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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:

Primary Cilia in Brain Development and Diseases
Yong Ha Youn, Young-Goo Han
American Journal Of Pathology (2017) Vol. 188, Iss. 1, pp. 11-22
Open Access | Times Cited: 141

Showing 1-25 of 141 citing articles:

The regulatory roles of motile cilia in CSF circulation and hydrocephalus
Vijay Kumar, Zobia Umair, Shiv Kumar, et al.
Fluids and Barriers of the CNS (2021) Vol. 18, Iss. 1
Open Access | Times Cited: 75
Cellular and evolutionary perspectives on organismal cognition: from unicellular to multicellular organisms
František Baluška, William B. Miller, Arthur S. Reber
Biological Journal of the Linnean Society (2022) Vol. 139, Iss. 4, pp. 503-513
Closed Access | Times Cited: 67
Exposure to cadmium induces neuroinflammation and impairs ciliogenesis in hESC-derived 3D cerebral organoids
Yan Huang, Yanping Dai, Min Li, et al.
The Science of The Total Environment (2021) Vol. 797, pp. 149043-149043
Closed Access | Times Cited: 60
Cellular and Molecular Mechanisms of Pathogenesis Underlying Inherited Retinal Dystrophies
Andrew Manley, Bahar I. Meshkat, Monica M. Jablonski, et al.
Biomolecules (2023) Vol. 13, Iss. 2, pp. 271-271
Open Access | Times Cited: 24
Neuronal and astrocytic primary cilia in the mature brain
Ashley Sterpka, Xuanmao Chen
Pharmacological Research (2018) Vol. 137, pp. 114-121
Open Access | Times Cited: 71
Long-read assembly of the Chinese rhesus macaque genome and identification of ape-specific structural variants
Yaoxi He, Xin Luo, Bin Zhou, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 70
TTBK2 and primary cilia are essential for the connectivity and survival of cerebellar Purkinje neurons
Emily Bowie, Sarah C. Goetz
eLife (2020) Vol. 9
Open Access | Times Cited: 68
Ciliary neuropeptidergic signaling dynamically regulates excitatory synapses in postnatal neocortical pyramidal neurons
Lauren Tereshko, Ya Gao, Brian Cary, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 41
Ciliary transition zone proteins coordinate ciliary protein composition and ectosome shedding
Liang Wang, Wen X, Zhengmao Wang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 31
Silver nanoparticles exposure induces developmental neurotoxicity in hiPSC-derived cerebral organoids
Yan Huang, Lulu Guo, Chulin Cao, et al.
The Science of The Total Environment (2022) Vol. 845, pp. 157047-157047
Closed Access | Times Cited: 30
TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system
Shyam K. Akula, Jack H. Marciano, Youngshin Lim, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 4
Open Access | Times Cited: 17
Permanent deconstruction of intracellular primary cilia in differentiating granule cell neurons
Carolyn Ott, Sandii Constable, Tri Nguyen, et al.
The Journal of Cell Biology (2024) Vol. 223, Iss. 10
Open Access | Times Cited: 7
Congenital hydrocephalus: a review of recent advances in genetic etiology and molecular mechanisms
Xiuyun Liu, Xin Song, Marek Czosnyka, et al.
Military Medical Research (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 6
The 5-HT6 receptor interactome: New insight in receptor signaling and its impact on brain physiology and pathologies
Séverine Chaumont‐Dubel, Vincent Dupuy, Joël Bockaert, et al.
Neuropharmacology (2019) Vol. 172, pp. 107839-107839
Open Access | Times Cited: 47
Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease
Ketu Mishra-Gorur, Tanyeri Barak, Leon D. Kaulen, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 16
Open Access | Times Cited: 13
The DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study
Christiane Ziegler, Franziska Grundner-Culemann, Miriam A. Schiele, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 38
Cilia in hereditary cerebral anomalies
Sophie Thomas, Lucile Boutaud, Madeline Louise Reilly, et al.
Biology of the Cell (2019) Vol. 111, Iss. 9, pp. 217-231
Open Access | Times Cited: 36
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders
Angelisa Frasca, Eleonora Spiombi, Michela Palmieri, et al.
EMBO Molecular Medicine (2020) Vol. 12, Iss. 6
Open Access | Times Cited: 34
MECP2 and the biology of MECP2 duplication syndrome
Santosh R. D’Mello
Journal of Neurochemistry (2021) Vol. 159, Iss. 1, pp. 29-60
Open Access | Times Cited: 29
Ciliogenesis defects after neurulation impact brain development and neuronal activity in larval zebrafish
Percival P D'Gama, Inyoung Jeong, Andreas Moe Nygård, et al.
iScience (2024) Vol. 27, Iss. 6, pp. 110078-110078
Open Access | Times Cited: 4
NUBP2 deficiency disrupts the centrosome‐check point in the brain and causes primary microcephaly
Rebecca Rushforth, Hanan E. Shamseldin, Nicole Costantino, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Co-Conservation of Synaptic Gene Expression and Circuitry in Collicular Neurons
Yuanming Liu, J McDaniel, Chen Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
A Novel Pathogenic Splicing Mutation of OFD1 is Responsible for a Boy with Joubert Syndrome Exhibiting Orofaciodigital Spectrum Anomalies, Polydactyly and Retinitis Pigmentosa
Liang Chen, Mei-Fang Zhao, Hongjun Deng, et al.
Pharmacogenomics and Personalized Medicine (2025) Vol. Volume 18, pp. 47-53
Open Access
Investigating the Role of the Zinc Finger Protein ZC2HC1C on Autism Spectrum Disorder Susceptibility
Simone Treccarichi, Mirella Vinci, Antonino Musumeci, et al.
Medicina (2025) Vol. 61, Iss. 4, pp. 574-574
Open Access
Tet2 loss and enhanced ciliogenesis suppress α-synuclein pathology
Quansah Emmanuel, Naman Vatsa, Elizabeth Ensink, et al.
Acta Neuropathologica Communications (2025) Vol. 13, Iss. 1
Open Access
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