Navegar por autor "Vega Gliemmo, Ana"

A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1

2014- Fachal Vilar, Laura; Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Sanchez Garcia, Manuel; Lobato Busto, Ramón; [et al.]

Abnormalities of thyroid C-cells in patients with PTEN-hamartoma tumour syndrome

2015- Cameselle Teijeiro, Jose Manuel; Vega Gliemmo, Ana; Abdulkader Nallib, Ihab; Reyes Santías, Rosa María; Cabezas Agrícola, José Manuel; [et al.]

About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants

2014- Vega Gliemmo, Ana

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.]

Annular elastolytic giant cell granuloma associated to late-onset erythtopoietic protoporphyria

2013- Alonso González, Julio; Gutierrez González, Enrique; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Garcia Martinez, Francisco Javier; [et al.]

Annular elastolytic giant cell granuloma associated to late-onset X-linked dominant protoporphyria

2013- Alonso González, Julio; Gutierrez González, Enrique; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Garcia Martinez, Francisco Javier; [et al.]

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.]

BRCA1 Circos: A visualisation resource for functional analysis of missense variants

2015- Vega Gliemmo, Ana

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 cancer genes: beyond BRCA1 and BRCA2

2013- Vega Gliemmo, Ana

Characterization of BRCA1 and BRCA2 splicing variants: A collaborative report by ENIGMA consortium members

2012- Fachal Vilar, Laura; Vega Gliemmo, Ana; Blanco Pérez, Ana

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.]

Clinical and molecular classification of ichthyosis

2012- Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Rodríguez Pazos, Laura

Evaluation of Rare Variants in the New Fanconi Anemia Gene ERCC4 (FANCQ) as Familial Breast/Ovarian Cancer Susceptibility Alleles

2013- Vega Gliemmo, Ana; Santamariña Pena, Marta

Ictiosis congénitas autosómicas recesivas

2013- Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Rodríguez Pazos, Laura

Identification of a Locus at 2q24 Associated With Susceptibility for Late Radiation Therapy Toxicity Through Performance of a 3-Stage Genome-Wide Association Study

2014- Fachal Vilar, Laura; Vega Gliemmo, Ana; Gómez Caamaño, Antonio

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis

2014- Fachal Vilar, Laura; Toribio Pérez, Jaime; Vega Gliemmo, Ana; Ginarte Val, Manuel Javier; Carracedo Álvarez, Ángel; [et al.]

Identification of Novel Susceptibility Loci and Genes for Prostate Cancer Risk: A Transcriptome-Wide Association Study in over 140,000 European Descendants

2019- Wu, L.; Wang, J. F.; Cai, Q. Y.; Cavazos, T. B.; Emami, N. C.; [et al.]

An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk

2020- Wu, L.; Yang, Y.; Guo, X.; Shu, X. O.; Cai, Q.; [et al.]

Repositorio digital RUNA

Navegar por autor "Vega Gliemmo, Ana"

A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1 ﻿

Abnormalities of thyroid C-cells in patients with PTEN-hamartoma tumour syndrome ﻿

About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants ﻿

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. ﻿

Annular elastolytic giant cell granuloma associated to late-onset erythtopoietic protoporphyria ﻿

Annular elastolytic giant cell granuloma associated to late-onset X-linked dominant protoporphyria ﻿

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

BRCA1 Circos: A visualisation resource for functional analysis of missense variants ﻿

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

Breast cancer genes: beyond BRCA1 and BRCA2 ﻿

Characterization of BRCA1 and BRCA2 splicing variants: A collaborative report by ENIGMA consortium members ﻿

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

Clinical and molecular classification of ichthyosis ﻿

Evaluation of Rare Variants in the New Fanconi Anemia Gene ERCC4 (FANCQ) as Familial Breast/Ovarian Cancer Susceptibility Alleles ﻿

Ictiosis congénitas autosómicas recesivas ﻿

Identification of a Locus at 2q24 Associated With Susceptibility for Late Radiation Therapy Toxicity Through Performance of a 3-Stage Genome-Wide Association Study ﻿

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis ﻿

Identification of Novel Susceptibility Loci and Genes for Prostate Cancer Risk: A Transcriptome-Wide Association Study in over 140,000 European Descendants ﻿

An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk ﻿

A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1

Abnormalities of thyroid C-cells in patients with PTEN-hamartoma tumour syndrome

About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants

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.

Annular elastolytic giant cell granuloma associated to late-onset erythtopoietic protoporphyria

Annular elastolytic giant cell granuloma associated to late-onset X-linked dominant protoporphyria

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

BRCA1 Circos: A visualisation resource for functional analysis of missense variants

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

Breast cancer genes: beyond BRCA1 and BRCA2

Characterization of BRCA1 and BRCA2 splicing variants: A collaborative report by ENIGMA consortium members

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

Clinical and molecular classification of ichthyosis

Evaluation of Rare Variants in the New Fanconi Anemia Gene ERCC4 (FANCQ) as Familial Breast/Ovarian Cancer Susceptibility Alleles

Ictiosis congénitas autosómicas recesivas

Identification of a Locus at 2q24 Associated With Susceptibility for Late Radiation Therapy Toxicity Through Performance of a 3-Stage Genome-Wide Association Study

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis

Identification of Novel Susceptibility Loci and Genes for Prostate Cancer Risk: A Transcriptome-Wide Association Study in over 140,000 European Descendants

An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk