Lista de obras -

A Multicenter Study to Validate the Reproducibility of MSI Testing With a Panel of 5 Quasimonomorphic Mononucleotide Repeats ⬇️

artículo científico publicado el 1 de diciembre de 2010

A subset of low-grade B cell lymphomas with a follicular growth pattern but without a BCL2 translocation shows features suggestive of nodal marginal zone lymphoma.

artículo científico

ARResT/Interrogate: an interactive immunoprofiler for IG/TR NGS data

artículo científico publicado en 2017

Activating mutations of the GNAQ gene: a frequent event in primary melanocytic neoplasms of the central nervous system

artículo científico publicado en 2010

Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity, and subcellular localization

artículo científico publicado en 2003

Clinical impact of recurrently mutated genes on lymphoma diagnostics: state-of-the-art and beyond

artículo científico publicado en 2016

Copy number variation analysis and methylome profiling of a GNAQ-mutant primary meningeal melanocytic tumor and its liver metastasis.

artículo científico publicado en 2016

Copy number variations as potential diagnostic and prognostic markers for CNS melanocytic neoplasms in neurocutaneous melanosis

artículo científico publicado en 2016

Epithelioid Hemangioendothelioma: clinicopathologic, immunhistochemical, and molecular genetic analysis of 39 cases

artículo científico publicado en 2014

Epstein-Barr virus in inflammatory bowel disease: the spectrum of intestinal lymphoproliferative disorders

artículo científico publicado en 2015

Guidance for laboratories performing molecular pathology for cancer patients

artículo científico publicado en 2014

High frequency of inactivating tetraspanin C D37 mutations in diffuse large B-cell lymphoma at immune-privileged sites

artículo científico publicado en 2019

High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage

artículo científico publicado en 2009

Hypermutation in Mantle Cell Lymphoma Does Not Indicate a Clinical or Biological Sub Entity. ⬇️

artículo científico publicado en 2006

Hypermutation in mantle cell lymphoma does not indicate a clinical or biological subentity

artículo científico publicado en 2009

Identification of IG-clonality status as a pre-treatment predictor for mortality in patients with immunodeficiency-associated Epstein-Barr virus-related lymphoproliferative disorders

artículo científico publicado en 2014

Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing.

artículo científico publicado en 2015

Immunohistochemical differentiation between follicular lymphoma and nodal marginal zone lymphoma--combined performance of multiple markers

artículo científico publicado en 2015

Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis.

artículo científico publicado en 2010

Integrated CGH- and Epression Array Profiling of Mantle Cell Lymphoma. ⬇️

artículo científico publicado en 2006

Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene-dosage regulated candidate genes.

artículo científico publicado en 2008

Is there a role for antigen selection in mantle cell lymphoma? Immunogenetic support from a series of 807 cases

artículo científico publicado en 2011

Lack of Bcl-2 expression in follicular lymphoma may be caused by mutations in the BCL2 gene or by absence of the t(14;18) translocation

artículo científico publicado en 2005

Memento for interprofessional learning

scientific article published on 08 April 2020

Molecular clonality assessment shows high performance to predict malignant B-cell non-Hodgkin's lymphoma using cytological smears

artículo científico

Multicentre validation study of nucleic acids extraction from FFPE tissues.

artículo científico publicado en 2010

Mutations in g protein encoding genes and chromosomal alterations in primary leptomeningeal melanocytic neoplasms.

artículo científico publicado en 2014

NRAS mutations are more prevalent than KIT mutations in melanoma of the female urogenital tract--a study of 24 cases from the Netherlands

artículo científico publicado en 2014

Next generation diagnostic molecular pathology: critical appraisal of quality assurance in Europe.

artículo científico

Next generation sequencing in synovial sarcoma reveals novel gene mutations

artículo científico publicado en 2015

Novel chromosomal imbalances in mantle cell lymphoma detected by genome-wide array-based comparative genomic hybridization

scientific article published on 21 October 2004

Pathways towards indolent B-cell lymphoma - Etiology and therapeutic strategies.

artículo científico

Pitfalls in TCR gene clonality testing: teaching cases.

artículo científico publicado en 2008

Podocyte changes upon induction of albuminuria in Thy-1.1 transgenic mice.

artículo científico publicado en 2003

Preparing pathology for personalized medicine: possibilities for improvement of the pre-analytical phase.

scientific article published on 11 April 2011

Primary melanocytic tumors of the central nervous system: a review with focus on molecular aspects

artículo científico publicado en 2015

Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytes.

artículo científico publicado en 2013

Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomas

artículo científico publicado en 2007

Protein profiling in pathology: Analysis and evaluation of 239 frozen tissue biopsies for diagnosis of B‐cell lymphomas ⬇️

artículo científico publicado el 26 de febrero de 2010

Protein profiling of B-cell lymphomas using tissue biopsies: A potential tool for small samples in pathology.

artículo científico publicado en 2008

Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomas.

artículo científico publicado en 2006

SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas

artículo científico publicado en 2016

Sequential immunohistochemistry: a promising new tool for the pathology laboratory.

artículo científico publicado en 2014

Solitary fibrous tumor - clinicopathologic, immunohistochemical and molecular analysis of 28 cases

artículo científico publicado en 2014

T-cell Landscape in a Primary Melanoma Predicts the Survival of Patients with Metastatic Disease after Their Treatment with Dendritic Cell Vaccines

artículo científico publicado en 2016

Teaching molecular genetics: Chapter 3--Proteomics in nephrology

artículo científico publicado en 2006

Tetraspanin CD37 protects against the development of B cell lymphoma

artículo científico publicado en 2016

Update on Molecular Pathology of Cutaneous Melanocytic Lesions: What is New in Diagnosis and Molecular Testing for Treatment?

artículo científico publicado en 2014

Whole-genome copy-number analysis identifies new leads for chromosomal aberrations involved in the oncogenesis and metastastic behavior of uveal melanomas

artículo científico

Lista de obras de

A Multicenter Study to Validate the Reproducibility of MSI Testing With a Panel of 5 Quasimonomorphic Mononucleotide Repeats ⬇️

A subset of low-grade B cell lymphomas with a follicular growth pattern but without a BCL2 translocation shows features suggestive of nodal marginal zone lymphoma.

ARResT/Interrogate: an interactive immunoprofiler for IG/TR NGS data

Activating mutations of the GNAQ gene: a frequent event in primary melanocytic neoplasms of the central nervous system

Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity, and subcellular localization

Clinical impact of recurrently mutated genes on lymphoma diagnostics: state-of-the-art and beyond

Copy number variation analysis and methylome profiling of a GNAQ-mutant primary meningeal melanocytic tumor and its liver metastasis.

Copy number variations as potential diagnostic and prognostic markers for CNS melanocytic neoplasms in neurocutaneous melanosis

Epithelioid Hemangioendothelioma: clinicopathologic, immunhistochemical, and molecular genetic analysis of 39 cases

Epstein-Barr virus in inflammatory bowel disease: the spectrum of intestinal lymphoproliferative disorders

Guidance for laboratories performing molecular pathology for cancer patients

High frequency of inactivating tetraspanin C D37 mutations in diffuse large B-cell lymphoma at immune-privileged sites

High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage

Hypermutation in Mantle Cell Lymphoma Does Not Indicate a Clinical or Biological Sub Entity. ⬇️

Hypermutation in mantle cell lymphoma does not indicate a clinical or biological subentity

Identification of IG-clonality status as a pre-treatment predictor for mortality in patients with immunodeficiency-associated Epstein-Barr virus-related lymphoproliferative disorders

Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing.

Immunohistochemical differentiation between follicular lymphoma and nodal marginal zone lymphoma--combined performance of multiple markers

Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis.

Integrated CGH- and Epression Array Profiling of Mantle Cell Lymphoma. ⬇️

Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene-dosage regulated candidate genes.

Is there a role for antigen selection in mantle cell lymphoma? Immunogenetic support from a series of 807 cases

Lack of Bcl-2 expression in follicular lymphoma may be caused by mutations in the BCL2 gene or by absence of the t(14;18) translocation

Memento for interprofessional learning

Molecular clonality assessment shows high performance to predict malignant B-cell non-Hodgkin's lymphoma using cytological smears

Multicentre validation study of nucleic acids extraction from FFPE tissues.

Mutations in g protein encoding genes and chromosomal alterations in primary leptomeningeal melanocytic neoplasms.

NRAS mutations are more prevalent than KIT mutations in melanoma of the female urogenital tract--a study of 24 cases from the Netherlands

Next generation diagnostic molecular pathology: critical appraisal of quality assurance in Europe.

Next generation sequencing in synovial sarcoma reveals novel gene mutations

Novel chromosomal imbalances in mantle cell lymphoma detected by genome-wide array-based comparative genomic hybridization

Pathways towards indolent B-cell lymphoma - Etiology and therapeutic strategies.

Pitfalls in TCR gene clonality testing: teaching cases.

Podocyte changes upon induction of albuminuria in Thy-1.1 transgenic mice.

Preparing pathology for personalized medicine: possibilities for improvement of the pre-analytical phase.

Primary melanocytic tumors of the central nervous system: a review with focus on molecular aspects

Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytes.

Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomas

Protein profiling in pathology: Analysis and evaluation of 239 frozen tissue biopsies for diagnosis of B‐cell lymphomas ⬇️

Protein profiling of B-cell lymphomas using tissue biopsies: A potential tool for small samples in pathology.

Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomas.

SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas

Sequential immunohistochemistry: a promising new tool for the pathology laboratory.

Solitary fibrous tumor - clinicopathologic, immunohistochemical and molecular analysis of 28 cases

T-cell Landscape in a Primary Melanoma Predicts the Survival of Patients with Metastatic Disease after Their Treatment with Dendritic Cell Vaccines

Teaching molecular genetics: Chapter 3--Proteomics in nephrology

Tetraspanin CD37 protects against the development of B cell lymphoma

Update on Molecular Pathology of Cutaneous Melanocytic Lesions: What is New in Diagnosis and Molecular Testing for Treatment?

Whole-genome copy-number analysis identifies new leads for chromosomal aberrations involved in the oncogenesis and metastastic behavior of uveal melanomas