P. Futreal

发表

T. Hubbard, M. Stratton, N. Rahman, 2004, Nature Reviews Cancer.

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

Antony V. Cox, R. Durbin, M. Hurles, 2008, Nature Genetics.

The landscape of cancer genes and mutational processes in breast cancer

A. Børresen-Dale, M. Stratton, M. J. van de Vijver, 2012, Nature.

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

Juliane C. Dohm, A. Valencia, R. Guigó, 2011, Nature.

Signatures of mutational processes in human cancer

David T. W. Jones, David C. Jones, M. Meyerson, 2013, Nature.

Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

Gurpreet W. Tang, Karl J. Dykema, M. Stratton, 2009, Nature.

Systematic identification of genomic markers of drug sensitivity in cancer cells

S. Ramaswamy, M. Stratton, P. Futreal, 2012, Nature.

Abstract 2206: Genomics of Drug Sensitivity in Cancer (GDSC): A resource for therapeutic biomarker discovery in cancer cells.

M. Stratton, P. Futreal, U. McDermott, 2013 .

The cancer genome

M. Stratton, P. Futreal, P. Campbell, 2009, Nature.

High-resolution analysis of DNA copy number using oligonucleotide microarrays.

M. Shapero, Jing Huang, K. W. Jones, 2004, Genome research.

Signatures of mutation and selection in the cancer genome

P. Deloukas, Fengtang Yang, S. Swamy, 2010, Nature.

The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

M. Stratton, P. Futreal, R. Wooster, 2004, British Journal of Cancer.

Mutational Processes Molding the Genomes of 21 Breast Cancers

A. Børresen-Dale, M. Stratton, P. Futreal, 2012, Cell.

Landscape of somatic mutations in 560 breast cancer whole genome sequences

David C. Jones, E. Birney, M. Ringnér, 2016, Nature.

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation.

J. Gécz, M. Stratton, P. Futreal, 2004, American journal of human genetics.

Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development

N. Carter, Fengtang Yang, M. Stratton, 2011, Cell.

Cancer and genomics

E. Birney, J. Mullikin, M. Stratton, 2001, Nature.

Patterns of somatic mutation in human cancer genomes

E. Birney, A. Nicholson, M. Stratton, 2007, Nature.

Recurrent KRAS codon 146 mutations in human colorectal cancer

Sarah Edkins, Simon Forbes, Helen Davies, 2006, Cancer biology & therapy.

The patterns and dynamics of genomic instability in metastatic pancreatic cancer

Andrew Menzies, Adam P. Butler, Jon W. Teague, 2010, Nature.

Mutations of the BRAF gene in human cancer

A. Nicholson, M. Stratton, P. Futreal, 2002, Nature.

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Andrew Menzies, Sarah Edkins, Sara Widaa, 2009, Nature Genetics.

COMPLEX LANDSCAPES OF SOMATIC REARRANGEMENT IN HUMAN BREAST CANCER GENOMES

A. Børresen-Dale, M. Stratton, H. Swerdlow, 2009, Nature.

International network of cancer genome projects

Gary D Bader, Benjamin J. Raphael, Joshua M. Stuart, 2010, Nature.

The Life History of 21 Breast Cancers

A. Børresen-Dale, M. Stratton, P. Futreal, 2012, Cell.

A comprehensive catalogue of somatic mutations from a human cancer genome

Tom Royce, D. Bentley, L. Chin, 2010, Nature.

Pan-cancer analysis of whole genomes

Steven J. M. Jones, Nuno A. Fonseca, Icgc, 2020, Nature.

Statistical Analysis of Pathogenicity of Somatic Mutations in Cancer

M. Stratton, P. Futreal, R. Wooster, 2006, Genetics.

A small cell lung cancer genome reports complex tobacco exposure signatures

E. Birney, K. McKernan, M. Stratton, 2009, Nature.

The topography of mutational processes in breast cancer genomes

E. Birney, A. Børresen-Dale, M. Stratton, 2016, Nature Communications.

JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis.

M. Stratton, P. Futreal, H. Lodish, 2007, The New England journal of medicine.

Estimation of rearrangement phylogeny for cancer genomes.

N. Carter, Fengtang Yang, M. Stratton, 2012, Genome research.

COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer

Gurpreet W. Tang, C. Cole, M. Stratton, 2009, Nucleic acids research.

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

Andrew D. Yates, Yvonne R Stephens, A. Nicholson, 2005, Nature Genetics.

Athletics: Momentous sprint at the 2156 Olympics?

Andrew D. Yates, Yvonne R Stephens, A. Nicholson, 2004, Nature.

Somatic mutations of the protein kinase gene family in human lung cancer.

Andrew D. Yates, Yvonne R Stephens, A. Nicholson, 2005, Cancer research.

COSMIC 2005

M. Stratton, P. Futreal, R. Wooster, 2006, British Journal of Cancer.

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

M. Stratton, P. Futreal, R. Wooster, 2006, Nature Genetics.

Heterogeneity of genomic evolution and mutational profiles in multiple myeloma

G. Parmigiani, P. Futreal, P. Campbell, 2014, Nature Communications.

1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis.

Shaying Zhao, Adam A. Margolin, Joel Greshock, 2003, Genome research.

The Life History of 21 Breast Cancers

Kenric Leung, Andrew Menzies, Adam P. Butler, 2015, Cell.

Mutational signatures of ionizing radiation in second malignancies

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

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

N. Rahman, P. Futreal, F. Muntoni, 2003, American journal of human genetics.

A survey of RNA editing in human brain.

Richard Wooster, Matthew Blow, Michael R Stratton, 2004, Genome research.

Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer

Carolyn Tregidgo, Albert J. Vilella, Peter J. Campbell, 2012, Cell.

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

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

Genetic screens using the piggyBac transposon

P. Futreal, A. Bradley, R. Rad, 2011, Methods.

Replacement of unfractionated heparin by low-molecular-weight heparin for postorthopedic surgery antithrombotic prophylaxis lowers the overall risk of symptomatic thrombosis because of a lower frequency of heparin-induced thrombocytopenia

P. Futreal, R. Wooster, P. Campbell, 2005 .

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

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

The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders.

M. Stratton, P. Futreal, R. Wooster, 2005, Blood.

M. Stratton, P. Futreal, R. Wooster, 2002, Cancer research.

DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome

A. Nicholson, M. Stratton, N. Rahman, 2011, Journal of Medical Genetics.

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

Keith W. Jones, Richard Wooster, Michael R Stratton, 2004, Human Genomics.

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.

Andrew Menzies, Keiran Raine, Sarah Edkins, 2007, American journal of human genetics.

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.

Andrew Menzies, Keiran Raine, Sarah Edkins, 2007, American journal of human genetics.

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution.

Andrew Menzies, Sarah Edkins, Richard Wooster, 2007, Genome research.

Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation

J. Gécz, M. Stratton, P. Futreal, 2010, European Journal of Human Genetics.

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.

Tracy T Batchelor, Richard Lugg, Andrew Menzies, 2006, Cancer research.

Patterns of somatic mutation in human cancer genomes

E. Birney, A. Nicholson, M. Stratton, 2007, Nature.

NIHMS662581-supplement-Supplementary data

Pardeep Kumar, Elizabeth Anderson, Jon W. Teague, 2016 .

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

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

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.

N. Rahman, P. Futreal, N. Norton, 2001, American journal of human genetics.

The Genomic Landscape of TEL-AML1+ (ETV6-RUNX1) Acute Lymphoblastic Leukaemia

M. Stratton, P. Futreal, P. Campbell, 2011 .

The BRAF gene is frequently mutated in malignant melanoma.

M. Stratton, P. Futreal, R. Wooster, 2004, Journal of drugs in dermatology : JDD.

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Peter Marynen, Rodney Scott, Patrick S Tarpey, 2008, American journal of human genetics.

Structural variants drive context-dependent oncogene activation in cancer

Jesse R. Dixon, P. Futreal, Graham P. McVicker, 2022, Nature.

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

Andrew Menzies, Sarah Edkins, Sara Widaa, 2008, Nature Genetics.

Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation

Stratton, J. Gécz, P. Futreal, 2007 .

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

M. Stratton, P. Futreal, S. Edkins, 2007, Journal of Medical Genetics.

Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells

Sridhar Ramaswamy, Howard Lightfoot, Nidhi Bindal, 2012, Nucleic Acids Res..

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

Mingming Jia, Nidhi Bindal, Rebecca Shepherd, 2010, Nucleic Acids Res..

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

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

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.

RNA editing of human microRNAs

Anton J. Enright, Richard Wooster, Michael R Stratton, 2006, Genome Biology.

Processed pseudogenes acquired somatically during cancer development

Andrew Menzies, Adam P. Butler, Jon W. Teague, 2014, Nature Communications.

A survey of homozygous deletions in human cancer genomes.

E. Birney, M. Stratton, P. Futreal, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

M. Stratton, P. Futreal, P. Campbell, 2013, Nature Genetics.

Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma

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

Sequence analysis of the protein kinase gene family in human testicular germ‐cell tumors of adolescents and adults

Richard Lugg, Andrew Menzies, Keiran Raine, 2006, Genes, chromosomes & cancer.

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

Andrew M. Jenkinson, C. Greenman, Rebecca Shepherd, 2007, Bioinform..

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

J. Gécz, M. Stratton, P. Futreal, 2007, Nature Genetics.

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.

J. Gécz, M. Stratton, P. Futreal, 2008, American journal of human genetics.

Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes

Andrew Menzies, Adam P. Butler, Jon W. Teague, 2014, Science.

Novel consensus DNA‐binding sequence for BRCA1 protein complexes

P. Futreal, D. Livingston, Leping Li, 2003, Molecular carcinogenesis.

Single-cell paired-end genome sequencing reveals structural variation per cell cycle

M. Stratton, P. Futreal, P. Campbell, 2013, Nucleic acids research.

Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes

M. Stratton, P. Futreal, P. Campbell, 2012, The Journal of pathology.

Recurrent PTPRB and PLCG1 mutations in angiosarcoma

M. Stratton, A. Protopopov, P. Futreal, 2014, Nature Genetics.

Breast cancer genome and transcriptome integration implicates specific mutational signatures with immune cell infiltration

E. Birney, M. Ringnér, A. Børresen-Dale, 2016, Nature Communications.

Tubio retrotransposition in cancer genomes Extensive transduction of nonrepetitive DNA mediated by L 1

M. Stratton, P. Futreal, P. Campbell, 2014 .

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set

Richard Lugg, Andrew Menzies, Michael R. Stratton, 2006, Molecular Cancer Therapeutics.

The Catalogue of Somatic Mutations in Cancer (COSMIC)

S A Forbes, G Bhamra, S Bamford, 2008, Current protocols in human genetics.

Polygenic in vivo validation of cancer mutations using transposons

Lia S. Campos, L. Chin, P. Futreal, 2014, Genome Biology.

Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Nuno A. Fonseca, Gary D Bader, Benjamin J. Raphael, 2020, Nature Communications.

BRCA2 mutations in primary breast and ovarian cancers

Sheila Seal, Richard Wooster, Alan Ashworth, 1996, Nature Genetics.

Genomic alterations link Rho family of GTPases to the highly invasive phenotype of pancreas cancer

Gerald C. Chu, L. Chin, W. Hahn, 2008, Proceedings of the National Academy of Sciences.

A Small Cell Lung Cancer Genome Reports Complex Tobacco Exposure Signatures Europe Pmc Funders Group

Minna, E. Birney, K. McKernan, 2022 .

Data mining using the Catalogue of Somatic Mutations in Cancer BioMart

Mingming Jia, Nidhi Bindal, Rebecca Shepherd, 2011, Database J. Biol. Databases Curation.

COSMIC, curating the cancer variome

Simon A. Forbes, Jon W. Teague, Michael R. Stratton, 2008, AIMM.

The continuing search for cancer-causing somatic mutations

P. Futreal, G. Dalgliesh, 2007, Breast Cancer Research.

Somatic mutations in human cancer: insights from resequencing the protein kinase gene family.

M. Stratton, P. Futreal, R. Wooster, 2005, Cold Spring Harbor symposia on quantitative biology.

Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability.

M. Shaw, J. Gécz, M. Stratton, 2010, American journal of human genetics.

Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

E. Birney, M. Ringnér, A. Børresen-Dale, 2019, Nature.

Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

M. Shaw, J. Gécz, M. Stratton, 2010, Nature Genetics.

COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer

Mingming Jia, Nidhi Bindal, Simon A. Forbes, 2009, Nucleic Acids Res..

Amplification and Overexpression of Hsa-miR-30b, Hsa-miR-30d and KHDRBS3 at 8q24.22-q24.23 in Medulloblastoma

P. Andrew Futreal, David W. Ellison, Graham R. Bignell, 2009, PloS one.

Predictive biomarker discovery through the parallel integration of clinical trial and functional genomics datasets

Z. Szallasi, P. Futreal, A. Eklund, 2010, Genome Medicine.

GLO1—A novel amplified gene in human cancer

M. Stratton, P. Futreal, T. Santarius, 2010, Genes, chromosomes & cancer.

Whole exome sequencing of adenoid cystic carcinoma.

M. Stratton, P. Futreal, P. Campbell, 2013, The Journal of clinical investigation.

Use of cancer‐specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors

M. Stratton, P. Futreal, P. Campbell, 2010, Genes, chromosomes & cancer.

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.

M. Stratton, P. Futreal, R. Wooster, 2006, Genomics.

Somatic structural rearrangements in genetically engineered mouse mammary tumors

M. Stratton, P. Futreal, P. Campbell, 2010, Genome Biology.

Breast cancer genome heterogeneity: a challenge to personalised medicine?

Charles Swanton, P. Futreal, C. Swanton, 2011, Breast Cancer Research.

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.

K. Friend, M. Shaw, J. Gécz, 2007, American journal of human genetics.

The driver landscape of sporadic chordoma

Matthew D. Young, M. Stratton, T. Nielsen, 2017, Nature Communications.

604 Cancer Genomics, Epigenetics and Genomic Instability. Mutational Processes Shaping the Genomes of Twenty-one Breast Cancers

M. Stratton, P. Futreal, P. Campbell, 2012 .

Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.

J. Gécz, M. Stratton, P. Futreal, 2008, American journal of human genetics.

Poon Application as a Screening Tool Genome-Wide Mutational Signatures of Aristolochic Acid and Its

M. Stratton, P. Futreal, W. Sung, 2013 .

The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

N. Rahman, P. Futreal, S. Edkins, 2002, American journal of human genetics.

Corrigendum: Signatures of mutational processes in human cancer

Roland Eils, Natalie Jäger, Adam P. Butler, 2013, Nature.

Author Correction: Pan-cancer analysis of whole genomes

Nuno A. Fonseca, Gary D Bader, Benjamin J. Raphael, 2023, Nature.

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.

J. Gécz, M. Stratton, P. Futreal, 2006, American journal of human genetics.

Sex differences in oncogenic mutational processes

Nuno A. Fonseca, Gary D Bader, Benjamin J. Raphael, 2019, Nature Communications.

Whole-genome sequencing identifies recurrent mutations in chronic lymphocyticleukaemia

A. Valencia, R. Guigó, X. Estivill, 2011 .

Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12.

N. Rahman, P. Futreal, C. Gumbs, 2001, Kidney international.

The driver landscape of sporadic chordoma

Matthew D. Young, M. Stratton, T. Nielsen, 2017, Nature Communications.

Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13.

N. Rahman, P. Futreal, G. Bignell, 2003, American journal of human genetics.

Supplementary file 1.

Jack A. Taylor, M. Stratton, D. Hayes, 2011 .

Stella-Cre Mice are Highly Efficient Cre Deleters

P. Futreal, A. Bradley, G. Vassiliou, 2011, Genesis.

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

P. A. Futreal, Karl J. Dykema, M. Stratton, 2010, Nature.

The topography of mutational processes in breast cancer genomes

E. Birney, A. Børresen-Dale, M. J. van de Vijver, 2016, Nature Communications.

Supplementary file 3.

Jack A. Taylor, M. Stratton, D. Hayes, 2014 .

Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers

L. Chin, M. Stratton, A. Protopopov, 2007, Nature.

The Catalogue of Somatic Mutations in Cancer

Gurpreet W. Tang, C. Cole, P. Futreal, 2009 .

Supplementary file 2.

Jack A. Taylor, D. Hayes, P. Futreal, 2014 .

Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations

Roland Eils, Rainer König, Rosario M. Piro, 2013, Acta Neuropathologica.

Supplementary file 1.

Jack A. Taylor, D. Hayes, P. Futreal, 2014 .

COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer

Gurpreet W. Tang, C. Cole, P. Futreal, 2010, Nucleic Acids Res..

Corrigendum: Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

M. Stratton, P. Futreal, P. Campbell, 2014, Nature Genetics.

Keratin 19: a key role player in the invasion of human hepatocellular carcinomas

Jack A. Taylor, D. Hayes, P. Futreal, 2013, Gut.

Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility.

Nazneen Rahman, Carel Meijers, Sheila Seal, 2003, American journal of human genetics.

A Multicenter Study of Cancer Incidence in CHEK2 1100delC Mutation Carriers

S. Seal, M. Stratton, N. Rahman, 2006, Cancer Epidemiology Biomarkers & Prevention.

Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

M. Stratton, P. Futreal, R. Wooster, 2011, Nature Genetics.

Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

E. Birney, M. Ringnér, A. Børresen-Dale, 2019, Nature.

Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.

P. A. Futreal, N. Nowak, P. Futreal, 1997, Genomics.

Cancer: Understanding the target

P. Futreal, M. Stratton, 2004, Nature.

Backseat Drivers Take the Wheel

P. Futreal, 2007, Cancer cell.

Supplementary file 1.

Jack A. Taylor, D. Hayes, P. Futreal, 2011 .

Mutations of the BRAF gene in human cancer

A. Nicholson, P. Futreal, R. Wooster, 2002, Nature.

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

S. Scherer, D. Merico, P. Nathan, 2015, Nature Genetics.

The landscape of cancer genes and mutational processes in breast cancer

A. Børresen-Dale, M. Stratton, M. J. van de Vijver, 2012, Nature.

Heterogeneity of genomic evolution and mutational profiles in multiple myeloma

G. Parmigiani, P. Futreal, J. Teague, 2014, Nature Communications.

Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability.

M. Shaw, J. Gécz, M. Stratton, 2010, American journal of human genetics.

Supplementary File 4

Jack A. Taylor, D. Hayes, P. Futreal, 2014 .

Ehlers-Danlos Syndrome with Severe Early-Onset Periodontal Disease ( EDS-VIII ) Is a Distinct , Heterogeneous Disorder with One Predisposition Gene at Chromosome 12 p 13

N. Rahman, P. Futreal, G. Bignell, 2007 .

Somatic mutation distributions in cancer genomes vary with three-dimensional chromatin structure

Jesse R. Dixon, R. Verhaak, P. Futreal, 2020, Nature genetics.

Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes

A. Børresen-Dale, M. Stratton, M. J. van de Vijver, 2014, Science.

Use of cancer‐specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors

M. Stratton, P. Futreal, P. Campbell, 2010, Genes, chromosomes & cancer.

Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

E. Birney, M. Ringnér, A. Børresen-Dale, 2019, Nature.

Supplementary File 4

Jack A. Taylor, D. Hayes, P. Futreal, 2014 .

Patterns of structural variants within TP53 introns and relocation of the TP53 promoter: a commentary†

Hannah C. Beird, P. Futreal, Alexander J Lazar, 2024, The Journal of pathology.

Identification of Novel Somatic Mutations in SF3B1, a Gene Encoding a Core Component of RNA Splicing Machinery, in Myelodysplasia with Ring Sideroblasts and Other Common Cancers

M. Stratton, P. Futreal, P. Campbell, 2011 .