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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:

Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy
Tirsa L.E. van Westering, Henrik J. Johansson, Britt Hanson, et al.
Molecular & Cellular Proteomics (2020) Vol. 19, Iss. 12, pp. 2047-2068
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

Therapeutic approaches for Duchenne muscular dystrophy
Thomas C. Roberts, Matthew J. A. Wood, Kay E. Davies
Nature Reviews Drug Discovery (2023) Vol. 22, Iss. 11, pp. 917-934
Closed Access | Times Cited: 60
CISD3/MiNT is required for complex I function, mitochondrial integrity, and skeletal muscle maintenance
Rachel Nechushtai, Linda Rowland, Ola Karmi, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 22
Open Access | Times Cited: 7
NLRP3 Contributes to Sarcopenia Associated to Dependency Recapitulating Inflammatory-Associated Muscle Degeneration
Eduardo Antuña, Yaiza Potes, Francisco Javier Baena-Huerta, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1439-1439
Open Access | Times Cited: 6
Complexity of skeletal muscle degeneration: multi-systems pathophysiology and organ crosstalk in dystrophinopathy
Kay Ohlendieck, Dieter Swandulla
Pflügers Archiv - European Journal of Physiology (2021) Vol. 473, Iss. 12, pp. 1813-1839
Open Access | Times Cited: 33
Mechanical loading is required for initiation of extracellular matrix deposition at the developing murine myotendinous junction
Sarah N. Lipp, Kathryn R. Jacobson, Haley A. Colling, et al.
Matrix Biology (2023) Vol. 116, pp. 28-48
Open Access | Times Cited: 12
Histopathology of Duchenne muscular dystrophy in correlation with changes in proteomic biomarkers.
Margit Zweyer, Hemmen Sabir, Paul Dowling, et al.
PubMed (2022) Vol. 37, Iss. 2, pp. 101-116
Closed Access | Times Cited: 19
Mass Spectrometric Profiling of Extraocular Muscle and Proteomic Adaptations in the mdx-4cv Model of Duchenne Muscular Dystrophy
Stephen Gargan, Paul Dowling, Margit Zweyer, et al.
Life (2021) Vol. 11, Iss. 7, pp. 595-595
Open Access | Times Cited: 17
Proteomic profiling of impaired excitation–contraction coupling and abnormal calcium handling in muscular dystrophy
Paul Dowling, Stephen Gargan, Dieter Swandulla, et al.
PROTEOMICS (2022) Vol. 22, Iss. 23-24
Open Access | Times Cited: 12
A deep redox proteome profiling workflow and its application to skeletal muscle of a Duchenne Muscular Dystrophy model
Nicholas Day, Tong Zhang, Matthew Gaffrey, et al.
Free Radical Biology and Medicine (2022) Vol. 193, pp. 373-384
Open Access | Times Cited: 12
Extracellular Matrix Proteomics: The mdx-4cv Mouse Diaphragm as a Surrogate for Studying Myofibrosis in Dystrophinopathy
Paul Dowling, Stephen Gargan, Margit Zweyer, et al.
Biomolecules (2023) Vol. 13, Iss. 7, pp. 1108-1108
Open Access | Times Cited: 7
The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases
Dèlia Yubero, Daniel Natera‐de Benito, Jordi Pijuan, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4274-4274
Open Access | Times Cited: 16
Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD
Britt Hanson, Sofia Stenler, Nina Ahlskog, et al.
Molecular Therapy — Nucleic Acids (2022) Vol. 30, pp. 379-397
Open Access | Times Cited: 11
Mass Spectrometry-Based Proteomic Technology and Its Application to Study Skeletal Muscle Cell Biology
Paul Dowling, Dieter Swandulla, Kay Ohlendieck
Cells (2023) Vol. 12, Iss. 21, pp. 2560-2560
Open Access | Times Cited: 6
How Can Proteomics Help to Elucidate the Pathophysiological Crosstalk in Muscular Dystrophy and Associated Multi-System Dysfunction?
Paul Dowling, Capucine Trollet, Elisa Négroni, et al.
Proteomes (2024) Vol. 12, Iss. 1, pp. 4-4
Open Access | Times Cited: 2
Proteomic Identification of Markers of Membrane Repair, Regeneration and Fibrosis in the Aged and Dystrophic Diaphragm
Stephen Gargan, Paul Dowling, Margit Zweyer, et al.
Life (2022) Vol. 12, Iss. 11, pp. 1679-1679
Open Access | Times Cited: 10
Proteome Profiling of the Dystrophic mdx Mice Diaphragm
Olga Mucha, Małgorzata Myszka, Paulina Podkalicka, et al.
Biomolecules (2023) Vol. 13, Iss. 11, pp. 1648-1648
Open Access | Times Cited: 5
Exon skipping induces uniform dystrophin rescue with dose-dependent restoration of serum miRNA biomarkers and muscle biophysical properties
Katarzyna Chwalenia, Jacopo Oieni, Joanna Zemła, et al.
Molecular Therapy — Nucleic Acids (2022) Vol. 29, pp. 955-968
Open Access | Times Cited: 8
Leucyl-tRNA Synthetase Contributes to Muscle Weakness through Mammalian Target of Rapamycin Complex 1 Activation and Autophagy Suppression in a Mouse Model of Duchenne Muscular Dystrophy
Jae‐Sung You, Kate Karaman, Adriana Reyes‐Ordoñez, et al.
American Journal Of Pathology (2024) Vol. 194, Iss. 8, pp. 1571-1580
Closed Access | Times Cited: 1
CISD3 is required for Complex I function, mitochondrial integrity, and skeletal muscle maintenance
Henri‐Baptiste Marjault, Ola Karmi, Linda Rowland, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Temporal Proteomic Profiling During Differentiation of Normal and Dystrophin-Deficient Human Muscle Cells
Mansi V. Goswami, Shefa M. Tawalbeh, Emily H. Canessa, et al.
Journal of Neuromuscular Diseases (2021) Vol. 8, Iss. s2, pp. S205-S222
Closed Access | Times Cited: 7
Caveolin-3 regulates the activity of Ca2+/calmodulin-dependent protein kinase II in C2C12 cells
Michio Matsunobe, Norio Motohashi, Eito Aoki, et al.
AJP Cell Physiology (2022) Vol. 323, Iss. 4, pp. C1137-C1148
Closed Access | Times Cited: 5
Is the fundamental pathology in Duchenne's muscular dystrophy caused by a failure of glycogenolysis–glycolysis in costameres?
Vishakha Nesari, Suresh Balakrishnan, Upendra Nongthomba
Journal of Genetics (2023) Vol. 102, Iss. 1
Closed Access | Times Cited: 2
Biochemical and proteomic insights into sarcoplasmic reticulum Ca 2+ -ATPase complexes in skeletal muscles
Paul Dowling, Dieter Swandulla, Kay Ohlendieck
Expert Review of Proteomics (2023) Vol. 20, Iss. 7-9, pp. 125-142
Closed Access | Times Cited: 2
Relative quantification of progressive changes in healthy and dysferlin‐deficient mouse skeletal muscle proteomes
Adriana E. Golding, Wenping Li, Paul S. Blank, et al.
Muscle & Nerve (2023) Vol. 68, Iss. 5, pp. 805-816
Closed Access | Times Cited: 2
Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD
Britt Hanson, Sofia Stenler, Nina Ahlskog, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
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