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Author Details

Michael R Stratton
Wellcome Sanger Institute
1987
347
140
Emma Lundberg (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36702998APOBEC mutagenesis is a common process in normal human small intestine.Nat Genet2023
37502962Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment.bioRxiv2023
38096571Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment.Bioinformatics2023
37079675The evolution of two transmissible cancers in Tasmanian devils.Science2023
36697836Author Correction: The repertoire of mutational signatures in human cancer.Nature2023
36539619Author Correction: Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro.Nat Genet2023
36388765Uncovering novel mutational signatures by <i>de novo</i> extraction with SigProfilerExtractor.Cell Genom2022
35803914Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.Nat Commun2022
35650442Clonal dynamics of haematopoiesis across the human lifespan.Nature2022
35581206Mutational landscape of normal epithelial cells in Lynch Syndrome patients.Nat Commun2022
35469014Functional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR ÿ LGR5 bispecific antibody with efficacy in epithelial tumors.Nat Cancer2022
35418684Somatic mutation rates scale with lifespan across mammals.Nature2022
35859169Mechanisms of APOBEC3 mutagenesis in human cancer cells.Nature2022
33318691Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing.Nat Protoc2021
33911282Somatic mutation landscapes at single-molecule resolution.Nature2021
34857954Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro.Nat Genet2021
34646017Convergent somatic mutations in metabolism genes in chronic liver disease.Nature2021
34433963Extensive phylogenies of human development inferred from somatic mutations.Nature2021
34433962The mutational landscape of human somatic and germline cells.Nature2021
34663923Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence.Nat Genet2021
34594041Increased somatic mutation burdens in normal human cells due to defective DNA polymerases.Nat Genet2021
32350471The mutational landscape of normal human endometrial epithelium.Nature2020
31996850Tobacco smoking and somatic mutations in human bronchial epithelium.Nature2020
31723001Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness.Cancer Res2020
31949161A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.Nat Commun2020
33232318Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils.PLoS Biol2020
33004514Extensive heterogeneity in somatic mutation and selection in the human bladder.Science2020
32673568Tissue-Biased Expansion of DNMT3A-Mutant Clones in a Mosaic Individual Is Associated with Conserved Epigenetic Erosion.Cell Stem Cell2020
33022221Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.Am J Hum Genet2020
32697969Somatic Evolution in Non-neoplastic IBD-Affected Colon.Cell2020
29602208Recurrent histone mutations in T-cell acute lymphoblastic leukaemia.Br J Haematol2019
31645730The landscape of somatic mutation in normal colorectal epithelial cells.Nature2019
31806814Embryonal precursors of Wilms tumor.Science2019
31548585Publisher Correction: Shared heritability and functional enrichment across six solid cancers.Nat Commun2019
31371581Somatic evolution and global expansion of an ancient transmissible cancer lineage.Science2019
30988298Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation.Nat Commun2019
30849372Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis.Cell2019
30683880Shared heritability and functional enrichment across six solid cancers.Nat Commun2019
29323295Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells.Nature2018
29915264Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants.Nat Commun2018
30185910Population dynamics of normal human blood inferred from somatic mutations.Nature2018
29858576Recurrent rearrangements of FOS and FOSB define osteoblastoma.Nat Commun2018
29906452Universal Patterns of Selection in Cancer and Somatic Tissues.Cell2018
30202019The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature.Nat Commun2018
30337457Somatic mutant clones colonize the human esophagus with age.Science2018
30559362Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.Nat Commun2018
29643510Intra-tumour diversification in colorectal cancer at the single-cell level.Nature2018
28904067Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency.Cancer Res2017
28112740A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.Nat Genet2017
28288110HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures.Nat Med2017
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Collaborators

The University of Texas MD Anderson Cancer Center
Co-authored papers 106
Wellcome Sanger Institute
Co-authored papers 89
University of Cambridge
Co-authored papers 76
Wellcome Trust Sanger Institute
Co-authored papers 56
Wellcome Sanger Institute
Co-authored papers 53
Wellcome Sanger Institute
Co-authored papers 53
Moores Cancer Center, university of california san diego
Co-authored papers 43
Wellcome Sanger Institute
Co-authored papers 43
Co-authored papers 42
Wellcome Sanger Institute
Co-authored papers 42
Early Cancer Institute, University of Cambridge
Co-authored papers 40
Wellcome Sanger Institute
Co-authored papers 38
Wellcome Sanger Institute
Co-authored papers 34
Manchester Cancer Research Centre, University of Manchester
Co-authored papers 32
Clinical Research Facility, Mercy University Hospital
Co-authored papers 29
University of East Anglia
Co-authored papers 29
The Francis Crick Institute
Co-authored papers 27
Basser Center for BRCA, Abramson Cancer Center, University of Pennsylvania
Co-authored papers 26
University of Queensland
Co-authored papers 25
Wellcome Trust Sanger Institute
Co-authored papers 24
University College London, UCL Cancer Institute
Co-authored papers 22
Wellcome Trust Sanger Institute
Co-authored papers 22
Inivata Ltd
Co-authored papers 21
Norwich Medical School, University of East Anglia
Co-authored papers 21
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University of Cambridge, UK Cambridge University Hospitals NHS Foundation Trust
Co-authored papers 20
Institute for Cancer Research, Oslo University Hospital
Co-authored papers 20
Murdoch Children's Research Institute, Royal Children's Hospital
Co-authored papers 19
University of Utah
Co-authored papers 18
Perelman School of Medicine, University of Pennsylvania, USA Abramson Cancer Center
Co-authored papers 18