Browse by Author "Carracedo Álvarez, Ángel"

Analysis of the SNPforID 52-plex markers in four Native American populations from Venezuela

2012- Carracedo Álvarez, Ángel

Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians

2013- Carracedo Álvarez, Ángel; Salas Ellacuriaga, Antonio; Gómez Carballa, Alberto; Pardo Seco, Jacobo José

Asesoramiento genético en Neurología: un problema complejo que necesita regulación.

2011- Prieto Formoso , María; Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Quintans Castro, Beatriz

Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric study

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

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

Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients

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

The association of germline variants with chronic lymphocytic leukemia outcome suggests the implication of novel genes and pathways in clinical evolution

2019- MOSQUERA ORGUEIRA, ADRIAN; Antelo Rodríguez, Beatriz; Alonso Vence, Natalia; Díaz Arias, José; Díaz Varela, Nicolás; [et al.]

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

2013- Pérez Carral, Celsa; Armisén Gil, Margarita; Carracedo Álvarez, Ángel; Vidal Pan, Carmen; Rodríguez Vázquez, Virginia; [et al.]

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

2012- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Ramos Rios, Ramón; Paz Silva, Eduardo; Suárez Rama, Jose Javier; [et al.]

Autism spectrum symptoms in Smith-Magenis syndrome and Williams syndrome: comparisons and contrasts

2015- Carracedo Álvarez, Ángel; Fernández Prieto, Montserrat

BDNF genetic variants and methylation: effects on cognition in major depressive disorder

2019- Ferrer, A.; Labad, J.; Salvat-Pujol, N.; Barrachina, M.; Costas Costas, Javier; [et al.]

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations

2013- Fernández Rozadilla, Ceres; Palles, C.; Carvajal-Carmona, L.; Peterlongo, P.; Nici, C.; [et al.]

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency

2013- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

BRCA1 mutations do not increase prostate cancer risk: Results from a meta-analysis including new data

2011- Fachal Vilar, Laura; Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Gómez Caamaño, Antonio; Peleteiro Higuero, Paula; [et al.]

Breast feeding, parity and breast cancer subtypes in a Spanish cohort

2012- Redondo Marey, Carmen Maria; Gago Dominguez, Manuela; Miranda Ponte, Sara; Enguix Castelo, Manuel; Jiang, Xuejuan; [et al.]

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.]

Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis

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

Case-control study for colorectal cancer genetic susceptibility in EPICOLON: Previously identified variants and mucins

2011- Cubiella Fernández, Joaquín; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Clofent Villaplana, Juan

Cerebral and cerebellar MRI volumes in Williams syndrome

2014- Carracedo Álvarez, Ángel; Fernández Prieto, Montserrat

RUNA digital repository

Browse by Author "Carracedo Álvarez, Ángel"

Analysis of the SNPforID 52-plex markers in four Native American populations from Venezuela ﻿

Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians ﻿

Asesoramiento genético en Neurología: un problema complejo que necesita regulación. ﻿

Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric study ﻿

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 ﻿

Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients ﻿

The association of germline variants with chronic lymphocytic leukemia outcome suggests the implication of novel genes and pathways in clinical evolution ﻿

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

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia ﻿

Autism spectrum symptoms in Smith-Magenis syndrome and Williams syndrome: comparisons and contrasts ﻿

BDNF genetic variants and methylation: effects on cognition in major depressive disorder ﻿

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations ﻿

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency ﻿

BRCA1 mutations do not increase prostate cancer risk: Results from a meta-analysis including new data ﻿

Breast feeding, parity and breast cancer subtypes in a Spanish cohort ﻿

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

Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis ﻿

Case-control study for colorectal cancer genetic susceptibility in EPICOLON: Previously identified variants and mucins ﻿

Cerebral and cerebellar MRI volumes in Williams syndrome ﻿

Analysis of the SNPforID 52-plex markers in four Native American populations from Venezuela

Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians

Asesoramiento genético en Neurología: un problema complejo que necesita regulación.

Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric study

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

Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients

The association of germline variants with chronic lymphocytic leukemia outcome suggests the implication of novel genes and pathways in clinical evolution

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

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

Autism spectrum symptoms in Smith-Magenis syndrome and Williams syndrome: comparisons and contrasts

BDNF genetic variants and methylation: effects on cognition in major depressive disorder

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency

BRCA1 mutations do not increase prostate cancer risk: Results from a meta-analysis including new data

Breast feeding, parity and breast cancer subtypes in a Spanish cohort

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

Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis

Case-control study for colorectal cancer genetic susceptibility in EPICOLON: Previously identified variants and mucins

Cerebral and cerebellar MRI volumes in Williams syndrome