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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:

Haplotype-aware analysis of somatic copy number variations from single-cell transcriptomes
Teng Gao, Ruslan Soldatov, Hirak Sarkar, et al.
Nature Biotechnology (2022) Vol. 41, Iss. 3, pp. 417-426
Closed Access | Times Cited: 91

Showing 26-50 of 91 citing articles:

Mutant IDH impairs chromatin binding by PDGFB to promote chromosome instability
Rachel Naomi Curry, Malcolm F. McDonald, Peihao He, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Benchmarking copy number aberrations inference tools using single-cell multi-omics datasets
Minfang Song, Shuai Ma, Gong Wang, et al.
Briefings in Bioinformatics (2025) Vol. 26, Iss. 2
Open Access
CNRein: an evolution-aware deep reinforcement learning algorithm for single-cell DNA copy number calling
Stefan Ivanovic, Mohammed El-Kebir
Genome biology (2025) Vol. 26, Iss. 1
Open 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
Clonal Evolution and Transcriptional Plasticity Shape Metastatic Dissemination Routes in Prostate Cancer
Joachim Weischenfeldt, Migle Mikutenaite, Evdoxia Karadoulama, et al.
Research Square (Research Square) (2025)
Closed Access
TeaCNV: decoding tumor somatic absolute copy number and clonal architecture from single cell chromatin accessibility data
Shaojun Zhang, Ying Wang, Yuhao Deng, et al.
Research Square (Research Square) (2025)
Closed Access
Deconvoluting clonal and cellular architecture in IDH-mutant acute myeloid leukemia
Maria Sirenko, Soobeom Lee, Zhengxi Sun, et al.
Cell stem cell (2025)
Closed Access
A pan-tissue survey of mosaic chromosomal alterations in 948 individuals
Teng Gao, Maria Eleni Kastriti, Viktor Ljungström, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1901-1911
Open Access | Times Cited: 9
STmut: a framework for visualizing somatic alterations in spatial transcriptomics data of cancer
Limin Chen, Darwin Chang, Bishal Tandukar, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 9
Coordinated Immune Cell Networks in the Bone Marrow Microenvironment Define the Graft versus Leukemia Response with Adoptive Cellular Therapy
Katie Maurer, Cameron Y. Park, Shouvik Mani, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Integrated electrophysiological and genomic profiles of single cells reveal spiking tumor cells in human glioma
Rachel Naomi Curry, Qianqian Ma, Malcolm F. McDonald, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Evolution-Aware Deep Reinforcement Learning for Single-Cell DNA Copy Number Calling
Stefan Ivanovic, Mohammed El-Kebir
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Phasing millions of samples achieves near perfect accuracy, enabling parent-of-origin classification of variants
Cole M. Williams, Jared O’Connell, William A. Freyman, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
HATCHet2: clone- and haplotype-specific copy number inference from bulk tumor sequencing data
Matthew A. Myers, Brian J. Arnold, Vineet Bansal, et al.
Genome biology (2024) Vol. 25, 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
Molecular Basis of Pancreatic Neuroendocrine Tumors
Alesia Maluchenko, Denis Maksimov, Zoya Antysheva, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 20, pp. 11017-11017
Open Access | Times Cited: 3
Clonal phylogenies inferred from bulk, single cell, and spatial transcriptomic analysis of epithelial cancers
Andrew Erickson, Sandy Figiel, Timothy Rajakumar, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0316475-e0316475
Open Access
Learning Phenotype Associated Signature in Spatial Transcriptomics with PASSAGE
C. Guo, Chen‐Rui Xia, Guangdun Peng, et al.
Small Methods (2025)
Open Access
Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression
Jelena Milosevic, Susanne Fransson, Johanna Svensson, et al.
Research Square (Research Square) (2025)
Open Access
Contribution of germline and somatic mutations to risk of neuromyelitis optica spectrum disorder
Tomohiro Yata, Go Sato, Kotaro Ogawa, et al.
Cell Genomics (2025), pp. 100776-100776
Open Access
The landscape of cell lineage tracing
Feng Ye, Liu Guang, Haiqing Li, et al.
Science China Life Sciences (2025)
Closed Access
New horizons at the interface of artificial intelligence and translational cancer research
Josephine Yates, Eliezer M. Van Allen
Cancer Cell (2025) Vol. 43, Iss. 4, pp. 708-727
Closed Access
Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression
Jelena Milosevic, Susanne Fransson, Johanna Svensson, et al.
Cancer Letters (2025), pp. 217769-217769
Open Access
Single-Cell Profiling in Multiple Myeloma: Insights, Problems, and Promises
Mehmet Samur, Raphaël Szalat, Nikhil Munshi
Blood (2023)
Closed Access | Times Cited: 6
Toward the functional interpretation of somatic structural variations: bulk- and single-cell approaches
Dohun Yi, Jin‐Wu Nam, Hyobin Jeong
Briefings in Bioinformatics (2023) Vol. 24, Iss. 5
Open Access | Times Cited: 6

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