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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.

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Showing 1-25 of 85 citing articles:

RING 3.0: fast generation of probabilistic residue interaction networks from structural ensembles
Damiano Clementel, Alessio Del Conte, Alexander Miguel Monzón, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. W1, pp. W651-W656
Open Access | Times Cited: 129
ACE2 and SCARF expression in human dorsal root ganglion nociceptors: implications for SARS-CoV-2 virus neurological effects
Stephanie Shiers, Pradipta Ray, Andi Wangzhou, et al.
Pain (2020) Vol. 161, Iss. 11, pp. 2494-2501
Open Access | Times Cited: 104
Molecular characteristics and structure–activity relationships of food-derived bioactive peptides
Fujia Yang, Xu Chen, Muchen Huang, et al.
Journal of Integrative Agriculture (2021) Vol. 20, Iss. 9, pp. 2313-2332
Open Access | Times Cited: 57
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Manuel Mattheisen, Jakob Grove, Thomas D. Als, et al.
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1470-1478
Open Access | Times Cited: 52
Single substitution in H3.3G34 alters DNMT3A recruitment to cause progressive neurodegeneration
Sima Khazaei, Carol Chen, Augusto Faria Andrade, et al.
Cell (2023) Vol. 186, Iss. 6, pp. 1162-1178.e20
Closed Access | Times Cited: 37
H3.3 contributes to chromatin accessibility and transcription factor binding at promoter-proximal regulatory elements in embryonic stem cells
Amanuel Tafessu, Ryan O’Hara, Sara Martire, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 30
Exploring noncoding variants in genetic diseases: from detection to functional insights
Ke Wu, Fengxiao Bu, Yang Wu, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2024) Vol. 51, Iss. 2, pp. 111-132
Open Access | Times Cited: 8
What can whiskers tell us about mammalian evolution, behaviour, and ecology?
Robyn A. Grant, V.G.A. Goss
Mammal Review (2021) Vol. 52, Iss. 1, pp. 148-163
Open Access | Times Cited: 46
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
Oncohistones: Exposing the nuances and vulnerabilities of epigenetic regulation
Michelle M. Mitchener, Tom W. Muir
Molecular Cell (2022) Vol. 82, Iss. 16, pp. 2925-2938
Open Access | Times Cited: 34
Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here?
Jacqueline Harris, Christine W. Gao, Jacquelyn Britton, et al.
Human Genetics (2023) Vol. 143, Iss. 4, pp. 607-624
Open Access | Times Cited: 22
Identification of epigenetic modulators as determinants of nuclear size and shape
Andreas Schibler, Predrag Jevtić, Gianluca Pegoraro, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 22
Histone variant H2BE enhances chromatin accessibility in neurons to promote synaptic gene expression and long-term memory
Emily R. Feierman, Sean Louzon, Nicholas Adrian Prescott, et al.
Molecular Cell (2024) Vol. 84, Iss. 15, pp. 2822-2837.e11
Open Access | Times Cited: 6
Multifunctional histone variants in genome function
Lee H. Wong, David J. Tremethick
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 6
Research progress on bulk nanobubbles
Le Sun, Fenghua Zhang, Xiaoming Guo, et al.
Particuology (2021) Vol. 60, pp. 99-106
Closed Access | Times Cited: 35
Extrusion bioprinting of hydroxyethylcellulose-based bioink for cervical tumor model
Antonina Gospodinova, Vladislav Nankov, С Томов, et al.
Carbohydrate Polymers (2021) Vol. 260, pp. 117793-117793
Closed Access | Times Cited: 34
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
Dong Li, Qin Wang, Allan Bayat, et al.
Journal of Clinical Investigation (2023) Vol. 134, Iss. 1
Open Access | Times Cited: 15
The cell-cycle choreography of H3 variants shapes the genome
Kamila Delaney, Nicole Weiss, Geneviève Almouzni
Molecular Cell (2023) Vol. 83, Iss. 21, pp. 3773-3786
Open Access | Times Cited: 14
Oncohistones: a roadmap to stalled development
Shriya Deshmukh, Adam Ptack, Brian Krug, et al.
FEBS Journal (2021) Vol. 289, Iss. 5, pp. 1315-1328
Open Access | Times Cited: 31
COVID-19 and the Acceleration of Behavioral Parent Training Telehealth: Current Status and Future Directions
Alexandra D. W. Sullivan, Rex Forehand, Juliana Acosta, et al.
Cognitive and Behavioral Practice (2021) Vol. 28, Iss. 4, pp. 618-629
Open Access | Times Cited: 31
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome
Federico Tessadori, Karen Duran, Karen Knapp, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 4, pp. 750-758
Open Access | Times Cited: 22
Characterizing crosstalk in epigenetic signaling to understand disease physiology
Joanna K. Lempiäinen, Benjamin A. García
Biochemical Journal (2023) Vol. 480, Iss. 1, pp. 57-85
Open Access | Times Cited: 12
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Dana E. Layo-Carris, Emily E. Lubin, Annabel K. Sangree, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 928-937
Open Access | Times Cited: 4
The ortholog of human DNAJC9 promotes histone H3–H4 degradation and is counteracted by Asf1 in fission yeast
Yan Ding, Jun Li, Hua Jiang, et al.
Nucleic Acids Research (2025) Vol. 53, Iss. 3
Open Access
Epigene functional diversity: isoform usage, disordered domain content, and variable binding partners
Leroy Bondhus, Aileen A. Nava, Isabelle S. Liu, et al.
Epigenetics & Chromatin (2025) Vol. 18, Iss. 1
Open Access
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