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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:

The clinical, histologic, and genotypic spectrum of SEPN1 -related myopathy
Rocío N. Villar‐Quiles, Maja von der Hagen, Corinne Métay, et al.
Neurology (2020) Vol. 95, Iss. 11
Open Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

Expanding the Frontiers of Guardian Antioxidant Selenoproteins in Cardiovascular Pathophysiology
Tommaso Angelone, Carmine Rocca, Vincenzo Lionetti, et al.
Antioxidants and Redox Signaling (2024) Vol. 40, Iss. 7-9, pp. 369-432
Closed Access | Times Cited: 18
Molecular and cellular basis of genetically inherited skeletal muscle disorders
James J. Dowling, Conrad C. Weihl, Melissa J. Spencer
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 11, pp. 713-732
Open Access | Times Cited: 80
SEPN1-related myopathy depends on the oxidoreductase ERO1A and is druggable with the chemical chaperone TUDCA
Serena Germani, Andrew Tri Van Ho, Alessandro Cherubini, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 3, pp. 101439-101439
Open Access | Times Cited: 13
Congenital muscular dystrophies: What is new?
Alberto A. Zambon, Francesco Muntoni
Neuromuscular Disorders (2021) Vol. 31, Iss. 10, pp. 931-942
Open Access | Times Cited: 48
Defining and identifying satellite cell-opathies within muscular dystrophies and myopathies
Massimo Ganassi, Francesco Muntoni, Peter S. Zammit
Experimental Cell Research (2021) Vol. 411, Iss. 1, pp. 112906-112906
Open Access | Times Cited: 44
Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy
Anne Filipe, Alexander Chernorudskiy, Sandrine Arbogast, et al.
Cell Death and Differentiation (2020) Vol. 28, Iss. 1, pp. 123-138
Open Access | Times Cited: 46
The Neurobiology of Selenium: Looking Back and to the Future
Ulrich Schweizer, Simon Bohleber, Wenchao Zhao, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 36
Historical Roles of Selenium and Selenoproteins in Health and Development: The Good, the Bad and the Ugly
Petra A. Tsuji, Didac Santesmasses, Byeong J. Lee, et al.
International Journal of Molecular Sciences (2021) Vol. 23, Iss. 1, pp. 5-5
Open Access | Times Cited: 35
Emerging roles of ER-resident selenoproteins in brain physiology and physiopathology
Cédric Jehan, Dorthe Cartier, Christine Bucharles, et al.
Redox Biology (2022) Vol. 55, pp. 102412-102412
Open Access | Times Cited: 28
A review of major causative genes in congenital myopathies
Masashi Ogasawara, Ichizo Nishino
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 215-225
Closed Access | Times Cited: 27
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 26
Hypoxia and Hypoxia-Inducible Factor Signaling in Muscular Dystrophies: Cause and Consequences
Thuy-Hang Nguyen, Stéphanie Conotte, Alexandra Belayew, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 13, pp. 7220-7220
Open Access | Times Cited: 28
SELENON-related myopathy with scoliosis and respiratory failure since early childhood diagnosed through reassessment during pediatric-to-adult healthcare transition: a case report
Yusuke Baba, Meiko Hashimoto Maeda, Kyosuke Muramatsu, et al.
Rinsho Shinkeigaku (2025)
Closed Access
SELENON-related myopathy as a cause of acute respiratory failure in middle age: a case report
Barbara Risi, Filomena Caria, Simona Damioli, et al.
Journal of Medical Case Reports (2025) Vol. 19, Iss. 1
Open Access
Zebrafish and cellular models of SELENON-Congenital myopathy exhibit novel embryonic and metabolic phenotypes
Pamela Barraza‐Flores, Behzad Moghadaszadeh, Won Lee, et al.
Skeletal Muscle (2025) Vol. 15, Iss. 1
Open Access
Disease Trajectories of a Large French Cohort of 142 Congenital Myopathy Patients in Adult Age
M. Bisciglia, Gianmarco Severa, Norma B. Romero, et al.
European Journal of Neurology (2025) Vol. 32, Iss. 4
Open Access
Congenital Myopathies
Ruchee Patel, Carsten G. Bönnemann
Elsevier eBooks (2025)
Closed Access
Mutations in proteins involved in E-C coupling and SOCE and congenital myopathies
Daniela Rossi, Maria Rosaria Catallo, Enrico Pierantozzi, et al.
The Journal of General Physiology (2022) Vol. 154, Iss. 9
Open Access | Times Cited: 16
Regulation of A-to-I RNA editing and stop codon recoding to control selenoprotein expression during skeletal myogenesis
Yuta Noda, Shunpei Okada, Tsutomu Suzuki
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 15
Not So Rare: Diseases Based on Mutant Proteins Controlling Endoplasmic Reticulum-Mitochondria Contact (MERC) Tethering
Tadashi Makio, Thomas Simmen
Contact (2024) Vol. 7
Open Access | Times Cited: 3
Calcium and Redox Liaison: A Key Role of Selenoprotein N in Skeletal Muscle
Ester Zito, Ana Ferreiro
Cells (2021) Vol. 10, Iss. 5, pp. 1116-1116
Open Access | Times Cited: 20
SELENON-Related Myopathy Across the Life Span, a Cross-Sectional Study for Preparing Trial Readiness
Karlijn Bouman, Jan T. Groothuis, Jonne Doorduin, et al.
Journal of Neuromuscular Diseases (2023) Vol. 10, Iss. 6, pp. 1055-1074
Open Access | Times Cited: 8
Natural history, outcome measures and trial readiness in LAMA2-related muscular dystrophy and SELENON-related myopathy in children and adults: protocol of the LAST STRONG study
Karlijn Bouman, Jan T. Groothuis, Jonne Doorduin, et al.
BMC Neurology (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 18
Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy
Karlijn Bouman, Madelief Gubbels, Frederik M.A. van den Heuvel, et al.
Neuromuscular Disorders (2022) Vol. 32, Iss. 8, pp. 635-642
Open Access | Times Cited: 11
ER stress and ERO1: Potential therapeutic targets for inherited myopathies
Anirban Roy, Aniket S. Joshi, Ashok Kumar
Cell Reports Medicine (2024) Vol. 5, Iss. 3, pp. 101462-101462
Open Access | Times Cited: 2
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