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Author Details
Full Name
Chris Greenman
Affiliation
University of East Anglia
ORCID
Career Start Year
2004
Papers
48
H Index
33
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
32450075
The complexity of genome rearrangement combinatorics under the infinite sites model.
J Theor Biol
2020
35221385
PDE MODELS OF ADDER MECHANISMS IN CELLULAR PROLIFERATION.
SIAM J Appl Math
2020
29662167
Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.
Nat Genet
2018
28282036
Heterarchy of transcription factors driving basal and luminal cell phenotypes in human urothelium.
Cell Death Differ
2017
25833184
Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process.
J Math Biol
2016
27335505
A Hierarchical Kinetic Theory of Birth, Death and Fission in Age-Structured Interacting Populations.
J Stat Phys
2016
26845763
Computational Cancer Biology: An Evolutionary Perspective.
PLoS Comput Biol
2016
26871029
Kinetic theory of age-structured stochastic birth-death processes.
Phys Rev E
2016
25728652
Exon Skipping Is Correlated with Exon Circularization.
J Mol Biol
2015
26571026
Inferring the Clonal Structure of Viral Populations from Time Series Sequencing.
PLoS Comput Biol
2015
26198836
Cardio-oncology: an ongoing evolution.
Future Oncol
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
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
25079870
Exact, time-independent estimation of clone size distributions in normal and mutated cells.
J R Soc Interface
2014
23762276
The relative timing of mutations in a breast cancer genome.
PLoS One
2013
21994251
Estimation of rearrangement phylogeny for cancer genomes.
Genome Res
2012
22767920
Cancer. Haploinsufficient gene selection in cancer.
Science
2012
22722201
The landscape of cancer genes and mutational processes in breast cancer.
Nature
2012
22460902
Systematic identification of genomic markers of drug sensitivity in cancer cells.
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
21215367
Massive genomic rearrangement acquired in a single catastrophic event during cancer development.
Cell
2011
21695067
Model-integrated estimation of normal tissue contamination for cancer SNP allelic copy number data.
Cancer Inform
2011
21441214
Germline fitness-based scoring of cancer mutations.
Genetics
2011
21248752
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.
Nature
2011
19837654
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data.
Biostatistics
2010
20544845
GLO1-A novel amplified gene in human cancer.
Genes Chromosomes Cancer
2010
20164919
Signatures of mutation and selection in the cancer genome.
Nature
2010
20054297
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes.
Nature
2010
20016488
A small-cell lung cancer genome with complex signatures of tobacco exposure.
Nature
2010
20016485
A comprehensive catalogue of somatic mutations from a human cancer genome.
Nature
2010
19165201
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition.
Br J Cancer
2009
20033038
Complex landscapes of somatic rearrangement in human breast cancer genomes.
Nature
2009
19330029
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
Nat Genet
2009
19377476
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
Nat Genet
2009
17485433
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.
Bioinformatics
2007
17675364
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution.
Genome Res
2007
17344846
Patterns of somatic mutation in human cancer genomes.
Nature
2007
16175573
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults.
Genes Chromosomes Cancer
2006
16783027
Statistical analysis of pathogenicity of somatic mutations in cancer.
Genetics
2006
16969076
Recurrent KRAS codon 146 mutations in human colorectal cancer.
Cancer Biol Ther
2006
16406726
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.
Genomics
2006
16618716
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.
Cancer Res
2006
15761058
A survey of homozygous deletions in human cancer genomes.
Proc Natl Acad Sci U S A
2005
16140923
Somatic mutations of the protein kinase gene family in human lung cancer.
Cancer Res
2005
15908952
A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer.
Nat Genet
2005
15457249
Lung cancer: intragenic ERBB2 kinase mutations in tumours.
Nature
2004
1 - 48 of 48
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