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:

Full length RTN3 regulates turnover of tubular endoplasmic reticulum via selective autophagy
Paolo Grumati, Giulio Morozzi, Soraya Hölper, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 373

Showing 26-50 of 373 citing articles:

A Genome-wide ER-phagy Screen Highlights Key Roles of Mitochondrial Metabolism and ER-Resident UFMylation
Jin Rui Liang, Emily Lingeman, Thao Luong, et al.
Cell (2020) Vol. 180, Iss. 6, pp. 1160-1177.e20
Open Access | Times Cited: 237

ER-Phagy: Quality Control and Turnover of Endoplasmic Reticulum
Haruka Chino, Noboru Mizushima
Trends in Cell Biology (2020) Vol. 30, Iss. 5, pp. 384-398
Open Access | Times Cited: 227

A selective ER ‐phagy exerts procollagen quality control via a Calnexin‐ FAM 134B complex
Alison Forrester, Chiara De Leonibus, Paolo Grumati, et al.
The EMBO Journal (2018) Vol. 38, Iss. 2
Open Access | Times Cited: 215

A cross-kingdom conserved ER-phagy receptor maintains endoplasmic reticulum homeostasis during stress
Madlen Stephani, Lorenzo Picchianti, Alexander Gajic, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 197

Curvature induction and membrane remodeling by FAM134B reticulon homology domain assist selective ER-phagy
Ramachandra M. Bhaskara, Paolo Grumati, Javier García‐Pardo, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 181

ER-phagy at a glance
Paolo Grumati, Ivan Ðikić, Alexandra Stolz
Journal of Cell Science (2018) Vol. 131, Iss. 17
Open Access | Times Cited: 177

ER ‐to‐lysosome‐associated degradation of proteasome‐resistant ATZ polymers occurs via receptor‐mediated vesicular transport
Ilaria Fregno, Elisa Fasana, Timothy J. Bergmann, et al.
The EMBO Journal (2018) Vol. 37, Iss. 17
Open Access | Times Cited: 172

Regulation of autophagy by canonical and non-canonical ER stress responses
Monika Bhardwaj, Nektaria Maria Leli, Constantinos Koumenis, et al.
Seminars in Cancer Biology (2019) Vol. 66, pp. 116-128
Open Access | Times Cited: 170

New insights regarding SNARE proteins in autophagosome-lysosome fusion
Xiaoyu Tian, Junlin Teng, Jianguo Chen
Autophagy (2020) Vol. 17, Iss. 10, pp. 2680-2688
Open Access | Times Cited: 158

A guide to the regulation of selective autophagy receptors
Andrea Gubaš, Ivan Ðikić
FEBS Journal (2021) Vol. 289, Iss. 1, pp. 75-89
Open Access | Times Cited: 158

Autophagy and organelle homeostasis in cancer
Dannah Miller, Andrew Thorburn
Developmental Cell (2021) Vol. 56, Iss. 7, pp. 906-918
Open Access | Times Cited: 155

The kinase PERK and the transcription factor ATF4 play distinct and essential roles in autophagy resulting from tunicamycin-induced ER stress
Morten Luhr, Maria Lyngaas Torgersen, Paula Szalai, et al.
Journal of Biological Chemistry (2019) Vol. 294, Iss. 20, pp. 8197-8217
Open Access | Times Cited: 152

Role and regulation of autophagy in cancer
Ravichandran Rakesh, Loganathan Chandramani PriyaDharshini, Kunnathur Murugesan Sakthivel, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2022) Vol. 1868, Iss. 7, pp. 166400-166400
Open Access | Times Cited: 121

ER-phagy: mechanisms, regulation, and diseases connected to the lysosomal clearance of the endoplasmic reticulum
Fulvio Reggiori, Maurizio Molinari
Physiological Reviews (2022) Vol. 102, Iss. 3, pp. 1393-1448
Open Access | Times Cited: 113

ER-Phagy, ER Homeostasis, and ER Quality Control: Implications for Disease
Susan Ferro‐Novick, Fulvio Reggiori, Jeffrey L. Brodsky
Trends in Biochemical Sciences (2021) Vol. 46, Iss. 8, pp. 630-639
Open Access | Times Cited: 112

The role of autophagy in viral infections
Tong Chen, Shaoyu Tu, Ling Ding, et al.
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 104

Ubiquitination regulates ER-phagy and remodelling of endoplasmic reticulum
Alexis González, Adriana Covarrubias‐Pinto, Ramachandra M. Bhaskara, et al.
Nature (2023) Vol. 618, Iss. 7964, pp. 394-401
Open Access | Times Cited: 101

ER remodeling via ER-phagy
Andrea Gubaš, Ivan Ðikić
Molecular Cell (2022) Vol. 82, Iss. 8, pp. 1492-1500
Open Access | Times Cited: 84

ER ‐phagy: selective autophagy of the endoplasmic reticulum
Keisuke Mochida, Hitoshi Nakatogawa
EMBO Reports (2022) Vol. 23, Iss. 8
Open Access | Times Cited: 83

Autophagy-Dependent Ferroptosis in Cancer
Fangquan Chen, Xiutao Cai, Rui Kang, et al.
Antioxidants and Redox Signaling (2023) Vol. 39, Iss. 1-3, pp. 79-101
Closed Access | Times Cited: 61

Selective autophagy in cancer: mechanisms, therapeutic implications, and future perspectives
Jiaxi Liu, Yongya Wu, Meng Sha, et al.
Molecular Cancer (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 44

Combinatorial selective ER-phagy remodels the ER during neurogenesis
Melissa Hoyer, Cristina Capitanio, Ian R. Smith, et al.
Nature Cell Biology (2024) Vol. 26, Iss. 3, pp. 378-392
Open Access | Times Cited: 18

Two FAM134B isoforms differentially regulate ER dynamics during myogenesis
Viviana Buonomo, Kateryna Lohachova, Alessio Reggio, et al.
The EMBO Journal (2025) Vol. 44, Iss. 4, pp. 1039-1073
Closed Access | Times Cited: 3

Hypoxia and Selective Autophagy in Cancer Development and Therapy
Ioanna Daskalaki, Ilias Gkikas, Nektarios Tavernarakis
Frontiers in Cell and Developmental Biology (2018) Vol. 6
Open Access | Times Cited: 150

ER homeostasis and autophagy
Matthew D. Smith, Simon Wilkinson
Essays in Biochemistry (2017) Vol. 61, Iss. 6, pp. 625-635
Open Access | Times Cited: 150

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