Lista de obras -

Assessment of a fully automated high-throughput DNA extraction method from formalin-fixed, paraffin-embedded tissue for KRAS, and BRAF somatic mutation analysis.

artículo científico publicado en 2012

B-cell lymphoblastic lymphoma with cutaneous involvement and a KMT2A gene rearrangement

scientific article published on 03 April 2020

BRCA1 Mutation Analysis in a Portuguese Population with Early-Onset Breast and/or Ovarian Cancer.

artículo científico publicado en 1999

Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.

artículo científico publicado en 2008

Colorectal carcinomas in MUTYH-associated polyposis display histopathological similarities to microsatellite unstable carcinomas

artículo científico publicado en 2009

Designing a high-throughput somatic mutation profiling panel specifically for gynaecological cancers

artículo científico publicado en 2014

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

artículo científico publicado en 2017

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

artículo científico publicado en 2017

Expression of HLA class I antigen, aspirin use, and survival after a diagnosis of colon cancer.

artículo científico publicado en 2014

Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype

artículo científico publicado en 2021

Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma.

artículo científico publicado en 2012

Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas.

artículo científico

High prevalence of MYD88 and CD79B mutations in intravascular large B-cell lymphoma

artículo científico publicado en 2018

Improved risk assessment of endometrial cancer by combined analysis of MSI, PI3K-AKT, Wnt/β-catenin and P53 pathway activation.

artículo científico publicado en 2012

Integral analysis of p53 and its value as prognostic factor in sporadic colon cancer

artículo científico publicado en 2013

Mass spectrometry-based loss of heterozygosity analysis of single-nucleotide polymorphism loci in paraffin embedded tumors using the MassEXTEND assay: single-nucleotide polymorphism loss of heterozygosity analysis of the protein tyrosine phosphatase

artículo científico publicado en 2005

Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2

scientific article published on 29 July 2018

Near-haploidization significantly associates with oncocytic adrenocortical, thyroid, and parathyroid tumors but not with mitochondrial DNA mutations.

artículo científico publicado en 2014

Progression and tumor heterogeneity analysis in early rectal cancer.

artículo científico publicado en 2008

Reliable High-Throughput Genotyping and Loss-of-Heterozygosity Detection in Formalin-Fixed, Paraffin-Embedded Tumors Using Single Nucleotide Polymorphism Arrays

artículo científico publicado en 2005

Somatic mutation profiles in primary colorectal cancers and matching ovarian metastases: Identification of driver and passenger mutations

artículo científico publicado en 2016

Statin Use After Diagnosis of Colon Cancer and Patient Survival

artículo científico publicado en 2017

Target-enriched next-generation sequencing reveals differences between primary and secondary ovarian tumors in formalin-fixed, paraffin-embedded tissue.

artículo científico publicado en 2014

The Influence of BRAF and KRAS Mutation Status on the Association between Aspirin Use and Survival after Colon Cancer Diagnosis

artículo científico publicado en 2017

The clinical value of HER-2 overexpression and PIK3CA mutations in the older breast cancer population: a FOCUS study analysis.

artículo científico publicado en 2016

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material

scientific article published on 15 October 2019

Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue

artículo científico publicado en 2018

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.

artículo científico publicado en 2014

Lista de obras de

Assessment of a fully automated high-throughput DNA extraction method from formalin-fixed, paraffin-embedded tissue for KRAS, and BRAF somatic mutation analysis.

B-cell lymphoblastic lymphoma with cutaneous involvement and a KMT2A gene rearrangement

BRCA1 Mutation Analysis in a Portuguese Population with Early-Onset Breast and/or Ovarian Cancer.

Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.

Colorectal carcinomas in MUTYH-associated polyposis display histopathological similarities to microsatellite unstable carcinomas

Designing a high-throughput somatic mutation profiling panel specifically for gynaecological cancers

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Expression of HLA class I antigen, aspirin use, and survival after a diagnosis of colon cancer.

Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype

Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma.

Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas.

High prevalence of MYD88 and CD79B mutations in intravascular large B-cell lymphoma

Improved risk assessment of endometrial cancer by combined analysis of MSI, PI3K-AKT, Wnt/β-catenin and P53 pathway activation.

Integral analysis of p53 and its value as prognostic factor in sporadic colon cancer

Mass spectrometry-based loss of heterozygosity analysis of single-nucleotide polymorphism loci in paraffin embedded tumors using the MassEXTEND assay: single-nucleotide polymorphism loss of heterozygosity analysis of the protein tyrosine phosphatase

Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2

Near-haploidization significantly associates with oncocytic adrenocortical, thyroid, and parathyroid tumors but not with mitochondrial DNA mutations.

Progression and tumor heterogeneity analysis in early rectal cancer.

Reliable High-Throughput Genotyping and Loss-of-Heterozygosity Detection in Formalin-Fixed, Paraffin-Embedded Tumors Using Single Nucleotide Polymorphism Arrays

Somatic mutation profiles in primary colorectal cancers and matching ovarian metastases: Identification of driver and passenger mutations

Statin Use After Diagnosis of Colon Cancer and Patient Survival

Target-enriched next-generation sequencing reveals differences between primary and secondary ovarian tumors in formalin-fixed, paraffin-embedded tissue.

The Influence of BRAF and KRAS Mutation Status on the Association between Aspirin Use and Survival after Colon Cancer Diagnosis

The clinical value of HER-2 overexpression and PIK3CA mutations in the older breast cancer population: a FOCUS study analysis.

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material

Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.