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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:

Abnormal neocortex arealization and Sotos-like syndrome–associated behavior in Setd2 mutant mice
Lichao Xu, Yue Zheng, Xuejing Li, et al.
Science Advances (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Structural and Functional Aspects of the Neurodevelopmental Gene NR2F1: From Animal Models to Human Pathology
Chiara Tocco, Michele Bertacchi, Michèle Studer
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 39
Interference of sympathetic overactivation restores limbal stem/progenitor cells function and accelerates corneal epithelial wound healing in diabetic mice
Zhenzhen Zhang, Lingling Yang, Ya Li, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 161, pp. 114523-114523
Open Access | Times Cited: 15
SETD2 deficiency accelerates sphingomyelin accumulation and promotes the development of renal cancer
Hanyu Rao, Changwei Liu, Aiting Wang, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 15
Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain development
Bo Chen, Chenyang Zhang, Hallgeir Rui, et al.
Human Genetics (2025)
Closed Access
A Ctnnb1 enhancer regulates neocortical neurogenesis by controlling the abundance of intermediate progenitors
Junbao Wang, Andi Wang, Kuan Tian, et al.
Cell Discovery (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 16
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
The role of histone methyltransferases in neurocognitive disorders associated with brain size abnormalities
Foster D. Ritchie, Sofia B. Lizarraga
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 8
Unraveling the genetic basis of epilepsy: Recent advances and implications for diagnosis and treatment
Rekha Dwivedi, Meenakshi Kaushik, Manjari Tripathi, et al.
Brain Research (2024) Vol. 1843, pp. 149120-149120
Closed Access | Times Cited: 3
An epigenetic circuit controls neurogenic programs during neocortex development
Andi Wang, Junbao Wang, Kuan Tian, et al.
Development (2021) Vol. 148, Iss. 22
Open Access | Times Cited: 18
Reprogramming of the epigenome in neurodevelopmental disorders
Khadija Wilson, Elizabeth G. Porter, Benjamin A. García
Critical Reviews in Biochemistry and Molecular Biology (2021) Vol. 57, Iss. 1, pp. 73-112
Open Access | Times Cited: 16
Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature
Alejandro Parra, Rachel Rabin, John Pappas, et al.
Genes (2023) Vol. 14, Iss. 6, pp. 1179-1179
Open Access | Times Cited: 7
A protocol for high-resolution episcopic microscopy and 3D volumetric analyses of the adult mouse brain
Benjamin Mitchell, Erica W. H. Mu, Laura Currey, et al.
Neuroscience Letters (2024) Vol. 824, pp. 137675-137675
Open Access | Times Cited: 2
The Landscape of Pediatric High-Grade Gliomas: The Virtues and Pitfalls of Pre-Clinical Models
Liam Furst, Enola M. Roussel, Ryan F. Leung, et al.
Biology (2024) Vol. 13, Iss. 6, pp. 424-424
Open Access | Times Cited: 2
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment
Jie Zhang, Gongcheng Hu, Yuli Lu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Human Accelerated Regions regulate gene networks implicated in apical-to-basal neural progenitor fate transitions
Mark Noble, Yu Ji, Kristina Yim, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
A Ctnnb1 enhancer transcriptionally regulates Wnt signaling dosage to balance homeostasis and tumorigenesis of intestinal epithelia
Xiaojiao Hua, Zhao Chen, Jianbo Tian, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 2
Catalytic activity of Setd2 is essential for embryonic development in mice: establishment of a mouse model harboring patient-derived Setd2 mutation
Shubei Chen, Dian‐Jia Liu, Bingyi Chen, et al.
Frontiers of Medicine (2024) Vol. 18, Iss. 5, pp. 831-849
Closed Access | Times Cited: 2
A Ctnnb1 enhancer transcriptionally regulates Wnt signaling dosage to balance homeostasis and tumorigenesis of intestinal epithelia
Xiaojiao Hua, Zhao Chen, Jianbo Tian, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 2
A novel SETD2 variant causing global development delay without overgrowth in a Chinese 3-year-old boy
Yuanyuan Wu, Fang Liu, Ruihua Wan, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 5
Epigenetic priming in neurodevelopmental disorders
Carl Ernst, Malvin Jefri
Trends in Molecular Medicine (2021) Vol. 27, Iss. 12, pp. 1106-1114
Closed Access | Times Cited: 12
Histone methyltransferase SETD2 is required for proper hippocampal lamination and neuronal maturation
Guangda Hu, Yue Zheng, Bo Zhang, et al.
Molecular Biology of the Cell (2024) Vol. 35, Iss. 4
Open Access | Times Cited: 1
Hypomagnetic Field Exposure Affecting Gut Microbiota, Reactive Oxygen Species Levels, and Colonic Cell Proliferation in Mice
Aisheng Zhan, Yukai Luo, Huafeng Qin, et al.
Bioelectromagnetics (2022) Vol. 43, Iss. 8, pp. 462-475
Closed Access | Times Cited: 4
Cellular and molecular functions of SETD2 in the central nervous system
Benjamin Mitchell, Stefan Thor, Michael Piper
Journal of Cell Science (2023) Vol. 136, Iss. 21
Open Access | Times Cited: 2
The E3 ubiquitin ligase RNF220 maintains hindbrainHoxexpression patterns through regulation of WDR5 stability
Huishan Wang, Xingyan Liu, Yamin Liu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
The E3 ubiquitin ligase RNF220 maintains hindbrain Hox expression patterns through regulation of WDR5 stability
Huishan Wang, Xingyan Liu, Yamin Liu, et al.
eLife (2024) Vol. 13
Open Access
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