Lista de obras - Wendy Winckler - Dominio Público Uruguay

A flexible rank-based framework for detecting copy number aberrations from array data

artículo científico publicado en 2009

A landscape of driver mutations in melanoma

artículo científico publicado en 2012

Absolute quantification of somatic DNA alterations in human cancer

artículo científico publicado en 2012

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

scientific article published on 01 August 2005

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

artículo científico publicado en 2005

Characterizing the cancer genome in lung adenocarcinoma

artículo científico publicado en 2007

Drug-sensitive FGFR2 mutations in endometrial carcinoma

artículo científico publicado en 2008

Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma

artículo científico publicado en 2014

Erratum: Corrigendum: High-throughput oncogene mutation profiling in human cancer

article

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

artículo científico publicado en 2012

Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.

artículo científico publicado en 2012

Genome-wide functional synergy between amplified and mutated genes in human breast cancer

artículo científico publicado en 2008

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

High-throughput oncogene mutation profiling in human cancer

article

Initial genome sequencing and analysis of multiple myeloma

artículo científico publicado en 2011

Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

artículo científico publicado en 2010

Integrative analysis of the melanoma transcriptome

artículo científico publicado en 2010

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Major copy proportion analysis of tumor samples using SNP arrays

artículo científico publicado en 2008

Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

artículo científico publicado en 2012

Melanoma genome sequencing reveals frequent PREX2 mutations

artículo científico publicado en 2012

Modeling genomic diversity and tumor dependency in malignant melanoma

artículo científico publicado en 2008

Mutational heterogeneity in cancer and the search for new cancer-associated genes

artículo científico publicado en 2013

Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancer

artículo científico publicado en 2011

Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions

scientific article published on 18 May 2009

Punctuated evolution of prostate cancer genomes

artículo científico publicado en 2013

RNA-SeQC: RNA-seq metrics for quality control and process optimization

artículo científico publicado en 2012

Somatic mutations affect key pathways in lung adenocarcinoma

artículo científico publicado en 2008

Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy

artículo científico publicado en 2010

The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people

artículo científico publicado en 2006

The genomic complexity of primary human prostate cancer

artículo científico publicado en 2011

The landscape of somatic copy-number alteration across human cancers

artículo científico publicado en 2010

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

artículo científico publicado en 2012

Toward performance-diverse small-molecule libraries for cell-based phenotypic screening using multiplexed high-dimensional profiling

artículo científico publicado en 2014

Lista de obras de Wendy Winckler

A flexible rank-based framework for detecting copy number aberrations from array data

A landscape of driver mutations in melanoma

Absolute quantification of somatic DNA alterations in human cancer

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

Characterizing the cancer genome in lung adenocarcinoma

Drug-sensitive FGFR2 mutations in endometrial carcinoma

Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma

Erratum: Corrigendum: High-throughput oncogene mutation profiling in human cancer

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.

Genome-wide functional synergy between amplified and mutated genes in human breast cancer

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

High-throughput oncogene mutation profiling in human cancer

Initial genome sequencing and analysis of multiple myeloma

Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

Integrative analysis of the melanoma transcriptome

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Major copy proportion analysis of tumor samples using SNP arrays

Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

Melanoma genome sequencing reveals frequent PREX2 mutations

Modeling genomic diversity and tumor dependency in malignant melanoma

Mutational heterogeneity in cancer and the search for new cancer-associated genes

Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancer

Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions

Punctuated evolution of prostate cancer genomes

RNA-SeQC: RNA-seq metrics for quality control and process optimization

Somatic mutations affect key pathways in lung adenocarcinoma

Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy

The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people

The genomic complexity of primary human prostate cancer

The landscape of somatic copy-number alteration across human cancers

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

Toward performance-diverse small-molecule libraries for cell-based phenotypic screening using multiplexed high-dimensional profiling