P Andrew Futreal

发表

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.

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.

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

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

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

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

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

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

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.

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.

Mutational signatures of ionizing radiation in second malignancies

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

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

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

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

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

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

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

Recurrent KRAS codon 146 mutations in human colorectal cancer

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

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

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

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.

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

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

RNA editing of human microRNAs

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

A survey of RNA editing in human brain.

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

Breast cancer genome heterogeneity: a challenge to personalised medicine?

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

Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma

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