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.

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Showing 1-25 of 35 citing articles:

The status of the human gene catalogue
Paulo Amaral, Sílvia Carbonell Sala, Francisco M. De La Vega, et al.
Nature (2023) Vol. 622, Iss. 7981, pp. 41-47
Open Access | Times Cited: 97

Unscrambling cancer genomes via integrated analysis of structural variation and copy number
Charles Shale, Daniel Cameron, Jonathan Baber, et al.
Cell Genomics (2022) Vol. 2, Iss. 4, pp. 100112-100112
Open Access | Times Cited: 66

Long-read sequencing uncovers a complex transcriptome topology in varicella zoster virus
István Prazsák, Norbert Moldován, Zsolt Balázs, et al.
BMC Genomics (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 64

Thioredoxin Domain Containing 5 (TXNDC5): Friend or Foe?
Seyed Hesamoddin Bidooki, María Á. Navarro, Susana C. M. Fernandes, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 4, pp. 3134-3163
Open Access | Times Cited: 5

Expression of the readthrough transcript CiDRE in alveolar macrophages boosts SARS-CoV-2 susceptibility and promotes COVID-19 severity
Yuichi Mitsui, Tatsuya Suzuki, Kanako Kuniyoshi, et al.
Immunity (2023) Vol. 56, Iss. 8, pp. 1939-1954.e12
Open Access | Times Cited: 13

Dysregulation of murine long noncoding single-cell transcriptome in nonalcoholic steatohepatitis and liver fibrosis
Kritika Karri, David J. Waxman
RNA (2023) Vol. 29, Iss. 7, pp. 977-1006
Open Access | Times Cited: 11

A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease
Gavin R. Oliver, Xiaojia Tang, Laura Schultz‐Rogers, et al.
PLoS ONE (2019) Vol. 14, Iss. 10, pp. e0223337-e0223337
Open Access | Times Cited: 27

Discovery of clinically relevant fusions in pediatric cancer
Stephanie LaHaye, James Fitch, Kyle Voytovich, et al.
BMC Genomics (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 22

Poly(A)‐Selected Intergenic Transcripts in In Vivo Developed Bovine Oocytes and Pre‐Implantation Embryos
Saurav Ranjitkar, Mohammad Shiri, Jiangwen Sun, et al.
Molecular Reproduction and Development (2025) Vol. 92, Iss. 2
Closed Access

Alternative Transcription at Venom Genes and Its Role as a Complementary Mechanism for the Generation of Venom Complexity in the Common House Spider
Robert A. Haney, Taylor Matte, FitzAnthony S. Forsyth, et al.
Frontiers in Ecology and Evolution (2019) Vol. 7
Open Access | Times Cited: 24

The Protein‐Coding Human Genome: Annotating High‐Hanging Fruits
Klas Hatje, Stefanie Mühlhausen, Dominic Simm, et al.
BioEssays (2019) Vol. 41, Iss. 11
Open Access | Times Cited: 24

Interstitial Deletions Generating Fusion Genes
Ioannis Panagopoulos, Sverre Heim
Cancer Genomics & Proteomics (2021) Vol. 18, Iss. 3, pp. 167-196
Open Access | Times Cited: 15

annoFuse: an R Package to annotate, prioritize, and interactively explore putative oncogenic RNA fusions
Krutika S. Gaonkar, Fédérico Marini, Komal S. Rathi, et al.
BMC Bioinformatics (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 10

Unscrambling cancer genomes via integrated analysis of structural variation and copy number
Charles Shale, Jonathan Baber, Daniel Cameron, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 9

MROH7‐TTC4 read‐through lncRNA suppresses vascular endothelial cell apoptosis and is upregulated by inhibition of ANXA7 GTPase activity
Xiaoying He, Xuan Zhao, Le Su, et al.
FEBS Journal (2019) Vol. 286, Iss. 24, pp. 4937-4950
Open Access | Times Cited: 8

Computational Detection of Known Pathogenic Gene Fusions in a Normal Tissue Database and Implications for Genetic Disease Research
Gavin R. Oliver, Garrett Jenkinson, Eric W. Klee
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 8

SNHG16 lncRNAs are overexpressed and may be oncogenic in human gastric cancer by regulating cell cycle progression
Juanjuan Zhao, Juanjuan Liu, Yunyuan Zhang, et al.
Neoplasma (2021) Vol. 69, Iss. 01, pp. 49-58
Open Access | Times Cited: 7

Intergenic transcription in in vivo developed bovine oocytes and pre-implantation embryos
Saurav Ranjitkar, Mohammad Shiri, Jiangwen Sun, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 2

Long-read Sequencing Uncovers a Complex Transcriptome Topology in Varicella Zoster Virus
István Prazsák, Norbert Moldován, Dóra Tombácz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 5

Rearrangements of ATP5L‐KMT2A in acute lymphoblastic leukaemia
Anna Ferrari, Andrea Ghelli Luserna di Rorà, Chiara Domizio, et al.
British Journal of Haematology (2020) Vol. 192, Iss. 6
Open Access | Times Cited: 4

Efficient system for upstream mRNA trans-splicing to generate covalent, head-to-tail, protein multimers
Hiroaki Mitsuhashi, Sachiko Homma, Mary Lou Beermann, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 3

RSPO2 abnormal transcripts result from read-through in liver tumours with high ß-catenin activation and CTNNB1 mutations
Quentin Bayard, Jean–Charles Nault, Jessica Zucman‐Rossi
Gut (2019) Vol. 69, Iss. 6, pp. 1152-1153
Open Access | Times Cited: 3

Versatile RNA: overlooked gems of the transcriptome
Murat Erdem, Mustafa Çiçek, Ayse Elif Erson‐Bensan
FEBS Journal (2023) Vol. 290, Iss. 20, pp. 4843-4851
Open Access | Times Cited: 1

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