Publicacións en colaboración con investigadores/as de Universidad Nacional de Córdoba (10)

2013

  1. Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians

    Forensic Science International: Genetics, Vol. 7, Núm. 5, pp. 537-542

  2. The Genetic Legacy of the Pre-Colonial Period in Contemporary Bolivians

    PLoS ONE, Vol. 8, Núm. 3

2012

  1. Typing short amplicon binary polymorphisms: Supplementary SNP and Indel genetic information in the analysis of highly degraded skeletal remains

    Forensic Science International: Genetics, Vol. 6, Núm. 4, pp. 469-476

2011

  1. The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genome

    BMC Genetics, Vol. 12

2010

  1. Hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) determination of cocaine and its metabolites benzoylecgonine, ecgonine methyl ester, and cocaethylene in hair samples

    Analytical and Bioanalytical Chemistry, Vol. 396, Núm. 5, pp. 1703-1712

2009

  1. A GEP-ISFG collaborative study on the optimization of an X-STR decaplex: Data on 15 Iberian and Latin American populations

    International Journal of Legal Medicine, Vol. 123, Núm. 3, pp. 227-234

2008

  1. 2006 GEP-ISFG collaborative exercise on mtDNA: reflections about interpretation, artefacts, and DNA mixtures

    Forensic Science International: Genetics, Vol. 2, Núm. 2, pp. 126-133

  2. Results of the GEP-ISFG collaborative study on an X-STR Decaplex

    Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 677-679

2007

  1. Erratum: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America (Journal of Human Genetics 51, (305-313) DOI: 10.1007/s10038-006-0362-0)

    Journal of Human Genetics

2006

  1. The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America

    Journal of Human Genetics, Vol. 51, Núm. 4, pp. 305-313