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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:

Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome
Emma Wakeling, Meriel McEntagart, Michael Bruccoleri, et al.
Human Genetics and Genomics Advances (2020) Vol. 2, Iss. 1, pp. 100015-100015
Open Access | Times Cited: 15

Showing 15 citing articles:

P3 site-directed mutagenesis: An efficient method based on primer pairs with 3’-overhangs
Negar Mousavi, Ethan Y. Zhou, Arezousadat Razavi, et al.
Journal of Biological Chemistry (2025), pp. 108219-108219
Open Access | Times Cited: 1
ADRAM is an experience-dependent long noncoding RNA that drives fear extinction through a direct interaction with the chaperone protein 14-3-3
Wei Wei, Qiongyi Zhao, Ziqi Wang, et al.
Cell Reports (2022) Vol. 38, Iss. 12, pp. 110546-110546
Open Access | Times Cited: 33
HDAC4 in cancer: A multitasking platform to drive not only epigenetic modifications
Emma Cuttini, Camilla Goi, Ester Pellarin, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 17
Phenotypic Manifestations of a New Variant in HDAC4 Gene
Monica Ianniello, Valentina De Angelis, Alessandro Ottaiano, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2025)
Closed Access
Molecular and clinical aspects of histone-related disorders
Mode Al Ojaimi, Bashar J. Banimortada, Abduljalil Alragheb, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders
Johann Lieberwirth, Benjamin Büttner, Chiara Klöckner, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 1795-1807
Open Access | Times Cited: 10
Genotype–Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review
Eva-Cristiana Gavril, Irina Nucă, Monica-Cristina Pânzaru, et al.
Genes (2023) Vol. 14, Iss. 2, pp. 465-465
Open Access | Times Cited: 5
Deciphering the roles of subcellular distribution and interactions involving the MEF2 binding region, the ankyrin repeat binding motif and the catalytic site of HDAC4 in Drosophila neuronal morphogenesis
Wei Jun Tan, Hannah R. Hawley, Sarah J. Wilson, et al.
BMC Biology (2024) Vol. 22, Iss. 1
Open Access
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies
Elisabetta Di Fede, Antonella Lettieri, Esi Taci, et al.
Human Genetics (2024) Vol. 143, Iss. 6, pp. 747-759
Open Access
De novo missense variants in HDAC3 leading to epigenetic machinery dysfunction are associated with a variable neurodevelopmental disorder
Jihoon G. Yoon, Seong-Kyun Lim, Hoseok Seo, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1588-1604
Open Access
De novo HDAC3variants leading to epigenetic machinery dysfunction are associated with a neurodevelopmental disorder
Jihoon G. Yoon, Seong-Kyun Lim, Hoseok Seo, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders
Johann Lieberwirth, Benjamin Büttner, Chiara Klöckner, et al.
Authorea (Authorea) (2022)
Open Access | Times Cited: 1
A family with brachydactyly mental retardation syndrome with a missense variant in <i>HDAC4</i>
Shinji Takeyari, Kenichi Yamamoto, Makoto Fujiwara, et al.
Clinical Pediatric Endocrinology (2023) Vol. 32, Iss. 2, pp. 105-109
Open Access
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders
Bernt Popp, Johann Lieberwirth, Benjamin Büttner, et al.
Authorea (Authorea) (2022)
Open Access
Ankyrin2 is required for neuronal morphogenesis and long-term memory and interacts genetically with HDAC4
Silvia Schwartz, Sarah J. Wilson, Tracy K. Hale, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
On the discovery of ADRAM, an experience-dependent long noncoding RNA that drives fear extinction through a direct interaction with the chaperone protein 14-3-3
Xiang Li, Qiongyi Zhao, Ziqi Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
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