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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:

Targeted in silico characterization of fusion transcripts in tumor and normal tissues via FusionInspector
Brian J. Haas, Alexander Dobin, Mahmoud Ghandi, et al.
Cell Reports Methods (2023) Vol. 3, Iss. 5, pp. 100467-100467
Open Access | Times Cited: 18

Showing 18 citing articles:

Comprehensive genomic characterization of early-stage bladder cancer
Frederik Prip, Philippe Lamy, Sia V. Lindskrog, et al.
Nature Genetics (2025)
Open Access | Times Cited: 2
Comparative analysis of RNA expression in a single institution cohort of pediatric cancer patients
Yvonne Vasquez, Holly C. Beale, Lauren Sanders, et al.
npj Precision Oncology (2025) Vol. 9, Iss. 1
Open Access | Times Cited: 1
Frequent lncRNA-derived fusions in pediatric neuroblastoma identified by LncFusion: potential biomarker and therapeutic implications
Zixiu Li, Joae Wu, Peng Zhou, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Effective Utilization of a Customized Targeted Hybrid Capture RNA Sequencing in the Routine Molecular Categorization of Adolescent and Adult B-Lineage Acute Lymphoblastic Leukemia: A Real-World Experience
Sreejesh Sreedharanunni, Venus Thakur, Anand Balakrishnan, et al.
Molecular Diagnosis & Therapy (2025)
Closed Access
Benchmarking mouse contamination removing protocols in patient-derived xenografts genomic profiling
Mukund Bhandari, Funan He, Anna Rogojina, et al.
npj Precision Oncology (2025) Vol. 9, Iss. 1
Open Access
Wnt/β-catenin activation by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary basal cell adenoma
Kim Wong, Justin A. Bishop, Ilan Weinreb, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Multi-omics profiling of papillary thyroid microcarcinoma reveals different somatic mutations and a unique transcriptomic signature
Qiang Li, Tienan Feng, Tengteng Zhu, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 9
CTAT-LR-fusion: accurate fusion transcript identification from long and short read isoform sequencing at bulk or single cell resolution
Qian Qin, Victoria Popic, Houlin Yu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Leveraging patient derived models of FGFR2 fusion positive intrahepatic cholangiocarcinoma to identify synergistic therapies
Michael E. Lidsky, Zechen Wang, Min Lu, et al.
npj Precision Oncology (2022) Vol. 6, Iss. 1
Open Access | Times Cited: 12
Anchored-fusion enables targeted fusion search in bulk and single-cell RNA sequencing data
Xilu Yuan, Haishuai Wang, Zhongquan Sun, et al.
Cell Reports Methods (2024) Vol. 4, Iss. 3, pp. 100733-100733
Open Access | Times Cited: 2
Misexpression of inactive genes in whole blood is associated with nearby rare structural variants
Thomas Vanderstichele, Katie L. Burnham, Niek de Klein, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1524-1543
Open Access | Times Cited: 2
Longitudinal characterization of primary osteosarcoma and derived subcutaneous and orthotopic relapsed patient-derived xenograft models
Maria Eugénia Marques Da Costa, Robin Droit, Pierre Khneisser, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 5
Characterization and evaluation of gene fusions as a measure of genetic instability and disease prognosis in prostate cancer
Carolin Schimmelpfennig, Michael Rade, Susanne Füssel, et al.
BMC Cancer (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 3
Misexpression of inactive genes in whole blood is associated with nearby rare structural variants
Thomas Vanderstichele, Katie L. Burnham, Niek de Klein, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Solitary fibrous tumor with IGF-II-induced non-islet cell tumor hypoglycemia: a case report and molecular characterization by next-generation sequencing
Helvijs Niedra, Ilze Konrāde, Raitis Pečulis, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 2
CDC42BPA::BRAF Represents a Novel Fusion in Desmoplastic Infantile Ganglioglioma/Desmoplastic Infantile Astrocytoma
Maria Isabel Barros Guinle, Jeffrey Nirschl, Yao Lulu Xing, et al.
Neuro-Oncology Advances (2024) Vol. 6, Iss. 1
Open Access
Activation of Wnt/β-catenin signalling by mutually exclusiveFBXW11andCTNNB1hotspot mutations drives salivary gland basal cell adenoma
Kim Wong, Justin A. Bishop, Ilan Weinreb, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Comparison of computational fusion detection methods for short-read RNA-seq data
Lucas Peres Oliveira, Victor Rigatto, Natacha Azussa Migita, et al.
(2024), pp. 24-35
Closed Access
Whole transcriptome sequencing reveals HOXD11-AGAP3, a novel fusion transcript in the Indian acute leukemia cohort
Sagar Desai, Febina Ravindran, Amey Panchal, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access
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