Navegar por autor "Brión Martínez, María José"

A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy

2013- Rojas, J.; Fernandez, I.; Pastor, J. C.; MacLaren, R. E.; Ramkissoon, Y.; [et al.]

Association between SNPs of Metalloproteinases and Prostaglandin F2 alpha Receptor Genes and Latanoprost Response in Open-Angle Glaucoma

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José

Association between SNPs of metalloproteinases and prostaglandin f2α receptor genes and latanoprost response in open-angle glaucoma

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José

Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio [et al.]

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

2015- Allegue, C.; Coll, M.; Mates, J.; Campuzano, O.; Iglesias, A.; [et al.]

Genetic association study of age-related macular degeneration in the Spanish population

2011- Carracedo Álvarez, Ángel; Brión Martínez, María José; Sanchez Salorio, Manuel; De La Fuente Freire, María; Pazos González, Belén; [et al.]

Genetic variants in genes related to lipid metabolism and atherosclerosis, dyslipidemia and atorvastatin response

2013- Carracedo Álvarez, Ángel; Brión Martínez, María José; Sobrino Rey, Beatríz

Increased clopidogrel response is associated with ABCC3 expression: A pilot study

2012- Carracedo Álvarez, Ángel; Brión Martínez, María José; Iñiguez Romo, Andres; Bravo Amaro, Marisol; Bastos Fernández, Guillermo [et al.]

Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population

2014- Corton, M.; Avila-Fernandez, A.; Vallespín, E.; López-Molina, M. I.; Almoguera, B.; [et al.]

Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José; Blanco Verea, Alejandro José; Sobrino Rey, Beatríz

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders

2014- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio; [et al.]

Next-generation sequencing data strengthens the involvement of cardiac structural diseases in Sudden Infant Death Syndrome (SIDS)

2014- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio [et al.]

Pharmacogenomics of anti-platelet therapy focused on peripheral blood cells of coronary arterial disease patients

2013- Carracedo Álvarez, Ángel; Brión Martínez, María José; Iñiguez Romo, Andres; Bravo Amaro, Marisol; Bastos Fernández, Guillermo [et al.]

Plan inspira saúde en Galicia 2023-2027: plan galego de actuación multidisciplinar en tabaquismo

2023- Aldama López, Guillermo; Alonso Fachado, Alfonso; Brión Martínez, María José; Carracedo Álvarez, Ángel María; Fernández Villar, José Alberto; [et al.]

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables.

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

2011- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio; [et al.]

PRKG1 mutations and thoracic aortic disease: Another candidate gene to consider during genetic diagnosis approach to non-syndromic cases

2015- Brión Martínez, María José; Blanco Verea, Alejandro José; Gago Díaz, Marina

Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility

2015- Carracedo Álvarez, Ángel; Brión Martínez, María José; Arrojo Romero, Manuel; Paz Silva, Eduardo; Suárez Rama, Jose Javier; [et al.]

Sarcomeric gene mutations in sudden infant death syndrome (SIDS)

2012- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio; [et al.]

Repositorio digital RUNA

Navegar por autor "Brión Martínez, María José"

A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy ﻿

Association between SNPs of Metalloproteinases and Prostaglandin F2 alpha Receptor Genes and Latanoprost Response in Open-Angle Glaucoma ﻿

Association between SNPs of metalloproteinases and prostaglandin f2α receptor genes and latanoprost response in open-angle glaucoma ﻿

Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood ﻿

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome ﻿

Genetic association study of age-related macular degeneration in the Spanish population ﻿

Genetic variants in genes related to lipid metabolism and atherosclerosis, dyslipidemia and atorvastatin response ﻿

Increased clopidogrel response is associated with ABCC3 expression: A pilot study ﻿

Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population ﻿

Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young ﻿

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders ﻿

Next-generation sequencing data strengthens the involvement of cardiac structural diseases in Sudden Infant Death Syndrome (SIDS) ﻿

Pharmacogenomics of anti-platelet therapy focused on peripheral blood cells of coronary arterial disease patients ﻿

Plan inspira saúde en Galicia 2023-2027: plan galego de actuación multidisciplinar en tabaquismo ﻿

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables ﻿

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables. ﻿

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases. ﻿

PRKG1 mutations and thoracic aortic disease: Another candidate gene to consider during genetic diagnosis approach to non-syndromic cases ﻿

Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility ﻿

Sarcomeric gene mutations in sudden infant death syndrome (SIDS) ﻿

A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy

Association between SNPs of Metalloproteinases and Prostaglandin F2 alpha Receptor Genes and Latanoprost Response in Open-Angle Glaucoma

Association between SNPs of metalloproteinases and prostaglandin f2α receptor genes and latanoprost response in open-angle glaucoma

Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

Genetic association study of age-related macular degeneration in the Spanish population

Genetic variants in genes related to lipid metabolism and atherosclerosis, dyslipidemia and atorvastatin response

Increased clopidogrel response is associated with ABCC3 expression: A pilot study

Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population

Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders

Next-generation sequencing data strengthens the involvement of cardiac structural diseases in Sudden Infant Death Syndrome (SIDS)

Pharmacogenomics of anti-platelet therapy focused on peripheral blood cells of coronary arterial disease patients

Plan inspira saúde en Galicia 2023-2027: plan galego de actuación multidisciplinar en tabaquismo

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables.

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

PRKG1 mutations and thoracic aortic disease: Another candidate gene to consider during genetic diagnosis approach to non-syndromic cases

Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility

Sarcomeric gene mutations in sudden infant death syndrome (SIDS)