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Author Details

Lucy A Stebbings
Wellcome Trust Sanger Institute
1998
34
30
PMIDPaper TitleJournal TitlePublished Year
29662167Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.Nat Genet2018
28179366Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations.Genome Res2017
27135926Landscape of somatic mutations in 560 breast cancer whole-genome sequences.Nature2016
27615322Mutational signatures of ionizing radiation in second malignancies.Nat Commun2016
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
26018901Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.Nat Genet2015
25999502Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin.Science2015
24413735RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.Nat Genet2014
23596509Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome.PLoS One2013
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
22608083The life history of 21 breast cancers.Cell2012
22608084Mutational processes molding the genomes of 21 breast cancers.Cell2012
21215367Massive genomic rearrangement acquired in a single catastrophic event during cancer development.Cell2011
21642962Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia.Nature2011
21248752Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.Nature2011
20016485A comprehensive catalogue of somatic mutations from a human cancer genome.Nature2010
20725990Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors.Genes Chromosomes Cancer2010
20942901Somatic structural rearrangements in genetically engineered mouse mammary tumors.Genome Biol2010
20981101The patterns and dynamics of genomic instability in metastatic pancreatic cancer.Nature2010
19948536Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.J Med Genet2010
20054297Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes.Nature2010
20016488A small-cell lung cancer genome with complex signatures of tobacco exposure.Nature2010
19330029Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.Nat Genet2009
20033038Complex landscapes of somatic rearrangement in human breast cancer genomes.Nature2009
18438408Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.Nat Genet2008
14681395HOMSTRAD: recent developments of the Homologous Protein Structure Alignment Database.Nucleic Acids Res2004
11960713Gap junctions in Drosophila: developmental expression of the entire innexin gene family.Mech Dev2002
10888681Two Drosophila innexins are expressed in overlapping domains and cooperate to form gap-junction channels.Mol Biol Cell2000
10079511Gap-Junctional communication between developing Drosophila muscles is essential for their normal development.Dev Genet1999
9769729Innexins: a family of invertebrate gap-junction proteins.Trends Genet1998
9799434A testis-specifically expressed gene is embedded within a cluster of maternally expressed genes at 89B in Drosophila melanogaster.Dev Genes Evol1998
9428764Drosophila Shaking-B protein forms gap junctions in paired Xenopus oocytes.Nature1998
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Collaborators

Wellcome Sanger Institute
Co-authored papers 23
Wellcome Sanger Institute
Co-authored papers 22
The University of Texas MD Anderson Cancer Center
Co-authored papers 19
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Co-authored papers 18
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Co-authored papers 17
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Co-authored papers 17
Wellcome Trust Sanger Institute
Co-authored papers 15
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Co-authored papers 13
Wellcome Sanger Institute
Co-authored papers 13
University of East Anglia
Co-authored papers 12
Early Cancer Institute, University of Cambridge
Co-authored papers 11
Wellcome Trust Sanger Institute
Co-authored papers 11
The Francis Crick Institute
Co-authored papers 10
Moores Cancer Center, university of california san diego
Co-authored papers 9
Manchester Cancer Research Centre, University of Manchester
Co-authored papers 9
Clinical Research Facility, Mercy University Hospital
Co-authored papers 8
Wellcome Trust Sanger Institute
Co-authored papers 8
Wellcome Sanger Institute
Co-authored papers 7
Institute of Cancer Sciences, University of Glasgow
Co-authored papers 7
Inivata Ltd
Co-authored papers 7
Co-authored papers 6
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Wellcome Sanger Institute
Co-authored papers 5
Memorial Sloan Kettering Cancer Center
Co-authored papers 5
Murdoch Children's Research Institute, Royal Children's Hospital
Co-authored papers 5
Wellcome Sanger Institute
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Wellcome Sanger Institute
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University of St Andrews
Co-authored papers 4