Lista de obras -

A Single-Nucleotide Substitution Mutator Phenotype Revealed by Exome Sequencing of Human Colon Adenomas

artículo científico publicado en 2012

A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH.

artículo científico publicado en 2007

A novel strategy for microarray quality control using Bayesian networks

artículo científico publicado en 2003

A strategy for identifying putative causes of gene expression variation in human cancers

article

Abnormal expression of apoptosis-related genes in haematological malignancies: overexpression of MYC is poor prognostic sign in mantle cell lymphoma.

artículo científico publicado en 2003

Aneuploidy facilitates oncogenic transformation via specific genetic alterations, including Twist2 upregulation

artículo científico publicado en 2013

Are data from different gene expression microarray platforms comparable?

artículo científico publicado en 2004

Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer

artículo científico publicado en 2009

Array-based gene expression, CGH and tissue data defines a 12q24 gain in neuroblastic tumors with prognostic implication

artículo científico publicado en 2010

CIP2A is associated with human breast cancer aggressivity

artículo científico publicado en 2009

Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemia

artículo científico publicado en 2018

Chimeric NUP98-NSD1 transcripts from the cryptic t(5;11)(q35.2;p15.4) in adult de novo acute myeloid leukemia.

artículo científico publicado en 2017

Data integration from two microarray platforms identifies bi-allelic genetic inactivation of RIC8A in a breast cancer cell line

artículo científico publicado en 2009

Drug-screening and genomic analyses of HER2-positive breast cancer cell lines reveal predictors for treatment response

artículo científico publicado en 2017

Enhanced serine production by bone metastatic breast cancer cells stimulates osteoclastogenesis

artículo científico publicado en 2010

Erratum to: Enhanced serine production by bone metastatic breast cancer cells stimulates osteoclastogenesis

scholarly article published in Breast Cancer Research and Treatment

Identification of fusion genes in breast cancer by paired-end RNA-sequencing

artículo científico publicado en 2011

Individualized systems medicine strategy to tailor treatments for patients with chemorefractory acute myeloid leukemia.

artículo científico publicado en 2013

Integrated breast cancer genomics

artículo científico publicado en 2006

Integrative functional genomics analysis of sustained polyploidy phenotypes in breast cancer cells identifies an oncogenic profile for GINS2

artículo científico publicado en 2010

Integrative genomic, transcriptomic, and RNAi analysis indicates a potential oncogenic role for FAM110B in castration-resistant prostate cancer

artículo científico publicado en 2011

Integrin trafficking regulated by Rab21 is necessary for cytokinesis

artículo científico publicado en 2008

Interactions between Notch- and hypoxia-induced transcriptomes in embryonic stem cells

article published in 2010

KRAS Oncogene Rearrangements and Gene Fusions: Unexpected Rare Encounters in Late-Stage Prostate Cancers: Table 1.

article

NMD microarray analysis for rapid genome-wide screen of mutated genes in cancer.

artículo científico publicado en 2005

Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing

artículo científico publicado en 2014

Optimized LOWESS normalization parameter selection for DNA microarray data

artículo científico publicado en 2004

Reanalysis of RNA-sequencing data reveals several additional fusion genes with multiple isoforms

artículo científico publicado en 2012

Somatic STAT3 mutations in large granular lymphocytic leukemia ⬇️

artículo científico publicado en 2012

Systematic analysis of microRNAs targeting the androgen receptor in prostate cancer cells

artículo científico publicado en 2011

Systematic bioinformatic analysis of expression levels of 17,330 human genes across 9,783 samples from 175 types of healthy and pathological tissues

artículo científico publicado en 2008

Systematic drug screening reveals specific vulnerabilities and co-resistance patterns in endocrine-resistant breast cancer

artículo científico publicado en 2016

TMPRSS2 fusions with oncogenic ETS factors in prostate cancer involve unbalanced genomic rearrangements and are associated with HDAC1 and epigenetic reprogramming

artículo científico publicado en 2006

The HER2 amplicon includes several genes required for the growth and survival of HER2 positive breast cancer cells

artículo científico publicado en 2012

Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors

artículo científico publicado en 2010

Lista de obras de

A Single-Nucleotide Substitution Mutator Phenotype Revealed by Exome Sequencing of Human Colon Adenomas

A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH.

A novel strategy for microarray quality control using Bayesian networks

A strategy for identifying putative causes of gene expression variation in human cancers

Abnormal expression of apoptosis-related genes in haematological malignancies: overexpression of MYC is poor prognostic sign in mantle cell lymphoma.

Aneuploidy facilitates oncogenic transformation via specific genetic alterations, including Twist2 upregulation

Are data from different gene expression microarray platforms comparable?

Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer

Array-based gene expression, CGH and tissue data defines a 12q24 gain in neuroblastic tumors with prognostic implication

CIP2A is associated with human breast cancer aggressivity

Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemia

Chimeric NUP98-NSD1 transcripts from the cryptic t(5;11)(q35.2;p15.4) in adult de novo acute myeloid leukemia.

Data integration from two microarray platforms identifies bi-allelic genetic inactivation of RIC8A in a breast cancer cell line

Drug-screening and genomic analyses of HER2-positive breast cancer cell lines reveal predictors for treatment response

Enhanced serine production by bone metastatic breast cancer cells stimulates osteoclastogenesis

Erratum to: Enhanced serine production by bone metastatic breast cancer cells stimulates osteoclastogenesis

Identification of fusion genes in breast cancer by paired-end RNA-sequencing

Individualized systems medicine strategy to tailor treatments for patients with chemorefractory acute myeloid leukemia.

Integrated breast cancer genomics

Integrative functional genomics analysis of sustained polyploidy phenotypes in breast cancer cells identifies an oncogenic profile for GINS2

Integrative genomic, transcriptomic, and RNAi analysis indicates a potential oncogenic role for FAM110B in castration-resistant prostate cancer

Integrin trafficking regulated by Rab21 is necessary for cytokinesis

Interactions between Notch- and hypoxia-induced transcriptomes in embryonic stem cells

KRAS Oncogene Rearrangements and Gene Fusions: Unexpected Rare Encounters in Late-Stage Prostate Cancers: Table 1.

NMD microarray analysis for rapid genome-wide screen of mutated genes in cancer.

Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing

Optimized LOWESS normalization parameter selection for DNA microarray data

Reanalysis of RNA-sequencing data reveals several additional fusion genes with multiple isoforms

Somatic STAT3 mutations in large granular lymphocytic leukemia ⬇️

Systematic analysis of microRNAs targeting the androgen receptor in prostate cancer cells

Systematic bioinformatic analysis of expression levels of 17,330 human genes across 9,783 samples from 175 types of healthy and pathological tissues

Systematic drug screening reveals specific vulnerabilities and co-resistance patterns in endocrine-resistant breast cancer

TMPRSS2 fusions with oncogenic ETS factors in prostate cancer involve unbalanced genomic rearrangements and are associated with HDAC1 and epigenetic reprogramming

The HER2 amplicon includes several genes required for the growth and survival of HER2 positive breast cancer cells

Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors