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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:

Applications of long-read sequencing to Mendelian genetics
Francesco Mastrorosa, Danny E. Miller, Evan E. Eichler
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 56

Showing 1-25 of 56 citing articles:

Unveiling microbial diversity: harnessing long-read sequencing technology
Daniel Paiva Agustinho, Yilei Fu, Vipin K. Menon, et al.
Nature Methods (2024) Vol. 21, Iss. 6, pp. 954-966
Closed Access | Times Cited: 29
A 25-year odyssey of genomic technology advances and structural variant discovery
David Porubský, Evan E. Eichler
Cell (2024) Vol. 187, Iss. 5, pp. 1024-1037
Closed Access | Times Cited: 26
Long read sequencing on its way to the routine diagnostics of genetic diseases
Giulia Olivucci, Emanuela Iovino, Giovanni Innella, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 19
Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection
Shloka Negi, Sarah L. Stenton, Seth Berger, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 2
Advances of high-throughput sequencing for unraveling biotechnological potential of microalgal-bacterial communities
Petr Zaytsev, Владимир Александрович Родин, Anna A. Zaytseva, et al.
Journal of Applied Phycology (2024) Vol. 36, Iss. 4, pp. 1901-1919
Closed Access | Times Cited: 9
Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes
Cate Paschal, Miranda Galey, Anita Beck, et al.
Journal of Molecular Diagnostics (2025)
Open Access | Times Cited: 1
Evolution of genome-wide methylation profiling technologies
Carolina Montaño, Winston Timp
Genome Research (2025) Vol. 35, Iss. 4, pp. 572-582
Closed Access | Times Cited: 1
The impact of long-read sequencing on human population-scale genomics
Tobias Rausch, Tobias Marschall, Jan O. Korbel
Genome Research (2025) Vol. 35, Iss. 4, pp. 593-598
Closed Access | Times Cited: 1
Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing
A Janssen, Rebekka M. Koeck, Rick Essers, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 7
Enhancing Clinical Utility: Utilization of International Standards and Guidelines for Metagenomic Sequencing in Infectious Disease Diagnosis
Chau-Ming Kan, Hin Fung Tsang, Xiao M. Pei, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 6, pp. 3333-3333
Open Access | Times Cited: 6
Closing the gap: Solving complex medically relevant genes at scale
Medhat Mahmoud, John Harting, Holly Corbitt, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Long-read sequencing improves the genetic diagnosis of retinitis pigmentosa by identifying an Alu retrotransposon insertion in the EYS gene
Elena Fernández-Suárez, María González‐del Pozo, Cristina Méndez‐Vidal, et al.
Mobile DNA (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Addressing diagnostic gaps and priorities of the global rare diseases community: Recommendations from the IRDiRC diagnostics scientific committee
David R. Adams, Clara D. van Karnebeek, Sergi Beltrán, et al.
European Journal of Medical Genetics (2024) Vol. 70, pp. 104951-104951
Open Access | Times Cited: 5
High-throughput assays to assess variant effects on disease
Kaiyue Ma, L. Gauthier, Frances Cheung, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 4
Decoding Complexity: The Role of Long-Read Sequencing in Unraveling Genetic Disease Etiologies
Ran Xu, Mengmeng Zhang, Xiaoming Yang, et al.
Mutation Research/Reviews in Mutation Research (2025) Vol. 795, pp. 108529-108529
Closed Access
High clinical utility of long-read sequencing for precise diagnosis of congenital adrenal hyperplasia in 322 probands
Yunpeng Wang, Gaohui Zhu, Dan‐Hua Li, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
Diagnostic utility of single-locus DNA methylation mark in Sotos syndrome developed by nanopore sequencing-based episignature
Takeshi Mizuguchi, Nobuhiko Okamoto, Taiki Hara, et al.
Clinical Epigenetics (2025) Vol. 17, Iss. 1
Open Access
A rapid and efficient zirconia bead-mediated ultrasonic strategy for DNA fragmentation up to 10 kbp
Pan Fu, Taowa Zhao, Pengyao Wei, et al.
RSC Advances (2025) Vol. 15, Iss. 8, pp. 6068-6075
Open Access
Identification ofde novovariants from parent-proband duos via long-read sequencing
Leandros Boukas, Emmanuèle C. Délot, Georgia Pitsava, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Charcot-marie-tooth disease: a review of clinical developments and its management - What’s new in 2025?
Amedeo De Grado, Paola Saveri, Paola Saveri, et al.
Expert Review of Neurotherapeutics (2025)
Closed Access
Sequencing the unseen: long-read metagenomics and the microbial frontier
Fatemeh Yaghoobizadeh
Elsevier eBooks (2025), pp. 65-97
Closed Access
Clinical Genetics and Genomics for the Immunologist
Maxwell Bannister, Xiao Peng
Immunology and Allergy Clinics of North America (2025)
Closed Access
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Long‐Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia
Thomas Wirth, Kishore R. Kumar, Michael Zech
Movement Disorders (2025)
Open Access
The advancements in precision medicine for Leber congenital amaurosis: Breakthroughs from genetic diagnosis to therapy
Pei Zhang, Zhuping Xu
Survey of Ophthalmology (2025)
Closed Access
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