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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:

Single-cell transcriptomics provides insights into hypertrophic cardiomyopathy
Martijn Wehrens, Anne E. de Leeuw, Maya Wright-Clark, et al.
Cell Reports (2022) Vol. 39, Iss. 6, pp. 110809-110809
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Single-cell RNA sequencing to identify cellular heterogeneity and targets in cardiovascular diseases: from bench to bedside
Xinjie Xu, Xiumeng Hua, Mo Han, et al.
Basic Research in Cardiology (2023) Vol. 118, Iss. 1
Closed Access | Times Cited: 23
Complex Analysis of Single-Cell RNA Sequencing Data
Anna A. Khozyainova, Anna A. Valyaeva, Mikhail Arbatsky, et al.
Biochemistry (Moscow) (2023) Vol. 88, Iss. 2, pp. 231-252
Open Access | Times Cited: 23
Cathepsin B as a key regulator of ferroptosis in microglia following intracerebral hemorrhage
Jinxin Lü, Haiying Li, Zhengquan Yu, et al.
Neurobiology of Disease (2024) Vol. 194, pp. 106468-106468
Open Access | Times Cited: 8
Pervasive nuclear envelope ruptures precede ECM signaling and disease onset without activating cGAS-STING in Lamin-cardiomyopathy mice
Atsuki En, Hanumakumar Bogireddi, Briana Thomas, et al.
Cell Reports (2024) Vol. 43, Iss. 6, pp. 114284-114284
Open Access | Times Cited: 8
Integrative analysis of transcriptome, DNA methylome, and chromatin accessibility reveals candidate therapeutic targets in hypertrophic cardiomyopathy
Junpeng Gao, Mengya Liu, Minjie Lu, et al.
Protein & Cell (2024) Vol. 15, Iss. 11, pp. 796-817
Open Access | Times Cited: 5
Incomplete-penetrant hypertrophic cardiomyopathy MYH7 G256E mutation causes hypercontractility and elevated mitochondrial respiration
Soah Lee, Alison S. Vander Roest, Cheavar A. Blair, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 19
Open Access | Times Cited: 4
Opportunities and challenges for the use of human samples in translational cardiovascular research: a scientific statement of the ESC Working Group on Cellular Biology of the Heart, the ESC Working Group on Cardiovascular Surgery, the ESC Council on Basic Cardiovascular Science, the ESC Scientists of Tomorrow, the European Association of Percutaneous Cardiovascular Interventions of the ESC, and the Heart Failure Association of the ESC
Sean M. Davidson, Ioanna Andreadou, Charalambos Antoniades, et al.
Cardiovascular Research (2025)
Closed Access
Genotype–phenotype correlations in inherited cardiomyopathies, their role in clinical decision-making, and implications in personalized cardiac medicine in multi-omics as well as disease modeling eras
Yaqob Samir Taleb, Paras Memon, Aftab Ahmed Jalbani, et al.
Saudi Journal for Health Sciences (2025) Vol. 14, Iss. 1, pp. 30-41
Open Access
Multi‐omic analyses and network biology in cardiovascular disease
Cristine J. Reitz, Uroš Kuzmanov, Anthony O. Gramolini
PROTEOMICS (2023) Vol. 23, Iss. 21-22
Open Access | Times Cited: 10
Feline myocardial transcriptome in health and in hypertrophic cardiomyopathy—A translational animal model for human disease
Jessica Joshua, Jeff Caswell, M. Lynne O’Sullivan, et al.
PLoS ONE (2023) Vol. 18, Iss. 3, pp. e0283244-e0283244
Open Access | Times Cited: 9
Single Nucleus RNA-sequencing Reveals Altered Intercellular Communication and Dendritic Cell Activation in Nonobstructive Hypertrophic Cardiomyopathy
Christina J. Codden, Amy Larson, Junya Awata, et al.
Cardiology and Cardiovascular Medicine (2022) Vol. 06, Iss. 04
Open Access | Times Cited: 12
New discoveries in the field of metabolism by applying single-cell and spatial omics
Baocai Xie, Dengfeng Gao, Biqiang Zhou, et al.
Journal of Pharmaceutical Analysis (2023) Vol. 13, Iss. 7, pp. 711-725
Open Access | Times Cited: 6
High‐resolution single‐cell transcriptomic survey of cardiomyocytes from patients with hypertrophic cardiomyopathy
Jiansen Lu, Jie Ren, Jie Liu, et al.
Cell Proliferation (2023) Vol. 57, Iss. 3
Open Access | Times Cited: 6
Advances in Hypertrophic Cardiomyopathy Disease Modelling Using hiPSC-Derived Cardiomyocytes
Saif Dababneh, Homa Hamledari, Yasaman Maaref, et al.
Canadian Journal of Cardiology (2023) Vol. 40, Iss. 5, pp. 766-776
Closed Access | Times Cited: 5
Recommendations for detection, validation, and evaluation of RNA editing events in cardiovascular and neurological/neurodegenerative diseases
Korina Karagianni, Alessia Bibi, Alisia Madè, et al.
Molecular Therapy — Nucleic Acids (2023) Vol. 35, Iss. 1, pp. 102085-102085
Open Access | Times Cited: 5
Mapping Cell Atlases at the Single‐Cell Level
Fang Ye, Jingjing Wang, Jiaqi Li, et al.
Advanced Science (2023) Vol. 11, Iss. 8
Open Access | Times Cited: 5
Studying Pathogenetic Contribution of a Variant of Unknown Significance, p.M659I (c.1977G > A) in MYH7, to the Development of Hypertrophic Cardiomyopathy Using CRISPR/Cas9-Engineered Isogenic Induced Pluripotent Stem Cells
С. В. Павлова, Angelina E. Shulgina, Suren M. Zakian, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8695-8695
Open Access | Times Cited: 1
Genotype-Phenotype Correlations in Inherited Cardiomyopathies, Their Role in Clinical Decision-Making and Implications in Personalized Cardiac Medicine in Multi-omics as Well as Disease Modelling Eras
Yaqob Samir Taleb, Paras Memon, Aftab Ahmed Jalbani, et al.
(2024)
Open Access | Times Cited: 1
Single-Cell RNA Sequencing and Combinatorial Approaches for Understanding Heart Biology and Disease
Le Wang, Bo Jin
Biology (2024) Vol. 13, Iss. 10, pp. 783-783
Open Access | Times Cited: 1
CVD Atlas: a multi-omics database of cardiovascular disease
Qiheng Qian, Ruikun Xue, Chenle Xu, et al.
Nucleic Acids Research (2024) Vol. 53, Iss. D1, pp. D1348-D1355
Open Access | Times Cited: 1
Strategy of Patient-Specific Therapeutics in Cardiovascular Disease Through Single-Cell RNA Sequencing
Yunseo Jung, Juyeong Kim, Ho-Won Jang, et al.
Korean Circulation Journal (2022) Vol. 53, Iss. 1, pp. 1-1
Open Access | Times Cited: 6
Application of Single-Cell Genomics in Cardiovascular Research
Xuejing Yu, Xianggui Yang, Jinjin Cao
Cardiology and Therapy (2023) Vol. 12, Iss. 1, pp. 101-125
Open Access | Times Cited: 3
A perspective on Notch signalling in progression and arrhythmogenesis in familial hypertrophic and dilated cardiomyopathies
Paulina Langa, Sanam Shafaattalab, Paul H. Goldspink, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2023) Vol. 378, Iss. 1879
Closed Access | Times Cited: 3
Single Cell Transcriptomic Analysis in a Mouse Model of Barth Syndrome Reveals Cell-Specific Alterations in Gene Expression and Intercellular Communication
Gayani Perera, Liam Power, Amy Larson, et al.
(2023)
Open Access | Times Cited: 3
Single Cell Transcriptomic Analysis in a Mouse Model of Barth Syndrome Reveals Cell-Specific Alterations in Gene Expression and Intercellular Communication
Gayani Perera, Liam Power, Amy Larson, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11594-11594
Open Access | Times Cited: 3
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