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:

PELI1 Selectively Targets Kinase-Active RIP3 for Ubiquitylation-Dependent Proteasomal Degradation
Seung-Won Choi, Han‐Hee Park, Soyeon Kim, et al.
Molecular Cell (2018) Vol. 70, Iss. 5, pp. 920-935.e7
Open Access | Times Cited: 94

Showing 1-25 of 94 citing articles:

Ubiquitination in the regulation of inflammatory cell death and cancer
Peter E. Cockram, Matthias Kist, Sumit Prakash, et al.
Cell Death and Differentiation (2021) Vol. 28, Iss. 2, pp. 591-605
Open Access | Times Cited: 310

Necroptosis molecular mechanisms: Recent findings regarding novel necroptosis regulators
Jinho Seo, Young Woo Nam, Seongmi Kim, et al.
Experimental & Molecular Medicine (2021) Vol. 53, Iss. 6, pp. 1007-1017
Open Access | Times Cited: 184

The therapeutic potential of targeting regulated non-apoptotic cell death
Kamyar Hadian, Brent R. Stockwell
Nature Reviews Drug Discovery (2023) Vol. 22, Iss. 9, pp. 723-742
Closed Access | Times Cited: 169

The role of Ubiquitination in Apoptosis and Necroptosis
Jamie Z. Roberts, Nyree Crawford, Daniel B. Longley
Cell Death and Differentiation (2021) Vol. 29, Iss. 2, pp. 272-284
Open Access | Times Cited: 139

Roles of RIPK3 in necroptosis, cell signaling, and disease
Michael J. Morgan, You‐Sun Kim
Experimental & Molecular Medicine (2022) Vol. 54, Iss. 10, pp. 1695-1704
Open Access | Times Cited: 98

Mediators of necroptosis: from cell death to metabolic regulation
Xiaoqin Wu, Laura E. Nagy, Jérémie Gautheron
EMBO Molecular Medicine (2024) Vol. 16, Iss. 2, pp. 219-237
Open Access | Times Cited: 20

The Structural Basis of Necroptotic Cell Death Signaling
Emma J. Petrie, Peter E. Czabotar, James M. Murphy
Trends in Biochemical Sciences (2018) Vol. 44, Iss. 1, pp. 53-63
Closed Access | Times Cited: 138

The role of necroptosis in cancer: A double-edged sword?
Xia Qin, Dan Ma, Yexiong Tan, et al.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (2019) Vol. 1871, Iss. 2, pp. 259-266
Closed Access | Times Cited: 110

Autophagy regulates inflammatory programmed cell death via turnover of RHIM-domain proteins
Junghyun Lim, Hyunjoo Park, Jason Heisler, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 104

Mechanisms of Severe Cutaneous Adverse Reactions: Recent Advances
Teresa Bellón
Drug Safety (2019) Vol. 42, Iss. 8, pp. 973-992
Closed Access | Times Cited: 95

Current translational potential and underlying molecular mechanisms of necroptosis
Tamás Molnár, Anett Mázló, Vera Tslaf, et al.
Cell Death and Disease (2019) Vol. 10, Iss. 11
Open Access | Times Cited: 93

The regulation of necroptosis by post-translational modifications
Yanxiang Meng, Jarrod J. Sandow, Peter E. Czabotar, et al.
Cell Death and Differentiation (2021) Vol. 28, Iss. 3, pp. 861-883
Open Access | Times Cited: 88

USP22 controls necroptosis by regulating receptor‐interacting protein kinase 3 ubiquitination
Jens Roedig, Lisa Kowald, Thomas Juretschke, et al.
EMBO Reports (2020) Vol. 22, Iss. 2
Open Access | Times Cited: 70

Ubiquitylation of MLKL at lysine 219 positively regulates necroptosis-induced tissue injury and pathogen clearance
Laura Ramos Garcia, Tencho Tenev, Richard Newman, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 62

Isoform- and cell-state-specific lipidation of ApoE in astrocytes
Karina Lindner, Katharina Beckenbauer, Larissa van Ek, et al.
Cell Reports (2022) Vol. 38, Iss. 9, pp. 110435-110435
Open Access | Times Cited: 50

Encephalitis and poor neuronal death–mediated control of herpes simplex virus in human inherited RIPK3 deficiency
Zhiyong Liu, Eduardo J. Garcia Reino, Oliver Harschnitz, et al.
Science Immunology (2023) Vol. 8, Iss. 82
Open Access | Times Cited: 26

Protein phosphorylation and kinases: Potential therapeutic targets in necroptosis
Yihui Shi, Chengkun Wu, Jiayi Shi, et al.
European Journal of Pharmacology (2024) Vol. 970, pp. 176508-176508
Closed Access | Times Cited: 8

Deubiquitination of RIPK3 by OTUB2 potentiates neuronal necroptosis after ischemic stroke
Fuqi Mei, Dongrui Deng, Zi-Jun Cao, et al.
EMBO Molecular Medicine (2025)
Open Access | Times Cited: 1

TRIM24-RIP3 axis perturbation accelerates osteoarthritis pathogenesis
Jimin Jeon, Hyunjin Noh, Hye‐Mi Lee, et al.
Annals of the Rheumatic Diseases (2020) Vol. 79, Iss. 12, pp. 1635-1643
Open Access | Times Cited: 64

RIPK3 signaling and its role in the pathogenesis of cancers
Shanhui Liu, Kanak Joshi, Mitchell F. Denning, et al.
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 23, pp. 7199-7217
Open Access | Times Cited: 43

E3 ligase TRIM25 ubiquitinates RIP3 to inhibit TNF induced cell necrosis
Pucheng Mei, Feiyan Xie, Jiasong Pan, et al.
Cell Death and Differentiation (2021) Vol. 28, Iss. 10, pp. 2888-2899
Open Access | Times Cited: 41

The resurrection of RIP kinase 1 as an early cell death checkpoint regulator—a potential target for therapy in the necroptosis era
Eunjin Ju, Kyeong Ah Park, Han‐Ming Shen, et al.
Experimental & Molecular Medicine (2022) Vol. 54, Iss. 9, pp. 1401-1411
Open Access | Times Cited: 28

Ubiquitination Links DNA Damage and Repair Signaling to Cancer Metabolism
Seo-Young Koo, Eun‐Ji Park, Hyun-Ji Noh, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8441-8441
Open Access | Times Cited: 20

PRMT1 reverts the immune escape of necroptotic colon cancer through RIP3 methylation
Lian Zhang, Yujiao He, Yi Jiang, et al.
Cell Death and Disease (2023) Vol. 14, Iss. 4
Open Access | Times Cited: 17

Caspase-8 in inflammatory diseases: a potential therapeutic target
Wangzheqi Zhang, Chenglong Zhu, Yan Liao, et al.
Cellular & Molecular Biology Letters (2024) Vol. 29, Iss. 1
Open Access | Times Cited: 7

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