Adam Shlien

发表

Combining exome and gene expression datasets in one graphical model of disease to empower the discovery of disease mechanisms pdf

Anna Goldenberg, Aziz M. Mezlini, Fabio Fuligni, 2015, ArXiv.

Processed pseudogenes acquired somatically during cancer development

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

The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models

Yves Moreau, Jeroen de Ridder, Keiran Raine, 2013, Genome Biology.

Principles Governing A-to-I RNA Editing in the Breast Cancer Transcriptome

David Gacquer, Peter J. Campbell, Christine Desmedt, 2015, bioRxiv.

Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes.

Gary D Bader, Adam Shlien, T. Paton, 2015, F1000Research.

The Life History of 21 Breast Cancers

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

Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden

Levi Garraway, Uri Tabori, James X. Sun, 2017, Genome Medicine.

Recurrent focal copy-number changes and loss of heterozygosity implicate two noncoding RNAs and one tumor suppressor gene at chromosome 3q13.31 in osteosarcoma.

David Malkin, Ana Novokmet, Adam Shlien, 2010, Cancer research.

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.

A proteomic chronology of gene expression through the cell cycle in human myeloid leukemia cells

Michael J. Emanuele, Michael R Stratton, Angus I Lamond, 2014, eLife.

Erratum: The Life History of 21 Breast Cancers (Cell 149 (994-1007))

Kenric Leung, Jon W. Teague, Peter J. Campbell, 2015 .

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

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

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

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

Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotyping.

Jinchuan Xing, Adam Shlien, L. Jorde, 2010, Genomics.

Excessive genomic DNA copy number variation in the Li–Fraumeni cancer predisposition syndrome

Uri Tabori, Christian R Marshall, Lars Feuk, 2008, Proceedings of the National Academy of Sciences.

Molecular Characterization of Choroid Plexus Tumors Reveals Novel Clinically Relevant Subgroups

Nada Jabado, Uri Tabori, Sanaa Choufani, 2014, Clinical Cancer Research.

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

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