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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:

In vivo characterization of human myofibrillar myopathy genes in zebrafish
John B. Bührdel, Sofia Hirth, Mirjam Keßler, et al.
Biochemical and Biophysical Research Communications (2015) Vol. 461, Iss. 2, pp. 217-223
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

The Role of Z-disc Proteins in Myopathy and Cardiomyopathy
Kirsty Wadmore, Amar J. Azad, Katja Gehmlich
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 6, pp. 3058-3058
Open Access | Times Cited: 46
Loss of the novel Vcp (valosin containing protein) interactor Washc4 interferes with autophagy-mediated proteostasis in striated muscle and leads to myopathy in vivo
Monika Kustermann, Linda Manta, Christoph Paone, et al.
Autophagy (2018) Vol. 14, Iss. 11, pp. 1911-1927
Open Access | Times Cited: 42
215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13–15 November 2015, Heemskerk, The Netherlands
Teresinha Evangelista, Conrad C. Weihl, Virginia Kimonis, et al.
Neuromuscular Disorders (2016) Vol. 26, Iss. 8, pp. 535-547
Open Access | Times Cited: 41
Modeling Human Muscular Dystrophies in Zebrafish: Mutant Lines, Transgenic Fluorescent Biosensors, and Phenotyping Assays
Chiara Tesoriero, Francesca Greco, Elena Cannone, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8314-8314
Open Access | Times Cited: 11
FGF8 rescues motor deficits in zebrafish model of limb-girdle muscular dystrophy R18
Zulvikar Syambani Ulhaq, Yukiko Ogino, William Ka Fai Tse
Biochemical and Biophysical Research Communications (2023) Vol. 652, pp. 76-83
Open Access | Times Cited: 10
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Sarah J. Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Human Molecular Genetics (2017) Vol. 27, Iss. 4, pp. 706-715
Open Access | Times Cited: 31
“Muscling” Throughout Life
Michelle F. Goody, Erin V. Carter, Elisabeth A. Kilroy, et al.
Current topics in developmental biology/Current Topics in Developmental Biology (2016), pp. 197-234
Open Access | Times Cited: 30
Atrogin-1 Deficiency Leads to Myopathy and Heart Failure in Zebrafish
Anja Bühler, Monika Kustermann, Tiziana Bummer, et al.
International Journal of Molecular Sciences (2016) Vol. 17, Iss. 2, pp. 187-187
Open Access | Times Cited: 27
Loss of αB-crystallin function in zebrafish reveals critical roles in the development of the lens and stress resistance of the heart
Sanjay Mishra, Shu-Yu Wu, Alexandra Fuller, et al.
Journal of Biological Chemistry (2017) Vol. 293, Iss. 2, pp. 740-753
Open Access | Times Cited: 27
Genetic compensation prevents myopathy and heart failure in an in vivo model of Bag3 deficiency
Federica Diofano, Karolina Weinmann, Isabelle Schneider, et al.
PLoS Genetics (2020) Vol. 16, Iss. 11, pp. e1009088-e1009088
Open Access | Times Cited: 22
Genetics of Cardiovascular Disease: Fishing for Causality
Christoph Paone, Federica Diofano, Deung-Dae Park, et al.
Frontiers in Cardiovascular Medicine (2018) Vol. 5
Open Access | Times Cited: 23
Does triclosan adsorption on polystyrene nanoplastics modify the toxicity of single contaminants?
Camilla Carla Parenti, Stefano Magni, Anna Ghilardi, et al.
Environmental Science Nano (2020) Vol. 8, Iss. 1, pp. 282-296
Open Access | Times Cited: 20
Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy
Nozomu Yoshioka, Masayuki Kurose, Masato Yano, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 10
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
Nir Pillar, Oren Pleniceanu, Mingyan Fang, et al.
Human Genetics (2017) Vol. 136, Iss. 7, pp. 835-845
Open Access | Times Cited: 17
Identifying Plectin Isoform Functions through Animal Models
M Castañón, Gerhard Wiche
Cells (2021) Vol. 10, Iss. 9, pp. 2453-2453
Open Access | Times Cited: 13
A zebrafish model for FHL1-opathy reveals loss-of-function effects of human FHL1 mutations
Mirjam Keßler, A. Kieltsch, Elham Kayvanpour, et al.
Neuromuscular Disorders (2018) Vol. 28, Iss. 6, pp. 521-531
Open Access | Times Cited: 15
Streamlining drug discovery assays for cardiovascular disease using zebrafish
Alexander Pott, Wolfgang Rottbauer, Steffen Just
Expert Opinion on Drug Discovery (2019) Vol. 15, Iss. 1, pp. 27-37
Open Access | Times Cited: 15
Human Mutated MYOT and CRYAB Genes Cause a Myopathic Phenotype in Zebrafish
Elena Cannone, Valeria Guglielmi, Giulia Marchetto, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11483-11483
Open Access | Times Cited: 4
Versatile Genome Engineering Techniques Advance Human Ocular Disease Researches in Zebrafish
Sisi Zheng, Ru‐Yi Han, Lue Xiang, et al.
Frontiers in Cell and Developmental Biology (2018) Vol. 6
Open Access | Times Cited: 12
CRISPR/Cas9-Mediated Constitutive Loss of VCP (Valosin-Containing Protein) Impairs Proteostasis and Leads to Defective Striated Muscle Structure and Function In Vivo
Philipp Voisard, Federica Diofano, Amelia A. Glazier, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 12, pp. 6722-6722
Open Access | Times Cited: 7
How the expression of green fluorescent protein and human cardiac actin in the heart influences cardiac function and aerobic performance in zebrafish Danio rerio
Sean R. Avey, Matiyo Ojehomon, John Dawson, et al.
Journal of Fish Biology (2017) Vol. 92, Iss. 1, pp. 177-189
Closed Access | Times Cited: 8
Semi-automated detection of fractional shortening in zebrafish embryo heart videos
Sara Nasrat, Daniel Marcato, Sofia Hirth, et al.
Current Directions in Biomedical Engineering (2016) Vol. 2, Iss. 1, pp. 233-236
Open Access | Times Cited: 7
A compactunc45b‐promoter drives muscle‐specific expression in zebrafish and mouse
Steven Rudeck, Christelle Etard, Muzamil Majid Khan, et al.
genesis (2016) Vol. 54, Iss. 8, pp. 431-438
Open Access | Times Cited: 5
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model
Emily A. McKaige, Clara Lee, Vanessa Calcinotto, et al.
Human Molecular Genetics (2024) Vol. 33, Iss. 14, pp. 1195-1206
Open Access
Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy
Nozomu Yoshioka, Masayuki Kurose, Masato Yano, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
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