The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Prediction of acute myeloid leukaemia risk in healthy individuals
Open accessAbstract
The incidence of acute myeloid leukaemia (AML) increases with age and mortality exceeds 90% when diagnosed after age 65. Most cases arise without any detectable early symptoms and patients usually present with the acute complications of bone marrow failure 1. The onset of such de novo AML cases is typically preceded by the accumulation of somatic mutations in preleukaemic haematopoietic stem and progenitor cells (HSPCs) that undergo clonal expansion 2,3. However, recurrent AML mutations also accumulate in HSPCs during ageing of healthy individuals who do not develop AML, a phenomenon referred to as age-related clonal haematopoiesis (ARCH)4-8. Here we use deep sequencing to analyse genes that are recurrently mutated in AML to distinguish between individuals who have a high risk of developing AML and those with benign ARCH. We analysed peripheral blood cells from 95 individuals that were obtained on average 6.3 years before AML diagnosis (pre-AML group), together with 414 unselected age- and gender-matched individuals (control group). Pre-AML cases were distinct from controls and had more mutations per sample, higher variant allele frequencies, indicating greater clonal expansion, and showed enrichment of mutations in specific genes. Genetic parameters were used to derive a model that accurately predicted AML-free survival; this model was validated in an independent cohort of 29 pre-AML cases and 262 controls. Because AML is rare, we also developed an AML predictive model using a large electronic health record database that identified individuals at greater risk. Collectively our findings provide proof-of-concept that it is possible to discriminate ARCH from pre-AML many years before malignant transformation. This could in future enable earlier detection and monitoring, and may help to inform intervention.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Furthermore, progression to hematological malignancies depends on the type and complexity of mutations in CHIP.2,5,6”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [5]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“CH-associated variants of the epigenetic writers and erasers Dnmt3a and Tet2, respectively, that affect the HSPC methylome have been shown to alter functions of monocyte-derived tissue M F and promote cardiovascular pathologies 31-34 .”
From Clonal hematopoiesis-associated motoric deficits caused by monocyte-derived microglia accumulating in aging mice (2025) · cites this paper as [34]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“CH prominently involves variants of epigenetic regulatory genes, such as DNMT3A and TET2, which constitute an increased risk for hematologic malignancies, cardiovascular events and stroke 34,45,70,71 .”
From Clonal hematopoiesis-associated motoric deficits caused by monocyte-derived microglia accumulating in aging mice (2025) · cites this paper as [34]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Clone size, which is approximated by the variant allele fraction (VAF), has previously been shown to be an important predictor of risk for blood cancer1,17 and cardiovascular outcomes8,9.”
From Clonal hematopoiesis is associated with protection from Alzheimer’s disease (2023) · cites this paper as [17]
The cited source says what the claim attributes to it.
In the citing paper
“CH prominently involves variants of epigenetic regulatory genes, such as DNMT3A and TET2, which constitute an increased risk for hematologic malignancies, cardiovascular events and stroke 34,45,70,71 .”
From Clonal hematopoiesis-associated motoric deficits caused by monocyte-derived microglia accumulating in aging mice (2025) · cites this paper as [34]
In the citing paper
“Both groups found that individuals with antecedent clonal hematopoiesis were at ~3 to 5-fold increased risk for developing AML in the subsequent years (Fig. 3A).”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [71]
In the citing paper
“The effect of specific gene variants on various outcomes may be quite different, as has been found in AML 71.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [71]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al. (2010) · Genome Research · doi:10.1101/gr.107524.110 · Cited by 27,895
BEDTools: a flexible suite of utilities for comparing genomic features
Quinlan, A. R., & Hall, I. M. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq033 · Cited by 27,437
Fast and accurate long-read alignment with Burrows-Wheeler transform.
Li, H., & Durbin, R. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp698 · Cited by 12,063
Arber, D. A., Orazi, A., Hasserjian, R., Thiele, J., Borowitz, M. J., Le Beau, M. M., Bloomfield, C. D., Cazzola, M., & Vardiman, J. W. (2016) · Blood · doi:10.1182/blood-2016-03-643544 · Cited by 10,119
Modeling Survival Data: Extending the Cox Model
Therneau, T. M., & Grambsch, P. M. (2000) · Statistics for Biology and Health · doi:10.1007/978-1-4757-3294-8 · Cited by 8,674
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencingPreprint
Koboldt, D. C., Zhang, Q., Larson, D. E., Shen, D., McLellan, M. D., Lin, L., Miller, C. A., Mardis, E. R., Ding, L., & Wilson, R. K. (2012) · Genome Research · doi:10.1101/gr.129684.111 · Cited by 4,954
Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841
Genomic classification and prognosis in acute myeloid leukemia
Papaemmanuil, E., Gerstung, M., Bullinger, L., Gaidzik, V. I., Paschka, P., Roberts, N. D., Potter, N. E., Heuser, M., Thol, F., Bolli, N., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1516192 · Cited by 4,350
Self-citationClonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
Genovese, G., Kähler, A. K., Handsaker, R. E., Lindberg, J., Rose, S. A., Bakhoum, S. F., Chambert, K., Mick, E., Neale, B. M., Fromer, M., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1409405 · Cited by 3,531
Cited by
Sorted by citations
Items 601–700 of 847
Jia, Z.-Y., Abulimiti, M., Wu, Y., Ma, L., Li, X., & Wang, J. (2025) · Heliyon · doi:10.1016/j.heliyon.2025.e42030 · Cited by 4
Benzene-induced hematotoxicity enhances the self-renewal ability of HSPCs in Mll-Af9 mice
Zhou, J., Sui, P., Zhao, J., Cheng, X., Tao, Y., Cui, S., Song, X., & Xing, C. (2025) · Toxicology · doi:10.1016/j.tox.2025.154061 · Cited by 3
Low WT1 Expression Identifies a Subset of Acute Myeloid Leukemia with a Distinct Genotype
Rondoni, M., Marconi, G., Nicoletti, A., Giannini, B., Zuffa, E., Giannini, M. B., Mianulli, A., Norata, M., Monaco, F., Zacheo, I., et al. (2025) · Cancers · doi:10.3390/cancers17071213 · Cited by 3
Guerrero, C., Larráyoz, M. J., Erdozain, I., Puig, N., Cedena, M., Maia, C., Mañú, A., Gordillo, N., Churruca, O., Alignani, D., et al. (2025) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-24-0274 · Cited by 3
Brogan, J., Kishtagari, A., Corty, R. W., Pershad, Y., Vlasschaert, C., Sharber, B., Heimlich, J. B., Luo, L. Y., Ferrell, P. B., Savona, M. R., et al. (2025) · EClinicalMedicine · doi:10.1016/j.eclinm.2025.103283 · Cited by 6
Hereditary Hematopoietic Malignancies: Considerations for Optimizing Diagnosis and Management
Trottier, A. M., Cunningham, L., & Godley, L. A. (2025) · Current Oncology Reports · doi:10.1007/s11912-025-01699-7 · Cited by 4
Emerging patterns in clonal haematopoiesis
Capo‐Chichi, J., Michaels, P. D., May, R. T.-L., Abelson, S., Hasserjian, R. P., & Xia, D. (2019) · Journal of Clinical Pathology · doi:10.1136/jclinpath-2019-205851 · Cited by 3
Systems Biology and Integrated Computational Methods for Cancer-Associated Mutation Analysis
Zia, A., & Rashid, S. (2020) · Springer eBooks · doi:10.1007/978-981-15-1067-0_13 · Cited by 3
Cellular Therapy in Follicular Lymphoma
Okosun, J., & Montoto, S. (2020) · Hematology/Oncology Clinics of North America · doi:10.1016/j.hoc.2020.02.006 · Cited by 3
Steensma, D. P. (2021) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2021.101327 · Cited by 3
Edahiro, T., Ureshino, H., Chishaki, R., Fujino, K., Mino, T., Yoshida, T., Fukushima, N., & Ichinohe, T. (2022) · Internal Medicine · doi:10.2169/internalmedicine.1069-22 · Cited by 3
The etiology of clonal mosaicism in human aging and disease
Massaar, S., & Sanders, M. A. (2023) · Aging and Cancer · doi:10.1002/aac2.12061 · Cited by 4
Craven, K. E., & Ewalt, M. D. (2023) · Clinics in Laboratory Medicine · doi:10.1016/j.cll.2023.06.001 · Cited by 3
AlJabban, A., & Alalsaidissa, J. N. J. (2024) · Iraqi Journal of Hematology · doi:10.4103/ijh.ijh_7_24 · Cited by 3
Management of vulnerable patient phenotypes and acute coronary syndrome mechanisms
Vito, L. D., Giusto, F. D., Mazzotta, S., Scalone, G., Bruscoli, F., Silenzi, S., Selimi, A., Angelini, M., Galieni, P., & Grossi, P. (2024) · International Journal of Cardiology · doi:10.1016/j.ijcard.2024.132365 · Cited by 4
Utilizing insights of DNA repair machinery to discover MMEJ deletions and novel mechanisms
Kadam, A., Shilo, S., Naor, H., Wainstein, A., Brilon, Y., Feldman, T., Minden, M. D., Kaushansky, N., Chapal-Ilani, N., & Shlush, L. I. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1132 · Cited by 3
Evolution of myeloproliferative neoplasms from normal blood stem cells
Hormoz, S., Sankaran, V. G., & Mullally, A. (2024) · Haematologica · doi:10.3324/haematol.2023.283951 · Cited by 3
MBD4: guardian of the epigenetic galaxy
Busque, L., & Godley, L. A. (2018) · Blood · doi:10.1182/blood-2018-08-867044 · Cited by 3
The Bone’s Role in Myeloid Neoplasia
Kazianka, L., & Staber, P. B. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134712 · Cited by 3
Dart, A. (2018) · Nature reviews. Cancer · doi:10.1038/s41568-018-0046-z · Cited by 3
On fitness: how do mutations shape the biology of cancer?
Majewski, I. J. (2019) · Biochemical Society Transactions · doi:10.1042/bst20180224 · Cited by 3
Leukemia’s Clonal Evolution in Development, Progression, and Relapse
Loh, J. W., & Khiabanian, H. (2019) · Current Stem Cell Reports · doi:10.1007/s40778-019-00157-y · Cited by 3
Plant homeodomain finger protein 6 in the regulation of normal and malignant hematopoiesis
Miyagi, S., & Iwama, A. (2020) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000588 · Cited by 3
Kinetics of pre‐myelodysplastic syndromes blood values correlate with disease risk and survival
Joffe, E., Greenbaum, U., Man‐El, G., Filanovsky, K., Oster, H. S., Levi, I., Raanani, P., Avivi, I. M., & Mittelman, M. (2020) · Hematological Oncology · doi:10.1002/hon.2777 · Cited by 3
Leukemia Stem Cells: Concept and Implications
Sánchez-Garcı́a, I., & Cobaleda, C. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0810-4_2 · Cited by 3
Li, Z., He, Z., Wang, J., & Kong, G. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiac015 · Cited by 3
Home and away: clonal hematopoiesis in sibling transplants
Fabre, M. A., & Vassiliou, G. S. (2020) · Blood · doi:10.1182/blood.2020005717 · Cited by 3
Karpova, D., Encabo, H. H., Donato, E., Kotova, I., Calderazzo, S., Leppä, A., Panten, J., Przbylla, A., Seifried, E., Kopp‐Schneider, A., et al. (2022) · medRxiv · doi:10.1101/2022.07.24.22277825 · Cited by 3
Uncovering the Gene Profile of Acute Myeloid Leukaemia Using Gradient Boosted TreesPreprint
Angelakis, A., Nathoe, R., & Filippakis, M. Ε. (2022) · Research Square · doi:10.21203/rs.3.rs-2374064/v1 · Cited by 3
Towards the Gene Profile of Acute Myeloid Leukaemia Using Machine Learning and Blood TranscriptomicsPreprint
Angelakis, A., Nathoe, R., & Filippakis, M. Ε. (2024) · Preprints.org · doi:10.20944/preprints202402.0593.v1 · Cited by 3
Risk of Incident Cytopenia in Clonal HematopoiesisPreprint
Brogan, J., Kishtagari, A., Corty, R. W., Pershad, Y., Vlasschaert, C., Sharber, B., Heimlich, J. B., Luo, L. Y., Xu, Y., & Bick, A. G. (2024) · medRxiv · doi:10.1101/2024.09.30.24314665 · Cited by 3
Clonal hematopoiesis: A challenge or opportunity in liquid biopsy?
Aran, V. (2025) · The Journal of Liquid Biopsy · doi:10.1016/j.jlb.2025.100292 · Cited by 2
Kim, J., Bae, S., Choi, J., Im, S.-W., Cha, B., Jung, G., Cho, S. W., Seo, E., Lee, Y. A., Paeng, J. C., et al. (2025) · Molecular Oncology · doi:10.1002/1878-0261.70078 · Cited by 2
Acute Leukemia Warning Model Combined CBC and CPD Data Based on Machine Learning
Gao, H., Wang, Y., Li, X., Liu, Z., Cai, J., Yang, W., Wang, F., Sun, Z., & You, C. (2025) · International Journal of Laboratory Hematology · doi:10.1111/ijlh.14538 · Cited by 2
The Impact of Splicing Factor Mutations on Clonal Hematopoiesis and Myeloid Neoplasm Progression
Izumi, T., Kawachi, A., & Yoshimi, A. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl38825 · Cited by 2
Of Barriers and Loops—How Evolution Limits Most Cancer Risks to Older Ages
Dominici, M. D., & DeGregori, J. V. (2026) · Cancer Discovery · doi:10.1158/2159-8290.cd-25-0779 · Cited by 3
Metformin Does Not Significantly Alter Longitudinal Dynamics of Clonal Hematopoiesis
Pareek, E., Pershad, Y., Zhao, K., Uddin, M. M., Xue, L., Vlasschaert, C., Mack, T., Haessler, J., Collins, J. M., Glick, E., et al. (2026) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-25-3606 · Cited by 2
Blood-based epigenetic instability linked to human aging and disease
Basrai, S., Nofech-Mozes, I., Detroja, R., Scolari, F. L., Bakhtiari, M., Arruda, A., Murphy, T., Bratman, S. V., Chan, S. M., Minden, M. D., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69430-z · Cited by 4
Beer, S. A., Huber, C., Nasyrov, E., Wolfram, L., Pietzsch, M., Schenk, A., Sommer, M., Wedrich, A., Lengerke, C., Doycheva, D., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-37804-4 · Cited by 2
The interplay of clonal hematopoiesis and cancer: Clinical implications in oncology
Tanguay, M., Tagliamento, M., Samaniego, J., Besse, B., Renneville, A., Bernard, E., & Micol, J. (2026) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2026.103109 · Cited by 3
Harnessing genomics for early cancer detection, risk stratification and prevention
Gu, M., Zhang, W. Z., Fitzgerald, R. C., Frankell, A. M., & Vassiliou, G. S. (2026) · Nature Genetics · doi:10.1038/s41588-026-02505-1 · Cited by 4
Prefibrotic bone marrow microenvironment is a hallmark of clonal hematopoiesis
Aguilar-Navarro, A. G., Edun, G., Gower, M., Kant, J. A., Li, X., Yang, D., Nader, M., Fernandez, M. M., Jahangiri, S., Tsao, E., et al. (2026) · Nature Immunology · doi:10.1038/s41590-026-02668-3 · Cited by 1
A single-cell lens into the co-evolution of genotypes and phenotypes in cancer
Izzo, F., Prieto, T., Potenski, C. J., & Landau, D. A. (2026) · Nature reviews. Cancer · doi:10.1038/s41568-026-00970-8 · Cited by 2
AML: Predicting the Unpredictable
Takahashi, K. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.07.005 · Cited by 2
Is the philosopher’s stone to rejuvenate blood stem cells an epigenetic regulator?
Svendsen, A. F., & de Haan, G. (2022) · Nature Aging · doi:10.1038/s43587-022-00305-w · Cited by 2
Can molecular patterns help to classify overlapping entities in myeloid neoplasms?
Hoermann, G., & Khoury, J. D. (2024) · Histopathology · doi:10.1111/his.15339 · Cited by 2
Alternative Splicing: A Potential Therapeutic Target in Hematological Malignancies
Temaj, G., Chichiarelli, S., Saha, S., Telkoparan‐Akillilar, P., Nuhii, N., Hadžiselimović, R., & Saso, L. (2024) · Hematology Reports · doi:10.3390/hematolrep16040066 · Cited by 2
Christopher, M. R., Nawas, M. T., & Reagan, J. L. (2024) · Bone Marrow Transplantation · doi:10.1038/s41409-024-02465-2 · Cited by 2
Understanding Human Oncogene Function and Cooperativity in Myeloid Malignancy Using iPSCs
Sarchi, M., & Doulatov, S. R. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104697 · Cited by 2
Lin, S., Li, Y. E., & Wang, Y. (2025) · Advanced Genetics · doi:10.1002/ggn2.202400047 · Cited by 2
Chien, K. S., Braish, J. S., Li, Z., Loghavi, S., Bataller, Á., Bravo, G. M., Sasaki, K., Kanagal‐Shamanna, R., Takahashi, K., Dinardo, C. D., et al. (2025) · Leukemia · doi:10.1038/s41375-025-02564-z · Cited by 2
Yao, X., Wang, H., & Yang, L. (2025) · Acta Haematologica · doi:10.1159/000545724 · Cited by 2
A case diagnosis as acute myeloid leukemia on a Family Medicine Policlinic
Tatar, S., & Öngel, K. (2019) · The Journal of Turkish Family Physician · doi:10.15511/tjtfp.19.00299 · Cited by 2
Clonal hematopoiesis sees Twin Peaks
Shlush, L. I. (2020) · Blood · doi:10.1182/blood.2019003869 · Cited by 2
Update on Clonal Hematopoiesis
Bolton, K. L. (2021) · Clinical Lymphoma Myeloma & Leukemia · doi:10.1016/s2152-2650(21)01199-x · Cited by 2
Yu, X., Qian, N., & Wang, Y. (2023) · Molecular Biology Reports · doi:10.1007/s11033-022-08118-1 · Cited by 2
Multiplicity of Time Scales in Blood Cell Formation and Leukemia
Stiehl, T. (2023) · Mathematics online first collections · doi:10.1007/16618_2023_73 · Cited by 2
New genetic loci associated with the risk of clonal hematopoiesis
(2022) · Nature Genetics · doi:10.1038/s41588-022-01125-9 · Cited by 2
The genomic landscape of clonal hematopoiesis in JapanPreprint
Terao, C. C., Suzuki, A., Momozawa, Y., Akiyama, M., Ishigaki, K., Yamamoto, K., Matsuda, K., Murakami, Y., McCarroll, S. A., Kubo, M., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/653733 · Cited by 2
Pseudo-mutant p53 as a targetable phenotype of DNMT3A -mutated pre-leukemiaPreprint
Tuval, A., Brilon, Y., Azogy, H., Moskovitz, Y., Biezuner, T., Leshkowitz, D., Salame, T. M., Minden, M. D., Tal, P., Rotter, V., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.30.446347 · Cited by 2
Detecting and quantifying clonal selection in somatic stem cellsPreprint
Körber, V., Ansari‐Pour, N., Jakobsen, N. A., Moore, R., Claudino, N., Metzner, M., Hörsch, F., Usukhbayar, B., Salazar, M. A., Newman, S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.15.472780 · Cited by 2
Dnmt3a -Mutant Hematopoietic Stem Cell Rewire IFNγ Signaling to Gain Clonal Advantage
Dominici, M. D., & DeGregori, J. V. (2022) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-22-0025 · Cited by 2
Microbial Signals May Drive Leukemia Development in Subjects With Clonal Hematopoiesis
Abdel-Wahab, O. I. (2018) · The Hematologist · doi:10.1182/hem.v15.5.8893 · Cited by 1
Regularized regression for two phase failure time studies
Soave, D. M., & Lawless, J. F. (2023) · Computational Statistics & Data Analysis · doi:10.1016/j.csda.2023.107703 · Cited by 1
Ronchini, C., Caprioli, C., Tunzi, G., D’Amico, F. F., Colombo, E., Giani, M., Foti, G., Conconi, D., Lavitrano, M., Passerini, R., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0282546 · Cited by 1
Kartal‐Kaess, M., Karow, A., Bacher, U., Pabst, T., Joncourt, R., Zweier, C., Kuehni, C. E., Porret, N. A., & Roessler, J. (2024) · Pediatric Hematology and Oncology · doi:10.1080/08880018.2024.2362885 · Cited by 2
Dezern, A. E., Goll, J. B., Jensen, T. L., Srivatsan, S. N., Gillis, N., Abel, G. A., Padron, E., Deeg, H. J., Baghdadi, T. A., Liu, J. J., et al. (2024) · Blood Neoplasia · doi:10.1016/j.bneo.2024.100026 · Cited by 1
Naddaf, L., & Li, S. (2025) · Aging and Cancer · doi:10.1002/aac2.12078 · Cited by 1
Wagner, S., Thielecke, L., & Glauche, I. (2025) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2025.111079 · Cited by 1
Induced pluripotent stem cell-based modelling of disease evolution in myeloid leukemia: MDS to AML
Boultwood, J. (2025) · Advances in Biological Regulation · doi:10.1016/j.jbior.2025.101119 · Cited by 1
Elucidating the risk factors and oncogene drivers of acute myeloid leukemia
Sanya, D. R. A., & Onésime, D. (2025) · Human Cell · doi:10.1007/s13577-025-01294-9 · Cited by 1
Clonal hematopoiesis of indeterminate potential and malignant neoplasms
Шевченко, В. Е., Kushnir, T., Gudkova, M. V., & Arnotskaya, N. E. (2025) · Advances in molecular oncology · doi:10.17650/2313-805x-2025-12-3-26-35 · Cited by 1
Steinauer, N., & Patnaik, M. M. (2025) · Current Hematologic Malignancy Reports · doi:10.1007/s11899-025-00763-0 · Cited by 1
Somatic mutations and clonal evolution in normal tissues and cancer development
Yoshida, K. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01592-0 · Cited by 4
Wang, L., Chien, W., Sheng‐Kai, K., Chung, C., Chen, Y., Tsai, W.-C., & Yang, B.-H. (2025) · PLoS Medicine · doi:10.1371/journal.pmed.1004646 · Cited by 1
LncRNA CISTR-ACT regulates cell size in human and mouse by guiding FOSL2
Kiriakopulos, K., Soleimanpour, K., McMurray, B. J., Moke, B.-I., Chalmers, J. J., Mokhtaridoost, M., Newton, J. D., Young, T. D., Delfosse, K., Ahmed, M. H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-67591-x · Cited by 2
Impact of Germline DNA Repair Mutations on Clonal Hematopoiesis and Myeloid Neoplasm Development
Fedorov, K., Luo, L. Y., Bick, A. G., & Savona, M. R. (2025) · Current Hematologic Malignancy Reports · doi:10.1007/s11899-025-00768-9 · Cited by 1
Park, S., Yi, K., Lee, J. L., Yang, M. J., Song, J.-H., Lim, J., Kim, T., Kim, S., Kim, S. M. (., Kim, H. S., et al. (2026) · Cancer Research · doi:10.1158/0008-5472.can-24-4977 · Cited by 2
Biomarkers and advances in AML-MRC: from bench to bedside
Meng, F., Al-Khafaji, Z., Muzammil, K., Sarbazjoda, E., Khaksari, M. N., Bayani, A., & Samarkhazan, H. S. (2026) · Annals of Hematology · doi:10.1007/s00277-026-06805-8 · Cited by 1
Song, Q., Meng, J., Li, H., Fu, W., Hong, K., Sj, S., Zhang, Z., Ding, S., Li, S., Zhang, Z., et al. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48030239 · Cited by 1
Ph-chromosome-negative myeloproliferative neoplasms: clonal dynamics are the name of the game
Noorafrooz, M., Noorafrooz, R., Barosi, G., & Gale, R. P. (2026) · Blood Reviews · doi:10.1016/j.blre.2026.101385 · Cited by 1
Aging mechanisms and rejuvenation strategies for hematopoietic stem cells
Zhang, Y., Xu, Y., Shi, W., Cao, D., Guo, D.-A., & Yue, R. (2026) · Genome biology · doi:10.1186/s13059-026-04119-6 · Cited by 1
Clonal hematopoiesis in the setting of sickle cell disease and its relevance to curative therapies
Weeks, L. D. (2026) · Seminars in Hematology · doi:10.1053/j.seminhematol.2026.05.008 · Cited by 1
FGF18 mediates fibroblast-leukemia cross talk to promote acute myeloid leukemia progression
Zhang, W., Ye, Z. L., Zhou, X., Xiong, P., Pan, Y., Qiu, J., Li, M., Shen, J., Li, Y., Lu, 姚., et al. (2026) · Blood · doi:10.1182/blood.2026033125 · Cited by 1
Dunn, W. G., Gu, M., Fabre, M. A., Cooper, J. L., Nomdedeu, J. F., Koumas, L., Nicolaou, K. A., Chi, J., Costeas, P., & Vassiliou, G. S. (2021) · Annals of Hematology · doi:10.1007/s00277-021-04472-5 · Cited by 1
Testa, U., Castelli, G., & Pelosi, E. (2022) · Hemato · doi:10.3390/hemato3030038 · Cited by 2
Leukemia - From Biology to Clinic
Guenova, M. L., & Balatzenko, G. N. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.100848 · Cited by 1
Klonale Hämatopoese – Ursachen und klinische Implikationen
Burchert, A. (2023) · Zeitschrift für Gerontologie und Geriatrie · doi:10.1007/s00391-023-02162-7 · Cited by 1
Johann Gregor Mendel: the victory of statistics over human imagination
Raudenská, M., Vičar, T., Gumulec, J., & Masařík, M. (2023) · European Journal of Human Genetics · doi:10.1038/s41431-023-01303-1 · Cited by 1
Katagiri, S., Furuya, N., Akahane, D., Chi, S., Minami, Y., Harada, Y., Harada, H., & Gotoh, A. (2023) · OncoTargets and Therapy · doi:10.2147/ott.s417137 · Cited by 1
Common in atherogenesis and carcinogenesis: clonal hematopoiesis
Слепцов, А. А., Nazarenko, M. S., & Puzyrev, V. P. (2023) · Russian Journal of Cardiology · doi:10.15829/1560-4071-2023-5511 · Cited by 4
Hutchcraft, M. L., Zhang, S., Lin, N., Pickarski, J., Belcher, E. A., Wei, S., Bocklage, T. J., Miller, R. W., Villano, J. L., Cavnar, M. J., et al. (2024) · JCO Precision Oncology · doi:10.1200/po.23.00266 · Cited by 1
Myeloid neoplasms in inflammatory bowel disease: A case series and review of the literature
Mueller, D. M., Nathan, D. I., Liu, A., Mascarenhas, J. O., & Marcellino, B. K. (2024) · Leukemia Research Reports · doi:10.1016/j.lrr.2024.100458 · Cited by 1
Al-Amrani, S., Zadjali, F., Jeelani, Y., AL-Jabri, Z., Bulushi, M. P. A., Rawahi, M. A., Alzaabi, A. A., Shekaili, J. A., Al-Huneini, M., & Al-Khabori, M. K. (2024) · Oman Medical Journal · doi:10.5001/omj.2024.80 · Cited by 1
Hua, W., Qi, J., Zhou, M., Han, S., Xu, X., Su, J., Pan, T., Wu, D., & Han, Y. (2024) · Annals of Hematology · doi:10.1007/s00277-024-05882-x · Cited by 1
Liu, Y., Desai, P. M., Nadeem, O., Woyach, J. A., & Alsouqi, A. (2025) · American Society of Clinical Oncology Educational Book · doi:10.1200/edbk-25-473650 · Cited by 1
CHIPing out PPM1D-mutant hematopoiesis
Kindler, T. (2018) · Blood · doi:10.1182/blood-2018-07-861716 · Cited by 1
dos Santos, W. M., Costa, A. F. O., Pinheiro, L. H. S., Silva, N. D. L., Sandes, A. F., Fleury Group, H. D., Nunes, M. A. P., Corrêa, C. B., Almeida, C. A. C., da Cruz, G. S., et al. (2019) · European Oncology & Haematology · doi:10.17925/eoh.2019.15.2.113 · Cited by 1
Shedding Light on Mutant Clonal Dynamics and Cancer Risk in the Skin
Dominici, M. D., & DeGregori, J. V. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-20-1644 · Cited by 1
Toward More Complete Prognostication for Patients with Clonal Hematopoiesis
Spitzer, B. G., & Levine, R. L. (2021) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-21-0025 · Cited by 1
Metadata
- Authors
- Abelson, S., Collord, G., Ng, S. W. K., Weissbrod, O., Mendelson Cohen, N., Niemeyer, E., Barda, N., Zuzarte, P. C., Heisler, L., Sundaravadanam, Y., Luben, R., Hayat, S., Wang, T. T., Zhao, Z., Cirlan, I., Pugh, T. J., Soave, D., Ng, K., Latimer, C., Hardy, C., Raine, K., Jones, D., Hoult, D., Britten, A., McPherson, J. D., Johansson, M., Mbabaali, F., Eagles, J., Miller, J. K., Pasternack, D., Timms, L., Krzyzanowski, P., Awadalla, P., Costa, R., Segal, E., Bratman, S. V., Beer, P., Behjati, S., Martincorena, I., Wang, J. C. Y., Bowles, K. M., Quirós, J. R., Karakatsani, A., La Vecchia, C., Trichopoulou, A., Salamanca-Fernández, E., Huerta, J. M., Barricarte, A., Travis, R. C., Tumino, R., Masala, G., Boeing, H., Panico, S., Kaaks, R., Krämer, A., Sieri, S., Riboli, E., Vineis, P., Foll, M., McKay, J., Polidoro, S., Sala, N., Khaw, K.-T., Vermeulen, R., Campbell, P. J., Papaemmanuil, E., Minden, M. D., Tanay, A., Balicer, R. D., Wareham, N. J., Gerstung, M., Dick, J. E., Brennan, P., Vassiliou, G. S., & Shlush, L. I.
- Affiliations
- University Health Network (CA)
- University of Cambridge (GB)
- University of Toronto (CA)
- Weizmann Institute of Science (IL)
- Clalit Health Services (IL)
- Ontario Institute for Cancer Research (CA)
- Wellcome Sanger Institute (GB)
- Centre international de recherche sur le cancer (FR)
- European Bioinformatics Institute (GB)
- University of East Anglia (GB)
- Gobierno del Principado de Asturias (ES)
- National and Kapodistrian University of Athens (GR)
- Hellenic Health Foundation (GR)
- Instituto Murciano de Investigación Biosanitaria (ES)
- Instituto de Salud Pública de Navarra (ES)
- University of Oxford (GB)
- Istituto per lo Studio e la Prevenzione Oncologica (IT)
- German Institute of Human Nutrition (DE)
- Federico II University Hospital (IT)
- German Cancer Research Center (DE)
- Fondazione IRCCS Istituto Nazionale dei Tumori (IT)
- Imperial College London (GB)
- Italian institute for Genomic Medicine (IT)
- Institut d'Investigació Biomédica de Bellvitge (ES)
- Utrecht University (NL)
- Memorial Sloan Kettering Cancer Center (US)
- World Health Organization (CH)
- Wellcome/MRC Cambridge Stem Cell Institute (GB)
- Corresponding author
- Gerstung, Moritz
- Dick, John E.
- Brennan, Paul
- Vassiliou, George S.
- Shlush, Liran I.
- ORCID
- Abelson, Sagi
- Collord, Grace
- Ng, Stanley W. K.
- Weissbrod, Omer
- Barda, Noam
- Zuzarte, Philip C.
- Heisler, Lawrence
- Sundaravadanam, Yogi
- Luben, Robert
- Hayat, Shabina
- Zhao, Zhen
- Cirlan, Iulia
- Pugh, Trevor J.
- Soave, David
- Ng, Karen
- Latimer, Calli
- Raine, Keiran
- Jones, David
- Britten, Abigail
- McPherson, John D.
- Johansson, Mattias
- Eagles, Jenna
- Miller, Jessica K.
- Krzyzanowski, Paul
- Awadalla, Philip
- Costa, Rui
- Segal, Eran
- Bratman, Scott V.
- Beer, Philip
- Behjati, Sam
- Wang, Jean C. Y.
- Bowles, Kristian M.
- Karakatsani, Anna
- Trichopoulou, Antonia
- Huerta, José M.
- Barricarte, Aurelio
- Travis, Ruth C.
- Tumino, Rosario
- Masala, Giovanna
- Boeing, Heiner
- Panico, Salvatore
- Kaaks, Rudolf
- Krämer, Alwin
- Sieri, Sabina
- Vineis, Paolo
- Foll, Matthieu
- McKay, James
- Polidoro, Silvia
- Sala, Núria
- Khaw, Kay-Tee
- Vermeulen, Roel
- Campbell, Peter J.
- Papaemmanuil, Elli
- Minden, Mark D.
- Tanay, Amos
- Balicer, Ran D.
- Wareham, Nicholas J.
- Gerstung, Moritz
- Dick, John E.
- Brennan, Paul
- Vassiliou, George S.
- Shlush, Liran I.
- Venue
- Nature
- Published
- 2018-07
- Volume
- 559
- Issue
- 7714
- Pages
- 400-404
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC6485381
- OpenAlex
- W2830196912
- Cited by
- 850
- References
- 49
- Citations by year
- 2026: 52 · 2025: 83 · 2024: 95 · 2023: 116 · 2022: 122 · 2021: 116 · 2020: 143 · 2019: 91 · 2018: 29
- FWCI
- 67.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RISalud Institutional Health Repository of Andalucía (submittedVersion, public-domain)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) (submittedVersion, public-domain)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- eScholarship (California Digital Library) (submittedVersion)
- Spiral (Imperial College London) (submittedVersion)
- Apollo (University of Cambridge) (submittedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion)
- Apollo
- Funders
- World Health Organization
- Leukemia and Lymphoma Society
- Wellcome Trust (WT 098051, WT095663MA)
- Cancer Research UK (23015, 14136, 16491, 21777)
- National Institute for Health and Care Research (NF-SI-0512-10114, NF-SI-0512-10135, NF-SI-0617-10149)
- Generalitat de Catalunya
- Associazione Italiana per la Ricerca sul Cancro
- Clalit Health Services
- Abisch-Frenkel-Stiftung
- Hellenic Health Foundation
- Medical Research Council (MC_UU_12015/1, MC_PC_13048, MC_PC_12009, MR/N003284/1)
- Agència de Gestió d'Ajuts Universitaris i de Recerca
- Instituto de Salud Carlos III (RD12/0036/0018)
- European Regional Development Fund
- National Cancer Institute (P30CA008748)
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
- Keywords
- acute myeloid leukemia, somatic mutations, clonal expansion, variant allele frequency
- MeSH terms
- Adult, Age Factors, Aged, Female, Health, Humans, Male, Middle Aged, Models, Genetic, Mutation, Leukemia, Myeloid, Acute, Prevalence, Mutagenesis, Disease Progression, Risk Assessment, Genetic Predisposition to Disease, Electronic Health Records
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review