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Author Details

Keiran Raine
Wellcome Sanger Institute
2004
64
54
PMIDPaper TitleJournal TitlePublished Year
34646017Convergent somatic mutations in metabolism genes in chronic liver disease.Nature2021
34824211Aberrant integration of Hepatitis B virus DNA promotes major restructuring of human hepatocellular carcinoma genome architecture.Nat Commun2021
33004514Extensive heterogeneity in somatic mutation and selection in the human bladder.Science2020
33028839Framework for quality assessment of whole genome cancer sequences.Nat Commun2020
30849372Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis.Cell2019
29656891Timing the Landmark Events in the Evolution of Clear Cell Renal Cell Cancer: TRACERx Renal.Cell2018
29988082Prediction of acute myeloid leukaemia risk in healthy individuals.Nature2018
29906452Universal Patterns of Selection in Cancer and Somatic Tissues.Cell2018
30039366Split-Read Indel and Structural Variant Calling Using PINDEL.Methods Mol Biol2018
29662167Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.Nat Genet2018
29789651Analysis of the genomic landscape of multiple myeloma highlights novel prognostic markers and disease subgroups.Leukemia2018
28810143Genomic Evolution of Breast Cancer Metastasis and Relapse.Cancer Cell2017
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
29056346Universal Patterns of Selection in Cancer and Somatic Tissues.Cell2017
29074948Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.Nat Genet2017
28945760Appraising the relevance of DNA copy number loss and gain in prostate cancer using whole genome DNA sequence data.PLoS Genet2017
27276561Genomic Classification and Prognosis in Acute Myeloid Leukemia.N Engl J Med2016
27615322Mutational signatures of ionizing radiation in second malignancies.Nat Commun2016
27588520A DNA target-enrichment approach to detect mutations, copy number changes and immunoglobulin translocations in multiple myeloma.Blood Cancer J2016
27930809ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data.Curr Protoc Bioinformatics2016
27930805cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data.Curr Protoc Bioinformatics2016
27498871Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer.Cell Rep2016
27135926Landscape of somatic mutations in 560 breast cancer whole-genome sequences.Nature2016
25730763Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.Nat Genet2015
26647970A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.Nat Commun2015
26678382cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing.Curr Protoc Bioinformatics2015
26099045Subclonal diversification of primary breast cancer revealed by multiregion sequencing.Nat Med2015
26018901Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.Nat Genet2015
24413735RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.Nat Genet2014
25260652Polygenic in vivo validation of cancer mutations using transposons.Genome Biol2014
25030888C. elegans whole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency.Genome Res2014
25082706Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.Science2014
24714652Processed pseudogenes acquired somatically during cancer development.Nat Commun2014
23770606Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.Nat Genet2013
24325359Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2.N Engl J Med2013
24182360Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs.Twin Res Hum Genet2013
24148783The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models.Genome Biol2013
24030381Clinical and biological implications of driver mutations in myelodysplastic syndromes.Blood2013
23630320Single-cell paired-end genome sequencing reveals structural variation per cell cycle.Nucleic Acids Res2013
23599896DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis.Elife2013
23778141Whole exome sequencing of adenoid cystic carcinoma.J Clin Invest2013
22341448Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer.Cell2012
22722201The landscape of cancer genes and mutational processes in breast cancer.Nature2012
22514011Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes.J Pathol2012
22608084Mutational processes molding the genomes of 21 breast cancers.Cell2012
22608083The life history of 21 breast cancers.Cell2012
22397650Intratumor heterogeneity and branched evolution revealed by multiregion sequencing.N Engl J Med2012
21248752Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.Nature2011
21995386Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.N Engl J Med2011
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Collaborators

Wellcome Sanger Institute
Co-authored papers 47
Wellcome Sanger Institute
Co-authored papers 46
Wellcome Sanger Institute
Co-authored papers 43
Wellcome Sanger Institute
Co-authored papers 41
Wellcome Sanger Institute
Co-authored papers 40
Wellcome Sanger Institute
Co-authored papers 34
The University of Texas MD Anderson Cancer Center
Co-authored papers 33
Clinical Research Facility, Mercy University Hospital
Co-authored papers 27
Wellcome Trust Sanger Institute
Co-authored papers 26
The Francis Crick Institute
Co-authored papers 25
Early Cancer Institute, University of Cambridge
Co-authored papers 24
Manchester Cancer Research Centre, University of Manchester
Co-authored papers 24
Inivata Ltd
Co-authored papers 23
Wellcome Trust Sanger Institute
Co-authored papers 19
Wellcome Trust Sanger Institute
Co-authored papers 19
Moores Cancer Center, university of california san diego
Co-authored papers 16
Murdoch Children's Research Institute, Royal Children's Hospital
Co-authored papers 16
University of East Anglia
Co-authored papers 15
Wellcome Sanger Institute
Co-authored papers 15
Co-authored papers 13
Wellcome Trust Sanger Institute
Co-authored papers 13
University of Cambridge
Co-authored papers 13
Institute of Cancer Sciences, University of Glasgow
Co-authored papers 13
Co-authored papers 12
Memorial Sloan Kettering Cancer Center
Co-authored papers 12
Co-authored papers 12
Co-authored papers 12
Co-authored papers 11
German Cancer Research Centre DKFZ
Co-authored papers 11
Wellcome Sanger Institute
Co-authored papers 10