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 1-25 of 91 citing articles:

Spatial transcriptomics reveals distinct and conserved tumor core and edge architectures that predict survival and targeted therapy response
Rohit Arora, Christian Cao, Mehul Kumar, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 95

Neuronal DNA double-strand breaks lead to genome structural variations and 3D genome disruption in neurodegeneration
Vishnu Dileep, Carles A. Boix, Hansruedi Mathys, et al.
Cell (2023) Vol. 186, Iss. 20, pp. 4404-4421.e20
Open Access | Times Cited: 68

Clonally resolved single-cell multi-omics identifies routes of cellular differentiation in acute myeloid leukemia
Sergi Beneyto‐Calabuig, Anne Kathrin Merbach, Jonas-Alexander Kniffka, et al.
Cell stem cell (2023) Vol. 30, Iss. 5, pp. 706-721.e8
Open Access | Times Cited: 54

Early Immune Remodeling Steers Clinical Response to First-Line Chemoimmunotherapy in Advanced Gastric Cancer
Minae An, Arnav Mehta, Byung‐Hoon Min, et al.
Cancer Discovery (2024) Vol. 14, Iss. 5, pp. 766-785
Open Access | Times Cited: 22

Deeper response predicts better outcomes in high-risk-smoldering-myeloma: results of the I-PRISM phase II clinical trial
Omar Nadeem, Michelle P. Aranha, Robert Redd, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2

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

Acquired resistance to a GPRC5D-directed T-cell engager in multiple myeloma is mediated by genetic or epigenetic target inactivation
Jennifer Derrien, Sarah Gastineau, Antoine Frigout, et al.
Nature Cancer (2023) Vol. 4, Iss. 11, pp. 1536-1543
Open Access | Times Cited: 42

Single-cell sequencing reveals the mechanisms of multiple myeloma progression: clarity or confusion?
Yunhui Xiang, Guokang Sun, Lvbo Tian, et al.
Annals of Hematology (2025)
Open Access | Times Cited: 1

Pan-cancer human brain metastases atlas at single-cell resolution
Xudong Xing, Jian Zhong, Jana Biermann, et al.
Cancer Cell (2025)
Closed Access | Times Cited: 1

Allele-specific transcriptional effects of subclonal copy number alterations enable genotype-phenotype mapping in cancer cells
Hongyu Shi, Marc Williams, Gryte Satas, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8

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.
Cancer Cell (2024)
Closed Access | Times Cited: 6

Somatic cancer driver mutations are enriched and associated with inflammatory states in Alzheimer’s disease microglia
August Yue Huang, Zinan Zhou, Maya Talukdar, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

Deciphering the heterogeneity and immunosuppressive function of regulatory T cells in osteosarcoma using single-cell RNA transcriptome
Debin Cheng, Zhao Zhang, Zhenzhou Mi, et al.
Computers in Biology and Medicine (2023) Vol. 165, pp. 107417-107417
Open Access | Times Cited: 13

Copy number alterations: a catastrophic orchestration of the breast cancer genome
Parastoo Shahrouzi, Farzaneh Forouz, Anthony Mathelier, et al.
Trends in Molecular Medicine (2024) Vol. 30, Iss. 8, pp. 750-764
Open Access | Times Cited: 4

Ongoing genome doubling promotes evolvability and immune dysregulation in ovarian cancer
Andrew McPherson, Ignacio Vázquez-Garćıa, Matthew A. Myers, et al.
(2024)
Closed Access | Times Cited: 4

Aneuploidy as a driver of human cancer
Eran Sdeor, Hajime Okada, Ron Saad, et al.
Nature Genetics (2024)
Closed Access | Times Cited: 4

Modeling specific aneuploidies: from karyotype manipulations to biological insights
My Anh Truong, Paula Cané‐Gasull, Susanne M.A. Lens
Chromosome Research (2023) Vol. 31, Iss. 3
Open Access | Times Cited: 10

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

Conserved patterns of transcriptional dysregulation, heterogeneity, and cell states in clear cell kidney cancer
Olivia Lombardi, Ran Li, Faiz Jabbar, et al.
Cell Reports (2025) Vol. 44, Iss. 1, pp. 115169-115169
Closed Access

Inactivation of TACC2 epigenetically represses CDKN1A and confers sensitivity to CDK inhibitors
Zhi-Rui Lin, Tian-Liang Xia, Mengyao Wang, et al.
Med (2025), pp. 100568-100568
Open Access

Three-dimensional patient-derived models of glioblastoma retain intra-tumoral heterogeneity
Zachery Moore, Claire Storey, Daniel V. Brown, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Detecting copy-number alterations from single-cell chromatin sequencing data by AtaCNA
Xiao-Chen Wang, Zijie Jin, Yang Shi, et al.
Cell Reports Methods (2025), pp. 100939-100939
Open Access

Coordinated immune networks in leukemia bone marrow microenvironments distinguish response to cellular therapy
Katie Maurer, Cameron Y. Park, Shouvik Mani, et al.
Science Immunology (2025) Vol. 10, Iss. 103
Closed Access

Deconvolution and Phylogeny Inference of Diverse Variant Types Integrating Bulk DNA-seq with Single-cell RNA-seq
Nishat Anjum Bristy, Russell Schwartz
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

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