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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:

Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
Fanny Kortüm, Viviana Caputo, Christiane K. Bauer, et al.
Nature Genetics (2015) Vol. 47, Iss. 6, pp. 661-667
Open Access | Times Cited: 197

Showing 1-25 of 197 citing articles:

Disorders of lysosomal acidification—The emerging role of v-ATPase in aging and neurodegenerative disease
Daniel J. Colacurcio, Ralph A. Nixon
Ageing Research Reviews (2016) Vol. 32, pp. 75-88
Open Access | Times Cited: 430
Endogenous Bioelectric Signaling Networks: Exploiting Voltage Gradients for Control of Growth and Form
Michael Levin, Giovanni Pezzulo, Joshua M. Finkelstein
Annual Review of Biomedical Engineering (2017) Vol. 19, Iss. 1, pp. 353-387
Open Access | Times Cited: 259
Lysosome trafficking and signaling in health and neurodegenerative diseases
Pearl P.Y. Lie, Ralph A. Nixon
Neurobiology of Disease (2018) Vol. 122, pp. 94-105
Open Access | Times Cited: 233
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
Bioelectric signaling as a unique regulator of development and regeneration
Matthew P. Harris
Development (2021) Vol. 148, Iss. 10
Open Access | Times Cited: 111
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Renzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 433-513
Open Access | Times Cited: 94
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa
Tim Van Damme, Thatjana Gardeitchik, Miski Mohamed, et al.
The American Journal of Human Genetics (2017) Vol. 100, Iss. 2, pp. 216-227
Open Access | Times Cited: 104
Gingival fibromatosis: clinical, molecular and therapeutic issues
Katarzyna Gawron, Katarzyna Łazarz‐Bartyzel, Jan Potempa, et al.
Orphanet Journal of Rare Diseases (2016) Vol. 11, Iss. 1
Open Access | Times Cited: 102
Clinical variability in inherited glycosylphosphatidylinositol deficiency disorders
Kara Bellai‐Dussault, Thi Tuyet Mai Nguyen, Nissan Vida Baratang, et al.
Clinical Genetics (2018) Vol. 95, Iss. 1, pp. 112-121
Closed Access | Times Cited: 98
Epigenetic maintenance of topological domains in the highly rearranged gibbon genome
Nathan H. Lazar, Kimberly A. Nevonen, Brendan L. O′Connell, et al.
Genome Research (2018) Vol. 28, Iss. 7, pp. 983-997
Open Access | Times Cited: 96
The Role of Early Bioelectric Signals in the Regeneration of Planarian Anterior/Posterior Polarity
Fallon Durant, Johanna Bischof, Chris Fields, et al.
Biophysical Journal (2019) Vol. 116, Iss. 5, pp. 948-961
Open Access | Times Cited: 89
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome
Christiane K. Bauer, Paolo Calligari, Francesca Clementina Radio, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 4, pp. 621-630
Open Access | Times Cited: 84
De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypes
Lina Liang, Xia Li, Sébastien Moutton, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 17, pp. 2937-2951
Open Access | Times Cited: 83
Genetic potassium channel-associated epilepsies: Clinical review of the Kv family
Nicholas M. Allen, Sarah Weckhuysen, Kathleen M. Gorman, et al.
European Journal of Paediatric Neurology (2019) Vol. 24, pp. 105-116
Open Access | Times Cited: 83
Origin and functional diversification of PAS domain, a ubiquitous intracellular sensor
Jiawei Xing, Vadim M. Gumerov, Igor B. Zhulin
Science Advances (2023) Vol. 9, Iss. 35
Open Access | Times Cited: 23
Aging as a loss of morphostatic information: A developmental bioelectricity perspective
Léo Pio-Lopez, Michael Levin
Ageing Research Reviews (2024) Vol. 97, pp. 102310-102310
Closed Access | Times Cited: 11
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 | Times Cited: 1
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
Steffen Syrbe, Frederike L. Harms, Elena Parrini, et al.
Brain (2017) Vol. 140, Iss. 9, pp. 2322-2336
Open Access | Times Cited: 85
Bioelectric gene and reaction networks: computational modelling of genetic, biochemical and bioelectrical dynamics in pattern regulation
Alexis Pietak, Michael Levin
Journal of The Royal Society Interface (2017) Vol. 14, Iss. 134, pp. 20170425-20170425
Open Access | Times Cited: 85
Syndromes with supernumerary teeth
Mark Lubinsky, Piranit Nik Kantaputra
American Journal of Medical Genetics Part A (2016) Vol. 170, Iss. 10, pp. 2611-2616
Open Access | Times Cited: 83
TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation
Jos C. Jansen, Sharita Timal, Monique van Scherpenzeel, et al.
The American Journal of Human Genetics (2016) Vol. 98, Iss. 2, pp. 322-330
Open Access | Times Cited: 82
HCN2 Rescues brain defects by enforcing endogenous voltage pre-patterns
Vaibhav P. Pai, Alexis Pietak, Valerie Willocq, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 82
De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy
Anna Fassio, Alessandro Esposito, Mitsuhiro Kato, et al.
Brain (2018) Vol. 141, Iss. 6, pp. 1703-1718
Open Access | Times Cited: 80
Ether‐à‐go‐go K+ channels: effective modulators of neuronal excitability
Christiane K. Bauer, Jürgen R. Schwarz
The Journal of Physiology (2018) Vol. 596, Iss. 5, pp. 769-783
Open Access | Times Cited: 74
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism
Frederike L. Harms, Katta M. Girisha, Andrew A. Hardigan, et al.
The American Journal of Human Genetics (2016) Vol. 100, Iss. 1, pp. 117-127
Open Access | Times Cited: 73
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