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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:

Epigenetic Inactivation of the Tumor Suppressor IRX1 Occurs Frequently in Lung Adenocarcinoma and Its Silencing Is Associated with Impaired Prognosis
Miriam M. Küster, Marc A. Schneider, Antje Richter, et al.
Cancers (2020) Vol. 12, Iss. 12, pp. 3528-3528
Open Access | Times Cited: 20

Showing 20 citing articles:

Correlation between chromatin epigenetic-related lncRNA signature (CELncSig) and prognosis, immune microenvironment, and immunotherapy in non-small cell lung cancer
Zhuolong Xiong, Zenglei Han, Weiyi Pan, et al.
PLoS ONE (2023) Vol. 18, Iss. 5, pp. e0286122-e0286122
Open Access | Times Cited: 12
ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenon
Sylvia Hartmann, Summaira Yasmeen, Benjamin Meir Jacobs, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 11
Epigenetically silenced apoptosis-associated tyrosine kinase (AATK) facilitates a decreased expression of Cyclin D1 and WEE1, phosphorylates TP53 and reduces cell proliferation in a kinase-dependent manner
Michelle L. Woods, Astrid Weiß, Anna M. Sokòl, et al.
Cancer Gene Therapy (2022) Vol. 29, Iss. 12, pp. 1975-1987
Open Access | Times Cited: 14
The Role of IRX Homeobox Genes in Hematopoietic Progenitors and Leukemia
Stefan Nagel
Genes (2023) Vol. 14, Iss. 2, pp. 297-297
Open Access | Times Cited: 8
The Hematopoietic TALE-Code Shows Normal Activity of IRX1 in Myeloid Progenitors and Reveals Ectopic Expression of IRX3 and IRX5 in Acute Myeloid Leukemia
Stefan Nagel, Claudia Pommerenke, Corinna Meyer, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 6, pp. 3192-3192
Open Access | Times Cited: 13
Genome-wide DNA methylation in relation to ARID1A deficiency in ovarian clear cell carcinoma
Shang Li, Gert Jan Meersma, Jolanta Kupryjańczyk, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Down-regulation of lncRNA MEG3 promotes chronic low dose cadmium exposure-induced cell transformation and cancer stem cell-like property
Hsuan-Pei Lin, Matthew Rea, Zhishan Wang, et al.
Toxicology and Applied Pharmacology (2021) Vol. 430, pp. 115724-115724
Open Access | Times Cited: 17
Exploring Differentially Methylated Genes in Vulvar Squamous Cell Carcinoma
Shatavisha Dasgupta, Patricia C. Ewing‐Graham, Sigrid Swagemakers, et al.
Cancers (2021) Vol. 13, Iss. 14, pp. 3580-3580
Open Access | Times Cited: 6
An integrative analysis of DNA methylation and gene expression to predict lung adenocarcinoma prognosis
Liexi Xu, Zhengrong Huang, Zihang Zeng, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 3
Identification and validation of a prognostic anoikis-related gene signature in papillary thyroid carcinoma by integrated analysis of single-cell and bulk RNA-sequencing
Ke Zheng, X. Zhang, Xin Yu, et al.
Medicine (2024) Vol. 103, Iss. 19, pp. e38144-e38144
Open Access
SIAH3 is frequently epigenetically silenced in cancer and regulates mitochondrial metabolism
Verena Deutschmeyer, Nico A. Schlaudraff, Sara K. Walesch, et al.
International Journal of Cancer (2024)
Open Access
Biomarker RIPK3 Is Silenced by Hypermethylation in Melanoma and Epigenetic Editing Reestablishes Its Tumor Suppressor Function
Sarah Arroyo Villora, Paula Silva, Tamara Zenz, et al.
Genes (2024) Vol. 15, Iss. 2, pp. 175-175
Open Access
Genetic and functional analysis of Raynaud’s syndrome implicates loci in vasculature and immunity
Anniina Tervi, Markus Ramste, Erik Abner, et al.
Cell Genomics (2024) Vol. 4, Iss. 9, pp. 100630-100630
Open Access
The α2A-adrenergic receptor (ADRA2A) modulates susceptibility to Raynaud’s syndrome
Anniina Tervi, Markus Ramste, Erik Abner, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
In‐silico selection of cancer blood plasma proteins by integrating genomic and proteomic databases
Gaurab Chatterjee, Bryn Ferris, Nikan Momenbeitollahi, et al.
PROTEOMICS (2021) Vol. 22, Iss. 4
Closed Access | Times Cited: 2
Innate differences in the molecular signature of normal inferior & superior human parathyroid glands: potential implications for parathyroid adenoma
Shipra Agarwal, Parmita Kar, Monikongkona Boruah, et al.
Molecular and Cellular Biochemistry (2023) Vol. 478, Iss. 10, pp. 2351-2359
Closed Access
Role of Iroquois homeobox 4 (IRX4) isoforms in prostate cancer
Achala Vitharanage
(2023)
Open Access
Genome-wide DNA methylation in relation to ARID1A deficiency in ovarian clear cell carcinoma
Shang Li, Gert Jan Meersma, Jolanta Kupryjańczyk, et al.
Research Square (Research Square) (2023)
Open Access
The α <sub>2A</sub>-Adrenergic Receptor ( <i>ADRA2A</i>) Modulates Susceptibility to Raynaud's Syndrome
Anniina Tervi, Markus Ramste, Erik Abner, et al.
(2023)
Closed Access
Iroquois homeobox gene 2 as a novel prognostic marker that dysregulated in lung adenocarcinoma
Zhen Huang, Ping Xiao, Bin Qu, et al.
Research Square (Research Square) (2022)
Open Access
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