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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 multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths
Mariela Cortés-López, Paulina Chamely, Allegra G. Hawkins, et al.
Cell stem cell (2023) Vol. 30, Iss. 9, pp. 1262-1281.e8
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Single-cell sequencing to multi-omics: technologies and applications
Xiangyu Wu, Xin Yang, Yunhan Dai, et al.
Biomarker Research (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 18
Cancer cell states: Lessons from ten years of single-cell RNA-sequencing of human tumors
Itay Tirosh, Mario L. Suvà
Cancer Cell (2024) Vol. 42, Iss. 9, pp. 1497-1506
Closed Access | Times Cited: 14
Integrative genotyping of cancer and immune phenotypes by long-read sequencing
Livius Penter, Mehdi Borji, Adi Nagler, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Single-cell and spatial transcriptomics: Bridging current technologies with long-read sequencing
Chengwei Ulrika Yuan, Fu Xiang Quah, Martin Hemberg
Molecular Aspects of Medicine (2024) Vol. 96, pp. 101255-101255
Closed Access | Times Cited: 6
Steering research on mRNA splicing in cancer towards clinical translation
Olga Anczuków, Frédéric H.‐T. Allain, Brittany Angarola, et al.
Nature reviews. Cancer (2024) Vol. 24, Iss. 12, pp. 887-905
Closed Access | Times Cited: 6
Single-cell genotype-phenotype mapping identifies therapeutic vulnerabilities in VEXAS syndrome
Saravanan Ganesan, Rebecca M. Murray, Jesús Alfonso López Sotélo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Mis-splicing of Mitotic Regulators Sensitizes SF3B1-Mutated Human HSCs to CHK1 Inhibition
Martina Sarchi, Courtnee Clough, Edie I. Crosse, et al.
Blood Cancer Discovery (2024) Vol. 5, Iss. 5, pp. 353-370
Open Access | Times Cited: 4
Strand Displacement-Enhanced CRISPR-Cas13a System for Ultra-Specific Detection of RNA Single Nucleotide Variation
Hao Hu, Haiyan Xue, Kejun Dong, et al.
Biosensors and Bioelectronics (2025), pp. 117445-117445
Closed Access
Clonal Hematopoiesis, a Risk Condition for Developing Myeloid Neoplasia
Ugo Testa, Germana Castelli, Elvira Pelosi
Hemato (2025) Vol. 6, Iss. 2, pp. 10-10
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
Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
Ashley Byrne, Daniel Le, Kostianna Sereti, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Decoding Cancer Evolution: Integrating Genetic and Non-Genetic Insights
Arghavan Ashouri, Chufan Zhang, Federico Gaiti
Genes (2023) Vol. 14, Iss. 10, pp. 1856-1856
Open Access | Times Cited: 7
Long-read transcriptome sequencing of CLL and MDS patients uncovers molecular effects ofSF3B1mutations
Alicja Pacholewska, Matthias Lienhard, Mirko Brüggemann, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 1832-1848
Closed Access | Times Cited: 2
Adenine base editor–mediated splicing remodeling activates noncanonical splice sites
Yuanyuan Liu, Qing Li, Tong Yan, et al.
Journal of Biological Chemistry (2023) Vol. 299, Iss. 12, pp. 105442-105442
Open Access | Times Cited: 4
Single-cell Rapid Capture Hybridization sequencing (scRaCH-seq) to reliably detect isoform usage and coding mutations in targeted genes at a single-cell level
Hongke Peng, Jafar S. Jabbari, Luyi Tian, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Competition of dual SF3B1mt clones in MDS-RS is associated with distinct RNA mis-splicing in hematopoietic stem cells
Pedro Luís Moura, Yasuhito Nannya, Affaf Aliouat, et al.
Deleted Journal (2024) Vol. 1, Iss. 2, pp. 100011-100011
Open Access | Times Cited: 1
RoCK and ROI: Single-cell transcriptomics with multiplexed enrichment of selected transcripts and region-specific sequencing
Giulia Moro, Izaskun Mallona, Joël Maillard, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Long-read RNA sequencing of archival tissues reveals novel genes and transcripts associated with clear cell renal cell carcinoma recurrence and immune evasion
Joshua Lee, Elizabeth A. Snell, Julia Brown, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 1849-1864
Closed Access | Times Cited: 1
Understanding MDS stem cells – advances and limitations
Sweta B. Patel, Daniel R Moskop, Craig T. Jordan, et al.
Seminars in Hematology (2024)
Closed Access | Times Cited: 1
RNA splicing as a therapeutic target in myelodysplastic syndromes
C.-C. Tseng, Esther A. Obeng
Seminars in Hematology (2024)
Open Access | Times Cited: 1
Cancer liquid biopsies by Oxford Nanopore Technologies sequencing of cell-free DNA: from basic research to clinical applications
Huaqi Si, Peng Wang, Fei Long, et al.
Molecular Cancer (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 1
Single-cell genomics in acquired bone marrow failure syndromes
Zhijie Wu, Neal S. Young
Blood (2023) Vol. 142, Iss. 14, pp. 1193-1207
Open Access | Times Cited: 3
Long-read RNA sequencing redefines the clear cell renal cell carcinoma transcriptome and reveals novel genes and transcripts associated with disease recurrence and immune evasion
Joshua Lee, Elizabeth A. Snell, Julia Brown, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Adding Splicing to the Cake: Enhancing Single-cell Multi-omics With Detection of Splicing Changes
Bethan Psaila
The Hematologist (2024) Vol. 21, Iss. 2
Open Access
Loss of hematopoietic progenitors heterogeneity is an adverse prognostic factor in lower-risk myelodysplastic neoplasms
Charles Dussiau, Thibault Comont, Camille Knosp, et al.
Leukemia (2024) Vol. 38, Iss. 5, pp. 1131-1142
Open Access
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