Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

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

Showing 1-25 of 46 citing articles:

Mitochondria Associated Membranes (MAMs): Architecture and physiopathological role
Lucia Barazzuol, Flavia Giamogante, Tito Calì
Cell Calcium (2021) Vol. 94, pp. 102343-102343
Closed Access | Times Cited: 107
Mitochondrial Properties in Skeletal Muscle Fiber
Han Dong, Shih‐Yin Tsai
Cells (2023) Vol. 12, Iss. 17, pp. 2183-2183
Open Access | Times Cited: 29
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
Calcium-mediated regulation of mitophagy: implications in neurodegenerative diseases
Fivos Borbolis, Christina Ploumi, Konstantinos Palikaras
npj Metabolic Health and Disease (2025) Vol. 3, Iss. 1
Open Access | Times Cited: 1
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
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
Neural dysregulation in post-COVID fatigue
Anne ME. Baker, Natalie J. Maffitt, Alessandro Del Vecchio, et al.
Brain Communications (2023) Vol. 5, Iss. 3
Open Access | Times Cited: 20
Mitochondria-SR interaction and mitochondrial fusion/fission in the regulation of skeletal muscle metabolism
Mauricio Castro‐Sepúlveda, Rodrigo Fernández‐Verdejo, Hermann Zbinden‐Foncea, et al.
Metabolism (2023) Vol. 144, pp. 155578-155578
Closed Access | Times Cited: 18
Pathways for Sensing and Responding to Hydrogen Peroxide at the Endoplasmic Reticulum
Jennifer M. Roscoe, Carolyn S. Sevier
Cells (2020) Vol. 9, Iss. 10, pp. 2314-2314
Open Access | Times Cited: 35
Beyond antioxidants: Selenium and skeletal muscle mitochondria
Lauren T Wesolowski, Pier L Semanchik, Sarah H White-Springer
Frontiers in Veterinary Science (2022) Vol. 9
Open Access | Times Cited: 21
Using mass spectrometry imaging to visualize age-related subcellular disruption
Kelly A. Hogan, Julianna D. Zeidler, Heather K. Beasley, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 12
Nogo-A Is Critical for Pro-Inflammatory Gene Regulation in Myocytes and Macrophages
H. M. Arif Ullah, Ahmed K. Elfadl, Sunyoung Park, et al.
Cells (2021) Vol. 10, Iss. 2, pp. 282-282
Open Access | Times Cited: 26
The aging of ER-mitochondria communication: A journey from undifferentiated to aged cells
Pablo Morgado-Cáceres, Gianella Liabeuf, Ximena Calle, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 17
Creatine transporter (SLC6A8) knockout mice exhibit reduced muscle performance, disrupted mitochondrial Ca2+ homeostasis, and severe muscle atrophy
Irene Pertici, Donato D’Angelo, Denis Vecellio Reane, et al.
Cell Death and Disease (2025) Vol. 16, Iss. 1
Open 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
Mitochondria associated membranes in dilated cardiomyopathy: connecting pathogenesis and cellular dysfunction
Pingge He, Hongbo Chang, Ying Qiu, et al.
Frontiers in Cardiovascular Medicine (2025) Vol. 12
Open Access
The MFN2 Q367H variant reveals a novel pathomechanism connected to mtDNA-mediated inflammation
Mashiat Zaman, Govinda Sharma, Walaa Almutawa, et al.
Life Science Alliance (2025) Vol. 8, Iss. 6, pp. e202402921-e202402921
Open Access
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
Endoplasmic reticulum-resident selenoproteins and their roles in glucose and lipid metabolic disorders
Zhan Shi, Ziyu Han, Jingyi Chen, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 6, pp. 167246-167246
Closed Access | Times Cited: 3
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
Page 1 - Next Page

Scroll to top