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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:

De novo detection of somatic mutations in high-throughput single-cell profiling data sets
Francesc Muyas, Carolin M. Sauer, Jose Espejo Valle-Inclán, et al.
Nature Biotechnology (2023) Vol. 42, Iss. 5, pp. 758-767
Open Access | Times Cited: 42

Showing 1-25 of 42 citing articles:

Profiling cell identity and tissue architecture with single-cell and spatial transcriptomics
Gunsagar S. Gulati, Jeremy Philip D’Silva, Yunhe Liu, et al.
Nature Reviews Molecular Cell Biology (2024) Vol. 26, Iss. 1, pp. 11-31
Closed Access | Times Cited: 34
Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 22
Human embryonic genetic mosaicism and its effects on development and disease
Sarah M. Waldvogel, Jennifer E. Posey, Margaret A. Goodell
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 13
Multiomic analysis reveals developmental dynamics of the human heart in health and disease
James Cranley, Kazumasa Kanemaru, Semih Bayraktar, et al.
(2024)
Open Access | Times Cited: 9
Single-cell genotyping and transcriptomic profiling in focal cortical dysplasia
Stéphanie Baulac, Sara Baldassari, Esther Klingler, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 5
Leveraging Single-Cell Populations to Uncover the Genetic Basis of Complex Traits
Mark A.A. Minow, Alexandre P. Marand, Robert J. Schmitz
Annual Review of Genetics (2023) Vol. 57, Iss. 1, pp. 297-319
Open Access | Times Cited: 11
Temporal recording of mammalian development and precancer
Mirazul Islam, Yilin Yang, Alan J. Simmons, et al.
Nature (2024) Vol. 634, Iss. 8036, pp. 1187-1195
Open Access | Times Cited: 4
Cell competition as an emerging mechanism and therapeutic target in cancer
Dakai Yang, Wenyue Sun, Lu Gao, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2025) Vol. 1871, Iss. 5, pp. 167769-167769
Closed Access
Identifying genetic errors of immunity due to mosaicism
Elizabeth G. Schmitz, Malachi Griffith, Obi L. Griffith, et al.
The Journal of Experimental Medicine (2025) Vol. 222, Iss. 5
Closed Access
Phertilizer: Growing a clonal tree from ultra-low coverage single-cell DNA sequencing of tumors
Leah L. Weber, Chuanyi Zhang, Idoia Ochoa, et al.
PLoS Computational Biology (2023) Vol. 19, Iss. 10, pp. e1011544-e1011544
Open Access | Times Cited: 10
Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometry
Dong‐Gi Mun, Firdous Ahmad Bhat, Neha Joshi, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 3
Detecting somatic mutations in single-cell data with SComatic
Tim H. H. Coorens
Nature reviews. Cancer (2025)
Closed Access
The Landscape of Malignant Transition: Unraveling Cancer Cell-of-Origin and Heterogeneous Tissue Microenvironment
Ruihan Luo, Jiajia Liu, Tiangang Wang, et al.
Cancer Letters (2025), pp. 217591-217591
Open Access
Comprehensive Integrated Analysis Reveals the Spatiotemporal Microevolution of Cancer Cells in Patients with Bone-Metastatic Prostate Cancer
Yinghua Feng, Xiuli Zhang, Guangpeng Wang, et al.
Biomedicines (2025) Vol. 13, Iss. 4, pp. 909-909
Open Access
Single-cell genotyping and transcriptomic profiling of mosaic focal cortical dysplasia
Sara Baldassari, Esther Klingler, Lucia Gomez Teijeiro, et al.
Nature Neuroscience (2025)
Open Access
Oncogene aberrations drive medulloblastoma progression, not initiation
Konstantin Okonechnikov, Piyush Joshi, Verena Körber, et al.
Nature (2025)
Open Access
Computing cell state discriminates the aberrant hematopoiesis and activated microenvironment in Myelodysplastic syndrome (MDS) through a single cell genomic study
Xinyu Guo, Wenyan Jin, Yuchen Wen, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 3
High‐confidence calling of normal epithelial cells allows identification of a novel stem‐like cell state in the colorectal cancer microenvironment
Tzu‐Ting Wei, Eric Blanc, Stefan Peidli, et al.
International Journal of Cancer (2024) Vol. 155, Iss. 9, pp. 1655-1669
Open Access | Times Cited: 3
A single cell RNAseq benchmark experiment embedding “controlled” cancer heterogeneity
Maddalena Arigoni, Maria Luisa Ratto, Federica Riccardo, et al.
Scientific Data (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 2
scTML: a pan-cancer single-cell landscape of multiple mutation types
Haochen Li, Tianxing Ma, Zetong Zhao, et al.
Nucleic Acids Research (2024) Vol. 53, Iss. D1, pp. D1547-D1556
Open Access | Times Cited: 2
stSNV: a comprehensive resource of SNVs in spatial transcriptome
Changbo Yang, Yujie Liu, Xiaohua Wang, et al.
Nucleic Acids Research (2024) Vol. 53, Iss. D1, pp. D1224-D1234
Open Access | Times Cited: 2
Refining SARS-CoV-2 intra-host variation by leveraging large-scale sequencing data
Fatima Mostefai, Jean‐Christophe Grenier, Raphaël Poujol, et al.
NAR Genomics and Bioinformatics (2024) Vol. 6, Iss. 4
Open Access | Times Cited: 2
Somatic mutation burden in relation to aging and functional life span: implications for cellular reprogramming and rejuvenation
Alexander Y. Maslov, Jan Vijg
Current Opinion in Genetics & Development (2023) Vol. 83, pp. 102132-102132
Open Access | Times Cited: 4
De novo identification of expressed cancer somatic mutations from single-cell RNA sequencing data
Tianyun Zhang, Hanying Jia, Tairan Song, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Identifying cancer cells from calling single-nucleotide variants in scRNA-seq data
Valérie Marot-Lassauzaie, Sergi Beneyto‐Calabuig, Benedikt Obermayer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
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