Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

The application of long-read sequencing in clinical settings
Josephine B. Oehler, Helen Wright, Zornitza Stark, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 60

Showing 1-25 of 60 citing articles:

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: 23
A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice
Cristina Méndez‐Vidal, Nereida Bravo‐Gil, Javier Pérez-Florido, et al.
Journal of Translational Medicine (2025) Vol. 23, Iss. 1
Open Access | Times Cited: 1
Unraveling the Genetic Landscape of Neurological Disorders: Insights into Pathogenesis, Techniques for Variant Identification, and Therapeutic Approaches
Zeba Firdaus, Xiaogang Li
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2320-2320
Open Access | Times Cited: 9
A comparison between full-length 16S rRNA Oxford nanopore sequencing and Illumina V3-V4 16S rRNA sequencing in head and neck cancer tissues
Kenny Yeo, James Connell, George Bouras, et al.
Archives of Microbiology (2024) Vol. 206, Iss. 6
Open Access | Times Cited: 6
Hybrid-Capture Target Enrichment in Human Pathogens: Identification, Evolution, Biosurveillance, and Genomic Epidemiology
Zheng Bin Randolph Quek, Sock Hoon Ng
Pathogens (2024) Vol. 13, Iss. 4, pp. 275-275
Open Access | Times Cited: 5
Advancements in HLA Typing Techniques and Their Impact on Transplantation Medicine
Jeethu Anu Geo, Reem Ameen, Salem Al Shemmari, et al.
Medical Principles and Practice (2024) Vol. 33, Iss. 3, pp. 215-231
Open Access | Times Cited: 5
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases
Ahmad Abou Tayoun, Shruti Sinha, Fatma Rabea, et al.
Research Square (Research Square) (2024)
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
Using New Technologies to Analyze Gut Microbiota and Predict Cancer Risk
Mohammad Amin Hemmati, Marzieh Monemi, Shima Asli, et al.
Cells (2024) Vol. 13, Iss. 23, pp. 1987-1987
Open Access | Times Cited: 5
SUMMER: an integrated nanopore sequencing pipeline for variants detection and clinical annotation on the human genome
Ran Li, Huashuo Chu, Kai Gao, et al.
Functional & Integrative Genomics (2025) Vol. 25, Iss. 1
Open Access
High‐Accuracy Long‐Read Sequencing of Mycobacterium tuberculosis PSNK363 Isolated From the Democratic People’s Republic of Korea
Thi Binh Dang, Nackmoon Sung, K. Lim, et al.
Canadian Journal of Infectious Diseases and Medical Microbiology (2025) Vol. 2025, Iss. 1
Open Access
Singleton rapid long-read genome sequencing as first tier genetic test for critically Ill children with suspected genetic diseases
Wuttichart Kamolvisit, Chanatjit Cheawsamoot, Wanna Chetruengchai, et al.
European Journal of Human Genetics (2025)
Closed 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
Targeted long-read sequencing facilitates effective carrier screening for complex monogenic diseases including spinal muscular atrophy, α-/β-thalassemia, 21-hydroxylase deficiency, and fragile-X syndrome
Shuyuan Li, Renyi Hua, Xu Han, et al.
Journal of Translational Medicine (2025) Vol. 23, Iss. 1
Open Access
Preliminary genomic data on fiveOrientia tsutsugamushistrains isolated in Vellore, India
Janaki Kumaraswamy, Agilandeeswari Kirubanathan, Karthik Gunasekaran, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
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: 4
Mechanisms and technologies in cancer epigenetics
Zaki A. Sherif, Olorunseun O. Ogunwobi, Habtom W. Ressom
Frontiers in Oncology (2025) Vol. 14
Open Access
Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocol
Amali Mallawaarachchi, Hugh J. McCarthy, Thomas Forbes, et al.
BMC Nephrology (2025) Vol. 26, Iss. 1
Open Access
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases
Shruti Sinha, Fatma Rabea, Sathishkumar Ramaswamy, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
ONT in Clinical Diagnostics of Repeat Expansion Disorders: Detection and Reporting Challenges
Ludmila Kaplun, Greice Krautz‐Peterson, Nir Neerman, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2725-2725
Open Access
“Aging Clocks” Based on Cell-Free DNA
Alexander V. Sergeev, О. V. Kisil, Andrey A. Eremin, et al.
Biochemistry (Moscow) (2025) Vol. 90, Iss. S1, pp. S342-S355
Closed Access
Preimplantation genetic testing: A remarkable history of pioneering, technical challenges, innovations, and ethical considerations
Keith E. Latham
Molecular Reproduction and Development (2024) Vol. 91, Iss. 1
Open Access | Times Cited: 3
Applications of Nanopore sequencing in precision cancer medicine
Sergey A. Dyshlovoy, Stefanie Paigin, Ann‐Kristin Afflerbach, et al.
International Journal of Cancer (2024) Vol. 155, Iss. 12, pp. 2129-2140
Open Access | Times Cited: 3
Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome
Ilaria Bestetti, M. Crippa, Alessandra Sironi, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
The Role of Genetic Testing in Adult CKD
N. Knoers, Albertien M. van Eerde
Journal of the American Society of Nephrology (2024) Vol. 35, Iss. 8, pp. 1107-1118
Closed Access | Times Cited: 2
Page 1 - Next Page

Scroll to top