Lista de obras -

A computational tool to detect DNA alterations tailored to formalin-fixed paraffin-embedded samples in cancer clinical sequencing.

artículo científico publicado en 2018

ASK1 and ASK2 differentially regulate the counteracting roles of apoptosis and inflammation in tumorigenesis.

artículo científico publicado en 2009

Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers.

artículo científico publicado en 2016

Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015

artículo científico publicado en 2016

Cardiac intimal sarcoma with PDGFRβ mutation and co-amplification of PDGFRα and MDM2: an autopsy case analyzed by whole-exome sequencing.

artículo científico publicado en 2017

Clinical Utility of Circulating Tumor DNA for Molecular Assessment and Precision Medicine in Pancreatic Cancer

artículo científico publicado en 2016

Clinical utility of circulating tumor DNA for molecular assessment in pancreatic cancer

artículo científico publicado en 2015

Comprehensive mutation profiling of mucinous gastric carcinoma

artículo científico publicado en 2016

DNA Adductome Analysis Identifies N-Nitrosopiperidine Involved in the Etiology of Esophageal Cancer in Cixian, China

scientific article published on 09 July 2019

Epigenetic landscape influences the liver cancer genome architecture.

artículo científico publicado en 2018

Epigenome mapping of human normal purified hepatocytes: personal epigenome variation and genome–epigenome correlation

Erratum: Corrigendum: Signatures of mutational processes in human cancer

artículo científico publicado en 2013

Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer

artículo científico publicado en 2016

Exploration of germline variants responsible for adverse events of crizotinib in anaplastic lymphoma kinase-positive non-small cell lung cancer by target-gene panel sequencing

scientific article published on 04 December 2018

Fibroblast growth factor receptor 2 tyrosine kinase fusions define a unique molecular subtype of cholangiocarcinoma

artículo científico publicado en 2014

GC-09GENOME-WIDE DNA METHYLATION AND TRANSCRIPTOMIC PROFILING IN PRIMARY CENTRAL NERVOUS SYSTEM GERM CELL TUMORS SUGGESTS A PRIMORDIAL GERM CELL ORIGIN FOR GERMINOMA.

artículo científico publicado en 2016

Genome-wide methylation profiles in primary intracranial germ cell tumors indicate a primordial germ cell origin for germinomas

artículo científico publicado en 2017

Genomic Sequencing Identifies ELF3 as a Driver of Ampullary Carcinoma

artículo científico publicado en 2016

Genomic and transcriptomic analysis of imatinib resistance in gastrointestinal stromal tumors

artículo científico publicado en 2016

Genomic spectra of biliary tract cancer.

artículo científico publicado en 2015

Highly recurrent H3F3A mutations with additional epigenetic regulator alterations in giant cell tumor of bone

artículo científico publicado en 2017

Initial and crucial genetic events in intestinal-type gastric intramucosal neoplasia

artículo científico publicado en 2019

Integrated genetic and epigenetic analysis of myxofibrosarcoma

artículo científico publicado en 2018

Integrated molecular analysis of adult T cell leukemia/lymphoma.

artículo científico publicado en 2015

Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency

artículo científico publicado en 2017

Involvement of telomerase reverse transcriptase in heterochromatin maintenance

artículo científico publicado en 2014

Mouse model for ROS1-rearranged lung cancer

artículo científico publicado en 2013

Post-mortem Plasma Cell-Free DNA Sequencing: Proof-of-Concept Study for the "Liquid Autopsy"

artículo científico publicado en 2020

Recurrent neomorphic mutations of MTOR in central nervous system and testicular germ cell tumors may be targeted for therapy

artículo científico publicado en 2016

Single-cell DNA and RNA sequencing reveals the dynamics of intra-tumor heterogeneity in a colorectal cancer model

artículo científico publicado en 2021

The potential application of PD-1 blockade therapy for early-stage biliary tract cancer

artículo científico publicado en 2020

Trans-ancestry mutational landscape of hepatocellular carcinoma genomes

artículo científico publicado en 2014

Unique mutation portraits and frequent COL2A1 gene alteration in chondrosarcoma

artículo científico publicado en 2014

Variegated RHOA mutations in adult T-cell leukemia/lymphoma.

artículo científico publicado en 2015

Whole exome sequencing to identify genetic markers for trastuzumab-induced cardiotoxicity.

artículo científico publicado en 2017

Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma.

artículo científico publicado en 2017

Whole-exome Sequencing Reveals New Potential Susceptibility Genes for Japanese Familial Pancreatic Cancer

artículo científico publicado en 2020

Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer.

artículo científico publicado en 2016

Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators

artículo científico publicado en 2012

Lista de obras de

A computational tool to detect DNA alterations tailored to formalin-fixed paraffin-embedded samples in cancer clinical sequencing.

ASK1 and ASK2 differentially regulate the counteracting roles of apoptosis and inflammation in tumorigenesis.

Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers.

Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015

Cardiac intimal sarcoma with PDGFRβ mutation and co-amplification of PDGFRα and MDM2: an autopsy case analyzed by whole-exome sequencing.

Clinical Utility of Circulating Tumor DNA for Molecular Assessment and Precision Medicine in Pancreatic Cancer

Clinical utility of circulating tumor DNA for molecular assessment in pancreatic cancer

Comprehensive mutation profiling of mucinous gastric carcinoma

DNA Adductome Analysis Identifies N-Nitrosopiperidine Involved in the Etiology of Esophageal Cancer in Cixian, China

Epigenetic landscape influences the liver cancer genome architecture.

Epigenome mapping of human normal purified hepatocytes: personal epigenome variation and genome–epigenome correlation

Erratum: Corrigendum: Signatures of mutational processes in human cancer

Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer

Exploration of germline variants responsible for adverse events of crizotinib in anaplastic lymphoma kinase-positive non-small cell lung cancer by target-gene panel sequencing

Fibroblast growth factor receptor 2 tyrosine kinase fusions define a unique molecular subtype of cholangiocarcinoma

GC-09GENOME-WIDE DNA METHYLATION AND TRANSCRIPTOMIC PROFILING IN PRIMARY CENTRAL NERVOUS SYSTEM GERM CELL TUMORS SUGGESTS A PRIMORDIAL GERM CELL ORIGIN FOR GERMINOMA.

Genome-wide methylation profiles in primary intracranial germ cell tumors indicate a primordial germ cell origin for germinomas

Genomic Sequencing Identifies ELF3 as a Driver of Ampullary Carcinoma

Genomic and transcriptomic analysis of imatinib resistance in gastrointestinal stromal tumors

Genomic spectra of biliary tract cancer.

Highly recurrent H3F3A mutations with additional epigenetic regulator alterations in giant cell tumor of bone

Initial and crucial genetic events in intestinal-type gastric intramucosal neoplasia

Integrated genetic and epigenetic analysis of myxofibrosarcoma

Integrated molecular analysis of adult T cell leukemia/lymphoma.

Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency

Involvement of telomerase reverse transcriptase in heterochromatin maintenance

Mouse model for ROS1-rearranged lung cancer

Post-mortem Plasma Cell-Free DNA Sequencing: Proof-of-Concept Study for the "Liquid Autopsy"

Recurrent neomorphic mutations of MTOR in central nervous system and testicular germ cell tumors may be targeted for therapy

Single-cell DNA and RNA sequencing reveals the dynamics of intra-tumor heterogeneity in a colorectal cancer model

The potential application of PD-1 blockade therapy for early-stage biliary tract cancer

Trans-ancestry mutational landscape of hepatocellular carcinoma genomes

Unique mutation portraits and frequent COL2A1 gene alteration in chondrosarcoma

Variegated RHOA mutations in adult T-cell leukemia/lymphoma.

Whole exome sequencing to identify genetic markers for trastuzumab-induced cardiotoxicity.

Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma.

Whole-exome Sequencing Reveals New Potential Susceptibility Genes for Japanese Familial Pancreatic Cancer

Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer.

Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators