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:

Whole genome sequencing in clinical practice
Frederik Otzen Bagger, Line Borgwardt, Andreas Sand Jespersen, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 42

Showing 1-25 of 42 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

Genome analysis of colistin-resistant Salmonella isolates from human sources in Guizhou of southwestern China, 2019–2023
Jingtong Wu, Yongxian Wen, Lv You, et al.
Frontiers in Microbiology (2025) Vol. 16
Open Access | Times Cited: 1

Advances in bioinformatics and multi-omics integration: transforming viral infectious disease research in veterinary medicine
Alyaa Elrashedy, Walid Mousa, Mohamed Nayel, et al.
Virology Journal (2025) Vol. 22, Iss. 1
Open Access | Times Cited: 1

mRNA vaccine platforms: linking infectious disease prevention and cancer immunotherapy
Dariush Haghmorad, Majid Eslami, Niloufar Orooji, et al.
Frontiers in Bioengineering and Biotechnology (2025) Vol. 13
Open Access | Times Cited: 1

Biocides as Drivers of Antibiotic Resistance: A Critical Review of Environmental Implications and Public Health Risks
Mariana Sousa, Idalina Machado, Lúcia C. Simões, et al.
Environmental Science and Ecotechnology (2025), pp. 100557-100557
Open Access | Times Cited: 1

Clinical Genetic and Genomic Testing in Congenital Heart Disease and Cardiomyopathy
Mahati Pidaparti, Gabrielle C. Geddes, Matthew D. Durbin
Journal of Clinical Medicine (2024) Vol. 13, Iss. 9, pp. 2544-2544
Open Access | Times Cited: 5

Should AI-Powered Whole-Genome Sequencing Be Used Routinely for Personalized Decision Support in Surgical Oncology—A Scoping Review
Kokiladevi Alagarswamy, Wenjie Shi, Aishwarya Boini, et al.
BioMedInformatics (2024) Vol. 4, Iss. 3, pp. 1757-1772
Open Access | Times Cited: 5

A Comprehensive Bioinformatics Approach to Analysis of Variants: Variant Calling, Annotation, and Prioritization
Merve Nur Köroğlu, Kaya Bilgüvar
Methods in molecular biology (2025), pp. 207-233
Closed Access

De la microscopía a la secuenciación genética: La evolución en las técnicas de diagnóstico de la Leucemia Linfoide Aguda
Dayana Fernanda Pico Sánchez, Daniela Alexandra Rosero Freire
Bionatura journal : (2025) Vol. 2, Iss. 1, pp. 1-21
Closed Access

The role of germline and somatic mutations in predicting cancer-associated thrombosis: a narrative review
Vincent Lanting, Marieke J Oskam, Hanneke Wilmink, et al.
Current Opinion in Hematology (2025)
Closed Access

PErsoNal Genome QUery IN Healthcare and Clinical Practice (PENGQUIN)
Elias Crum
Lecture notes in computer science (2025), pp. 23-32
Closed Access

Molecular features and clinical actionability of gene fusions in colorectal cancer
Francesco Giulio Sullo, Simon Garinet, Hélène Blons, et al.
Critical Reviews in Oncology/Hematology (2025) Vol. 208, pp. 104656-104656
Closed Access

Translational Advances in Oncogene and Tumor-Suppressor Gene Research
Radoslav Stojchevski, Edward Agus Sutanto, R. Sutanto, et al.
Cancers (2025) Vol. 17, Iss. 6, pp. 1008-1008
Open Access

A novel TRKB-activating internal tandem duplication characterizes a new mechanism of receptor tyrosine kinase activation
Lauren M. Brown, Gábor Tax, Pablo Acera Mateos, et al.
Research Square (Research Square) (2025)
Closed Access

Expanded Carrier Screening for Prevention of Genetic Recessive Diseases
Maurizio Poli, Lucrezia Pilenzi, Roberta Giansante, et al.
Elsevier eBooks (2025)
Closed Access

Genetics of canine cancer: a guide for the veterinary oncologist
Maja L. Arendt, A. Heiden, Raphaela Pensch, et al.
Veterinary oncology. (2025) Vol. 2, Iss. 1
Open Access

Current methods in the diagnosis of invasive meningococcal disease
Ergi̇n Çi̇ftçi̇, Duygu Öcal, Ayper Somer, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access

Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract
Lisanne Vendrig, Mayke A C Ten Hoor, Benthe H König, et al.
Pediatric Nephrology (2024)
Open Access | Times Cited: 3

The role of NHS genomic associates, assistants, and practitioners in England: Demographics, career plans and challenges faced
Bethany Lumborg, Stephen P. Lake, Andrew Patton
Research Square (Research Square) (2025)
Closed Access

From haystack to high precision: advanced sequencing methods to unraveling circulating tumor DNA mutations
Tamires Ferreira da Silva, Juscelino Carvalho de Azevedo, Eliel Barbosa Teixeira, et al.
Frontiers in Molecular Biosciences (2024) Vol. 11
Closed Access | Times Cited: 1

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