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Author Details
Full Name
Peter J Campbell
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
2003
Papers
278
H Index
123
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
32341528
Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers.
Nat Genet
2023
37884686
Effects of psoriasis and psoralen exposure on the somatic mutation landscape of the skin.
Nat Genet
2023
37608017
Convergent somatic evolution commences in utero in a germline ribosomopathy.
Nat Commun
2023
37973947
Clonal selection of hematopoietic stem cells after gene therapy for sickle cell disease.
Nat Med
2023
36993727
Positive selection of somatically mutated clones identifies adaptive pathways in metabolic liver disease.
bioRxiv
2023
37040760
Positive selection of somatically mutated clones identifies adaptive pathways in metabolic liver disease.
Cell
2023
36697832
Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.
Nature
2023
36849600
Author Correction: Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing.
Nat Protoc
2023
36702998
APOBEC mutagenesis is a common process in normal human small intestine.
Nat Genet
2023
36326980
Demystifying the black box: from ignorance to observation to mechanism in cancer research.
Eur J Epidemiol
2023
32047324
Publisher Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers.
Nat Genet
2023
35228729
Author Correction: Inherent mosaicism and extensive mutation of human placentas.
Nature
2022
35803914
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.
Nat Commun
2022
35650444
The longitudinal dynamics and natural history of clonal haematopoiesis.
Nature
2022
35650442
Clonal dynamics of haematopoiesis across the human lifespan.
Nature
2022
35379892
Bayesian networks elucidate complex genomic landscapes in cancer.
Commun Biol
2022
35581206
Mutational landscape of normal epithelial cells in Lynch Syndrome patients.
Nat Commun
2022
35790747
Interrogating breast cancer heterogeneity using single and pooled circulating tumor cell analysis.
NPJ Breast Cancer
2022
35363872
Molecular subclusters of follicular lymphoma: a report from the United Kingdom's Haematological Malignancy Research Network.
Blood Adv
2022
35418684
Somatic mutation rates scale with lifespan across mammals.
Nature
2022
36778659
The eternal quest for self-improvement of somatic cells.
Cell Genom
2022
36423636
Mapping single-cell transcriptomes in the intra-tumoral and associated territories of kidney cancer.
Cancer Cell
2022
36450981
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.
Nature
2022
35941135
Unified classification and risk-stratification in Acute Myeloid Leukemia.
Nat Commun
2022
35953718
Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.
Nat Med
2022
35953478
Clonal diversification and histogenesis of malignant germ cell tumours.
Nat Commun
2022
36352222
Spatial genomics maps the structure, nature and evolution of cancer clones.
Nature
2022
35948631
Diverse mutational landscapes in human lymphocytes.
Nature
2022
33318691
Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing.
Nat Protoc
2021
33911282
Somatic mutation landscapes at single-molecule resolution.
Nature
2021
33767199
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities.
Nat Commun
2021
33905417
Protection of the C. elegans germ cell genome depends on diverse DNA repair pathways during normal proliferation.
PLoS One
2021
33649505
Publisher Correction: Chromothripsis drives the evolution of gene amplification in cancer.
Nature
2021
33692543
Inherent mosaicism and extensive mutation of human placentas.
Nature
2021
33657416
Development, maturation, and maintenance of human prostate inferred from somatic mutations.
Cell Stem Cell
2021
34824211
Aberrant integration of Hepatitis B virus DNA promotes major restructuring of human hepatocellular carcinoma genome architecture.
Nat Commun
2021
34646017
Convergent somatic mutations in metabolism genes in chronic liver disease.
Nature
2021
34614038
C. elegans genome-wide analysis reveals DNA repair pathways that act cooperatively to preserve genome integrity upon ionizing radiation.
PLoS One
2021
34433963
Extensive phylogenies of human development inferred from somatic mutations.
Nature
2021
34433962
The mutational landscape of human somatic and germline cells.
Nature
2021
34594041
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases.
Nat Genet
2021
33981037
Lineage tracing of human development through somatic mutations.
Nature
2021
33054126
<i>CDKN2A</i> deletion is a frequent event associated with poor outcome in patients with peripheral T-cell lymphoma not otherwise specified (PTCL-NOS).
Haematologica
2021
33361815
Chromothripsis drives the evolution of gene amplification in cancer.
Nature
2021
32317634
Timing the initiation of multiple myeloma.
Nat Commun
2020
31996850
Tobacco smoking and somatic mutations in human bronchial epithelium.
Nature
2020
31932696
Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution.
Nat Genet
2020
32024997
Comprehensive molecular characterization of mitochondrial genomes in human cancers.
Nat Genet
2020
32051610
Author Correction: Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution.
Nat Genet
2020
33028839
Framework for quality assessment of whole genome cancer sequences.
Nat Commun
2020
1 - 50 of 278
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Patrick S Tarpey
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Andrew Menzies
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Laura Mudie
Wellcome Trust Sanger Institute
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David Jones
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Clinical Research Facility, Mercy University Hospital
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Lucy A Stebbings
Wellcome Trust Sanger Institute
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Stuart McLaren
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