about
A landscape of driver mutations in melanomaMutational heterogeneity in cancer and the search for new cancer-associated genesIntegrative analysis of the melanoma transcriptomeMelanoma genome sequencing reveals frequent PREX2 mutationsExome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancerThe genomic complexity of primary human prostate cancerInitial genome sequencing and analysis of multiple myelomaSomatic mutations affect key pathways in lung adenocarcinomaCharacterizing the cancer genome in lung adenocarcinoma.Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancer.Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesMapping the hallmarks of lung adenocarcinoma with massively parallel sequencingGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityThe landscape of somatic copy-number alteration across human cancers.Major copy proportion analysis of tumor samples using SNP arrays.A flexible rank-based framework for detecting copy number aberrations from array data.Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma.Toward performance-diverse small-molecule libraries for cell-based phenotypic screening using multiplexed high-dimensional profiling.Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy.RNA-SeQC: RNA-seq metrics for quality control and process optimizationAbsolute quantification of somatic DNA alterations in human cancerThe metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people.Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.Drug-sensitive FGFR2 mutations in endometrial carcinomaPunctuated evolution of prostate cancer genomes.Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions.Genome-wide functional synergy between amplified and mutated genes in human breast cancer.Modeling genomic diversity and tumor dependency in malignant melanoma.
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description
onderzoeker
@nl
name
Wendy Winckler
@en
Wendy Winckler
@es
Wendy Winckler
@sl
type
label
Wendy Winckler
@en
Wendy Winckler
@es
Wendy Winckler
@sl
prefLabel
Wendy Winckler
@en
Wendy Winckler
@es
Wendy Winckler
@sl
P106
P21
P31
P6634
wendy-winckler-5876608