Lista de obras - Barbara Hutter - Dominio Público Uruguay

A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.

artículo científico publicado en 2015

A comprehensive multicenter comparison of whole genome sequencing pipelines using a uniform tumor-normal sample pair

Author Correction: The landscape of genomic alterations across childhood cancers

artículo científico publicado en 2018

BRAF inhibitor-associated ERK activation drives development of chronic lymphocytic leukemia

artículo científico publicado en 2014

Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia

artículo científico publicado en 2020

Cooperation of BRAF(F595L) and mutant HRAS in histiocytic sarcoma provides new insights into oncogenic BRAF signaling

artículo científico publicado en 2015

Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies

artículo científico publicado en 2013

Defective homologous recombination DNA repair as therapeutic target in advanced chordoma

scientific article published on 09 April 2019

Dissecting the genomic complexity underlying medulloblastoma

artículo científico publicado en 2012

Divergence of imprinted genes during mammalian evolution

artículo científico publicado en 2010

Erratum: Corrigendum: Signatures of mutational processes in human cancer

artículo científico publicado en 2013

Genomic footprints of activated telomere maintenance mechanisms in cancer

artículo científico publicado en 2020

Hypermutation of the inactive X chromosome is a frequent event in cancer

artículo científico publicado en 2013

ICGC PedBrain - dissecting the genomic complexity underlying medulloblastoma using whole-genome sequencing.

artículo científico publicado en 2012

Identification and characterization of a BRAF fusion oncoprotein with retained autoinhibitory domains

scientific article published on 26 September 2019

Identifying CpG islands by different computational techniques

artículo científico publicado en 2009

Imprinted genes show unique patterns of sequence conservation

artículo científico publicado en 2010

Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer

artículo científico publicado en 2013

Integrative genomic and transcriptomic analysis of leiomyosarcoma.

artículo científico publicado en 2018

Metastatic adult pancreatoblastoma: Multimodal treatment and molecular characterization of a very rare disease

artículo científico publicado en 2020

NRG1 Fusions in KRAS Wild-type Pancreatic Cancer.

artículo científico publicado en 2018

Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study

artículo científico publicado en 2016

Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.

artículo científico publicado en 2015

Recurrent CDKN1B (p27) mutations in hairy cell leukemia

artículo científico publicado en 2015

Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

artículo científico publicado en 2013

Repetitive elements in imprinted genes.

artículo científico publicado en 2006

Signatures of mutational processes in human cancer

artículo científico publicado en 2013

TB-17A COMPREHENSIVE PAN-CANCER ANALYSIS OF CHILDHOOD MALIGNANCIES.

artículo científico publicado en 2016

Tandem repeats in the CpG islands of imprinted genes

article

Targetable ERBB2 mutations identified in neurofibroma/schwannoma hybrid nerve sheath tumors

scientific article published on 04 February 2020

Targeting Fibroblast Growth Factor Receptor 1 for Treatment of Soft-Tissue Sarcoma

artículo científico publicado en 2016

The landscape of chromothripsis across adult cancer types

artículo científico publicado en 2020

The landscape of genomic alterations across childhood cancers

artículo científico publicado en 2018

The whole-genome landscape of medulloblastoma subtypes

artículo científico publicado en 2017

Whole genome sequencing puts forward hypotheses on metastasis evolution and therapy in colorectal cancer

artículo científico publicado en 2018

Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies

artículo científico publicado en 2021

Lista de obras de Barbara Hutter

A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.

A comprehensive multicenter comparison of whole genome sequencing pipelines using a uniform tumor-normal sample pair

Author Correction: The landscape of genomic alterations across childhood cancers

BRAF inhibitor-associated ERK activation drives development of chronic lymphocytic leukemia

Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia

Cooperation of BRAF(F595L) and mutant HRAS in histiocytic sarcoma provides new insights into oncogenic BRAF signaling

Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies

Defective homologous recombination DNA repair as therapeutic target in advanced chordoma

Dissecting the genomic complexity underlying medulloblastoma

Divergence of imprinted genes during mammalian evolution

Erratum: Corrigendum: Signatures of mutational processes in human cancer

Genomic footprints of activated telomere maintenance mechanisms in cancer

Hypermutation of the inactive X chromosome is a frequent event in cancer

ICGC PedBrain - dissecting the genomic complexity underlying medulloblastoma using whole-genome sequencing.

Identification and characterization of a BRAF fusion oncoprotein with retained autoinhibitory domains

Identifying CpG islands by different computational techniques

Imprinted genes show unique patterns of sequence conservation

Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer

Integrative genomic and transcriptomic analysis of leiomyosarcoma.

Metastatic adult pancreatoblastoma: Multimodal treatment and molecular characterization of a very rare disease

NRG1 Fusions in KRAS Wild-type Pancreatic Cancer.

Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study

Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.

Recurrent CDKN1B (p27) mutations in hairy cell leukemia

Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

Repetitive elements in imprinted genes.

Signatures of mutational processes in human cancer

TB-17A COMPREHENSIVE PAN-CANCER ANALYSIS OF CHILDHOOD MALIGNANCIES.

Tandem repeats in the CpG islands of imprinted genes

Targetable ERBB2 mutations identified in neurofibroma/schwannoma hybrid nerve sheath tumors

Targeting Fibroblast Growth Factor Receptor 1 for Treatment of Soft-Tissue Sarcoma

The landscape of chromothripsis across adult cancer types

The landscape of genomic alterations across childhood cancers

The whole-genome landscape of medulloblastoma subtypes

Whole genome sequencing puts forward hypotheses on metastasis evolution and therapy in colorectal cancer

Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies