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Author Details
Full Name
Michael R Stratton
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
1987
Papers
347
H Index
140
Expertise
CM4AI Collaborator
Emma Lundberg (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36702998
APOBEC mutagenesis is a common process in normal human small intestine.
Nat Genet
2023
37502962
Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment.
bioRxiv
2023
38096571
Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment.
Bioinformatics
2023
37079675
The evolution of two transmissible cancers in Tasmanian devils.
Science
2023
36697836
Author Correction: The repertoire of mutational signatures in human cancer.
Nature
2023
36539619
Author Correction: Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro.
Nat Genet
2023
36388765
Uncovering novel mutational signatures by <i>de novo</i> extraction with SigProfilerExtractor.
Cell Genom
2022
35803914
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.
Nat Commun
2022
35650442
Clonal dynamics of haematopoiesis across the human lifespan.
Nature
2022
35581206
Mutational landscape of normal epithelial cells in Lynch Syndrome patients.
Nat Commun
2022
35469014
Functional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR ÿ LGR5 bispecific antibody with efficacy in epithelial tumors.
Nat Cancer
2022
35418684
Somatic mutation rates scale with lifespan across mammals.
Nature
2022
35859169
Mechanisms of APOBEC3 mutagenesis in human cancer cells.
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
34857954
Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro.
Nat Genet
2021
34646017
Convergent somatic mutations in metabolism genes in chronic liver disease.
Nature
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
34663923
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence.
Nat Genet
2021
34594041
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases.
Nat Genet
2021
32350471
The mutational landscape of normal human endometrial epithelium.
Nature
2020
31996850
Tobacco smoking and somatic mutations in human bronchial epithelium.
Nature
2020
31723001
Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness.
Cancer Res
2020
31949161
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
Nat Commun
2020
33232318
Evolution and lineage dynamics of a transmissible cancer in Tasmanian devils.
PLoS Biol
2020
33004514
Extensive heterogeneity in somatic mutation and selection in the human bladder.
Science
2020
32673568
Tissue-Biased Expansion of DNMT3A-Mutant Clones in a Mosaic Individual Is Associated with Conserved Epigenetic Erosion.
Cell Stem Cell
2020
33022221
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.
Am J Hum Genet
2020
32697969
Somatic Evolution in Non-neoplastic IBD-Affected Colon.
Cell
2020
29602208
Recurrent histone mutations in T-cell acute lymphoblastic leukaemia.
Br J Haematol
2019
31645730
The landscape of somatic mutation in normal colorectal epithelial cells.
Nature
2019
31806814
Embryonal precursors of Wilms tumor.
Science
2019
31548585
Publisher Correction: Shared heritability and functional enrichment across six solid cancers.
Nat Commun
2019
31371581
Somatic evolution and global expansion of an ancient transmissible cancer lineage.
Science
2019
30988298
Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation.
Nat Commun
2019
30849372
Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis.
Cell
2019
30683880
Shared heritability and functional enrichment across six solid cancers.
Nat Commun
2019
29323295
Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells.
Nature
2018
29915264
Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants.
Nat Commun
2018
30185910
Population dynamics of normal human blood inferred from somatic mutations.
Nature
2018
29858576
Recurrent rearrangements of FOS and FOSB define osteoblastoma.
Nat Commun
2018
29906452
Universal Patterns of Selection in Cancer and Somatic Tissues.
Cell
2018
30202019
The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature.
Nat Commun
2018
30337457
Somatic mutant clones colonize the human esophagus with age.
Science
2018
30559362
Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.
Nat Commun
2018
29643510
Intra-tumour diversification in colorectal cancer at the single-cell level.
Nature
2018
28904067
Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency.
Cancer Res
2017
28112740
A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.
Nat Genet
2017
28288110
HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures.
Nat Med
2017
1 - 50 of 347
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David C Wedge
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The Francis Crick Institute
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