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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:

Chromatin regulation of transcriptional enhancers and cell fate by the Sotos syndrome gene NSD1
Zhen Sun, Yuan Lin, Mohammed T. Islam, et al.
Molecular Cell (2023) Vol. 83, Iss. 14, pp. 2398-2416.e12
Open Access | Times Cited: 18

Showing 18 citing articles:

NSD family proteins: Rising stars as therapeutic targets
Lin He, Yiping Cao, Luyang Sun
Cell Insight (2024) Vol. 3, Iss. 2, pp. 100151-100151
Open Access | Times Cited: 6
Macrophage-derived ectosomal miR-350-3p promotes osteoarthritis progression through downregulating chondrocyte H3K36 methyltransferase NSD1
Rengui Lin, Jianbin Yin, Jia-Luo Huang, et al.
Cell Death Discovery (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 4
Genomic context-dependent histone H3K36 methylation by three Drosophila methyltransferases and implications for dedicated chromatin readers
Muhunden Jayakrishnan, M Havlová, Václav Veverka, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 13, pp. 7627-7649
Open Access | Times Cited: 4
Inhibition of DEK restores hematopoietic stem cell function in Fanconi anemia
Zhe Chen, Feng Wu, Yan Li, et al.
The Journal of Experimental Medicine (2025) Vol. 222, Iss. 3
Closed Access
Incorporating multiscale methylation effects into nucleosome-resolution chromatin models for simulating mesoscale fibers
Zilong Li, Stephanie Portillo‐Ledesma, M Padma Janani, et al.
The Journal of Chemical Physics (2025) Vol. 162, Iss. 9
Closed Access
The Sotos syndrome gene Nsd1 safeguards developmental gene enhancers poised for transcription by maintaining the precise deposition of histone methylation
Jie Li, Zhucui Li, Jiekai Yin, et al.
Journal of Biological Chemistry (2025), pp. 108423-108423
Open Access
Role and mechanisms of histone methylation in osteogenic/odontogenic differentiation of dental mesenchymal stem cells
Meijun Hu, Zhipeng Fan
International Journal of Oral Science (2025) Vol. 17, Iss. 1
Open Access
Histone methylation mediated by NSD1 is required for the establishment and maintenance of neuronal identities
Yue Zheng, Chen Zhao, Qiulin Song, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113496-113496
Open Access | Times Cited: 9
Genomic context-dependent histone H3K36 methylation by threeDrosophilamethyltransferases and implications for dedicated chromatin readers
Muhunden Jayakrishnan, M Havlová, Václav Veverka, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Systematic perturbations of SETD2, NSD1, NSD2, NSD3 and ASH1L reveals their distinct contributions to H3K36 methylation
Gerry A. Shipman, Reinnier Padilla, Cynthia Horth, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome
Giulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
Diagnostics (2024) Vol. 14, Iss. 6, pp. 594-594
Open Access | Times Cited: 1
H3K36 Methylation - a Guardian of Epigenome Integrity
Reinnier Padilla, Gerry A. Shipman, Cynthia Horth, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Systematic perturbations of SETD2, NSD1, NSD2, NSD3, and ASH1L reveal their distinct contributions to H3K36 methylation
Gerry A. Shipman, Reinnier Padilla, Cynthia Horth, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Transposable element activity captures human pluripotent cell states
Florencia Levin-Ferreyra, Srikanth Kodali, Yingzhi Cui, et al.
EMBO Reports (2024)
Open Access | Times Cited: 1
Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice
Shiori Kinoshita, Kazuaki Kojima, Eriko Ohnishi, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
H3K36 methyltransferase SMYD2 affects cell proliferation and migration in Hirschsprung's disease by regulating METTL3
Xinwei Hou, Yang� Yang, Chen Wang, et al.
Journal of Cellular Physiology (2024) Vol. 239, Iss. 9
Closed Access
Magnetic resonance imaging evaluation and nuclear receptor binding SET domain protein 1 mutation in the Sotos syndrome with attention-deficit/hyperactivity disorder
Wei Zhu
World Journal of Clinical Cases (2024) Vol. 13, Iss. 2
Closed Access
The interplay between H3K36 methylation and DNA methylation in cancer
Jiameng Dan, Zeling Du, Jinghong Zhang, et al.
Cancer Biology and Medicine (2023), pp. 1-8
Open Access | Times Cited: 1
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