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Michael R. Stratton

Researcher Next ID · RN-028570

Researcher · Biochemistry, Genetics and Molecular Biology

Wellcome Sanger Institute

Cambridge, United States

Not currently recruitingFunding unknown
Works count
654
Citation count
202,269
H-index
182
i10-index
399

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Cancer Genomics and Diagnostics
Genetic factors in colorectal cancer
BRCA gene mutations in cancer
DNA Repair Mechanisms
Genomic variations and chromosomal abnormalities

Publications

  • Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro

    Nature Genetics · 2021 · 10.1038/s41588-021-00972-2

  • Somatic mutant clones colonize the human esophagus with age

    Science · 2018 · 10.1126/science.aau3879

  • The Repertoire of Mutational Signatures in Human Cancer

    bioRxiv (Cold Spring Harbor Laboratory) · 2018 · https://doi.org/10.1101/322859

  • Genomic Evolution of Breast Cancer Metastasis and Relapse

    Cancer Cell · 2017 · https://doi.org/10.1016/j.ccell.2017.07.005

  • HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures

    Nature Medicine · 2017 · https://doi.org/10.1038/nm.4292

  • Universal Patterns of Selection in Cancer and Somatic Tissues

    Cell · 2017 · 10.1016/j.cell.2017.09.042

  • Mutational signatures associated with tobacco smoking in human cancer

    Science · 2016 · https://doi.org/10.1126/science.aag0299

  • Landscape of somatic mutations in 560 breast cancer whole-genome sequences

    Nature · 2016 · 10.1038/nature17676

  • A Landscape of Pharmacogenomic Interactions in Cancer

    Cell · 2016 · https://doi.org/10.1016/j.cell.2016.06.017

  • Clock-like mutational processes in human somatic cells

    Nature Genetics · 2015 · 10.1038/ng.3441

  • Prospective Derivation of a Living Organoid Biobank of Colorectal Cancer Patients

    Cell · 2015 · 10.1016/j.cell.2015.03.053

  • Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets

    Nature Genetics · 2015 · 10.1038/ng.3252

  • High burden and pervasive positive selection of somatic mutations in normal human skin

    Science · 2015 · 10.1126/science.aaa6806

  • High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4+ T cells in human melanoma

    Nature Medicine · 2014 · 10.1038/nm.3773

  • COSMIC: exploring the world's knowledge of somatic mutations in human cancer

    Nucleic Acids Research · 2014 · 10.1093/nar/gku1075

  • Deciphering Signatures of Mutational Processes Operative in Human Cancer

    Cell Reports · 2013 · 10.1016/j.celrep.2012.12.008

  • Signatures of mutational processes in human cancer

    Nature · 2013 · https://doi.org/10.1038/nature12477

  • Clinical and biological implications of driver mutations in myelodysplastic syndromes

    Blood · 2013 · 10.1182/blood-2013-08-518886

  • Tumor Exome Analysis Reveals Neoantigen-Specific T-Cell Reactivity in an Ipilimumab-Responsive Melanoma

    Journal of Clinical Oncology · 2013 · 10.1200/jco.2012.47.7521

  • The landscape of cancer genes and mutational processes in breast cancer

    Nature · 2012 · 10.1038/nature11017

  • Systematic identification of genomic markers of drug sensitivity in cancer cells

    Nature · 2012 · 10.1038/nature11005

  • Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells

    Nucleic Acids Research · 2012 · https://doi.org/10.1093/nar/gks1111

  • The Life History of 21 Breast Cancers

    Cell · 2012 · 10.1016/j.cell.2012.04.023

  • Mutational Processes Molding the Genomes of 21 Breast Cancers

    Cell · 2012 · 10.1016/j.cell.2012.04.024

  • Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

    Nature · 2011 · 10.1038/nature10113

  • SomaticSF3B1Mutation in Myelodysplasia with Ring Sideroblasts

    New England Journal of Medicine · 2011 · 10.1056/nejmoa1103283

  • Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

    Nature · 2011 · 10.1038/nature09639

  • Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development

    Cell · 2011 · 10.1016/j.cell.2010.11.055

  • Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

    Nature · 2010 · 10.1038/nature08979

  • International network of cancer genome projects

    Nature · 2010 · 10.1038/nature08987

  • COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

    Nucleic Acids Research · 2010 · 10.1093/nar/gkq929

  • The patterns and dynamics of genomic instability in metastatic pancreatic cancer

    Nature · 2010 · 10.1038/nature09460

  • Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

    Nature · 2010 · 10.1038/nature08672

  • A comprehensive catalogue of somatic mutations from a human cancer genome

    Nature · 2009 · 10.1038/nature08658

  • Complex landscapes of somatic rearrangement in human breast cancer genomes

    Nature · 2009 · 10.1038/nature08645

  • A small-cell lung cancer genome with complex signatures of tobacco exposure

    Nature · 2009 · 10.1038/nature08629

  • The cancer genome

    Nature · 2009 · https://doi.org/10.1038/nature07943

  • The Catalogue of Somatic Mutations in Cancer (COSMIC)

    Current Protocols in Human Genetics · 2008 · 10.1002/0471142905.hg1011s57

  • JAK2 Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis

    New England Journal of Medicine · 2007 · 10.1056/nejmoa065202

  • Genome-wide association study identifies novel breast cancer susceptibility loci

    Nature · 2007 · 10.1038/nature05887

  • Patterns of somatic mutation in human cancer genomes

    Nature · 2007 · 10.1038/nature05610

  • PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

    Nature Genetics · 2006 · 10.1038/ng1959

  • Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype

    Clinical Cancer Research · 2005 · 10.1158/1078-0432.ccr-04-2424

  • A census of human cancer genes

    Nature reviews. Cancer · 2004 · 10.1038/nrc1299

  • Intragenic ERBB2 kinase mutations in tumours

    Nature · 2004 · 10.1038/431525b

  • Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations

    Nature Genetics · 2002 · 10.1038/ng879

  • BRAF and RAS mutations in human lung cancer and melanoma.

    PubMed · 2002

  • Mutations of the BRAF gene in human cancer

    Nature · 2002 · https://doi.org/10.1038/nature00766

  • Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families

    The American Journal of Human Genetics · 1998 · 10.1086/301749

  • Identification of the breast cancer susceptibility gene BRCA2

    Nature · 1995 · https://doi.org/10.1038/378789a0

  • Localization of a Breast Cancer Susceptibility Gene, BRCA2 , to Chromosome 13q12-13

    Science · 1994 · 10.1126/science.8091231

Current projects

    No projects listed.