Publications en collaboration avec des chercheurs de Universidad de Málaga (12)

2024

  1. NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

    Movement Disorders

2018

  1. Phenotype-loci associations in networks of patients with rare disorders: application to assist in the diagnosis of novel clinical cases

    European Journal of Human Genetics, Vol. 26, Núm. 10, pp. 1451-1461

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. Biocomputational resources useful for drug discovery against compartmentalized targets

    Current Pharmaceutical Design, Vol. 20, Núm. 2, pp. 293-300

  2. 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. Regulatory cross-talk of mouse liver polyamine and methionine metabolic pathways: A systemic approach to its physiopathological consequences

    Amino Acids, Vol. 42, Núm. 2-3, pp. 577-595

  4. 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

2009

  1. Systems biology metabolic modeling assistant: An ontology-based tool for the integration of metabolic data in kinetic modeling

    Bioinformatics, Vol. 25, Núm. 6, pp. 834-835