Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Extensive phylogenies of human development inferred from somatic mutations
Tim H. H. Coorens, Luiza Moore, Philip S. Robinson, et al.
Nature (2021) Vol. 597, Iss. 7876, pp. 387-392
Open Access | Times Cited: 129

Showing 26-50 of 129 citing articles:

The somatic mutation landscape of normal gastric epithelium
Tim H. H. Coorens, Grace Collord, Hyungchul Jung, et al.
Nature (2025)
Open Access | Times Cited: 1
Somatic variation in normal tissues: friend or foe of cancer early detection?
Amelia Acha‐Sagredo, Piyali Ganguli, Francesca D. Ciccarelli
Annals of Oncology (2022) Vol. 33, Iss. 12, pp. 1239-1249
Open Access | Times Cited: 29
Prenatal BRCA1 epimutations contribute significantly to triple-negative breast cancer development
Oleksii Nikolaienko, Hans Petter Eikesdal, Elisabet Ognedal, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 18
Somatic mutations in human ageing: New insights from DNA sequencing and inherited mutations
Kasit Chatsirisupachai, João Pedro de Magalhães
Ageing Research Reviews (2024) Vol. 96, pp. 102268-102268
Open Access | Times Cited: 8
Mitochondrial DNA mosaicism in normal human somatic cells
Jisong An, Chang Hyun Nam, Ryul Kim, et al.
Nature Genetics (2024) Vol. 56, Iss. 8, pp. 1665-1677
Open Access | Times Cited: 7
A statistical method for quantifying progenitor cells reveals incipient cell fate commitments
Shanjun Deng, Han Gong, Di Zhang, et al.
Nature Methods (2024) Vol. 21, Iss. 4, pp. 597-608
Open Access | Times Cited: 6
MQuad enables clonal substructure discovery using single cell mitochondrial variants
Aaron Wing Cheung Kwok, Chen Qiao, Rongting Huang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 28
Quantitative fate mapping: A general framework for analyzing progenitor state dynamics via retrospective lineage barcoding
Weixiang Fang, Claire Bell, Abel Sapirstein, et al.
Cell (2022) Vol. 185, Iss. 24, pp. 4604-4620.e32
Open Access | Times Cited: 23
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations
Peter J. Campbell, Michael Spencer Chapman, C. Matthias Wilk, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 16
Previously reported and here added cases demonstrate euploid pregnancies followed by PGT-A as “mosaic” as well as “aneuploid” designated embryos
Norbert Gleicher, Pasquale Patrizio, Lyka Mochizuki, et al.
Reproductive Biology and Endocrinology (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 15
Clonal origin of KMT2A wild-type lineage-switch leukemia following CAR-T cell and blinatumomab therapy
Tim H. H. Coorens, Grace Collord, Taryn D. Treger, et al.
Nature Cancer (2023) Vol. 4, Iss. 8, pp. 1095-1101
Open Access | Times Cited: 14
Mapping recurrent mosaic copy number variation in human neurons
Chen Sun, Kunal Kathuria, Sarah B. Emery, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Cancer-Causative Mutations Occurring in Early Embryogenesis
Fresia Pareja, Ryan Ptashkin, David Brown, et al.
Cancer Discovery (2021) Vol. 12, Iss. 4, pp. 949-957
Open Access | Times Cited: 29
Somatic Mutation: What Shapes the Mutational Landscape of Normal Epithelia?
Joanna C. Fowler, Philip H. Jones
Cancer Discovery (2022) Vol. 12, Iss. 7, pp. 1642-1655
Open Access | Times Cited: 22
Embryonic and extraembryonic tissues during mammalian development: shifting boundaries in time and space
Shifaan Thowfeequ, Shankar Srinivas
Philosophical Transactions of the Royal Society B Biological Sciences (2022) Vol. 377, Iss. 1865
Open Access | Times Cited: 19
Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
Albert Herms, Philip H. Jones
Annual Review of Cancer Biology (2023) Vol. 7, Iss. 1, pp. 189-205
Open Access | Times Cited: 11
Mitochondrial mutation, drift and selection during human development and ageing
Peter J. Campbell, Michael Spencer Chapman, Moritz J. Przybilla, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 11
Reconstructing phylogenetic trees from genome-wide somatic mutations in clonal samples
Tim H. H. Coorens, Michael Spencer Chapman, Nicholas Williams, et al.
Nature Protocols (2024) Vol. 19, Iss. 6, pp. 1866-1886
Closed Access | Times Cited: 4
Characterization of clonal dynamics using duplex sequencing in donor-recipient pairs decades after hematopoietic cell transplantation
Masumi Ueda, Jacob E. Higgins, Isaac Jenkins, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 770
Closed Access | Times Cited: 4
Applying single-cell and single-nucleus genomics to studies of cellular heterogeneity and cell fate transitions in the nervous system
Igor Adameyko, Trygve E. Bakken, Aparna Bhaduri, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 12, pp. 2278-2291
Closed Access | Times Cited: 4
Reconstructing Progenitor State Hierarchy and Dynamics Using Lineage Barcoding Data
Weixiang Fang, Yi-Jung Yang, Hongkai Ji, et al.
Methods in molecular biology (2025), pp. 177-199
Closed Access
Landscape of human protein-coding somatic mutations across tissues and individuals
Huixin Xu, Rob Bierman, Dayna T. Akey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Single-cell DNA sequencing reveals pervasive positive selection throughout preleukemic evolution
Gladys Y. P. Poon, Aditi Vedi, Mathijs A. Sanders, et al.
Cell Genomics (2025), pp. 100744-100744
Open Access
Bone Marrow Niche in Cardiometabolic Disease: Mechanisms and Therapeutic Potential
Zachary A. Kohutek, Heather L. Caslin, Daniel J. Fehrenbach, et al.
Circulation Research (2025) Vol. 136, Iss. 3, pp. 325-353
Closed Access
ScisTree2: An Improved Method for Large-Scale Inference of Cell Lineage Trees and Genotype Calling from Noisy Single Cell Data
Haotian Zhang, Yiming Zhang, Teng Gao, et al.
Lecture notes in computer science (2025), pp. 277-280
Closed Access

Scroll to top