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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:

Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes
Wataru Nakamura, Makoto Hirata, Satoyo Oda, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 12

Showing 12 citing articles:

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
Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders
Laura Ivete Rudaks, Igor Stevanovski, Dennis Yeow, et al.
Annals of Clinical and Translational Neurology (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
Innovations in Transgene Integration Analysis: A Comprehensive Review of Enrichment and Sequencing Strategies in Biotechnology
Zaobing Zhu, Shengtao Lu, Hongchun Wang, et al.
ACS Applied Materials & Interfaces (2025) Vol. 17, Iss. 2, pp. 2716-2735
Closed Access
Nanopore adaptive sampling accurately detects nucleotide variants and improves the characterization of large‐scale rearrangement for the diagnosis of cancer predisposition
Sandy Chevrier, Corentin Richard, M.-L. Mille, et al.
Clinical and Translational Medicine (2025) Vol. 15, Iss. 1
Open Access
Establishment of a high-risk pediatric AML-derived cell line YCU-AML2 with genetic and metabolic vulnerabilities
Junji Ikeda, Norio Shiba, Shota Kato, et al.
International Journal of Hematology (2025)
Closed Access
Mosaicism in Short Tandem Repeat Disorders: A Clinical Perspective
Rose M. Doss, Susana Lopez-Ignacio, Anna Dischler, et al.
Genes (2025) Vol. 16, Iss. 2, pp. 216-216
Open Access
Genetics, genomics and clinical features of adenomatous polyposis
Jihoon E. Joo, Julen Viana-Errasti, Daniel D. Buchanan, et al.
Familial Cancer (2025) Vol. 24, Iss. 2
Open Access
Genome profiling with targeted adaptive sampling long-read sequencing for pediatric leukemia
Shota Kato, Aiko Sato‐Otsubo, Wataru Nakamura, et al.
Blood Cancer Journal (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Capturing clinically relevant Campylobacter attributes through direct whole genome sequencing of stool
Bilal Djeghout, Thanh Le-Viet, Leonardo de Oliveira Martins, et al.
Microbial Genomics (2024) Vol. 10, Iss. 8
Open Access | Times Cited: 1
Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
Laura Ivete Rudaks, Igor Stevanovski, Dennis Yeow, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access
Methods to investigate somatic structural variants in synucleinopathies
Caoimhe Morley, Christos Proukakis
Elsevier eBooks (2024), pp. 75-100
Closed Access
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