Browse by Author "Carracedo Álvarez, Ángel"

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.]

Nucleocytoplasmic transport and gene expression in patients with heart failure

2012- González Juanatey, José Ramón; Carracedo Álvarez, Ángel; Vidal Figueroa, Anxo

P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

2011- Carracedo Álvarez, Ángel; Blanco Arias, Patricia; Arias Gómez, Manuel; Pardo Fernández, Julio; Guijarro del Amo, Mónica [et al.]

Patterns of Y-STR variation in Italy

2012- Carracedo Álvarez, Ángel

Pharmacogenetics of OATP transporters reveals that SLCO1B1 c.388a>G variant is determinant of increased atorvastatin response

2011- Carracedo Álvarez, Ángel; Salas Ellacuriaga, Antonio; Phillips, Cristopher Paul; Rodrigues, AC; Rodrigues, Alice C; [et al.]

Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration.

2013- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Candamio Folgar, Sonia; [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.]

Population genetics of 17 Y-STR markers in West Libya (Tripoli region)

2013- Carracedo Álvarez, Ángel; Sánchez Diz, Paula; Rey González, Daniel

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.]

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.]

SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests?

2012- Carracedo Álvarez, Ángel; Salas Ellacuriaga, Antonio

SNPS in DNA repair and damage detection genes and acute normal tissue toxicity in prostate cancer patients

2012- Fachal Vilar, Laura; Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Sanchez Garcia, Manuel; Lobato Busto, Ramón; [et al.]

The CYP1A2 -163C>A polymorphism is associated with clozapine-induced generalized tonic-clonic seizures in Brazilian schizophrenia patients

2013- Carracedo Álvarez, Ángel

The value of genetic polymorphisms to predict toxicity in metastatic colorectal patients with irinotecan-based regimens

2012- Carracedo Álvarez, Ángel; Mosquera Leal, Ana; Candamio Folgar, Sonia; López López, Rafael; Barros Angueira, Francisco; [et al.]

Tumor Profiling at the Service of Cancer Therapy

2021- Fernández Rozadilla, Ceres; Santos Simoes, Ana Rita; Lleonart, M. E.; Carnero, A.; Carracedo Álvarez, Ángel [et al.]

Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage

2012- Carracedo Álvarez, Ángel

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

2014- Carracedo Álvarez, Ángel; Brión Martínez, María José; Blanco Verea, Alejandro José; Sobrino Rey, Beatríz; Amigo Lechuga, Jorge; [et al.]

RUNA digital repository

Browse by Author "Carracedo Álvarez, Ángel"

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) ﻿

Nucleocytoplasmic transport and gene expression in patients with heart failure ﻿

P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K) ﻿

Patterns of Y-STR variation in Italy ﻿

Pharmacogenetics of OATP transporters reveals that SLCO1B1 c.388a>G variant is determinant of increased atorvastatin response ﻿

Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration. ﻿

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

Population genetics of 17 Y-STR markers in West Libya (Tripoli region) ﻿

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. ﻿

Sarcomeric gene mutations in sudden infant death syndrome (SIDS) ﻿

SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests? ﻿

SNPS in DNA repair and damage detection genes and acute normal tissue toxicity in prostate cancer patients ﻿

The CYP1A2 -163C>A polymorphism is associated with clozapine-induced generalized tonic-clonic seizures in Brazilian schizophrenia patients ﻿

The value of genetic polymorphisms to predict toxicity in metastatic colorectal patients with irinotecan-based regimens ﻿

Tumor Profiling at the Service of Cancer Therapy ﻿

Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage ﻿

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease ﻿

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)

Nucleocytoplasmic transport and gene expression in patients with heart failure

P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Patterns of Y-STR variation in Italy

Pharmacogenetics of OATP transporters reveals that SLCO1B1 c.388a>G variant is determinant of increased atorvastatin response

Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration.

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

Population genetics of 17 Y-STR markers in West Libya (Tripoli region)

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.

Sarcomeric gene mutations in sudden infant death syndrome (SIDS)

SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests?

SNPS in DNA repair and damage detection genes and acute normal tissue toxicity in prostate cancer patients

The CYP1A2 -163C>A polymorphism is associated with clozapine-induced generalized tonic-clonic seizures in Brazilian schizophrenia patients

The value of genetic polymorphisms to predict toxicity in metastatic colorectal patients with irinotecan-based regimens

Tumor Profiling at the Service of Cancer Therapy

Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease