Closed Access

Structural Predictions of the SNX-RGS Proteins Suggest They Belong to a New Class of Lipid Transfer Proteins
Blessy Paul, Saroja Weeratunga, Vikas A. Tillu, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 25

Lysosomal phospholipase A2 contributes to the biosynthesis of the atypical late endosome lipid bis(monoacylglycero)phosphate
Jacinda Chen, Amaury Cazenave‐Gassiot, Yimeng Xu, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 14

Targeting membrane contact sites to mediate lipid dynamics: innovative cancer therapies
Jie Wang, Meifeng Wang, X. Zeng, et al.
Cell Communication and Signaling (2025) Vol. 23, Iss. 1
Open Access

Systematic interrogation of functional genes underlying cholesterol and lipid homeostasis
Hai-Huan Shan, Shuangshuang Fan, Qifeng Li, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access

The (social) lives, deaths, and biophysical phases of lipid droplets
W. Mike Henne
Current Opinion in Cell Biology (2023) Vol. 82, pp. 102178-102178
Open Access | Times Cited: 11

PtdIns4P exchange at endoplasmic reticulum-autolysosome contacts is essential for autophagy and neuronal homeostasis
Hao Liu, Wenxia Shao, Wei Liu, et al.
Autophagy (2023) Vol. 19, Iss. 10, pp. 2682-2701
Open Access | Times Cited: 10

Endolysosomal cholesterol export: More than just NPC1
Albert Lu
BioEssays (2022) Vol. 44, Iss. 10
Open Access | Times Cited: 15

Engineering membrane architecture for biotechnological applications
Zimo Jin, Asia Vighi, Yueming Dong, et al.
Biotechnology Advances (2023) Vol. 64, pp. 108118-108118
Closed Access | Times Cited: 8

Lysosomal membrane contact sites: Integrative hubs for cellular communication and homeostasis
Sumit Bandyopadhyay, Daniel Adebayo, Eseiwi Obaseki, et al.
Current topics in membranes (2024), pp. 85-116
Closed Access | Times Cited: 2

The role of lysosomes in lipid homeostasis
Florian Fröhlich, Ayelén González Montoro
Biological Chemistry (2023) Vol. 404, Iss. 5, pp. 455-465
Closed Access | Times Cited: 6

Filling in the gaps: SNX-RGS proteins as multiorganelle tethers
Hanaa Hariri, W. Mike Henne
The Journal of Cell Biology (2022) Vol. 221, Iss. 5
Open Access | Times Cited: 9

Targeting the lysosome: Mechanisms and treatments for nonalcoholic fatty liver disease
Jing Pu
Journal of Cellular Biochemistry (2022) Vol. 123, Iss. 10, pp. 1624-1633
Open Access | Times Cited: 8

Cholesterol Metabolism in Neurodegenerative Diseases
Keqiang He, Zhiwei Zhao, Juan Zhang, et al.
Antioxidants and Redox Signaling (2024)
Closed Access | Times Cited: 1

CRISPR screening in cardiovascular research
Hai-Huan Shan, Fei Teng
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 3

The GARP complex prevents sterol accumulation at the trans-Golgi network during dendrite remodeling
Caitlin E. O’Brien, Susan Younger, Lily Yeh Jan, et al.
The Journal of Cell Biology (2022) Vol. 222, Iss. 1
Open Access | Times Cited: 4

Transmembrane Membrane Readers form a Novel Class of Proteins That Include Peripheral Phosphoinositide Recognition Domains and Viral Spikes
Michael Overduin, Anh Tran, Dominic Eekels, et al.
Membranes (2022) Vol. 12, Iss. 11, pp. 1161-1161
Open Access | Times Cited: 4

Organelle-selective click labeling coupled with flow cytometry allows high-throughput CRISPR screening of genes involved in phosphatidylcholine metabolism
Masaki Tsuchiya, Nobuhiko Tachibana, Kohjiro Nagao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Closed Access | Times Cited: 3

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