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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:

KCTD15 deregulation is associated with alterations of the NF-κB signaling in both pathological and physiological model systems
Giovanni Smaldone, Luigi Coppola, Katia Pane, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 8

Showing 8 citing articles:

Molecular Mechanisms of Ferroptosis and Its Roles in Hematologic Malignancies
Yan Zhao, Zineng Huang, Hongling Peng
Frontiers in Oncology (2021) Vol. 11
Open Access | Times Cited: 46
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome
Kerry A. Miller, David A. Cruz Walma, Daniel M. Pinkas, et al.
Journal of Medical Genetics (2024), pp. jmg-109531
Open Access | Times Cited: 8
Alphafold Predictions Provide Insights into the Structural Features of the Functional Oligomers of All Members of the KCTD Family
Luciana Esposito, Nicole Balasco, Luigi Vitagliano
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13346-13346
Open Access | Times Cited: 11
A Comprehensive Analysis of the Expression Profiles of KCTD Proteins in Acute Lymphoblastic Leukemia: Evidence of Selective Expression of KCTD1 in T-ALL
Lorena Buono, Concetta Iside, Giovanni Pecoraro, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 11, pp. 3669-3669
Open Access | Times Cited: 5
KCTD15 Is Overexpressed in her2+ Positive Breast Cancer Patients and Its Silencing Attenuates Proliferation in SKBR3 CELL LINE
Luigi Coppola, Simona Baselice, Francesco Messina, et al.
Diagnostics (2022) Vol. 12, Iss. 3, pp. 591-591
Open Access | Times Cited: 9
Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction
Nicole Balasco, Alessia Ruggiero, Giovanni Smaldone, et al.
International Journal of Biological Macromolecules (2024) Vol. 277, pp. 134390-134390
Open Access | Times Cited: 1
An overview of Synlab SDN Biobank’s quality control system
Luigi Coppola, Anna Grimaldi, Ginevra Sarnacchiaro, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction
Nicole Balasco, Alessia Ruggiero, Giovanni Smaldone, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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