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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.

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Showing 1-25 of 46 citing articles:

Clinical utility of serum biomarkers in Duchenne muscular dystrophy
Yetrib Hathout, Haeri Seol, M H Han, et al.
Clinical Proteomics (2016) Vol. 13, Iss. 1
Open Access | Times Cited: 74
Progressive muscle proteome changes in a clinically relevant pig model of Duchenne muscular dystrophy
Thomas Fröhlich, Elisabeth Kemter, Florian Flenkenthaler, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 65
The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle
Sandra Murphy, Kay Ohlendieck
Computational and Structural Biotechnology Journal (2015) Vol. 14, pp. 20-27
Open Access | Times Cited: 52
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
Proteomic analysis of dystrophin deficiency and associated changes in the aged mdx-4cv heart model of dystrophinopathy-related cardiomyopathy
Sandra Murphy, Paul Dowling, Margit Zweyer, et al.
Journal of Proteomics (2016) Vol. 145, pp. 24-36
Closed Access | Times Cited: 46
Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis
Ashling Holland, Sandra Murphy, Paul Dowling, et al.
PROTEOMICS (2015) Vol. 16, Iss. 2, pp. 345-366
Closed Access | Times Cited: 41
Myoscaffolds reveal laminin scarring is detrimental for stem cell function while sarcospan induces compensatory fibrosis
Kristen M. Stearns-Reider, Michael R. Hicks, Katherine G. Hammond, et al.
npj Regenerative Medicine (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 12
Proteomic analysis of the sarcolemma-enriched fraction from dystrophic mdx-4cv skeletal muscle
Sandra Murphy, Margit Zweyer, Michael Henry, et al.
Journal of Proteomics (2018) Vol. 191, pp. 212-227
Open Access | Times Cited: 38
Proteomic profiling of the dystrophin complex and membrane fraction from dystrophic mdx muscle reveals decreases in the cytolinker desmoglein and increases in the extracellular matrix stabilizers biglycan and fibronectin
Sandra Murphy, Heinrich Brinkmeier, Mirjam Krautwald, et al.
Journal of Muscle Research and Cell Motility (2017) Vol. 38, Iss. 2, pp. 251-268
Closed Access | Times Cited: 37
Proteomic profiling of the mouse diaphragm and refined mass spectrometric analysis of the dystrophic phenotype
Sandra Murphy, Margit Zweyer, Maren Raucamp, et al.
Journal of Muscle Research and Cell Motility (2019) Vol. 40, Iss. 1, pp. 9-28
Open Access | Times Cited: 35
Proteomic profiling of mdx-4cv serum reveals highly elevated levels of the inflammation-induced plasma marker haptoglobin in muscular dystrophy
Sandra Murphy, Paul Dowling, Margit Zweyer, et al.
International Journal of Molecular Medicine (2017) Vol. 39, Iss. 6, pp. 1357-1370
Open Access | Times Cited: 34
Distribution and Expression of Vimentin and Desmin in Broiler Pectoralis major Affected by the Growth-Related Muscular Abnormalities
Francesca Soglia, Maurizio Mazzoni, Martina Zappaterra, et al.
Frontiers in Physiology (2020) Vol. 10
Open Access | Times Cited: 30
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
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
Label-free proteomic analysis of Duchenne and Becker muscular dystrophy showed decreased sarcomere proteins and increased ubiquitination-related proteins
João Silva, María Xesús Nogueira Pereira, Yara Martins da Silva, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Concurrent Label-Free Mass Spectrometric Analysis of Dystrophin Isoform Dp427 and the Myofibrosis Marker Collagen in Crude Extracts from mdx-4cv Skeletal Muscles
Sandra Murphy, Margit Zweyer, Rustam R. Mundegar, et al.
Proteomes (2015) Vol. 3, Iss. 3, pp. 298-327
Open Access | Times Cited: 30
Label-free mass spectrometric analysis reveals complex changes in the brain proteome from the mdx-4cv mouse model of Duchenne muscular dystrophy
Sandra Murphy, Margit Zweyer, Michael Henry, et al.
Clinical Proteomics (2015) Vol. 12, Iss. 1
Open Access | Times Cited: 29
Emerging proteomic biomarkers of X-linked muscular dystrophy
Paul Dowling, Sandra Murphy, Margit Zweyer, et al.
Expert Review of Molecular Diagnostics (2019) Vol. 19, Iss. 8, pp. 739-755
Open Access | Times Cited: 26
Multi-omics analysis of sarcospan overexpression in mdx skeletal muscle reveals compensatory remodeling of cytoskeleton-matrix interactions that promote mechanotransduction pathways
Jackie L. McCourt, Kristen M. Stearns-Reider, Hafsa Mamsa, et al.
Skeletal Muscle (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 9
Uncovering the exercise‐related proteome signature in skeletal muscle
Ana Isabel Padrão, Rita Ferreira, Francisco Amado, et al.
PROTEOMICS (2015) Vol. 16, Iss. 5, pp. 816-830
Closed Access | Times Cited: 26
Proteomic profiling of liver tissue from the mdx-4cv mouse model of Duchenne muscular dystrophy
Sandra Murphy, Margit Zweyer, Michael Henry, et al.
Clinical Proteomics (2018) Vol. 15, Iss. 1
Open Access | Times Cited: 26
Differential YAP nuclear signaling in healthy and dystrophic skeletal muscle
Shama R. Iyer, Sameer B. Shah, Christopher W. Ward, et al.
AJP Cell Physiology (2019) Vol. 317, Iss. 1, pp. C48-C57
Open Access | Times Cited: 25
Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation
Heidi R. Fuller, Laura C. Graham, Maica Llavero Hurtado, et al.
Expert Review of Proteomics (2016) Vol. 13, Iss. 7, pp. 659-671
Open Access | Times Cited: 23
Molekulare Pathogenese der Fibrose bei Muskeldystrophie vom Typ Duchenne
Kay Ohlendieck, Dieter Swandulla
Der Pathologe (2017) Vol. 38, Iss. 1, pp. 21-29
Open Access | Times Cited: 22
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
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