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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:

SETD5 Regulates Chromatin Methylation State and Preserves Global Transcriptional Fidelity during Brain Development and Neuronal Wiring
Alessandro Sessa, Luca Fagnocchi, Giuseppina Mastrototaro, et al.
Neuron (2019) Vol. 104, Iss. 2, pp. 271-289.e13
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

Epigenetics and beyond: targeting writers of protein lysine methylation to treat disease
Kamakoti P. Bhat, H. Ümit Kanıskan, Jian Jin, et al.
Nature Reviews Drug Discovery (2021) Vol. 20, Iss. 4, pp. 265-286
Open Access | Times Cited: 177
The role of histone modifications: from neurodevelopment to neurodiseases
Jisu Park, Kyubin Lee, Kyunghwan Kim, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 156
Aging-induced tRNAGlu-derived fragment impairs glutamate biosynthesis by targeting mitochondrial translation-dependent cristae organization
Dingfeng Li, Xinyi Gao, Xiaolin Ma, et al.
Cell Metabolism (2024) Vol. 36, Iss. 5, pp. 1059-1075.e9
Closed Access | Times Cited: 23
Genetic and Epigenetic Etiology Underlying Autism Spectrum Disorder
Sang Hoon Yoon, Joonhyuk Choi, Won Yong Lee, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 4, pp. 966-966
Open Access | Times Cited: 125
SETD5-Coordinated Chromatin Reprogramming Regulates Adaptive Resistance to Targeted Pancreatic Cancer Therapy
Zhentian Wang, Simone Hausmann, Ruitu Lyu, et al.
Cancer Cell (2020) Vol. 37, Iss. 6, pp. 834-849.e13
Open Access | Times Cited: 75
Chromatin-mediated alternative splicing regulates cocaine-reward behavior
Song-Jun Xu, Sonia I. Lombroso, Delaney K. Fischer, et al.
Neuron (2021) Vol. 109, Iss. 18, pp. 2943-2966.e8
Open Access | Times Cited: 59
A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation
Jiayang Chen, Mary E. Lambo, Xia Ge, et al.
Neuron (2021) Vol. 109, Iss. 23, pp. 3775-3792.e14
Open Access | Times Cited: 56
Transcriptional linkage analysis with in vivo AAV-Perturb-seq
António J. Santinha, Esther Klingler, Maria Kuhn, et al.
Nature (2023) Vol. 622, Iss. 7982, pp. 367-375
Open Access | Times Cited: 39
Role of histone modifications in neurogenesis and neurodegenerative disease development
Anqi Zhao, Wenhong Xu, Rui Han, et al.
Ageing Research Reviews (2024) Vol. 98, pp. 102324-102324
Closed Access | Times Cited: 13
Fish models to explore epigenetic determinants of hypoxia-tolerance
William Johnston, Sally Adil, Catherine Cao, et al.
Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology (2025) Vol. 302, pp. 111811-111811
Closed Access | Times Cited: 1
H3K36 trimethylation-mediated biological functions in cancer
Xiao Chu, Tao Fan, He Tian, et al.
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 44
ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder
Yuze Yan, Miaomiao Tian, Meng Li, et al.
Neuron (2022) Vol. 110, Iss. 7, pp. 1156-1172.e9
Open Access | Times Cited: 34
SETD2: from chromatin modifier to multipronged regulator of the genome and beyond
Thom M. Molenaar, Fred van Leeuwen
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 6
Open Access | Times Cited: 32
A new Bayesian factor analysis method improves detection of genes and biological processes affected by perturbations in single-cell CRISPR screening
Yifan Zhou, Kaixuan Luo, Lifan Liang, et al.
Nature Methods (2023) Vol. 20, Iss. 11, pp. 1693-1703
Open Access | Times Cited: 18
DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders
Diana L. Christian, Dennis Y. Wu, Jenna R. Martin, et al.
Cell Reports (2020) Vol. 33, Iss. 8, pp. 108416-108416
Open Access | Times Cited: 49
The autism-associated protein CHD8 is required for cerebellar development and motor function
Atsuki Kawamura, Yuta Katayama, Wataru Kakegawa, et al.
Cell Reports (2021) Vol. 35, Iss. 1, pp. 108932-108932
Open Access | Times Cited: 36
Placental DNA methylation profile as predicting marker for autism spectrum disorder (ASD)
Amin Ravaei, Marco Emanuele, G. Nazzaro, et al.
Molecular Medicine (2023) Vol. 29, Iss. 1
Open Access | Times Cited: 15
Inhibition of EHMT1/2 rescues synaptic damage and motor impairment in a PD mouse model
Zhixiong Zhang, Rui Wang, Hui Zhou, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 5
New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders
Mariana Moysés‐Oliveira, Rachita Yadav, Serkan Erdin, et al.
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 195-206
Closed Access | Times Cited: 39
H3K36 Methylation in Neural Development and Associated Diseases
Mattia Zaghi, Vania Broccoli, Alessandro Sessa
Frontiers in Genetics (2020) Vol. 10
Open Access | Times Cited: 35
Epigenetic evidence for distinct contributions of resident and acquired myonuclei during long-term exercise adaptation using timed in vivo myonuclear labeling
Kevin A. Murach, Cory M. Dungan, Ferdinand von Walden, et al.
AJP Cell Physiology (2021) Vol. 322, Iss. 1, pp. C86-C93
Open Access | Times Cited: 32
Dysregulation of the chromatin environment leads to differential alternative splicing as a mechanism of disease in a human model of autism spectrum disorder
Calvin S. Leung, Shoshana J Rosenzweig, Brian Yoon, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 10, pp. 1634-1646
Open Access | Times Cited: 11
Knockout mice with pituitary malformations help identify human cases of hypopituitarism
Julian Martinez-Mayer, Michelle L. Brinkmeier, Sean P. O’Connell, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 4
Histone Variants and Histone Modifications in Neurogenesis
Mengtian Zhang, Jinyue Zhao, Yuqing Lv, et al.
Trends in Cell Biology (2020) Vol. 30, Iss. 11, pp. 869-880
Closed Access | Times Cited: 28
CHD8suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing
Emanuela Kerschbamer, Michele Arnoldi, Takshashila Tripathi, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 22, pp. 12809-12828
Open Access | Times Cited: 17
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