Navegar por autor "Carracedo Álvarez, Ángel"

Longitudinal analysis on parasite diversity in honeybee colonies: new taxa, high frequency of mixed infections and seasonal patterns of variation

2020- Bartolomé Husson, Carolina; Buendía-Abad, M.; Benito, M.; Sobrino Rey, Beatríz; Amigo Lechuga, Jorge; [et al.]

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

2013- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; García Murias, María; Prieto González, José María; Ordoñez Ugalde, Andrés [et al.]

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing.

2011- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Barros Angueira, Francisco; Campos Balea, Begoña; Quintans Castro, Beatriz; [et al.]

Neuropsychological assessment in SCA36: 'Costa da Morte' ataxia

2014- Pumar Cebreiro, José Manuel; Carracedo Álvarez, Ángel; Labella Caballero, Torcuato; Sobrido Gómez, María Jesús; Fernández Prieto, Montserrat; [et al.]

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response

2011- Echarri Piudo, Ana; Castro Alvariño, Javier; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; [et al.]

Population pharmacokinetic/pharmacogenetic model of lopinavir/ritonavir in HIV-infected patients

2014- Carracedo Álvarez, Ángel

Prevalence of Somatic MutL Homolog 1 Promoter Hypermethylation in Lynch Syndrome Colorectal Cancer

2015- Carracedo Álvarez, Ángel

Publications and letters related to the forensic genetic analysis of low amounts of DNA

2011- Carracedo Álvarez, Ángel

RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families

2014- Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Santamariña Pena, Marta; Blanco Pérez, Ana

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.

2015- Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

2014- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Ramos Rios, Ramón; Costas Costas, Javier

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.]

Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation

2013- Rodríguez-Soler, María; Pérez-Carbonell, Lucía; Guarinos, Carla; Zapater, Pedro; Castillejo, Adela; [et al.]

Seeking genetic susceptibility variants for colorectal cancer: The EPICOLON consortium experience

2012- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

Supercomplex Assembly Determines Electron Flux in the Mitochondrial Electron Transport Chain

2013- Carracedo Álvarez, Ángel; Cruz Guerrero, Raquel

Synaptic, transcriptional and chromatin genes disrupted in autism

2014- Carracedo Álvarez, Ángel

The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Transcriptome and genome sequencing uncovers functional variation in humans

2013- Carracedo Álvarez, Ángel

X-ray cross-complementing group 1 and thymidylate synthase polymorphisms might predict response to chemoradiotherapy in rectal cancer patients

2012- Lamas Díaz, María Jesús; Durán Piñeiro, Goretti; Gómez Caamaño, Antonio; Balboa Beltrán, Emilia; Anido Herranz, Urbano; [et al.]

Repositorio digital RUNA

Navegar por autor "Carracedo Álvarez, Ángel"

Longitudinal analysis on parasite diversity in honeybee colonies: new taxa, high frequency of mixed infections and seasonal patterns of variation ﻿

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice ﻿

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing. ﻿

Neuropsychological assessment in SCA36: 'Costa da Morte' ataxia ﻿

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response ﻿

Population pharmacokinetic/pharmacogenetic model of lopinavir/ritonavir in HIV-infected patients ﻿

Prevalence of Somatic MutL Homolog 1 Promoter Hypermethylation in Lynch Syndrome Colorectal Cancer ﻿

Publications and letters related to the forensic genetic analysis of low amounts of DNA ﻿

RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families ﻿

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer. ﻿

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain ﻿

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 ﻿

Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation ﻿

Seeking genetic susceptibility variants for colorectal cancer: The EPICOLON consortium experience ﻿

Supercomplex Assembly Determines Electron Flux in the Mitochondrial Electron Transport Chain ﻿

Synaptic, transcriptional and chromatin genes disrupted in autism ﻿

The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals ﻿

Transcriptome and genome sequencing uncovers functional variation in humans ﻿

X-ray cross-complementing group 1 and thymidylate synthase polymorphisms might predict response to chemoradiotherapy in rectal cancer patients ﻿

Longitudinal analysis on parasite diversity in honeybee colonies: new taxa, high frequency of mixed infections and seasonal patterns of variation

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing.

Neuropsychological assessment in SCA36: 'Costa da Morte' ataxia

Pharmacogenetics study of TPMT and ITPA genes in patients with inflammatory bowel disease treated with azathioprine detects relation between ITPase deficiency and clinical response

Population pharmacokinetic/pharmacogenetic model of lopinavir/ritonavir in HIV-infected patients

Prevalence of Somatic MutL Homolog 1 Promoter Hypermethylation in Lynch Syndrome Colorectal Cancer

Publications and letters related to the forensic genetic analysis of low amounts of DNA

RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain

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

Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation

Seeking genetic susceptibility variants for colorectal cancer: The EPICOLON consortium experience

Supercomplex Assembly Determines Electron Flux in the Mitochondrial Electron Transport Chain

Synaptic, transcriptional and chromatin genes disrupted in autism

The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals

Transcriptome and genome sequencing uncovers functional variation in humans

X-ray cross-complementing group 1 and thymidylate synthase polymorphisms might predict response to chemoradiotherapy in rectal cancer patients