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:
A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity
Kevin M. Flanigan, Megan A. Waldrop, Paul T. Martin, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 6, pp. 663-673
Open Access | Times Cited: 8
Kevin M. Flanigan, Megan A. Waldrop, Paul T. Martin, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 6, pp. 663-673
Open Access | Times Cited: 8
Showing 8 citing articles:
2023 in the European Journal of Human Genetics
Alisdair McNeill
European Journal of Human Genetics (2024) Vol. 32, Iss. 2, pp. 135-137
Open Access | Times Cited: 180
Alisdair McNeill
European Journal of Human Genetics (2024) Vol. 32, Iss. 2, pp. 135-137
Open Access | Times Cited: 180
Muscle-specific increased expression ofJAG1improves skeletal muscle phenotype in dystrophin-deficient mice.
Felipe de Souza Leite, Matthias Lambert, Tracy Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Felipe de Souza Leite, Matthias Lambert, Tracy Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Is it time for genetic modifiers to predict prognosis in Duchenne muscular dystrophy?
Luca Bello, Eric P. Hoffman, Elena Pegoraro
Nature Reviews Neurology (2023) Vol. 19, Iss. 7, pp. 410-423
Closed Access | Times Cited: 9
Luca Bello, Eric P. Hoffman, Elena Pegoraro
Nature Reviews Neurology (2023) Vol. 19, Iss. 7, pp. 410-423
Closed Access | Times Cited: 9
Emerging Perspectives on Gene Therapy Delivery for Neurodegenerative and Neuromuscular Disorders
Cintia Gomez Limia, Megan Baird, M. Schwartz, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 12, pp. 1979-1979
Open Access | Times Cited: 11
Cintia Gomez Limia, Megan Baird, M. Schwartz, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 12, pp. 1979-1979
Open Access | Times Cited: 11
GNE myopathy: can homozygous asymptomatic subjects give a clue for the identification of protective factors?
Stella Mitrani‐Rosenbaum, Ruben Attali, Zohar Argov
Neuromuscular Disorders (2023) Vol. 33, Iss. 10, pp. 762-768
Closed Access | Times Cited: 5
Stella Mitrani‐Rosenbaum, Ruben Attali, Zohar Argov
Neuromuscular Disorders (2023) Vol. 33, Iss. 10, pp. 762-768
Closed Access | Times Cited: 5
Transcriptomic analysis of paired healthy human skeletal muscles to identify modulators of disease severity in DMD
Shirley Nieves‐Rodriguez, Florian Barthélémy, Jeremy D. Woods, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
Shirley Nieves‐Rodriguez, Florian Barthélémy, Jeremy D. Woods, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
The complex genomics of single gene disorders
Alisdair McNeill
European Journal of Human Genetics (2023) Vol. 31, Iss. 6, pp. 609-610
Open Access
Alisdair McNeill
European Journal of Human Genetics (2023) Vol. 31, Iss. 6, pp. 609-610
Open Access
Elucidation of bioinformatic-guided high-prospect drug repositioning candidates for DMD via Swanson linking of target-focused latent knowledge from text-mined categorical metadata
J. Wes Ulm, Florian Barthélémy, Stanley F. Nelson
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access
J. Wes Ulm, Florian Barthélémy, Stanley F. Nelson
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access
