Related references
Note: Only part of the references are listed.The Pfam protein families database: towards a more sustainable future
Robert D. Finn et al.
NUCLEIC ACIDS RESEARCH (2016)
MEGSA: A Powerful and Flexible Framework for Analyzing Mutual Exclusivity of Tumor Mutations
Xing Hua et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Oncotator: Cancer Variant Annotation Tool
Alex H. Ramos et al.
HUMAN MUTATION (2015)
Recurrent somatic mutations in regulatory regions of human cancer genomes
Collin Melton et al.
NATURE GENETICS (2015)
Loss of AT-Rich Interactive Doman 1A Expression in Gastrointestinal Malignancies
Soo Young Lee et al.
ONCOLOGY (2015)
Comprehensive assessment of cancer missense mutation clustering in protein structures
Atanas Kamburov et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Systematic analysis of somatic mutations impacting gene expression in 12 tumour types
Jiarui Ding et al.
NATURE COMMUNICATIONS (2015)
Loss of ARID1A expression in colorectal carcinoma is strongly associated with mismatch repair deficiency
Angela Chou et al.
HUMAN PATHOLOGY (2014)
Asp120Asn mutation impairs the catalytic activity of NDM-1 metallo-β-lactamase: experimental and computational study
Jiao Chen et al.
PHYSICAL CHEMISTRY CHEMICAL PHYSICS (2014)
A comparative survey of functional footprints of EGFR pathway mutations in human cancers
A. Lane et al.
ONCOGENE (2014)
The Nrf2 regulatory network provides an interface between redox and intermediary metabolism
John D. Hayes et al.
TRENDS IN BIOCHEMICAL SCIENCES (2014)
A pan-cancer proteomic perspective on The Cancer Genome Atlas
Rehan Akbani et al.
NATURE COMMUNICATIONS (2014)
DawnRank: discovering personalized driver genes in cancer
Jack P. Hou et al.
GENOME MEDICINE (2014)
Identifying driver mutations in sequenced cancer genomes: computational approaches to enable precision medicine
Benjamin J. Raphael et al.
GENOME MEDICINE (2014)
OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes
David Tamborero et al.
BIOINFORMATICS (2013)
Discovering causal pathways linking genomic events to transcriptional states using Tied Diffusion Through Interacting Events (TieDIE)
Evan O. Paull et al.
BIOINFORMATICS (2013)
Integrative eQTL-Based Analyses Reveal the Biology of Breast Cancer Risk Loci
Qiyuan Li et al.
CELL (2013)
The emerging role of the Nrf2-Keap1 signaling pathway in cancer
Melba C. Jaramillo et al.
GENES & DEVELOPMENT (2013)
Copy neutral loss of heterozygosity is more frequent in older ovarian cancer patients
Brent S. Pedersen et al.
GENES CHROMOSOMES & CANCER (2013)
Detection of FLT3 Internal Tandem Duplication in Targeted, Short-Read-Length, Next-Generation Sequencing Data
David H. Spencer et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2013)
Systematic analysis of somatic mutations in phosphorylation signaling predicts novel cancer drivers
Jueri Reimand et al.
MOLECULAR SYSTEMS BIOLOGY (2013)
Mutational heterogeneity in cancer and the search for new cancer-associated genes
Michael S. Lawrence et al.
NATURE (2013)
Mutational landscape and significance across 12 major cancer types
Cyriac Kandoth et al.
NATURE (2013)
Pan-cancer patterns of somatic copy number alteration
Travis I. Zack et al.
NATURE GENETICS (2013)
Computational approaches to identify functional genetic variants in cancer genomes
Abel Gonzalez-Perez et al.
NATURE METHODS (2013)
TCPA: a resource for cancer functional proteomics data
Jun Li et al.
NATURE METHODS (2013)
Emerging patterns of somatic mutations in cancer
Ian R. Watson et al.
NATURE REVIEWS GENETICS (2013)
Loss of heterozygosity preferentially occurs in early replicating regions in cancer genomes
Brent S. Pedersen et al.
NUCLEIC ACIDS RESEARCH (2013)
Nrf2 Pathway Regulates Multidrug-Resistance-Associated Protein 1 in Small Cell Lung Cancer
Lili Ji et al.
PLOS ONE (2013)
Identification of Mutations in Distinct Regions of p85 Alpha in Urothelial Cancer
Rebecca L. Ross et al.
PLOS ONE (2013)
Exploring TCGA Pan-Cancer Data at the UCSC Cancer Genomics Browser
Melissa S. Cline et al.
SCIENTIFIC REPORTS (2013)
Interpretation of Genomic Variants Using a Unified Biological Network Approach
Ekta Khurana et al.
PLOS COMPUTATIONAL BIOLOGY (2013)
PARADIGM-SHIFT predicts the function of mutations in multiple cancers using pathway impact analysis
Sam Ng et al.
BIOINFORMATICS (2012)
Comprehensive molecular characterization of human colon and rectal cancer
Donna M. Muzny et al.
NATURE (2012)
Integrative Subtype Discovery in Glioblastoma Using iCluster
Ronglai Shen et al.
PLOS ONE (2012)
Cancer syndromes and therapy by stop-codon readthrough
Renata Bordeira-Carrico et al.
TRENDS IN MOLECULAR MEDICINE (2012)
DriverNet: uncovering the impact of somatic driver mutations on transcriptional networks in cancer
Ali Bashashati et al.
GENOME BIOLOGY (2012)
Hallmarks of Cancer: The Next Generation
Douglas Hanahan et al.
CELL (2011)
Predicting the functional impact of protein mutations: application to cancer genomics
Boris Reva et al.
NUCLEIC ACIDS RESEARCH (2011)
GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers
Craig H. Mermel et al.
GENOME BIOLOGY (2011)
The Control of the Metabolic Switch in Cancers by Oncogenes and Tumor Suppressor Genes
Arnold J. Levine et al.
SCIENCE (2010)
Dysfunctional KEAP1-NRF2 interaction in non-small-cell lung cancer
Anju Singh et al.
PLOS MEDICINE (2006)
Oncogenic transformation by inhibitor-sensitive and -resistant EGFR mutants
H Greulich et al.
PLOS MEDICINE (2005)
A strategy for disease gene identification through nonsense-mediated mRNA decay inhibition
EN Noensie et al.
NATURE BIOTECHNOLOGY (2001)
Share Paper
