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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:

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

Showing 18 citing articles:

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
Preparing for Patient-Customized N-of-1 Antisense Oligonucleotide Therapy to Treat Rare Diseases
Harry Wilton-Clark, Eric Yan, Toshifumi Yokota
Genes (2024) Vol. 15, Iss. 7, pp. 821-821
Open Access | Times Cited: 5
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 possible genetic predisposition to suspected hypoxic-ischaemic encephalopathy
Megan A. Holborn, Juanita Mellet, Fourie Joubert, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2025) Vol. 1871, Iss. 4, pp. 167732-167732
Open 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
Preparing for patient-customized N-of-1 Antisense Oligonucleotide Therapy to Treat Rare Diseases
Harry Wilton-Clark, Eric Yan, Toshifumi Yokota
(2024)
Open Access | Times Cited: 3
Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications
Sara Mansoorshahi, Anji T. Yetman, Malenka M. Bissell, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 10, pp. 2219-2231
Open Access | Times Cited: 3
Peripheral mechanisms of peripheral neuropathic pain
Paola Pacifico, James S. Coy-Dibley, Richard J. Miller, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 7
Genotypic and phenotypic analysis of 173 patients with extremely rare pathogenic mutations who applied for experimental antisense oligonucleotide treatment
Stanley T. Crooke, Tracy Cole, Jeffrey B. Carroll, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Kif1a and intact microtubules maintain synaptic‐vesicle populations at ribbon synapses in zebrafish hair cells
Sandeep David, Katherine Pinter, Keziah‐Khue Nguyen, et al.
The Journal of Physiology (2024)
Open Access | Times Cited: 1
Whole Exome Sequencing Uncovers the Genetic Complexity of Bicuspid Aortic Valve in Families with Early Onset Complications
Sara Mansoorshahi, Anji T. Yetman, Malenka M. Bissell, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Genetic Alterations in a Large Population of Italian Patients Affected by Neurodevelopmental Disorders
Annaluisa Ranieri, Ilaria La Monica, Maria Rosaria Di Iorio, et al.
Genes (2024) Vol. 15, Iss. 4, pp. 427-427
Open Access
Long‐term clinical observation of patients with heterozygous KIF1A variants
Aritomo Kawashima, Kaori Kodama, Yukimune Okubo, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 10
Closed Access
Kif1a and intact microtubules maintain synaptic-vesicle populations at ribbon synapses in zebrafish hair cells
Sandeep David, Katherine Pinter, Keziah‐Khue Nguyen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Striving for inclusivity: the crucial function of neurorehabilitation in the management of KIF1A syndrome
Seema Saini, Neelam Hitesh Tejani, Amrutkuvar Rayjade
Frontiers in Neurology (2024) Vol. 15
Open Access
Integrative ceRNA network analysis identifies unique and shared molecular signatures in Bipolar Disorder and Schizophrenia
Rachayita Bharadwaj, Prangan Nath, Jadab Kishore Phukan, et al.
Journal of Psychiatric Research (2024) Vol. 176, pp. 47-57
Closed Access
Feature Reviews in Pharmaceutical Technology
Silviya P. Zustiak, Era Jain
Pharmaceuticals (2023) Vol. 16, Iss. 10, pp. 1336-1336
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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