Publicacións nas que colabora con Ana Vega Gliemmo (23)

2024

  1. Host gene expression signatures to identify infection type and organ dysfunction in children evaluated for sepsis: a multicentre cohort study

    The Lancet Child and Adolescent Health, Vol. 8, Núm. 5, pp. 325-338

2019

  1. Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

    Scientific Reports, Vol. 9, Núm. 1

  2. Identification of regulatory variants associated with genetic susceptibility to meningococcal disease

    Scientific Reports, Vol. 9, Núm. 1

  3. Plasma lipid profiles discriminate bacterial from viral infection in febrile children

    Scientific Reports, Vol. 9, Núm. 1

2016

  1. Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies

    Scientific Reports, Vol. 6

2015

  1. No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 168, Núm. 1, pp. 54-65

2014

  1. Evaluating the role of mitochondrial DNA variation to the genetic predisposition to radiation-induced toxicity

    Radiotherapy and Oncology, Vol. 111, Núm. 2, pp. 199-205

  2. No association between typical European mitochondrial variation and prostate cancer risk in a Spanish cohort

    Journal of Human Genetics, Vol. 59, Núm. 7, pp. 411-414

2013

  1. Indian Signatures in the Westernmost Edge of the European Romani Diaspora: New Insight from Mitogenomes

    PLoS ONE, Vol. 8, Núm. 10

2012

  1. Multiple local and recent founder effects of TGM1 in Spanish families.

    PloS one, Vol. 7, Núm. 4

2010

  1. The genomics serving pediatrics in the investigation of the multifactorial disease

    Acta Pediatrica Espanola, Vol. 68, Núm. 2, pp. 55-60

2009

  1. Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: A two-stage Spanish case-control study

    Gynecologic Oncology, Vol. 112, Núm. 1, pp. 210-214

  2. High mitochondrial DNA stability in B-Cell chronic lymphocytic leukemia

    PLoS ONE, Vol. 4, Núm. 11

  3. Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease

    PLoS ONE, Vol. 4, Núm. 12

2008

  1. Is mitochondrial DNA variation associated with sporadic breast cancer risk?

    Cancer Research

  2. The ‘Pokemon’ (ZBTB7) gene: No evidence of association with sporadic breast cancer

    Clinical Medicine: Oncology, Vol. 2, pp. 357-362

2006

  1. Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes

    Human Genetics, Vol. 118, Núm. 6, pp. 669-679

  2. Mutation spectra of ABCC8 gene in Spanish patients with Hyperinsulinism of Infancy (HI).

    Human mutation, Vol. 27, Núm. 2, pp. 214

2005

  1. A critical reassessment of the role of mitochondria in tumorigenesis

    PLoS Medicine, Vol. 2, Núm. 11, pp. 1158-1166

2004

  1. mtDNA mutations in tumors of the central nervous system reflect the neutral evolution of mtDNA in populations

    Oncogene, Vol. 23, Núm. 6, pp. 1314-1320