Navegar por "Fundación pública Galega de Medicina Xenómica"

A study of East Timor variability using the SNPforID 52-plex SNP panel

2011- Carracedo Álvarez, Ángel

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.]

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

A Xq21.31 duplication without features of Prader-Willi syndrome

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura

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

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

2014- Gutierrez-Enriquez, S; Bonache, S; de Garibay, GR; Osorio, A; Santamariña Pena, Marta; [et al.]

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4

2014- Arrojo Romero, Manuel; Ramos Rios, Ramón; Paz Silva, Eduardo; Agra Romero, Santiago; Brenlla González, Julio; [et al.]

Acromesomelic dysplasia type Maroteaux: Broadening the spectrum of NPR2 mutations

2012- Leis Trabazo, María Rosaura; Loidi Fernández, Lourdes; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; Castro Feijoo, Lidia; [et al.]

Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study

2012- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel

Adaptive selection of an incretin gene in Eurasian populations

2011- Amigo Lechuga, Jorge

Additional trisomies amongst patients with chronic lymphocytic leukemia carrying trisomy 12: The partner chromosome makes a difference

2015- González Martínez, María Teresa

Admixture and genetic relationships of Mexican Mestizos regarding Latin American and Caribbean populations based on 13 CODIS-STRs

2015- Sánchez Diz, Paula

Adrenomyeloneuropathy diagnosed in a young female with spastic paraparesis after full exome sequencing

2014- Sobrido Gómez, María Jesús; Quintans Castro, Beatriz; Pardo Fernández, Julio; Ordoñez Ugalde, Andrés

affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling

2015- Carracedo Álvarez, Ángel; Quintela García, Inés

Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases

2014- Ali, A. M.; Schmidt, M. K.; Bolla, M. K.; Wang, Q.; Gago-Dominguez, M.; [et al.]

Allele frequencies of 20 STRs from Northwest Spain (Galicia)

2012- Carracedo Álvarez, Ángel

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders

2015- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Ramos Rios, Ramón; Paz Silva, Eduardo; Agra Romero, Santiago; [et al.]

An update on primary familial brain calcification

2013- Rodrígues de Lemos, Roberta

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

2012- Carracedo Álvarez, Ángel; Quintela García, Inés

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types

2015- Gago Dominguez, Manuela

Repositorio digital RUNA

Navegar por "Fundación pública Galega de Medicina Xenómica"

A study of East Timor variability using the SNPforID 52-plex SNP panel ﻿

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

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

A Xq21.31 duplication without features of Prader-Willi syndrome ﻿

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

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

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4 ﻿

Acromesomelic dysplasia type Maroteaux: Broadening the spectrum of NPR2 mutations ﻿

Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study ﻿

Adaptive selection of an incretin gene in Eurasian populations ﻿

Additional trisomies amongst patients with chronic lymphocytic leukemia carrying trisomy 12: The partner chromosome makes a difference ﻿

Admixture and genetic relationships of Mexican Mestizos regarding Latin American and Caribbean populations based on 13 CODIS-STRs ﻿

Adrenomyeloneuropathy diagnosed in a young female with spastic paraparesis after full exome sequencing ﻿

affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling ﻿

Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases ﻿

Allele frequencies of 20 STRs from Northwest Spain (Galicia) ﻿

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders ﻿

An update on primary familial brain calcification ﻿

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

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types ﻿

A study of East Timor variability using the SNPforID 52-plex SNP panel

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

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

A Xq21.31 duplication without features of Prader-Willi syndrome

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

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

Absence of low frequency variants associated with schizophrenia at the ultraconserved non-coding region of TCF4

Acromesomelic dysplasia type Maroteaux: Broadening the spectrum of NPR2 mutations

Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study

Adaptive selection of an incretin gene in Eurasian populations

Additional trisomies amongst patients with chronic lymphocytic leukemia carrying trisomy 12: The partner chromosome makes a difference

Admixture and genetic relationships of Mexican Mestizos regarding Latin American and Caribbean populations based on 13 CODIS-STRs

Adrenomyeloneuropathy diagnosed in a young female with spastic paraparesis after full exome sequencing

affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling

Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases

Allele frequencies of 20 STRs from Northwest Spain (Galicia)

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders

An update on primary familial brain calcification

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

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types