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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:

Pancreatic cancers require autophagy for tumor growth
Shenghong Yang, Xiaoxu Wang, Gianmarco Contino, et al.
Genes & Development (2011) Vol. 25, Iss. 7, pp. 717-729
Open Access | Times Cited: 1385

Showing 1-25 of 1385 citing articles:

Autophagy: Renovation of Cells and Tissues
Noboru Mizushima, Masaaki Komatsu
Cell (2011) Vol. 147, Iss. 4, pp. 728-741
Open Access | Times Cited: 5658
Autophagy in Human Health and Disease
Augustine M.K. Choi, Stefan W. Ryter, Beth Levine
New England Journal of Medicine (2013) Vol. 368, Iss. 7, pp. 651-662
Closed Access | Times Cited: 2441
Mechanism and medical implications of mammalian autophagy
Ivan Ðikić, Zvulun Elazar
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 6, pp. 349-364
Closed Access | Times Cited: 2378
Targeting autophagy in cancer
Jean M. Mulcahy Levy, Christina G. Towers, Andrew Thorburn
Nature reviews. Cancer (2017) Vol. 17, Iss. 9, pp. 528-542
Open Access | Times Cited: 2159
Pancreatic Adenocarcinoma
David P. Ryan, Theodore S. Hong, Nabeel Bardeesy
New England Journal of Medicine (2014) Vol. 371, Iss. 11, pp. 1039-1049
Closed Access | Times Cited: 2158
Dynamics and functions of lipid droplets
James A. Olzmann, Pedro Carvalho
Nature Reviews Molecular Cell Biology (2018) Vol. 20, Iss. 3, pp. 137-155
Open Access | Times Cited: 2032
Drugging the undruggable RAS: Mission Possible?
Adrienne D. Cox, Stephen W. Fesik, Alec C. Kimmelman, et al.
Nature Reviews Drug Discovery (2014) Vol. 13, Iss. 11, pp. 828-851
Open Access | Times Cited: 1776
Glutamine supports pancreatic cancer growth through a KRAS-regulated metabolic pathway
Jaekyoung Son, Costas A. Lyssiotis, Haoqiang Ying, et al.
Nature (2013) Vol. 496, Iss. 7443, pp. 101-105
Open Access | Times Cited: 1757
ROS signalling in the biology of cancer
Jennifer N. Moloney, Thomas G. Cotter
Seminars in Cell and Developmental Biology (2017) Vol. 80, pp. 50-64
Closed Access | Times Cited: 1637
Deconvoluting the context-dependent role for autophagy in cancer
Eileen White
Nature reviews. Cancer (2012) Vol. 12, Iss. 6, pp. 401-410
Open Access | Times Cited: 1614
Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy
Joseph D. Mancias, Xiaoxu Wang, Steven P. Gygi, et al.
Nature (2014) Vol. 509, Iss. 7498, pp. 105-109
Open Access | Times Cited: 1568
Pancreatic cancer
Jörg Kleeff, Murray Korc, Minoti V. Apte, et al.
Nature Reviews Disease Primers (2016) Vol. 2, Iss. 1
Closed Access | Times Cited: 1559
Autophagy modulation as a potential therapeutic target for diverse diseases
David C. Rubinsztein, Patrice Codogno, Beth Levine
Nature Reviews Drug Discovery (2012) Vol. 11, Iss. 9, pp. 709-730
Open Access | Times Cited: 1369
NRF2 and the Hallmarks of Cancer
Montserrat Rojo de la Vega, Eli Chapman, Donna D. Zhang
Cancer Cell (2018) Vol. 34, Iss. 1, pp. 21-43
Open Access | Times Cited: 1332
Metabolic pathways promoting cancer cell survival and growth
Lindsey K. Boroughs, Ralph J. DeBerardinis
Nature Cell Biology (2015) Vol. 17, Iss. 4, pp. 351-359
Open Access | Times Cited: 1296
Autophagy and autophagy-related proteins in cancer
Xiaohua Li, Shikun He, Binyun Ma
Molecular Cancer (2020) Vol. 19, Iss. 1
Open Access | Times Cited: 1276
Autophagy-Dependent Anticancer Immune Responses Induced by Chemotherapeutic Agents in Mice
Mickaël Michaud, Isabelle Martins, Abdul Qader Sukkurwala, et al.
Science (2011) Vol. 334, Iss. 6062, pp. 1573-1577
Closed Access | Times Cited: 1253
Activated Ras requires autophagy to maintain oxidative metabolism and tumorigenesis
Jessie Yanxiang Guo, Hsin-Yi Chen, Robin Mathew, et al.
Genes & Development (2011) Vol. 25, Iss. 5, pp. 460-470
Open Access | Times Cited: 1237
The role for autophagy in cancer
Eileen White
Journal of Clinical Investigation (2015) Vol. 125, Iss. 1, pp. 42-46
Open Access | Times Cited: 1167
The Role of Autophagy in Cancer: Therapeutic Implications
Zhineng J. Yang, Cheng Ean Chee, Shengbing Huang, et al.
Molecular Cancer Therapeutics (2011) Vol. 10, Iss. 9, pp. 1533-1541
Open Access | Times Cited: 1133
Oncogene ablation-resistant pancreatic cancer cells depend on mitochondrial function
Andrea Viale, Piergiorgio Pettazzoni, Costas A. Lyssiotis, et al.
Nature (2014) Vol. 514, Iss. 7524, pp. 628-632
Open Access | Times Cited: 1110
Autophagy in malignant transformation and cancer progression
Lorenzo Galluzzi, Federico Pietrocola, José Manuel Bravo‐San Pedro, et al.
The EMBO Journal (2015) Vol. 34, Iss. 7, pp. 856-880
Open Access | Times Cited: 1090
PAMPs and DAMPs: signal 0s that spur autophagy and immunity
Daolin Tang, Rui Kang, Carolyn B. Coyne, et al.
Immunological Reviews (2012) Vol. 249, Iss. 1, pp. 158-175
Open Access | Times Cited: 1061
Mitochondria and Cancer
Wei‐Xing Zong, Joshua D. Rabinowitz, Eileen White
Molecular Cell (2016) Vol. 61, Iss. 5, pp. 667-676
Open Access | Times Cited: 1051
p53 in survival, death and metabolic health: a lifeguard with a licence to kill
Flore Kruiswijk, Christiaan F. Labuschagne, Karen H. Vousden
Nature Reviews Molecular Cell Biology (2015) Vol. 16, Iss. 7, pp. 393-405
Closed Access | Times Cited: 994
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