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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:

Genotype and defects in microtubule-based motility correlate with clinical severity in KIF1A-associated neurological disorder
Lia Boyle, Lu Rao, Simranpreet Kaur, et al.
Human Genetics and Genomics Advances (2021) Vol. 2, Iss. 2, pp. 100026-100026
Open Access | Times Cited: 67

Showing 1-25 of 67 citing articles:

Pathogenic mutations in the kinesin-3 motor KIF1A diminish force generation and movement through allosteric mechanisms
Breane Budaitis, Shashank Jariwala, Lu Rao, et al.
The Journal of Cell Biology (2021) Vol. 220, Iss. 4
Open Access | Times Cited: 78
Microtubule lattice spacing governs cohesive envelope formation of tau family proteins
Valerie Siahaan, Ruensern Tan, Tereza Humhalová, et al.
Nature Chemical Biology (2022) Vol. 18, Iss. 11, pp. 1224-1235
Open Access | Times Cited: 45
De novo mutations in KIF1A-associated neuronal disorder (KAND) dominant-negatively inhibit motor activity and axonal transport of synaptic vesicle precursors
Yuzu Anazawa, Tomoki Kita, Rei Iguchi, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 32
Open Access | Times Cited: 43
An ALS‐associated KIF5A mutant forms oligomers and aggregates and induces neuronal toxicity
Juri Nakano, Kyoko Chiba, Shinsuke Niwa
Genes to Cells (2022) Vol. 27, Iss. 6, pp. 421-435
Open Access | Times Cited: 40
Insight into the regulation of axonal transport from the study of KIF1A-associated neurological disorder
Kyoko Chiba, Tomoki Kita, Yuzu Anazawa, et al.
Journal of Cell Science (2023) Vol. 136, Iss. 5
Open Access | Times Cited: 30
Phosphatidylinositol 3,5-bisphosphate facilitates axonal vesicle transport and presynapse assembly
Filiz Sila Rizalar, Max Thomas Lucht, Astrid G. Petzoldt, et al.
Science (2023) Vol. 382, Iss. 6667, pp. 223-230
Open Access | Times Cited: 24
Neurogenetic disorders across the lifespan: from aberrant development to degeneration
Richard A. Hickman, Sarah A. O’Shea, Mark F. Mehler, et al.
Nature Reviews Neurology (2022) Vol. 18, Iss. 2, pp. 117-124
Open Access | Times Cited: 34
KIF1A-Associated Neurological Disorder: An Overview of a Rare Mutational Disease
Ayushi Nair, Alosh Greeny, Rajalakshmi Rajendran, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 2, pp. 147-147
Open Access | Times Cited: 18
Antisense oligonucleotide therapy in an individual with KIF1A-associated neurological disorder
Alban Ziegler, Joanne Carroll, Jennifer Bain, et al.
Nature Medicine (2024) Vol. 30, Iss. 10, pp. 2782-2786
Closed Access | Times Cited: 7
A highly conserved 3 10 helix within the kinesin motor domain is critical for kinesin function and human health
Aileen J. Lam, Lu Rao, Yuzu Anazawa, et al.
Science Advances (2021) Vol. 7, Iss. 18
Open Access | Times Cited: 40
Presynaptic perspective: Axonal transport defects in neurodevelopmental disorders
Gui-Jing Xiong, Zu‐Hang Sheng
The Journal of Cell Biology (2024) Vol. 223, Iss. 6
Open Access | Times Cited: 5
Mechanism and regulation of kinesin motors
Ahmet Yıldız
Nature Reviews Molecular Cell Biology (2024)
Closed Access | Times Cited: 5
Comparative analysis of two Caenorhabditis elegans kinesins KLP-6 and UNC-104 reveals a common and distinct activation mechanism in kinesin-3
Tomoki Kita, Kyoko Chiba, Jiye Wang, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 11
Cryo-EM unveils kinesin KIF1A’s processivity mechanism and the impact of its pathogenic variant P305L
Matthieu P. M. H. Benoit, Lu Rao, Ana B. Asenjo, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
The de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Turkish casein a case
S. Barış, Efe Can
Research Square (Research Square) (2025)
Open Access
A Two-Heads-Bound State Drives KIF1A Superprocessivity
Lu Rao, Jan Otto Wirth, Jessica Matthias, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
The Huntingtin Transport Complex
Emily N. P. Prowse, Brooke A. Turkalj, Lale Gursu, et al.
Biochemistry (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
Modular photostable fluorescent DNA blocks dissect the effects of pathogenic mutant kinesin on collective transport
Tomoki Kita, Ryota Sugie, Yuki Suzuki, et al.
Cell Reports Physical Science (2025), pp. 102440-102440
Open Access
Distinct Clinical Phenotypes in KIF1A-Associated Neurological Disorders Result from Different Amino Acid Substitutions at the Same Residue in KIF1A
Lu Rao, Wenxing Li, Yufeng Shen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Insights on the Shared Genetic Landscape of Neurodevelopmental and Movement Disorders
Elisabetta Indelicato, Michael Zech, Anja Eberl, et al.
Current Neurology and Neuroscience Reports (2025) Vol. 25, Iss. 1
Open Access
Novel KIF1A Variant in a Patient with Cerebellar Atrophy and Ataxia: A Case Report
Sema Akkuş, Ayuko A Iverson, Winona Tse
The Cerebellum (2025) Vol. 24, Iss. 3
Closed Access
A plant flavonol and genetic suppressors rescue a pathogenic mutation associated with kinesin in neurons
Yongping Chai, Dong Li, Weibin Gong, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 5
Open Access | Times Cited: 3
Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A-associated neurological disorder
Khemika K. Sudnawa, Wenxing Li, Sean Calamia, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 8, pp. 101169-101169
Open Access | Times Cited: 3
Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, Alessandra Tessa, Claudia Dosi, et al.
Journal of Neurology (2021) Vol. 269, Iss. 1, pp. 437-450
Closed Access | Times Cited: 18
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