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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:

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability
Weihao Zhao, Xue Gao, Shiwei Qiu, et al.
EBioMedicine (2019) Vol. 45, pp. 408-421
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

The emerging roles of vacuolar-type ATPase-dependent Lysosomal acidification in neurodegenerative diseases
Qiao‐Yun Song, Bo Meng, Haidong Xu, et al.
Translational Neurodegeneration (2020) Vol. 9, Iss. 1
Open Access | Times Cited: 148
The H+-ATPase (V-ATPase): from proton pump to signaling complex in health and disease
Amity F. Eaton, Maria Merkulova, Dennis Brown
AJP Cell Physiology (2020) Vol. 320, Iss. 3, pp. C392-C414
Open Access | Times Cited: 114
Determinants, maintenance, and function of organellar pH
Spencer A. Freeman, Sergio Grinstein, John Orlowski
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 515-606
Closed Access | Times Cited: 50
Bioinformatics Analysis of Next Generation Sequencing Data Identifies Molecular Biomarkers Associated With Type 2 Diabetes Mellitus
Varun Alur, Varshita Raju, Basavaraj Vastrad, et al.
Clinical Medicine Insights Endocrinology and Diabetes (2023) Vol. 16
Open Access | Times Cited: 17
Single Administration of AAV‐mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2‐Induced Lysosomal Dysfunction in Hair Cells
Guanghua Wei, Shiwei Qiu, Xue Gao, et al.
Advanced Science (2025)
Open Access
Nsp2 has the potential to be a drug target revealed by global identification of SARS-CoV-2 Nsp2-interacting proteins
Yun-xiao Zheng, Lei Wang, Wei-Sha Kong, et al.
Acta Biochimica et Biophysica Sinica (2021) Vol. 53, Iss. 9, pp. 1134-1141
Closed Access | Times Cited: 27
V-ATPase Dysfunction in the Brain: Genetic Insights and Therapeutic Opportunities
Antonio Falace, Greta Volpedo, Marcello Scala, et al.
Cells (2024) Vol. 13, Iss. 17, pp. 1441-1441
Open Access | Times Cited: 4
Malate initiates a proton-sensing pathway essential for pH regulation of inflammation
Yujianan Chen, Ruihua Shi, Yan Xiang, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 4
DOORS syndrome and a recurrent truncating ATP6V1B2 variant
Éliane Beauregard‐Lacroix, G. Pacheco-Cuellar, Norbert Fonya Ajeawung, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 149-154
Open Access | Times Cited: 25
Time-resolved transcriptomics in neural stem cells identifies a v-ATPase/Notch regulatory loop
Sebastian Wissel, Heike Harzer, François Bonnay, et al.
The Journal of Cell Biology (2018) Vol. 217, Iss. 9, pp. 3285-3300
Open Access | Times Cited: 24
ATP6V1A is required for synaptic rearrangements and plasticity in murine hippocampal neurons
Alessandro Esposito, Sara Pepe, Maria Sabina Cerullo, et al.
Acta Physiologica (2024) Vol. 240, Iss. 8
Open Access | Times Cited: 2
Effects of Pyridoxine Deficiency on Hippocampal Function and Its Possible Association with V-Type Proton ATPase Subunit B2 and Heat Shock Cognate Protein 70
Hyo Young Jung, Woosuk Kim, Kyu Ri Hahn, et al.
Cells (2020) Vol. 9, Iss. 5, pp. 1067-1067
Open Access | Times Cited: 17
Molecular Mechanisms and Biological Functions of Autophagy for Genetics of Hearing Impairment
Ken Hayashi, Yuna Suzuki, Chisato Fujimoto, et al.
Genes (2020) Vol. 11, Iss. 11, pp. 1331-1331
Open Access | Times Cited: 17
Comparative analyses of hypothalamus transcriptomes reveal fertility-, growth-, and immune-related genes and signal pathways in different ploidy cyprinid fish
Shengnan Li, Yi Zhou, Conghui Yang, et al.
Genomics (2021) Vol. 113, Iss. 2, pp. 595-605
Closed Access | Times Cited: 15
Gene4HL: An Integrated Genetic Database for Hearing Loss
Shasha Huang, Guihu Zhao, Jie Wu, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 12
Clinicopathological Relationships in an Aged Case of DOORS Syndrome With a p.Arg506X Mutation in the ATP6V1B2 Gene
Dénes Zádori, Levente Szalárdy, Zita Reisz, et al.
Frontiers in Neurology (2020) Vol. 11
Open Access | Times Cited: 12
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms
Danai Veltra, Faidon‐Nikolaos Tilemis, Nikolaos M. Marinakis, et al.
Expert Review of Molecular Diagnostics (2023) Vol. 23, Iss. 1, pp. 85-103
Closed Access | Times Cited: 4
NOVEL MUTATIONS IN THE NON-STRUCTURE PROTEIN 2 OF SARS-CoV-2
Mohsen Nakhaei, Zohreh‐al‐sadat Ghoreshi, Mohammad Rezaei Zadeh Rukerd, et al.
Mediterranean Journal of Hematology and Infectious Diseases (2023) Vol. 15, Iss. 1, pp. e2023059-e2023059
Open Access | Times Cited: 4
ATP6V1B2‐related epileptic encephalopathy
Luciana Midori Inuzuka, Lúcia Inês Macedo‐Souza, Bruno Della‐Rippa, et al.
Epileptic Disorders (2020) Vol. 22, Iss. 3, pp. 317-322
Open Access | Times Cited: 11
Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant
Éliane Beauregard‐Lacroix, G. Pacheco-Cuellar, Norbert Fonya Ajeawung, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 237-237
Open Access | Times Cited: 10
Loss of neurodevelopmental-associated miR-592 impairs neurogenesis and causes social interaction deficits
Yu Fu, Yang Zhou, Yuanlin Zhang, et al.
Cell Death and Disease (2022) Vol. 13, Iss. 4
Open Access | Times Cited: 6
A novel pathogenic ATP6V1B2 variant: Widening the genotypic spectrum of the epileptic neurodevelopmental phenotype
Danai Veltra, Konstantina Kosma, Antigoni Papavasiliou, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 12, pp. 3563-3566
Closed Access | Times Cited: 6
The ATP6V1B2 DDOD/DOORS-Associated p.Arg506* Variant Causes Hyperactivity and Seizures in Mice
Justine Rousseau, Samuel Boris Tene Tadoum, Marisol Lavertu Jolin, et al.
Genes (2023) Vol. 14, Iss. 8, pp. 1538-1538
Open Access | Times Cited: 3
Case Report: Exome Sequencing Identified Variants in Three Candidate Genes From Two Families With Hearing Loss, Onychodystrophy, and Epilepsy
Yuan Li, Jianjun Xiong, Yi Zhang, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 6
Protein-protein networks analysis of differentially expressed genes unveils the key phenomenon of biological process with respect to reproduction in endangered catfish, C. Magur
Basdeo Kushwaha, Neha Srivastava, Sanjeev Kumar, et al.
Gene (2023) Vol. 860, pp. 147235-147235
Closed Access | Times Cited: 2
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