Publications by the researcher in collaboration with Jorge Amigo Lechuga (21)

2020

  1. A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel

    Forensic Science International: Genetics, Vol. 46

  2. Broadening the Applicability of a Custom Multi-Platform Panel of Microhaplotypes: Bio-Geographical Ancestry Inference and Expanded Reference Data

    Frontiers in Genetics, Vol. 11

  3. Building a custom large-scale panel of novel microhaplotypes for forensic identification using MiSeq and Ion S5 massively parallel sequencing systems

    Forensic Science International: Genetics, Vol. 45

2017

  1. Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus Disease

    Scientific Reports, Vol. 7, Núm. 1

2015

  1. Completion of a worldwide reference panel of samples for an ancestry informative Indel assay

    Forensic Science International: Genetics, Vol. 17, pp. 75-80

  2. Mitogenomes from The 1000 Genome Project reveal new Near Eastern features in present-day Tuscans

    PLoS ONE, Vol. 10, Núm. 3

  3. Tetra-allelic SNPs: Informative forensic markers compiled from public whole-genome sequence data

    Forensic Science International: Genetics, Vol. 19, pp. 100-106

2014

  1. A genome-wide study of modern-day Tuscans: Revisiting Herodotus's theory on the origin of the Etruscans

    PLoS ONE, Vol. 9, Núm. 9

  2. Global population variability in Qiagen Investigator HDplex STRs

    Forensic Science International: Genetics, Vol. 8, Núm. 1, pp. 36-43

2013

  1. A Generalized Model to Estimate the Statistical Power in Mitochondrial Disease Studies Involving 2×k Tables

    PLoS ONE, Vol. 8, Núm. 9

2012

  1. GDF: Dealing with high-throughput genotyping multiplatform data for medical and population genetic applications

    Journal of Proteomics and Bioinformatics, Vol. 5, Núm. 1, pp. 1-6

2011

  1. Analysis of global variability in 15 established and 5 new European Standard Set (ESS) STRs using the CEPH human genome diversity panel

    Forensic Science International: Genetics, Vol. 5, Núm. 3, pp. 155-169

  2. Call for participation in the neurogenetics consortium within the Human Variome Project

    Neurogenetics, Vol. 12, Núm. 3, pp. 169-173

  3. ENGINES: Exploring single nucleotide variation in entire human genomes

    BMC Bioinformatics, Vol. 12

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

    BMC Genetics, Vol. 12

2010

  1. A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups

    PLoS ONE, Vol. 5, Núm. 5

2009

  1. Viability of in-house datamarting approaches for population genetics analysis of SNP genotypes

    BMC Bioinformatics

  2. pop.STR-An online population frequency browser for established and new forensic STRs

    Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 361-362

2008

  1. SPSmart: Adapting population based SNP genotype databases for fast and comprehensive web access

    BMC Bioinformatics, Vol. 9

  2. The SNPforID browser: An online tool for query and display of frequency data from the SNPforID project

    International Journal of Legal Medicine, Vol. 122, Núm. 5, pp. 435-440