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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:

Application of long-read sequencing to the detection of structural variants in human cancer genomes
Yoshitaka Sakamoto, Suzuko Zaha, Yutaka Suzuki, et al.
Computational and Structural Biotechnology Journal (2021) Vol. 19, pp. 4207-4216
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

A guide for the diagnosis of rare and undiagnosed disease: beyond the exome
Shruti Marwaha, Joshua W. Knowles, Euan A. Ashley
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 228
Porechop_ABI: discovering unknown adapters in Oxford Nanopore Technology sequencing reads for downstream trimming
Quentin Bonenfant, Laurent Noé, Hélène Touzet
Bioinformatics Advances (2022) Vol. 3, Iss. 1
Open Access | Times Cited: 55
Transposable Elements and Human Diseases: Mechanisms and Implication in the Response to Environmental Pollutants
Benoı̂t Chénais
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 5, pp. 2551-2551
Open Access | Times Cited: 42
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Tobias Rausch, René Snajder, Adrien Léger, et al.
Cell Genomics (2023) Vol. 3, Iss. 4, pp. 100281-100281
Open Access | Times Cited: 30
A survey of algorithms for the detection of genomic structural variants from long-read sequencing data
Mian Umair Ahsan, Qian Liu, Jonathan E. Perdomo, et al.
Nature Methods (2023) Vol. 20, Iss. 8, pp. 1143-1158
Open Access | Times Cited: 30
The Current State of Nanopore Sequencing
Jonathan Pugh
Methods in molecular biology (2023), pp. 3-14
Closed Access | Times Cited: 25
Linear time complexity de novo long read genome assembly with GoldRush
Johnathan Wong, Lauren Coombe, Vladimir Nikolić, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 18
Comparison of structural variant callers for massive whole-genome sequence data
Soobok Joe, Jong‐Lyul Park, Jun Kim, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 6
Phasing analysis of lung cancer genomes using a long read sequencer
Yoshitaka Sakamoto, Shuhei Miyake, Miho Oka, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 22
Towards understanding cancer dormancy over strategic hitching up mechanisms to technologies
Sumin Yang, Jieun Seo, Jeong‐Hyeon Choi, et al.
Molecular Cancer (2025) Vol. 24, Iss. 1
Open Access
Genome assembly resources of genitourinary cancers for chromosomal aberration at the single nucleotide level
Hyun Ho Han, Hyung Ho Lee, Min Kim, et al.
Scientific Data (2025) Vol. 12, Iss. 1
Open Access
Deciphering IGH rearrangement complexity and detection strategies in acute lymphoblastic leukaemia
Ashlee Thomson, Jacqueline Rehn, David T Yeung, et al.
npj Precision Oncology (2025) Vol. 9, Iss. 1
Open Access
Unravelling the tumour genome: The evolutionary and clinical impacts of structural variants in tumourigenesis
Alhafidz Hamdan, Ailith Ewing
The Journal of Pathology (2022) Vol. 257, Iss. 4, pp. 479-493
Open Access | Times Cited: 15
Resolving complex structural variants via nanopore sequencing
Simone Romagnoli, Niccolò Bartalucci, Alessandro M. Vannucchi
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 9
Cytogenetics in the management of hematological malignancies: An overview of alternative technologies for cytogenetic characterization
Valentin Lestringant, Hélène Guermouche-Flament, Mélanie Jimenez-Pocquet, et al.
Current Research in Translational Medicine (2024) Vol. 72, Iss. 3, pp. 103440-103440
Open Access | Times Cited: 3
Population-scale genotyping of structural variation in the era of long-read sequencing
Cheng Quan, Hao Lu, Yiming Lu, et al.
Computational and Structural Biotechnology Journal (2022) Vol. 20, pp. 2639-2647
Open Access | Times Cited: 12
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
Mariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, et al.
Life Science Alliance (2024) Vol. 7, Iss. 8, pp. e202302481-e202302481
Open Access | Times Cited: 2
Systematic evaluation of multiple NGS platforms for structural variants detection
Xuan Meng, Miao Wang, Mingjie Luo, et al.
Journal of Biological Chemistry (2023) Vol. 299, Iss. 12, pp. 105436-105436
Open Access | Times Cited: 6
Identification of 121 variants of honey bee Vitellogenin protein sequences with structural differences at functional sites
Vilde Leipart, Jane Ludvigsen, Matthew Kent, et al.
Protein Science (2022) Vol. 31, Iss. 7
Open Access | Times Cited: 7
Porechop_ABI: discovering unknown adapters in ONT sequencing reads for downstream trimming
Quentin Bonenfant, Laurent Noé, Hélène Touzet
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
De Novo Structural Variations of Escherichia coli Detected by Nanopore Long-Read Sequencing
Xia Zhou, Jiao Pan, Yaohai Wang, et al.
Genome Biology and Evolution (2023) Vol. 15, Iss. 6
Open Access | Times Cited: 4
Can long-read sequencing tackle the barriers, which the next-generation could not? A review
Nikolett Szakállas, Barbara Kinga Barták, Gábor Valcz, et al.
Pathology & Oncology Research (2024) Vol. 30
Open Access | Times Cited: 1
Addressing Technical Pitfalls in Pursuit of Molecular Factors That Mediate Immunoglobulin Gene Regulation
Eric Engelbrecht, Oscar L. Rodriguez, Corey T. Watson
The Journal of Immunology (2024) Vol. 213, Iss. 5, pp. 651-662
Open Access | Times Cited: 1
Toward understanding the role of genomic repeat elements in neurodegenerative diseases
Zhengyu An, Aidi Jiang, Jingqi Chen
Neural Regeneration Research (2024) Vol. 20, Iss. 3, pp. 646-659
Open Access | Times Cited: 1
Comprehensive detection of structural variation and transposable element differences between wild type laboratory lineages ofC. elegans
Zachary D. Bush, Alice F. S. Naftaly, Devin Dinwiddie, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
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