Navegar por autor "Carracedo Álvarez, Ángel"

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

2014- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Couce Pico, María Luz; Balboa Beltran, Emilia; Pérez Muñuzuri, Alejandro; [et al.]

A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22

2011- Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

Allele frequencies of 20 STRs from Northwest Spain (Galicia)

2012- Carracedo Álvarez, Ángel

Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data

2012- Carracedo Álvarez, Ángel; Quintela García, Inés

Analysis of PALB2 Gene in BRCA1/BRCA2 Negative Spanish Hereditary Breast/Ovarian Cancer Families with Pancreatic Cancer Cases

2013- Graña Suárez, Begoña; Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Blanco Pérez, Ana

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

2011- Fachal Vilar, Laura; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Carracedo Álvarez, Ángel; [et al.]

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

2012- Carracedo Álvarez, Ángel

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 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.]

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

2015- Carracedo Álvarez, Ángel; Fernández Prieto, Montserrat

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

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

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.]

Cerebral and cerebellar MRI volumes in Williams syndrome

2014- Carracedo Álvarez, Ángel; Fernández Prieto, Montserrat

CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families

2013- Fachal Vilar, Laura; Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Santamariña Pena, Marta; Blanco Pérez, Ana [et al.]

Colorectal cancer eqtls as susceptibility loci Candidates

2012- Ruiz Ponte, Clara; Carracedo Álvarez, Ángel

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

2011- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Costas Costas, Javier; Mattheisen ?, Manuel

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

2012- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Ruiz Ponte, Clara; De Castro Parga, María Luisa

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

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Correlación fenotipo neuroanatómico y neurocognitivo en el síndrome de Williams

2013- Carracedo Álvarez, Ángel; Fernández Prieto, Montserrat

Repositorio digital RUNA

Navegar por autor "Carracedo Álvarez, Ángel"

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease ﻿

A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22 ﻿

Allele frequencies of 20 STRs from Northwest Spain (Galicia) ﻿

Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data ﻿

Analysis of PALB2 Gene in BRCA1/BRCA2 Negative Spanish Hereditary Breast/Ovarian Cancer Families with Pancreatic Cancer Cases ﻿

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects. ﻿

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

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

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 ﻿

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

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

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

Cerebral and cerebellar MRI volumes in Williams syndrome ﻿

CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families ﻿

Colorectal cancer eqtls as susceptibility loci Candidates ﻿

Common variants at VRK2 and TCF4 conferring risk of schizophrenia ﻿

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer ﻿

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

Correlación fenotipo neuroanatómico y neurocognitivo en el síndrome de Williams ﻿

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22

Allele frequencies of 20 STRs from Northwest Spain (Galicia)

Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data

Analysis of PALB2 Gene in BRCA1/BRCA2 Negative Spanish Hereditary Breast/Ovarian Cancer Families with Pancreatic Cancer Cases

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

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

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

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

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

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

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

Cerebral and cerebellar MRI volumes in Williams syndrome

CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families

Colorectal cancer eqtls as susceptibility loci Candidates

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

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

Correlación fenotipo neuroanatómico y neurocognitivo en el síndrome de Williams