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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:

Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia
Claudia Schob, Maja Hempel, Dana Šafka Brožková, et al.
Annals of Neurology (2021) Vol. 90, Iss. 5, pp. 738-750
Open Access | Times Cited: 9

Showing 9 citing articles:

Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia
Wei Qiao, Wenlu Fan, Hong‐Fu Li, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2025)
Closed Access
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia
Yiqiang Zhi, Yan Shi, Danping Lu, et al.
CNS Neuroscience & Therapeutics (2025) Vol. 31, Iss. 2
Open Access
Genetic regulation of gene expression across multiple tissues in chickens
Dailu Guan, Zhonghao Bai, Xiaoning Zhu, et al.
Nature Genetics (2025)
Closed Access
Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up
Aliénor Jaillard, Stéphanie Valence, Saskia Vande Perre, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 1, pp. 35-48
Open Access | Times Cited: 3
Communicating pain: emerging axonal signaling in peripheral neuropathic pain
Livia Testa, Sofia Dotta, Alessandro Vercelli, et al.
Frontiers in Neuroanatomy (2024) Vol. 18
Open Access | Times Cited: 2
KPNA3 regulates histone locus body formation by modulating condensation and nuclear import of NPAT
Shui Bo Xu, Xiu Kui Gao, Hanghua Liang, et al.
The Journal of Cell Biology (2024) Vol. 224, Iss. 1
Closed Access | Times Cited: 1
Long-read sequencing revealing intragenic deletions in exome-negative spastic paraplegias
Hiromi Fukuda, Takeshi Mizuguchi, Hiroshi Doi, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 10, pp. 689-697
Closed Access | Times Cited: 3
A Recurrent KPNA3 Missense Variant Causing Infantile Pure Spastic Paraplegia
Jonathan De Winter, Liedewei Van de Vondel, Stephan Züchner, et al.
Annals of Neurology (2022) Vol. 91, Iss. 2, pp. 298-299
Open Access | Times Cited: 1
Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia
Yijun Chen, Mengwen Wang, Yusen Qiu, et al.
Movement Disorders (2023) Vol. 38, Iss. 9, pp. 1750-1755
Closed Access
Heterozygous De Novo KPNA3 Mutations Cause Complex Hereditary Spastic Paraplegia
Mehrdad A. Estiar, Gurnoor Lail, David A. Dyment, et al.
Annals of Neurology (2021) Vol. 91, Iss. 5, pp. 730-732
Closed Access
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