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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:

FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention
Jack Humphrey, Nicol Birsa, Carmelo Milioto, et al.
Nucleic Acids Research (2020) Vol. 48, Iss. 12, pp. 6889-6905
Open Access | Times Cited: 90

Showing 1-25 of 90 citing articles:

TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
Anna‐Leigh Brown, Oscar G. Wilkins, Matthew J. Keuss, et al.
Nature (2022) Vol. 603, Iss. 7899, pp. 131-137
Open Access | Times Cited: 313
Antisense oligonucleotide silencing of FUS expression as a therapeutic approach in amyotrophic lateral sclerosis
Vladislav A. Korobeynikov, Alexander K. Lyashchenko, Beatriz Blanco-Redondo, et al.
Nature Medicine (2022) Vol. 28, Iss. 1, pp. 104-116
Open Access | Times Cited: 186
Alternative splicing in neurodegenerative disease and the promise of RNA therapies
David Nikom, Sika Zheng
Nature reviews. Neuroscience (2023) Vol. 24, Iss. 8, pp. 457-473
Closed Access | Times Cited: 81
RNA dysregulation in neurodegenerative diseases
Yini Li, Shuying Sun
The EMBO Journal (2025) Vol. 44, Iss. 3, pp. 613-638
Open Access | Times Cited: 3
Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implications
Thomas G. Moens, Sandrine Da Cruz, Manuela Neumann, et al.
The Lancet Neurology (2025) Vol. 24, Iss. 2, pp. 166-178
Closed Access | Times Cited: 3
The role of hnRNPs in frontotemporal dementia and amyotrophic lateral sclerosis
Alexander Bampton, Lauren M. Gittings, Pietro Fratta, et al.
Acta Neuropathologica (2020) Vol. 140, Iss. 5, pp. 599-623
Open Access | Times Cited: 95
Gene architecture directs splicing outcome in separate nuclear spatial regions
Luna Tammer, Ofir Hameiri, Ifat Keydar, et al.
Molecular Cell (2022) Vol. 82, Iss. 5, pp. 1021-1034.e8
Open Access | Times Cited: 52
Lost in local translation: TDP-43 and FUS in axonal/neuromuscular junction maintenance and dysregulation in amyotrophic lateral sclerosis
Diana Piol, Tessa Robberechts, Sandrine Da Cruz
Neuron (2023) Vol. 111, Iss. 9, pp. 1355-1380
Open Access | Times Cited: 26
Nuclear pore dysfunction and disease: a complex opportunity
Charlotte M. Fare, Jeffrey D. Rothstein
Nucleus (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
Targeting common disease pathomechanisms to treat amyotrophic lateral sclerosis
Kiterie M. E. Faller, Helena Chaytow, Thomas H. Gillingwater
Nature Reviews Neurology (2025) Vol. 21, Iss. 2, pp. 86-102
Closed Access | Times Cited: 1
Aberrant interaction of FUS with the U1 snRNA provides a molecular mechanism of FUS induced amyotrophic lateral sclerosis
Daniel Jutzi, Sébastien Campagne, Ralf Schmidt, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 60
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
Nicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Science Advances (2021) Vol. 7, Iss. 30
Open Access | Times Cited: 52
Synaptic dysfunction in ALS and FTD: anatomical and molecular changes provide insights into mechanisms of disease
Pauline A. Gelon, Paul A. Dutchak, Chantelle F. Sephton
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 35
Widespread intron retention impairs protein homeostasis in C9orf72 ALS brains
Qingqing Wang, Erin G. Conlon, James L. Manley, et al.
Genome Research (2020) Vol. 30, Iss. 12, pp. 1705-1715
Open Access | Times Cited: 41
HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing
Alexander Bampton, Ariana Gatt, Jack Humphrey, et al.
Acta Neuropathologica (2021) Vol. 142, Iss. 4, pp. 609-627
Open Access | Times Cited: 36
Transposable element sequence fragments incorporated into coding and noncoding transcripts modulate the transcriptome of human pluripotent stem cells
Isaac A. Babarinde, Gang Ma, Yuhao Li, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 16, pp. 9132-9153
Open Access | Times Cited: 35
Pathological insights from amyotrophic lateral sclerosis animal models: comparisons, limitations, and challenges
Longhong Zhu, Shihua Li, Xiao‐Jiang Li, et al.
Translational Neurodegeneration (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 14
Disruption of MAM integrity in mutant FUS oligodendroglial progenitors from hiPSCs
Yingli Zhu, Thibaut Burg, Katrien Neyrinck, et al.
Acta Neuropathologica (2024) Vol. 147, Iss. 1
Open Access | Times Cited: 5
Disruption of nuclear speckle integrity dysregulates RNA splicing in C9ORF72-FTD/ALS
Rong Wu, Yingzhi Ye, Daoyuan Dong, et al.
Neuron (2024) Vol. 112, Iss. 20, pp. 3434-3451.e11
Closed Access | Times Cited: 5
ALS-related FUS mutations alter axon growth in motoneurons and affect HuD/ELAVL4 and FMRP activity
Maria Giovanna Garone, Nicol Birsa, Maria Rosito, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 31
Where and Why Modeling Amyotrophic Lateral Sclerosis
Francesco Liguori, Susanna Amadio, Cinzia Volonté
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 3977-3977
Open Access | Times Cited: 27
Prematurely terminated intron-retaining mRNAs invade axons in SFPQ null-driven neurodegeneration and are a hallmark of ALS
Richard Taylor, Fursham Hamid, Triona Fielding, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 19
G-quadruplexes control hepatitis B virus replication by promoting cccDNA transcription and phase separation in hepatocytes
Guillaume Giraud, Mélanie Rodà, Pélagie Huchon, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. 5, pp. 2290-2305
Open Access | Times Cited: 12
FUS Alters circRNA Metabolism in Human Motor Neurons Carrying the ALS-Linked P525L Mutation
Alessio Colantoni, Davide Capauto, Vincenzo Alfano, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3181-3181
Open Access | Times Cited: 11
Molecular mechanisms of amyotrophic lateral sclerosis as broad therapeutic targets for gene therapy applications utilizing adeno‐associated viral vectors
Jessica Merjane, Roger S. Chung, Rickie Patani, et al.
Medicinal Research Reviews (2023) Vol. 43, Iss. 4, pp. 829-854
Open Access | Times Cited: 11
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