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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:

Glycine-alanine dipeptide repeats spread rapidly in a repeat length- and age-dependent manner in the fly brain
Javier Morón-Oset, Tessa Supèr, Jacqueline Eßer, et al.
Acta Neuropathologica Communications (2019) Vol. 7, Iss. 1
Open Access | Times Cited: 19

Showing 19 citing articles:

Molecular Chaperones: A Double-Edged Sword in Neurodegenerative Diseases
Jessica Tittelmeier, Eliana Nachman, Carmen Nussbaum‐Krammer
Frontiers in Aging Neuroscience (2020) Vol. 12
Open Access | Times Cited: 78
Intercellular transmission of pathogenic proteins in ALS: Exploring the pathogenic wave
Frederick J. Arnold, Ashlie Nguyen, Richard Bedlack, et al.
Neurobiology of Disease (2023) Vol. 184, pp. 106218-106218
Open Access | Times Cited: 15
Co-expression of C9orf72 related dipeptide-repeats over 1000 repeat units reveals age- and combination-specific phenotypic profiles in Drosophila
Ryan J. H. West, Joanne L. Sharpe, André Voelzmann, et al.
Acta Neuropathologica Communications (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 33
Fly for ALS: Drosophila modeling on the route to amyotrophic lateral sclerosis modifiers
Francesco Liguori, Susanna Amadio, Cinzia Volonté
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 17-18, pp. 6143-6160
Open Access | Times Cited: 30
Amyotrophic Lateral Sclerosis Genes in Drosophila melanogaster
Sophie Layalle, Laetitia They, Sarah Ourghani, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 2, pp. 904-904
Open Access | Times Cited: 25
Inducible expression of human C9ORF72 36× G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice
Fréderike W. Riemslagh, Esmay C. van der Toorn, Rob F. M. Verhagen, et al.
Disease Models & Mechanisms (2021) Vol. 14, Iss. 2
Open Access | Times Cited: 18
RAN proteins in neurodegenerative disease: Repeating themes and unifying therapeutic strategies
Shu Guo, Lien Nguyen, Laura P.W. Ranum
Current Opinion in Neurobiology (2021) Vol. 72, pp. 160-170
Open Access | Times Cited: 16
Promising animal models for amyotrophic lateral sclerosis drug discovery: a comprehensive update
Léa Lescouzères, Scott B. Patten
Expert Opinion on Drug Discovery (2024) Vol. 19, Iss. 10, pp. 1213-1233
Open Access | Times Cited: 2
Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity
Craig L. Bennett, Somasish Ghosh Dastidar, Frederick J. Arnold, et al.
Acta Neuropathologica Communications (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 5
Prion-like properties of the mutant huntingtin protein in living organisms: the evidence and the relevance
Melanie Alpaugh, Hélèna L. Denis, Francesca Cicchetti
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 269-280
Closed Access | Times Cited: 12
Toxicity ofC9orf72-associated dipeptide repeat peptides is modified by commonly used protein tags
Javier Morón-Oset, Lilly KS Fischer, Mireia Carcolé, et al.
Life Science Alliance (2023) Vol. 6, Iss. 9, pp. e202201739-e202201739
Open Access | Times Cited: 4
Repeat length of C9orf72-associated glycine–alanine polypeptides affects their toxicity
Javier Morón-Oset, Lilly Katharina Sophie Fischer, Nathalie Jauré, et al.
Acta Neuropathologica Communications (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 4
Drosophila appear resistant to trans-synaptic tau propagation
James H. Catterson, Edmond N Mouofo, Inés López De Toledo Soler, et al.
Brain Communications (2024) Vol. 6, Iss. 4
Open Access | Times Cited: 1
C9ORF72-derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons
Paolo Marchi, Lara Marrone, Laurent Brasseur, et al.
Life Science Alliance (2022) Vol. 5, Iss. 9, pp. e202101276-e202101276
Open Access | Times Cited: 7
Conformational dynamics in the disordered region of human CPEB3 linked to memory consolidation
Daniel Ramírez de Mingo, David Pantoja‐Uceda, Rubén Hervás, et al.
BMC Biology (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 7
Modeling C9orf72-Related Frontotemporal Dementia and Amyotrophic Lateral Sclerosis in Drosophila
Joanne L. Sharpe, Nikki S. Harper, Duncan R. Garner, et al.
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 7
Preferred conformations in the disordered region of human CPEB3, a functional amyloid linked to memory consolidation
Daniel Ramírez de Mingo, David Pantoja‐Uceda, Rubén Hervás, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 6
Inducible expression of human C9ORF72 36x G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice
Fréderike W. Riemslagh, Esmay C. van der Toorn, Rob F. M. Verhagen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access
C9orf72-derived poly-GA DPRs undergo endocytic uptake in iNPC-derived astrocytes and spread to motor neurons
Paolo Marchi, Lara Marrone, Laurent Brasseur, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
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