Navegar por autor "Carracedo Álvarez, Ángel"

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization

2012- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; García Murias, María; Quintans Castro, Beatriz; [et al.]

Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: A study in Spanish and Italian populations and meta-analysis

2011- Fernández Sueiro, José Luis; Carracedo Álvarez, Ángel

Development of a novel forensic STR multiplex for ancestry analysis and extended identity testing

2013- Carracedo Álvarez, Ángel

Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach

2019- Alemany-Navarro, M.; Costas Costas, Javier; Real, E.; Segalàs, C.; Bertolín, S.; [et al.]

Enhanced localization of genetic samples through linkage-disequilibrium correction

2013- Baran, Y.; Quintela García, Inés; Carracedo Álvarez, Ángel; Pasaniuc, B.; Halperin, E. [et al.]

Estimating Exposome Score for Schizophrenia Using Predictive Modeling Approach in Two Independent Samples: The Results From the EUGEI Study

2019- Pries, L. K.; Lage-Castellanos, A.; Delespaul, P.; Kenis, G.; Luykx, J. J.; [et al.]

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome

2011- Castillejo, A; Guarinos, C; Martínez-Canto, A; Barbera VM; Egoavil C; [et al.]

Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes.

2011- Gómez-Carballa, Alberto; Cerezo, María; Balboa Beltrán, Emilia; Heredia Ramírez, Claudia Emilia; Castro Feijoo, Lidia; [et al.]

Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion

2015- Carracedo Álvarez, Ángel; Gómez Guerrero, Lorena María; Fernández Prieto, Montserrat

Fine mapping of the myosin light chain kinase (MYLK) gene replicates the association with asthma in populations of Spanish descent

2015- Carracedo Álvarez, Ángel

First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families

2012- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; Cacheiro Martínez, Pilar; García Murias, María; [et al.]

GDF: Dealing with high-throughput genotyping multiplatform data for medical and population genetic applications

2012- Carracedo Álvarez, Ángel; Costas Costas, Javier

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 QT interval highlights role for calcium signaling pathways in myocardial repolarization

2014- Carracedo Álvarez, Ángel

Genetic susceptibility variants associated with colorectal cancer prognosis

2013- Cubiella Fernández, Joaquín; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Clofent Villaplana, Juan [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

Genetic variants related to nicotine dependence

2011- Corradini, B; Sánchez-Diz, P; Alú, M; Estany Gestal, Ana; Carracedo Álvarez, Ángel; [et al.]

Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project

2019- Moreno-Grau, S.; de Rojas, I.; Hernández, I.; Quintela, I.; Montrreal, L.; [et al.]

Genome-wide association study of germline variants and breast cancer-specific mortality

2019- Escala-Garcia, M.; Guo, Q.; Dörk, T.; Canisius, S.; Keeman, R.; [et al.]

Global population variability in Qiagen Investigator HDplex STRs

2014- Carracedo Álvarez, Ángel; Amigo Lechuga, Jorge

O repositorio dixital RUNA

Navegar por autor "Carracedo Álvarez, Ángel"

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization ﻿

Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: A study in Spanish and Italian populations and meta-analysis ﻿

Development of a novel forensic STR multiplex for ancestry analysis and extended identity testing ﻿

Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach ﻿

Enhanced localization of genetic samples through linkage-disequilibrium correction ﻿

Estimating Exposome Score for Schizophrenia Using Predictive Modeling Approach in Two Independent Samples: The Results From the EUGEI Study ﻿

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome ﻿

Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes. ﻿

Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion ﻿

Fine mapping of the myosin light chain kinase (MYLK) gene replicates the association with asthma in populations of Spanish descent ﻿

First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families ﻿

GDF: Dealing with high-throughput genotyping multiplatform data for medical and population genetic applications ﻿

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

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

Genetic susceptibility variants associated with colorectal cancer prognosis ﻿

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

Genetic variants related to nicotine dependence ﻿

Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project ﻿

Genome-wide association study of germline variants and breast cancer-specific mortality ﻿

Global population variability in Qiagen Investigator HDplex STRs ﻿

'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization

Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: A study in Spanish and Italian populations and meta-analysis

Development of a novel forensic STR multiplex for ancestry analysis and extended identity testing

Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach

Enhanced localization of genetic samples through linkage-disequilibrium correction

Estimating Exposome Score for Schizophrenia Using Predictive Modeling Approach in Two Independent Samples: The Results From the EUGEI Study

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome

Evolutionary analyses of entire genomes do not support the association of mtdna mutations with ras/mapk pathway syndromes.

Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion

Fine mapping of the myosin light chain kinase (MYLK) gene replicates the association with asthma in populations of Spanish descent

First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families

GDF: Dealing with high-throughput genotyping multiplatform data for medical and population genetic applications

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

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

Genetic susceptibility variants associated with colorectal cancer prognosis

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

Genetic variants related to nicotine dependence

Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project

Genome-wide association study of germline variants and breast cancer-specific mortality

Global population variability in Qiagen Investigator HDplex STRs