Campbell, Peter J.
Wellcome Sanger Institute
68 papers on CoChatORCID 0000-0002-3921-0510
Most cited papers
- Verified
V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis
Campbell, P. J. (2006) · Blood
Myeloproliferative Neoplasms: Diagnosis and TreatmentPlatelet Disorders and Treatments
Cited by 224
- Verified
Genomic patterns of progression in smoldering multiple myeloma
Bolli, N., Maura, F., Minvielle, S., Gloznik, D., Szalat, R., Fullam, A., Martincorena, I., Dawson, K. J., Samur, M. K., Zamora, J., et al. (2018) · Nature Communications
Multiple Myeloma Research and TreatmentsCancer Genomics and Diagnostics
Cited by 222
- Verified
Convergent somatic mutations in metabolism genes in chronic liver disease
Ng, S. W. K., Rouhani, F. J., Brunner, S. F., Brzozowska, N., Aitken, S. J., Yang, M., Abascal, F., Moore, L., Nikitopoulou, E., Chappell, L., et al. (2021) · Nature
Cancer Genomics and DiagnosticsLiver Disease Diagnosis and Treatment
Cited by 190
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A practical guide for mutational signature analysis in hematological malignancies
Maura, F., Degasperi, A., Nadeu, F., Leongamornlert, D., Davies, H., Moore, L., Royo, R., Ziccheddu, B., Puente, X. S., Avet-Loiseau, H., et al. (2019) · Nature Communications
Cancer Genomics and DiagnosticsAcute Myeloid Leukemia Research
Cited by 184
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Increased somatic mutation burdens in normal human cells due to defective DNA polymerases
Robinson, P. S., Coorens, T. H. H., Palles, C., Mitchell, E., Abascal, F., Olafsson, S., Lee, B. C. H., Lawson, A. R. J., Lee-Six, H., Moore, L., et al. (2021) · Nature Genetics
Cancer Genomics and DiagnosticsDNA Repair Mechanisms
Cited by 173
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Timing the Initiation of Multiple Myeloma
Rustad, E. H., Yellapantula, V., Leongamornlert, D., Bolli, N., Ledergor, G., Nadeu, F., Angelopoulos, N., Dawson, K. J., Mitchell, T. J., Osborne, R. J., et al. (2020) · Nature Communications
Multiple Myeloma Research and TreatmentsCancer Genomics and Diagnostics
Cited by 165
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The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders
Scott, L. M., Campbell, P. J., Baxter, E. J., Todd, T., Stephens, P., Edkins, S., Wooster, R., Stratton, M. R., Futreal, P. A., & Green, A. R. (2005) · Blood
Myeloproliferative Neoplasms: Diagnosis and TreatmentAcute Myeloid Leukemia Research
Cited by 158
- Verified
Intensive insulin therapy and weight gain in IDDM
Carlson, M. G., & Campbell, P. J. (1993) · Diabetes
Diabetes Management and ResearchDiabetes, Cardiovascular Risks, and Lipoproteins
Cited by 155
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Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities
Oben, B., Froyen, G., Maclachlan, K. H., Leongamornlert, D., Abascal, F., Zheng-Lin, B., Yellapantula, V., Derkach, A., Geerdens, E., Diamond, B. T., et al. (2021) · Nature Communications
Multiple Myeloma Research and TreatmentsCancer Genomics and Diagnostics
Cited by 129
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Diverse mutational landscapes in human lymphocytes
Machado, H. E., Mitchell, E., Øbro, N. F., Kübler, K., Davies, M., Leongamornlert, D., Cull, A., Maura, F., Sanders, M. A., Cagan, A. T. J., et al. (2022) · Nature
Cancer Genomics and DiagnosticsDNA Repair Mechanisms
Cited by 116
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Single-cell mutational profiling and clonal phylogeny in cancer
Potter, N. E., Ermini, L., Papaemmanuil, E., Cazzaniga, G., Vijayaraghavan, G., Titley, I., Ford, A., Campbell, P., Kearney, L., & Greaves, M. (2013) · Genome Research
Cancer Genomics and DiagnosticsSingle-cell and spatial transcriptomics
Cited by 107
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A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers
Glodzik, D., Morganella, S., Davies, H., Simpson, P. T., Li, Y., Zou, X., Diez-Perez, J., Staaf, J., Alexandrov, L. B., Smid, M., et al. (2017) · Nature Genetics
Cancer Genomics and DiagnosticsBRCA gene mutations in cancer
Cited by 84
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Positive selection of somatically mutated clones identifies adaptive pathways in metabolic liver disease
Wang, Z., Zhu, S., Jia, Y., Wang, Y., Kubota, N., Fujiwara, N., Gordillo, R., Lewis, C., Zhu, M., Sharma, T., et al. (2023) · Cell
Liver Disease Diagnosis and TreatmentLiver physiology and pathology
Cited by 72
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Genome Sequencing during a Patient’s Journey through Cancer
Nangalia, J., & Campbell, P. J. (2019) · New England Journal of Medicine
Cancer Genomics and DiagnosticsBRCA gene mutations in cancer
Cited by 66
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Clonal dynamics after allogeneic haematopoietic cell transplantation
Spencer Chapman, M., Wilk, C. M., Boettcher, S., Mitchell, E., Dawson, K., Williams, N., Müller, J., Kovtonyuk, L., Jung, H., Caiado, F., et al. (2024) · Nature
Hematopoietic Stem Cell TransplantationAcute Myeloid Leukemia Research
Cited by 60
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The somatic mutation landscape of normal gastric epithelium
Coorens, T. H. H., Collord, G., Jung, H., Wang, Y., Moore, L., Hooks, Y., Mahbubani, K., Law, S. Y. K., Yan, H. H. N., Yuen, S. T., et al. (2025) · Nature
Cancer Genomics and DiagnosticsGenetic factors in colorectal cancer
Cited by 57
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Tissue-Biased Expansion of DNMT3A-Mutant Clones in a Mosaic Individual Is Associated with Conserved Epigenetic Erosion
Tovy, A., Reyes, J. M., Gundry, M. C., Brunetti, L., Lee-Six, H., Petljak, M., Park, H. J., Guzman, A. G., Rosas, C., Jeffries, A. R., et al. (2020) · Cell Stem Cell
Acute Myeloid Leukemia ResearchEpigenetics and DNA Methylation
Cited by 30
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Genomics define malignant transformation in myeloma precursor conditions
Maura, F., Bergsagel, P. L., Ziccheddu, B., Kumar, S., Maclachlan, K., Derkach, A., Garces, J.-J., Firestone, R., Braggio, E., Asmann, Y., et al. (2026) · Journal of Clinical Oncology
Multiple Myeloma Research and TreatmentsChronic Lymphocytic Leukemia Research
Cited by 18
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Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles
Bolli, N., Barcella, M., Salvi, E., D'Avila, F., Vendramin, A., De Philippis, C., Munshi, N. C., Avet‐Loiseau, H., Campbell, P. J., Mussetti, A., et al. (2017) · Cancer
Multiple Myeloma Research and TreatmentsGenomics and Rare Diseases
Cited by 17
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Selection for somatic escape variants in SERPINA1 in the liver of patients with alpha-1 antitrypsin deficiency
Brzozowska, N., Wu, L. Y. D., Khodzhaeva, V., Griffiths, W. J., Duckworth, A., Jung, H., Coorens, T. H. H., Hooks, Y., Chambers, J. E., Campbell, P. J., et al. (2025) · Nature Genetics
Genomics and Rare DiseasesEvolution and Genetic Dynamics
Cited by 11
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