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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:

Applying genomic and transcriptomic advances to mitochondrial medicine
William L. Macken, Jana Vandrovcová, Michael G. Hanna, et al.
Nature Reviews Neurology (2021) Vol. 17, Iss. 4, pp. 215-230
Open Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

Hallmarks of aging: An expanding universe
Carlos López-Otı́n, Marı́a A. Blasco, Linda Partridge, et al.
Cell (2023) Vol. 186, Iss. 2, pp. 243-278
Open Access | Times Cited: 2747
Meta-hallmarks of aging and cancer
Carlos López-Otı́n, Federico Pietrocola, David Roiz‐Valle, et al.
Cell Metabolism (2023) Vol. 35, Iss. 1, pp. 12-35
Open Access | Times Cited: 264
Nanopore DNA sequencing technologies and their applications towards single-molecule proteomics
Adam Dorey, Stefan Howorka
Nature Chemistry (2024) Vol. 16, Iss. 3, pp. 314-334
Closed Access | Times Cited: 38
Mitochondrial diseases: from molecular mechanisms to therapeutic advances
Hu Wen, Hui Deng, Bingyan Li, et al.
Signal Transduction and Targeted Therapy (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 4
Direct Nanopore Sequencing of Individual Full Length tRNA Strands
Niki K. Thomas, Vinay Chaitanya Poodari, Miten Jain, et al.
ACS Nano (2021) Vol. 15, Iss. 10, pp. 16642-16653
Open Access | Times Cited: 90
Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease
Christopher J. Record, Menelaos Pipis, Mariola Skorupinska, et al.
Brain (2024) Vol. 147, Iss. 9, pp. 3144-3156
Open Access | Times Cited: 11
The Complicated Nature of Somatic mtDNA Mutations in Aging
Mónica Sánchez-Contreras, Scott R. Kennedy
Frontiers in Aging (2022) Vol. 2
Open Access | Times Cited: 33
Nanopore long-read next-generation sequencing for detection of mitochondrial DNA large-scale deletions
Chiara Frascarelli, Nadia Zanetti, Alessia Nasca, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 19
Functional genomics and small molecules in mitochondrial neurodevelopmental disorders
Daniel G. Calame, Lisa Emrick
Neurotherapeutics (2024) Vol. 21, Iss. 1, pp. e00316-e00316
Open Access | Times Cited: 7
Analyzing Modern Biomolecules: The Revolution of Nucleic-Acid Sequencing – Review
Gabriel Dorado, Sergio Gálvez, Teresa E. Rosales Tham, et al.
Biomolecules (2021) Vol. 11, Iss. 8, pp. 1111-1111
Open Access | Times Cited: 38
The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies
Anna Grether, Ivan Ivanovski, Martina Russo, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 5
Open Access | Times Cited: 13
Challenges and opportunities to bridge translational to clinical research for personalized mitochondrial medicine
Andrea Gropman, Martine Uittenbogaard, Anne Chiaramello
Neurotherapeutics (2024) Vol. 21, Iss. 1, pp. e00311-e00311
Open Access | Times Cited: 5
TOWARDS TRANSCRIPTOMICS AS A PRIMARY TOOL FOR RARE DISEASE INVESTIGATION
Stephen B. Montgomery, Jonathan A. Bernstein, Matthew T. Wheeler
Molecular Case Studies (2022), pp. mcs.a006198-mcs.a006198
Open Access | Times Cited: 22
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Ieva Keraite, Philipp Becker, Davide Canevazzi, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 20
Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing
William L. Macken, Micol Falabella, Caroline McKittrick, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 16
Omics-based approaches for the systematic profiling of mitochondrial biology
Jasmin Schäfer, F.X. Reymond Sutandy, Christian Münch
Molecular Cell (2023) Vol. 83, Iss. 6, pp. 911-926
Open Access | Times Cited: 9
Enhanced mitochondrial genome analysis: bioinformatic and long-read sequencing advances and their diagnostic implications
William L. Macken, Micol Falabella, Chiara Pizzamiglio, et al.
Expert Review of Molecular Diagnostics (2023) Vol. 23, Iss. 9, pp. 797-814
Open Access | Times Cited: 9
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases
Olivia V. Poole, Chiara Pizzamiglio, David Murphy, et al.
Annals of Neurology (2021) Vol. 89, Iss. 6, pp. 1240-1247
Open Access | Times Cited: 22
Use of Next-Generation Sequencing for Identifying Mitochondrial Disorders
Shafi Mahmud, Suvro Biswas, Shamima Afrose, et al.
Current Issues in Molecular Biology (2022) Vol. 44, Iss. 3, pp. 1127-1148
Open Access | Times Cited: 14
Laboratory testing for mitochondrial diseases: biomarkers for diagnosis and follow-up
Abraham J. Paredes‐Fuentes, Clara Oliva, Roser Urreizti, et al.
Critical Reviews in Clinical Laboratory Sciences (2023) Vol. 60, Iss. 4, pp. 270-289
Closed Access | Times Cited: 7
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
Ismail Gouiza, Meriem Hechmi, Abir Zioudi, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 2
Approaches and challenges in identifying, quantifying, and manipulating dynamic mitochondrial genome variations
Fei Li, Run Xiang, Yue Liu, et al.
Cellular Signalling (2024) Vol. 117, pp. 111123-111123
Closed Access | Times Cited: 2
Young small extracellular vesicles rejuvenate replicative senescence by remodeling Drp1 translocation-mediated mitochondrial dynamics
Yingying Peng, Tingting Zhao, Shuxuan Rong, et al.
Journal of Nanobiotechnology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
A clinical approach to diagnosis and management of mitochondrial myopathies
Hui‐Lin Chin, Poh San Lai, S K Tay
Neurotherapeutics (2023) Vol. 21, Iss. 1, pp. e00304-e00304
Open Access | Times Cited: 4
A Two-Genome Portrayal of Mitochondrial Disorders: A Review with Clinical Presentations
Jude Abadie
Frontiers in Bioscience-Scholar (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
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