Clonal hematopoiesis: Mutation-specific adaptation to environmental change

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

Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases

Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891

Clonal 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

Clonal hematopoiesis and risk of atherosclerotic cardiovascular disease

Jaiswal, S., Natarajan, P., Silver, A. J., Gibson, C. J., Bick, A. G., Shvartz, E., McConkey, M., Gupta, N., Gabriel, S., Ardissino, D., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1701719 · Cited by 2,683

Frequent pathway mutations of splicing machinery in myelodysplasia

Yoshida, K., Sanada, M., Shiraishi, Y., Nowak, D., Nagata, Y., Yamamoto, R., Sato, Y., Sato-Otsubo, A., Kon, A., Nagasaki, M., et al. (2011) · Nature · doi:10.1038/nature10496 · Cited by 2,029

DNMT3A Mutations in Acute Myeloid Leukemia

Ley, T. J., Ding, L., Walter, M. J., McLellan, M. D., Lamprecht, T., Larson, D. E., Kandoth, C., Payton, J. E., Baty, J., Welch, J., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1005143 · Cited by 1,983

Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes

Steensma, D. P., Bejar, R., Jaiswal, S., Lindsley, R. C., Sekeres, M. A., Hasserjian, R. P., & Ebert, B. L. (2015) · Blood · doi:10.1182/blood-2015-03-631747 · Cited by 1,971

Age-related mutations associated with clonal hematopoietic expansion and malignancies

Xie, M., Lu, C., Wang, J., McLellan, M. D., Johnson, K. J., Wendl, M. C., McMichael, J. F., Schmidt, H. K., Yellapantula, V., Miller, C. A., et al. (2014) · Nature Medicine · doi:10.1038/nm.3733 · Cited by 1,874

Clinical and biological implications of driver mutations in myelodysplastic syndromes

Papaemmanuil, E., Gerstung, M., Malcovati, L., Tauro, S., Gundem, G., Van Loo, P., Yoon, C. J., Ellis, P., Wedge, D. C., Pellagatti, A., et al. (2013) · Blood · doi:10.1182/blood-2013-08-518886 · Cited by 1,832

Mutation in TET2 in Myeloid Cancers

Delhommeau, F., Dupont, S., Valle, V. D., James, C., Trannoy, S., Massé, A., Kosmider, O., Le Couedic, J.-P., Robert, F., Alberdi, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0810069 · Cited by 1,776

Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging

Jakobsen, N. A., Turkalj, S., Zeng, A. G. X., Stoilova, B., Metzner, M., Rahmig, S., Nagree, M. S., Shah, S., Moore, R., Usukhbayar, B., et al. (2024) · Cell Stem Cell · doi:10.1016/j.stem.2024.05.010 · Cited by 130

Clonal hematopoiesis driven by mutated DNMT3A promotes inflammatory bone loss

Wang, H., Divaris, K., Pan, B., Li, X., Lim, J., Saha, G., Barovic, M., Giannakou, D., Korostoff, J. M., Bing, Y., et al. (2024) · Cell · doi:10.1016/j.cell.2024.05.003 · Cited by 122

The evolutionary theory of cancer: challenges and potential solutions

Laplane, L., & Maley, C. C. (2024) · Nature reviews. Cancer · doi:10.1038/s41568-024-00734-2 · Cited by 89

Clonal hematopoiesis and inflammation – the perpetual cycle

Avagyan, S., & Zon, L. I. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.12.001 · Cited by 79

Loss of TET2 in human hematopoietic stem cells alters the development and function of neutrophils

Encabo, H. H., Aramburu, I. V., Albornoz, M. G., Piganeau, M., Wood, H. J., Song, A., Ferrelli, A., Sharma, A., Minutti, C. M., Domart, M., et al. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.05.004 · Cited by 85

Clonal dynamics and somatic evolution of haematopoiesis in mouse

Kapadia, C. D., Williams, N., Dawson, K. J., Watson, C. J., Yousefzadeh, M. J., Le, D. T., Nyamondo, K., Kodavali, S., Cagan, A., Waldvogel, S. M., et al. (2025) · Nature · doi:10.1038/s41586-025-08625-8 · Cited by 48

Blood and guts: how the intestinal microbiome shapes hematopoiesis and treatment of hematologic disease

Sanchez, J. F., Maknojia, A., & King, K. Y. (2024) · Blood · doi:10.1182/blood.2023021174 · Cited by 41

IL-1 in aging and pathologies of hematopoietic stem cells

Caiado, F., & Manz, M. G. (2024) · Blood · doi:10.1182/blood.2023023105 · Cited by 40

Forged in the fire: Lasting impacts of inflammation on hematopoietic progenitors

Cao, R., Thatavarty, A., & King, K. Y. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104215 · Cited by 38

Donor-Derived Malignancy and Transplantation Morbidity: Risks of Patient and Donor Genetics in Allogeneic Hematopoietic Stem Cell Transplantation

Williams, L. S., Williams, K. M., Gillis, N., Bolton, K. L., Damm, F., Deuitch, N. T., Farhadfar, N., Gergis, U. S., Keel, S., Michelis, F. V., et al. (2023) · Transplantation and Cellular Therapy · doi:10.1016/j.jtct.2023.10.018 · Cited by 35

Role of TET dioxygenases in the regulation of both normal and pathological hematopoiesis

Joshi, K., Zhang, L., Breslin, P., Kini, A. R., & Zhang, J. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02496-x · Cited by 31

Bone marrow niches for hematopoietic stem cells

Pereira, A. L., Galli, S., & Nombela‐Arrieta, C. (2024) · HemaSphere · doi:10.1002/hem3.133 · Cited by 35

Telomere attrition becomes an instrument for clonal selection in aging hematopoiesis and leukemogenesis

McLoughlin, M. A., Kovilakam, S. C., Dunn, W. G., Gu, M., Tobin, J., Pershad, Y., Williams, N., Leongamornlert, D. A., Dawson, K. J., Bond, L., et al. (2025) · Nature Genetics · doi:10.1038/s41588-025-02296-x · Cited by 32

Inflammageing and clonal haematopoiesis interplay and their impact on human disease

Hajishengallis, G., & Chavakis, T. (2026) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00936-y · Cited by 37

Periodontal Medicine Rewired: Mechanisms Linking Periodontitis to Systemic Diseases

Romandini, M., Hajishengallis, G., Curtis, M. A., & Baima, G. (2026) · Journal of Periodontal Research · doi:10.1111/jre.70099 · Cited by 36

Metabolic regulation of stress erythropoiesis, outstanding questions, and possible paradigms

Ruan, B., & Paulson, R. F. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2022.1063294 · Cited by 30

Clonal Hematopoiesis and Its Cardiovascular Implications: A Scientific Statement From the American Heart Association

Rhee, J., Bolton, K. L., Gupta, D., Weeks, L. D., Bick, A. G., Tall, A. R., Walsh, K. X., Fuster, J. J., & Natarajan, P. (2026) · Circulation · doi:10.1161/cir.0000000000001404 · Cited by 31

TET2-mutant myeloid cells mitigate Alzheimer’s disease progression via CNS infiltration and enhanced phagocytosis in mice

Matatall, K. A., Wathan, T. K., Nguyen, M., Chen, H., McDonald, A., Qi, G., Belk, J. A., Florez, M. A., Le, D. T., Olarinde, T., et al. (2025) · Cell Stem Cell · doi:10.1016/j.stem.2025.06.006 · Cited by 23

Hematopoietic stem and progenitor cells as a reservoir for trained immunity

Tran, B. T., Jeyanathan, V., Cao, R., Kaufmann, E., & King, K. Y. (2025) · eLife · doi:10.7554/elife.106610 · Cited by 25

CHIP: a clonal odyssey of the bone marrow niche

Schleicher, W. E., Hoag, B., Dominici, M. D., DeGregori, J. V., & Pietras, E. M. (2024) · Journal of Clinical Investigation · doi:10.1172/jci180068 · Cited by 23

The impact of age and number of mutations on the size of clonal hematopoiesis

Wang, K., Zhang, W., Yi, L., Zhao, M., Li, P.-Y., Fu, M.-H., Lin, R., Zhu, Y., Li, J., Yang, W., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319364121 · Cited by 24

Causes of Clonal Hematopoiesis: a Review

Joo, L., Bradley, C. C., Lin, S. H., Scheet, P. A., & Nead, K. T. (2023) · Current Oncology Reports · doi:10.1007/s11912-023-01362-z · Cited by 23

Atherosclerotic cardiovascular disease in aging and the role of advanced cardiovascular imaging

Wong, J. J., Hong, R., Teo, L. L. Y., Tan, R., & Koh, A. S.-M. (2024) · npj Cardiovascular Health · doi:10.1038/s44325-024-00012-y · Cited by 20

The IL-1β inhibitor canakinumab in previously treated lower-risk myelodysplastic syndromes: a phase 2 clinical trial

Rodríguez‐Sevilla, J. J., Ademà, V., Chien, K. S., Loghavi, S., Ma, F., Yang, H., Bravo, G. M., Huang, X., Calvo, X., Joseph, J., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54290-2 · Cited by 21

All that glitters is not LGL Leukemia

Semenzato, G., Teramo, A., Calabretto, G., Gasparini, V. R., & Zambello, R. (2022) · Leukemia · doi:10.1038/s41375-022-01695-x · Cited by 22

Epigenetic Modification of Cytosines in Hematopoietic Differentiation and Malignant Transformation

An, J., & Ko, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021727 · Cited by 21

Chronic inflammation can transform the fate of normal and mutant hematopoietic stem cells

Li, J., Malouf, C., Miles, L. A., Willis, M., Pietras, E. M., & King, K. Y. (2023) · Experimental Hematology · doi:10.1016/j.exphem.2023.08.008 · Cited by 18

Tissue mosaicism following stem cell aging: blood as an exemplar

Kapadia, C. D., & Goodell, M. A. (2024) · Nature Aging · doi:10.1038/s43587-024-00589-0 · Cited by 18

Inflammation in myelodysplastic syndrome pathogenesis

Rodríguez‐Sevilla, J. J., & Colla, S. (2024) · Seminars in Hematology · doi:10.1053/j.seminhematol.2024.09.005 · Cited by 20

Insights into the Molecular Mechanisms of Genetic Predisposition to Hematopoietic Malignancies: The Importance of Gene–Environment Interactions

Cobaleda, C., Godley, L. A., Nichols, K. E., Włodarski, M. W., & Sánchez-Garcı́a, I. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-1091 · Cited by 17

Ten‐Eleven Translocation Family Proteins: Structure, Biological Functions, Diseases, and Targeted Therapy

Liang, J., Na, X., Meng, L., He, L., Shu, T., Fang, Y., Zhang, B., Zhao, Z., Guo, C., Li, J., et al. (2025) · MedComm · doi:10.1002/mco2.70245 · Cited by 15

Transcriptional and functional consequences of Oncostatin M signaling on young Dnmt3a-mutant hematopoietic stem cells

Schwartz, L. S., Young, K. A., Stearns, T. M., Boyer, N., Mujica, K. D., & Trowbridge, J. J. (2023) · Experimental Hematology · doi:10.1016/j.exphem.2023.11.005 · Cited by 15

Cigarette smoke impairs the hematopoietic supportive property of mesenchymal stem cells via the production of reactive oxygen species and NLRP3 activation

Park, H. S., Lee, B., Chae, D., Yu, A., Park, J. H., Heo, J., Han, M. H., Cho, K., Lee, J. W., Jung, J., et al. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03731-2 · Cited by 15

Genetic and environmental risks for clonal hematopoiesis and cancer

Franco, S., & Godley, L. A. (2024) · The Journal of Experimental Medicine · doi:10.1084/jem.20230931 · Cited by 15

STING mediates increased self-renewal and lineage skewing in DNMT3A-mutated hematopoietic stem/progenitor cells

Huang, J., Xie, J., Wang, Y., Sheng, M., Sun, Y., Chen, P., Rong, S., Yin, D., Wang, Y., Zhu, P., et al. (2025) · Leukemia · doi:10.1038/s41375-025-02542-5 · Cited by 16

PU.1 is required to restrain myelopoiesis during chronic inflammatory stress

Chavez, J. S., Rabe, J. L., Niño, K. E., Wells, H. H., Gessner, R. L., Mills, T. S., Hernandez, G., & Pietras, E. M. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1204160 · Cited by 14

Emerging Insights into Molecular Mechanisms of Inflammation in Myelodysplastic Syndromes

Vallelonga, V., Gandolfi, F., Ficara, F., Porta, M. G. D., & Ghisletti, S. (2023) · Biomedicines · doi:10.3390/biomedicines11102613 · Cited by 15

Germline variants in acquired aplastic anemia: current knowledge and future perspectives

Wang, P., Jiang, W., Lai, T., Liu, Q., Shen, Y., Ye, B., & Wu, D. (2024) · Haematologica · doi:10.3324/haematol.2023.284312 · Cited by 16

Aging and Cancer—Inextricably Linked Across the Lifespan

DeGregori, J. V., Seidl, K. J., & Montano, M. A. (2025) · Aging Cell · doi:10.1111/acel.14483 · Cited by 12

Hematologic DNMT3A reduction and high-fat diet synergize to promote weight gain and tissue inflammation

Reyes, J. M., Tovy, A., Zhang, L., Bortoletto, A. S., Rosas, C., Chen, C.-W. D., Waldvogel, S. M., Guzman, A. G., Aguilar, R., Gupta, S., et al. (2024) · iScience · doi:10.1016/j.isci.2024.109122 · Cited by 14

From complexity to clarity: aging bone marrow niche in bone and blood regeneration and malignancy

Roy, N., Liu, H., Horenberg, A. L., Pathak, A. P., Chen, J., Ramasamy, S. K., Cohen-Solal, M. E., Bözec, A., Grayson, W. L., & Kusumbe, A. P. (2026) · Bone Research · doi:10.1038/s41413-026-00543-3 · Cited by 11

Single-Cell DNA Sequencing Reveals an Evolutionary Pattern of CHIP in Transplant Eligible Multiple Myeloma Patients

Borsi, E., Vigliotta, I., Poletti, A., Mazzocchetti, G., Solli, V., Zazzeroni, L., Martello, M., Armuzzi, S., Taurisano, B., Kanapari, A., et al. (2024) · Cells · doi:10.3390/cells13080657 · Cited by 11

Considering clonal hematopoiesis of indeterminate potential in space radiation risk analysis for hematologic cancers and cardiovascular disease

Werneth, C. M., Patel, Z. S., Thompson, M. S., Blattnig, S. R., & Huff, J. L. (2024) · Communications Medicine · doi:10.1038/s43856-023-00408-4 · Cited by 13

Clonal Hematopoiesis and Solid Cancers

Nguyen, Y. T. M., Fujisawa, M., Ishikawa, S., & Sakata‐Yanagimoto, M. (2025) · Cancer Science · doi:10.1111/cas.70097 · Cited by 12

Clonal Hematopoiesis and Risk of Heart Failure After Autologous Hematopoietic Cell Transplantation for Lymphoma

Rhee, J., Pillai, R. K., Chen, S., Bosworth, A., Oganesyan, A., Atencio, L., Freeman, K., Estrada, C., Guzman, T., Lukas, K., et al. (2024) · JACC CardioOncology · doi:10.1016/j.jaccao.2024.10.006 · Cited by 9

Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential

Leiser, C. L., Whitsel, E. A., Reiner, A. P., Rich, S. S., Rotter, J. I., Taylor, K. D., Tracy, R. P., Kooperberg, C. L., Smith, A. V., Manson, J. E., et al. (2023) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-23-0305 · Cited by 7

Decoding Clonal Hematopoiesis: Emerging Themes and Novel Mechanistic Insights

Pendse, S., & Loeffler, D. (2024) · Cancers · doi:10.3390/cancers16152634 · Cited by 8

Clonal hematopoiesis of indeterminate potential: contribution to disease and promising interventions

Li, C., Zhang, C., & Li, X. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05261-8 · Cited by 8

Epigenetic inflammatory memory and periodontal disease: Mechanisms and clinical significance for comorbidities

Hajishengallis, G. (2025) · Journal of Periodontology · doi:10.1002/jper.70040 · Cited by 9

Dangerous Liaisons between Tet2 Mutation, Inflammatory Monocytes, and Leukemogenesis

Pietras, E. M., & DeGregori, J. V. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-22-0846 · Cited by 8

Somatic mutations in tumor-infiltrating lymphocytes impact on antitumor immunity

Mukohara, F., Iwata, K., Ishino, T., Inozume, T., Nagasaki, J., Ueda, Y., Suzawa, K., Ueno, T., Ikeda, H., Kawase, K., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2320189121 · Cited by 9

Clinical Significance of TP53 -Mutant Clonal Hematopoiesis Across Diseases

Usui, Y., Endo, M., Iwasaki, Y., Iijima, H., Nakagawa, H., Matsuda, K., & Momozawa, Y. (2025) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-24-0355 · Cited by 8

Hematopoietic aging: Cellular, molecular, and related mechanisms

Ye, L., Tian, C., Li, Y., Pan, H., Hu, J., Shu, L., & Pan, X. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002871 · Cited by 9

Microbiome and Hemato-immune Aging

Johansson, A., Ho, N. P. Y., & Takizawa, H. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104685 · Cited by 7

Impact of Clonal Hematopoiesis–Associated Mutations in Phase I Patients Treated for Solid Tumors: An Analysis of the STING Trial

Rodriguez, J. E., Baldini, C., Bayle, A., Pagès, A., Danlos, F., Vasseur, D., Rouleau, É., Lacroix, L., de Castro, B. A., Goldschmidt, V., et al. (2024) · JCO Precision Oncology · doi:10.1200/po.23.00631 · Cited by 6

Ferulic Acid Promotes Hematopoietic Stem Cell Maintenance in Homeostasis and Injury Through Diminishing Ferroptosis Susceptibility

Zhang, S., Zhang, Y., Le, J., Yu, K., Chen, X., Chen, J., Chen, M., Wu, Y., Yang, X., Wang, S., et al. (2025) · Antioxidants · doi:10.3390/antiox14091053 · Cited by 6

Clonal hematopoiesis of indeterminate potential and risk of autoimmune thyroid disease

Zhang, X. J., Wang, Y., Xue, H., Zhao, Y., Liu, M.-C., Wei, H., & Liu, Q. (2025) · BMC Medicine · doi:10.1186/s12916-025-04077-z · Cited by 6

Immune-driven clonal cell selection at the intersection among cancer, infections, autoimmunity and senescence

Pagliuca, S., & Ferraro, F. (2024) · Seminars in Hematology · doi:10.1053/j.seminhematol.2024.01.002 · Cited by 6

Clonal Hematopoiesis of Indeterminate Potential and Cardiovascular Risk in Patients with Chronic Kidney Disease without Previous Cardiac Pathology

Kislikova, M., Lopez, M. A. B., Salinas, F. J. F., Blanco, J. A. P., Molina, M. P. G.-B., Fernandez, A. A., Haces, V. C. P., García‐Unzueta, M. T., Benito‐Hernández, A., Ruiz, J. C., et al. (2023) · Life · doi:10.3390/life13091801 · Cited by 5

Age-related micro-environmental changes as drivers of clonal hematopoiesis

Bacharach, T., Kaushansky, N., & Shlush, L. I. (2023) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000798 · Cited by 6

Dynamically adjusted cell fate decisions and resilience to mutant invasion during steady-state hematopoiesis revealed by an experimentally parameterized mathematical model

Komarova, N. L., Rignot, C., Fleischman, A. G., & Wodarz, D. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2321525121 · Cited by 5

TNF Receptors Choose HSC Fate in Supporting Dnmt3a -Mutant Clonal Hematopoiesis

Niño, K. E., & Pietras, E. M. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-22-1022 · Cited by 5

Exploring the intricate cross-talk between clonal expansion and the bone marrow niche

Ngo, S. D., Papazoglou, D., Encabo, H. H., & Bonnet, D. A. (2024) · Frontiers in Hematology · doi:10.3389/frhem.2024.1334807 · Cited by 4

Clonal heamatopoiesis and associated cardiovascular diseases

Tajiri, K., Suehara, Y., Suzuki, T., & Sekine, I. (2023) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyac210 · Cited by 4

Clones of aging: When better fitness can be dangerous

Marongiu, F., Cheri, S., & Laconi, E. (2023) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2023.151340 · Cited by 4

Regulators of clonal hematopoiesis and physiological consequences of this condition

Park, E., Evans, M. A., & Walsh, K. X. (2023) · The Journal of Cardiovascular Aging · doi:10.20517/jca.2023.39 · Cited by 4

Clonal Hematopoiesis in Nonmalignant Disease: Functional Consequences of Mutated Immune Cells by Clonal Hematopoiesis in the Diseased Tissue

Koh, Y., Tengesdal, I. W., & Jaiswal, S. (2025) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-111523-023442 · Cited by 3

DNA mutation rates in evolution, longevity, and disease: An evolutionary and biological trade-off

Cao, D., Zeng, C., & Ren, R. (2026) · Cell investigation. · doi:10.1016/j.clnves.2026.100061 · Cited by 3

Association of infection frequency and incident clonal hematopoiesis of indeterminant potential

Lapite, A., Burk, V. A., DeCuir, J., Ishigami, J., Saadatagah, S., Natarajan, P., Ballantyne, C. M., Platz, E. A., & King, K. Y. (2026) · Experimental Hematology · doi:10.1016/j.exphem.2026.105420 · Cited by 4

Understanding MDS stem cells: Advances and limitations

Patel, S. B., Moskop, D. R., Jordan, C. T., & Pietras, E. M. (2024) · Seminars in Hematology · doi:10.1053/j.seminhematol.2024.09.007 · Cited by 3

Cancer Clones Revised

Laplane, L. (2024) · Biological Theory · doi:10.1007/s13752-024-00484-2 · Cited by 4

Increased Clonal Hematopoiesis in Long-term Survivors of Pediatric Hematopoietic Cell Transplantation

Müskens, K. F., Wieringa, N., van Bergen, M. G. J. M., Bense, J. E., Pas, B. M. T., de Pagter, A. P. J., Lankester, A. C., Bierings, M., Neuberg, D. S., Haitjema, S., et al. (2025) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-24-0136 · Cited by 5

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

Clonal Hematopoietic Mutations in Plasma Cell Disorders: Clinical Subgroups and Shared Pathogenesis

Wang, X., Zuo, L., Yu, Y. C., Xiong, X., Xu, J., Qiao, B., Chen, J., Cai, H., Yan, Q., Han, H.-X., et al. (2025) · Genomics Proteomics & Bioinformatics · doi:10.1093/gpbjnl/qzaf027 · Cited by 3

Clinical progression of clonal hematopoiesis is determined by a combination of mutation timing, fitness, and clonal structurePreprint

Crespo, E. L., Robertson, N., Kosebent, E. G., MacGillivray, L., Murphy, L., Uddin, M. M., Whitsel, E. A., Honigberg, M. C., Bick, A. G., Reiner, A. P., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.28.640879 · Cited by 4

Association of clonal haematopoiesis with severe postoperative complications in patients undergoing radical oesophagectomy

Wang, H., Yan, H., Chen, W., Tang, H., Pei, Y.-Z., Shan, Q., Cang, J., Miao, C., Tan, L., & Tan, L. (2023) · British Journal of Anaesthesia · doi:10.1016/j.bja.2023.10.035 · Cited by 2

Clonal hematopoiesis of indeterminate potential and heart failure

Lyasnikova, E. A., Ivanchenko, L. Y., Козлова, С. Н., Sitnikova, M. Y., Kostareva, A. A., & Shlyakhto, E. V. (2024) · Russian Journal of Cardiology · doi:10.15829/1560-4071-2024-6016 · Cited by 3

The phenomenon of clonal hematopoiesis: etiology, classification and its prognostic role

Kunevich, E. O., Mikhaleva, M., Крысюк, О. Б., Bogdanov, A. N., Zherniakova, A., & Волошин, С. В. (2025) · Oncohematology · doi:10.17650/1818-8346-2025-20-1-28-54 · Cited by 2

Association of high‐dose radioactive iodine therapy with PPM1D ‐mutated clonal hematopoiesis in older individuals

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