Publicaciones en colaboración con investigadores/as de Centro de Investigación Biomédica en Red sobre Enfermedades Raras (7)

2016

  1. Systematic identification of phenotypically enriched loci using a patient network of genomic disorders

    BMC Genomics, Vol. 17, Núm. 1

2015

  1. Kpath: Integration of metabolic pathway linked data

    Database, Vol. 2015

2014

  1. PhenUMA: A tool for integrating the biomedical relationships among genes and diseases

    BMC Bioinformatics, Vol. 15, Núm. 1

2013

  1. Global Analysis of the Human Pathophenotypic Similarity Gene Network Merges Disease Module Components

    PLoS ONE, Vol. 8, Núm. 2

2012

  1. A combined model of hepatic polyamine and sulfur amino acid metabolism to analyze S-adenosyl methionine availability

    Amino Acids, Vol. 42, Núm. 2-3, pp. 597-610

  2. Histamine: An undercover agent in multiple rare diseases?

    Journal of Cellular and Molecular Medicine, Vol. 16, Núm. 9, pp. 1947-1960

  3. What is known on angiogenesis-related rare diseases? A systematic review of literature

    Journal of Cellular and Molecular Medicine, Vol. 16, Núm. 12, pp. 2872-2893