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Author Details
Full Name
Keiran Raine
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
2004
Papers
64
H Index
54
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34646017
Convergent somatic mutations in metabolism genes in chronic liver disease.
Nature
2021
34824211
Aberrant integration of Hepatitis B virus DNA promotes major restructuring of human hepatocellular carcinoma genome architecture.
Nat Commun
2021
33004514
Extensive heterogeneity in somatic mutation and selection in the human bladder.
Science
2020
33028839
Framework for quality assessment of whole genome cancer sequences.
Nat Commun
2020
30849372
Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis.
Cell
2019
29656891
Timing the Landmark Events in the Evolution of Clear Cell Renal Cell Cancer: TRACERx Renal.
Cell
2018
29988082
Prediction of acute myeloid leukaemia risk in healthy individuals.
Nature
2018
29906452
Universal Patterns of Selection in Cancer and Somatic Tissues.
Cell
2018
30039366
Split-Read Indel and Structural Variant Calling Using PINDEL.
Methods Mol Biol
2018
29662167
Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.
Nat Genet
2018
29789651
Analysis of the genomic landscape of multiple myeloma highlights novel prognostic markers and disease subgroups.
Leukemia
2018
28810143
Genomic Evolution of Breast Cancer Metastasis and Relapse.
Cancer Cell
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
29056346
Universal Patterns of Selection in Cancer and Somatic Tissues.
Cell
2017
29074948
Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.
Nat Genet
2017
28945760
Appraising the relevance of DNA copy number loss and gain in prostate cancer using whole genome DNA sequence data.
PLoS Genet
2017
27276561
Genomic Classification and Prognosis in Acute Myeloid Leukemia.
N Engl J Med
2016
27615322
Mutational signatures of ionizing radiation in second malignancies.
Nat Commun
2016
27588520
A DNA target-enrichment approach to detect mutations, copy number changes and immunoglobulin translocations in multiple myeloma.
Blood Cancer J
2016
27930809
ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data.
Curr Protoc Bioinformatics
2016
27930805
cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data.
Curr Protoc Bioinformatics
2016
27498871
Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer.
Cell Rep
2016
27135926
Landscape of somatic mutations in 560 breast cancer whole-genome sequences.
Nature
2016
25730763
Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
Nat Genet
2015
26647970
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.
Nat Commun
2015
26678382
cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing.
Curr Protoc Bioinformatics
2015
26099045
Subclonal diversification of primary breast cancer revealed by multiregion sequencing.
Nat Med
2015
26018901
Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
Nat Genet
2015
24413735
RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.
Nat Genet
2014
25260652
Polygenic in vivo validation of cancer mutations using transposons.
Genome Biol
2014
25030888
C. elegans whole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency.
Genome Res
2014
25082706
Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.
Science
2014
24714652
Processed pseudogenes acquired somatically during cancer development.
Nat Commun
2014
23770606
Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.
Nat Genet
2013
24325359
Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2.
N Engl J Med
2013
24182360
Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs.
Twin Res Hum Genet
2013
24148783
The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models.
Genome Biol
2013
24030381
Clinical and biological implications of driver mutations in myelodysplastic syndromes.
Blood
2013
23630320
Single-cell paired-end genome sequencing reveals structural variation per cell cycle.
Nucleic Acids Res
2013
23599896
DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis.
Elife
2013
23778141
Whole exome sequencing of adenoid cystic carcinoma.
J Clin Invest
2013
22341448
Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer.
Cell
2012
22722201
The landscape of cancer genes and mutational processes in breast cancer.
Nature
2012
22514011
Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes.
J Pathol
2012
22608084
Mutational processes molding the genomes of 21 breast cancers.
Cell
2012
22608083
The life history of 21 breast cancers.
Cell
2012
22397650
Intratumor heterogeneity and branched evolution revealed by multiregion sequencing.
N Engl J Med
2012
21248752
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.
Nature
2011
21995386
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.
N Engl J Med
2011
1 - 50 of 64
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Elaine R Mardis
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Patrick S Tarpey
Wellcome Trust Sanger Institute
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Serena Nik-Zainal
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23
Laura Mudie
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Stuart McLaren
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Ludmil B Alexandrov
Moores Cancer Center, university of california san diego
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Rebecca Shepherd
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Chris Greenman
University of East Anglia
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Inigo Martincorena
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Sarah Edkins
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Lucy A Stebbings
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Douglas F Easton
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