Peter J Campbell

发表

cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data

David Jones, Keiran M Raine, Helen Davies, 2016, Current protocols in bioinformatics.

Precision oncology for acute myeloid leukemia using a knowledge bank approach

Inigo Martincorena, Verena I Gaidzik, Peter J Campbell, 2017, Nature Genetics.

Bone marrow pathology in essential thrombocythemia: interobserver reliability and utility for identifying disease subtypes.

Peter J Campbell, Wendy N Erber, Keith Wheatley, 2008, Blood.

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

Peter J Campbell, Michael R Stratton, Luca Malcovati, 2011, Blood.

Prediction of acute myeloid leukaemia risk in healthy individuals

Paolo Vineis, Zhen Zhao, Amos Tanay, 2018, Nature.

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

Roberta Spinelli, Rocco Piazza, Torsten Haferlach, 2012, Nature Genetics.

cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing

Keiran M Raine, Helen Davies, Adam P Butler, 2015, Current protocols in bioinformatics.

Somatic mutations of the histone H3K27 demethylase, UTX, in human cancer

Bin Tean Teh, Chai Yin Kok, Andrew Menzies, 2009, Nature Genetics.

Mutational signatures of ionizing radiation in second malignancies

Christophe Badie, Rebecca Shepherd, David Jones, 2016, Nature Communications.

Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer

Adam P Butler, Serena Nik-Zainal, Peter J Campbell, 2014, Nature Genetics.

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Roland Arnold, Richard G Grundy, Daniele Merico, 2015, Nature Genetics.

Mutational signatures are jointly shaped by DNA damage and repair

Iñigo Martincorena, Peter J Campbell, Federico Abascal, 2019, bioRxiv.

Subclonal diversification of primary breast cancer revealed by multiregion sequencing

Andrew Menzies, Keiran Raine, Young Seok Ju, 2015, Nature Medicine.

Corrigendum: Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.

Carlos Caldas, Fengtang Yang, Rosalind Eeles, 2016, Genome research.

DNMT3A mutations occur early or late in patients with myeloproliferative neoplasms and mutation order influences phenotype

Peter J Campbell, David C Wedge, Anthony R Green, 2015, Haematologica.

Somatic mutations and clonal dynamics in healthy and cirrhotic human liver

Inigo Martincorena, Peter J Campbell, Michael R Stratton, 2019, Nature.

Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma

Daniel Baumhoer, Inigo Martincorena, Roberto Tirabosco, 2017, Nature Communications.

ABSOLUTE cancer genomics

Peter Van Loo, Peter J Campbell, P. Campbell, 2012, Nature Biotechnology.

Effect of mutation order on myeloproliferative neoplasms.

Paola Guglielmelli, George S Vassiliou, Beatriz Bellosillo, 2015, The New England journal of medicine.

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer

Bin Tean Teh, Andrew Menzies, Keiran Raine, 2014, eLife.

Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

Carlos Caldas, Fengtang Yang, Rosalind Eeles, 2015, Genome research.

Primary myelofibrosis (PMF), post polycythemia vera myelofibrosis (post-PV MF), post essential thrombocythemia myelofibrosis (post-ET MF), blast phase PMF (PMF-BP): Consensus on terminology by the international working group for myelofibrosis research and treatment (IWG-MRT).

Francisco Cervantes, Giovanni Barosi, Juergen Thiele, 2007, Leukemia research.

Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma

David Beare, Andrew Menzies, Keiran Raine, 2013, Nature Genetics.