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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:

Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A ( KIF1A )
Simranpreet Kaur, Nicole J. Van Bergen, Kristen J. Verhey, et al.
Human Mutation (2020) Vol. 41, Iss. 10, pp. 1761-1774
Open Access | Times Cited: 24

Showing 24 citing articles:

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
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
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
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
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
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
Axonal mRNA translation in neurological disorders
Julie Qiaojin Lin, Francesca W. van Tartwijk, Christine E. Holt
RNA Biology (2020) Vol. 18, Iss. 7, pp. 936-961
Open Access | Times Cited: 27
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
Ophthalmic findings in the KIF1A-associated neurological disorder (KAND)
Aliaa H. Abdelhakim, Scott E. Brodie, Wendy K. Chung
American Journal of Ophthalmology (2024) Vol. 268, pp. 247-257
Closed Access | Times Cited: 2
Kinesins in Mammalian Spermatogenesis and Germ Cell Transport
Mingxia Yao, Haoyang Qu, Yating Han, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 10
Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics
Govinda Sharma, Gerald Pfeffer, Timothy E. Shutt
Biology (2021) Vol. 10, Iss. 4, pp. 268-268
Open Access | Times Cited: 14
The Novel KIF1A Missense Variant (R169T) Strongly Reduces Microtubule Stimulated ATPase Activity and Is Associated With NESCAV Syndrome
Cinthia Aguilera, Stefan Hümmer, Marc Masanas, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 14
Kinesin-3 motors are fine-tuned at the molecular level to endow distinct mechanical outputs
Pushpanjali Soppina, Nishaben Patel, Dipeshwari J. Shewale, et al.
BMC Biology (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 9
Expanding the Knowledge of KIF1A-Dependent Disorders to a Group of Polish Patients
Justyna Paprocka, Aleksandra Jezela‐Stanek, Robert Śmigiel, et al.
Genes (2023) Vol. 14, Iss. 5, pp. 972-972
Open Access | Times Cited: 5
Multiple layers of spatial regulation coordinate axonal cargo transport
Eitan Erez Zahavi, Casper C. Hoogenraad
Current Opinion in Neurobiology (2021) Vol. 69, pp. 241-246
Open Access | Times Cited: 11
Roles of four targets in the pathogenesis of graves' orbitopathy
Ziqiang Ren, Hailing Zhang, Haiwen Yu, et al.
Heliyon (2023) Vol. 9, Iss. 9, pp. e19250-e19250
Open Access | Times Cited: 4
Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract
Mauro Lecca, Lucia Mauri, Simone Gana, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 403-412
Closed Access | Times Cited: 1
Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement
Min‐Yu Lan, Chin‐Song Lu, Shey‐Lin Wu, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 3
Genotype and defects in microtubule-based motility correlate with clinical severity in KIF1A Associated Neurological Disorder
Lia Boyle, Lu Rao, Simranpreet Kaur, et al.
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2
A Highly Conserved 310-Helix Within the Kinesin Motor Domain is Critical for Kinesin Function and Human Health
Aileen J. Lam, Lu Rao, Yuzu Anazawa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2
Enfermedad neurológica asociada al gen KIF1A: correlación genotipo/fenotipo
Ana Ortiz‐Ortigosa, Rocío Calvo Medina, C. Ruiz-García, et al.
Revista de Neurología (2023) Vol. 77, Iss. 06, pp. 141-141
Open Access
Autosomal dominant neurodevelopmental disorders associated with <italic>KIF1A</italic> gene variants in 6 pediatric patients
Jingqi Lin, Niu Li, Ruen Yao, et al.
Journal of Zhejiang University (Medical Sciences) (2023) Vol. 52, Iss. 6, pp. 693-700
Open Access
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