Lista de obras - Maria Torres - Dominio Público Uruguay

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

artículo científico publicado en 2016

A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system

artículo científico publicado en 2010

Analyses of variants located in estrogen metabolism genes (ESR1, ESR2, COMT and APOE) and schizophrenia

article

Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects

artículo científico publicado en 2003

Analysis of BRCA1 and BRCA2 in breast and breast/ovarian cancer families shows population substructure in the Iberian peninsula

scientific article published on 01 January 2002

Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction

artículo científico publicado en 2007

Association of thromboxane A1 synthase (TBXAS1) gene polymorphism with acute urticaria induced by nonsteroidal anti-inflammatory drugs

artículo científico publicado en 2013

Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set.

artículo científico publicado en 2014

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

artículo científico publicado en 2010

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

artículo científico publicado en 2017

Development of a Panel of Genome-Wide Ancestry Informative Markers to Study Admixture Throughout the Americas

artículo científico publicado en 2012

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic variation in the nuclear factor kappaB pathway in relation to susceptibility to rheumatoid arthritis.

artículo científico publicado en 2008

Identification of a novel mutation in the humanPDE6Agene in autosomal recessive retinitis pigmentosa: homology with thenmf28/nmf28mice model

article

Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

artículo científico publicado en 2014

Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS)

article

New technologies in the genetic approach to sudden cardiac death in the young.

artículo científico publicado en 2010

Relative efficiency of the linkage disequilibrium mapping approach in detecting candidate genes for schizophrenia in different European populations

artículo científico publicado en 2005

Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications

artículo científico publicado en 2014

Lista de obras de Maria Torres

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system

Analyses of variants located in estrogen metabolism genes (ESR1, ESR2, COMT and APOE) and schizophrenia

Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects

Analysis of BRCA1 and BRCA2 in breast and breast/ovarian cancer families shows population substructure in the Iberian peninsula

Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction

Association of thromboxane A1 synthase (TBXAS1) gene polymorphism with acute urticaria induced by nonsteroidal anti-inflammatory drugs

Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set.

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

Development of a Panel of Genome-Wide Ancestry Informative Markers to Study Admixture Throughout the Americas

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Genetic variation in the nuclear factor kappaB pathway in relation to susceptibility to rheumatoid arthritis.

Identification of a novel mutation in the humanPDE6Agene in autosomal recessive retinitis pigmentosa: homology with thenmf28/nmf28mice model

Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS)

New technologies in the genetic approach to sudden cardiac death in the young.

Relative efficiency of the linkage disequilibrium mapping approach in detecting candidate genes for schizophrenia in different European populations

Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications

Sequenom MassArray™ application in the long QT syndrome mutation detection