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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:

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
Alistair T. Pagnamenta, Rauan Kaiyrzhanov, Yaqun Zou, et al.
Brain (2020) Vol. 144, Iss. 2, pp. 584-600
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics
Sanjog R. Chintalaphani, Sandy S. Pineda, Ira W. Deveson, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 125
Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing
Igor Stevanovski, Sanjog R. Chintalaphani, Hasindu Gamaarachchi, et al.
Science Advances (2022) Vol. 8, Iss. 9
Open Access | Times Cited: 125
Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences
Terence Gall-Duncan, Nozomu Sato, Ryan K. C. Yuen, et al.
Genome Research (2021) Vol. 32, Iss. 1, pp. 1-27
Open Access | Times Cited: 63
Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease
Christopher J. Record, Menelaos Pipis, Mariola Skorupinska, et al.
Brain (2024) Vol. 147, Iss. 9, pp. 3144-3156
Open Access | Times Cited: 11
Acrolein-inducing ferroptosis contributes to impaired peripheral neurogenesis in zebrafish
Haozhe Qi, Kejia Kan, Carsten Sticht, et al.
Frontiers in Neuroscience (2023) Vol. 16
Open Access | Times Cited: 13
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards
Jevin Parmar, Nigel G. Laing, Marina Kennerson, et al.
Journal of Neurology Neurosurgery & Psychiatry (2024) Vol. 95, Iss. 11, pp. 992-1001
Open Access | Times Cited: 5
The impact of inversions across 33,924 families with rare disease from a national genome sequencing project
Alistair T. Pagnamenta, Jing Yu, Susan Walker, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 6, pp. 1140-1164
Open Access | Times Cited: 5
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Congenital Spinal Muscular Atrophy, Autosomal Dominant (SMA-LED)
Alberto A. Zambon, Stefano C. Previtali
Elsevier eBooks (2025)
Closed Access
Analysis of targeted and whole genome sequencing of PacBio HiFi reads for a comprehensive genotyping of gene-proximal and phenotype-associated Variable Number Tandem Repeats
Sara Javadzadeh, Aaron W. Adamson, Jonghun Park, et al.
PLoS Computational Biology (2025) Vol. 21, Iss. 4, pp. e1012885-e1012885
Open Access
Seizure-like behavior and hyperactivity in napb knockout zebrafish as a model for autism and epilepsy
Kyung Chul Shin, Waseem Hasan, Gowher Ali, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Clinical and Genetic Analysis of Patients With TK2 Deficiency
Francisco C. Ceballos, Pablo Serrano‐Lorenzo, Laura Bermejo‐Guerrero, et al.
Neurology Genetics (2024) Vol. 10, Iss. 2
Open Access | Times Cited: 3
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Engineering cell-derived extracellular matrix for peripheral nerve regeneration
Yingxi Xu, Xianbo Liu, Muhammad Arslan Ahmad, et al.
Materials Today Bio (2024) Vol. 27, pp. 101125-101125
Open Access | Times Cited: 3
Early onset hereditary neuronopathies: an update on non-5qmotor neuron diseases
Alberto A. Zambon, Veronica Pini, Luca Bosco, et al.
Brain (2022) Vol. 146, Iss. 3, pp. 806-822
Open Access | Times Cited: 14
Hereditary motor neuropathies
Marina Frasquet, Teresa Sevilla
Current Opinion in Neurology (2022)
Closed Access | Times Cited: 12
Proteomic studies in VWA1‐related neuromyopathy allowed new pathophysiological insights and the definition of blood biomarkers
M. Athamneh, Nassam Daya, Andreas Hentschel, et al.
Journal of Cellular and Molecular Medicine (2024) Vol. 28, Iss. 8
Open Access | Times Cited: 2
Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish
Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 15
vwa1 Knockout in Zebrafish Causes Abnormal Craniofacial Chondrogenesis by Regulating FGF Pathway
Xiaomin Niu, Fuyu Zhang, Lu Ping, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 838-838
Open Access | Times Cited: 6
Riboflavin transporter deficiency

Definitions (2020)
Open Access | Times Cited: 12
Charcot–Marie–Tooth disease due to MORC2 mutations in Spain
Rafael Sivera, Vincenzo Lupo, Marina Frasquet, et al.
European Journal of Neurology (2021) Vol. 28, Iss. 9, pp. 3001-3011
Open Access | Times Cited: 11
RNA Gain-of-Function Mechanisms in Short Tandem Repeat Diseases
Mackenzie L. Davenport, Maurice S. Swanson
RNA (2024), pp. rna.080277.124-rna.080277.124
Closed Access | Times Cited: 1
Methylome and Transcriptome-Based Integration Analysis Identified Molecular Signatures Associated With Meningitis Induced by Glaesserella parasuis
Ling Guo, Hongxin Chen, Shulin Fu, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 7
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome: genetic and clinical insights
Roisin Sullivan, Rauan Kaiyrzhanov, Henry Houlden
Current Opinion in Neurology (2021) Vol. 34, Iss. 4, pp. 556-564
Open Access | Times Cited: 9
Genetic characterization of non-5q proximal spinal muscular atrophy in a French cohort: the place of whole exome sequencing
Julian Theuriet, Gorka Fernández‐Eulate, Philippe Latour, et al.
European Journal of Human Genetics (2023)
Open Access | Times Cited: 3
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