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:

Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models
Anny Devoy, Georgia Price, Francesca De Giorgio, et al.
iScience (2021) Vol. 24, Iss. 12, pp. 103463-103463
Open Access | Times Cited: 13

Showing 13 citing articles:

Opinion: more mouse models and more translation needed for ALS
Elizabeth Fisher, Linda Greensmith, Andrea Malaspina, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 24

Generation ofC9orf72h370mice, an intron 1 humanisedC9orf72repeat-expansion knock-in model
R. Nair, Mireia Carcolé, David Thompson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Drug repurposing in amyotrophic lateral sclerosis (ALS)
Emily Carroll, Jakub Scaber, K. Huber, et al.
Expert Opinion on Drug Discovery (2025)
Open Access

The power of mouse models in the diagnostic odyssey of patients with rare congenital anomalies
Stephen R.F. Twigg, Nicholas D. E. Greene, Deborah J. Henderson, et al.
Mammalian Genome (2025)
Open Access

Humanized rodent models of neurodegenerative diseases and other brain disorders
X.B Zhang, Jianxiang Wang, Jiewen Zhang, et al.
Neuroscience & Biobehavioral Reviews (2025), pp. 106112-106112
Closed Access

Challenges of modelling TDP-43 pathology in mice
José Miguel Brito Armas, Lucas Taoro-González, Elizabeth Fisher, et al.
Mammalian Genome (2025)
Open Access

Metabolic alterations in the absence of a detectable neuromuscular phenotype in novel genomically humanisedSOD1A4Vmice.
David Thompson, Chloe Williams, Andrew P. Tosolini, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Taf1 knockout is lethal in embryonic male mice and heterozygous females show weight and movement disorders
Elisa M. Crombie, Andrea J. Korecki, Karen Cleverley, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 7
Open Access | Times Cited: 3

Modern Approaches to Mouse Genome Editing Using the CRISPR-Cas Toolbox and Their Applications in Functional Genomics and Translational Research
Cíntia J. Monteiro, David M. Heery, Jonathan B. Whitchurch
Advances in experimental medicine and biology (2023), pp. 13-40
Closed Access | Times Cited: 6

Sectioning and Counting of Motor Neurons in the L3 to L6 Region of the Adult Mouse Spinal Cord
Adele Austin, Lynn Beresford, Georgia Price, et al.
Current Protocols (2022) Vol. 2, Iss. 5
Open Access | Times Cited: 6

A humanized knock-inCol6a1mouse recapitulates a deep-intronic splice-activating variant
Véronique Bolduc, Fady Guirguis, Berit Lubben, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Theme 4 In Vivo Experimental Models

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (2024) Vol. 25, Iss. sup1, pp. 136-157
Open Access

Mouse Models of Amyotrophic Lateral Sclerosis
Eva de Lago, Carmen Rodríguez‐Cueto, Javier Fernández‐Ruíz
Neuromethods (2024), pp. 341-363
Closed Access

Editorial: Peripheral nerve anatomy in health and disease
James N. Sleigh
Journal of Anatomy (2022) Vol. 241, Iss. 5, pp. 1083-1088
Open Access | Times Cited: 2

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