| Genome-wide identification of hypoxia-inducible factor binding sites and target genes by a probabilistic model integrating transcription-profiling data and in silico binding … A Ortiz-Barahona, D Villar, N Pescador, J Amigo, L Del Peso Nucleic acids research 38 (7), 2332-2345, 2010 | 246 | 2010 |
| BigBWA: Approaching the Burrows-Wheeler Aligner to Big Data Technologies. JM Abuín, JC Pichel, TF Pena, J Amigo Bioinformatics, 2015 | 160 | 2015 |
| Analysis of global variability in 15 established and 5 new European Standard Set (ESS) STRs using the CEPH human genome diversity panel C Phillips, L Fernandez-Formoso, M Garcia-Magarinos, L Porras, ... Forensic Science International: Genetics 5 (3), 155-169, 2011 | 128 | 2011 |
| SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access J Amigo, A Salas, C Phillips, Á Carracedo BMC bioinformatics 9 (1), 428, 2008 | 128 | 2008 |
| SparkBWA: speeding up the alignment of high-throughput DNA sequencing data JM Abuín, JC Pichel, TF Pena, J Amigo PloS one 11 (5), e0155461, 2016 | 102 | 2016 |
| The impact of modern migrations on present-day multi-ethnic Argentina as recorded on the mitochondrial DNA genome ML Catelli, V Álvarez-Iglesias, A Gómez-Carballa, A Mosquera-Miguel, ... BMC genetics 12 (1), 77, 2011 | 98 | 2011 |
| SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data C Morcillo-Suarez, J Alegre, R Sangros, E Gazave, R De Cid, R Milne, ... Bioinformatics 24 (14), 1643-1644, 2008 | 82 | 2008 |
| The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project J Amigo, C Phillips, M Lareu, Á Carracedo International journal of legal medicine 122 (5), 435-440, 2008 | 71 | 2008 |
| Genetic analysis of arrhythmogenic diseases in the era of NGS: the complexity of clinical decision-making in Brugada syndrome C Allegue, M Coll, J Mates, O Campuzano, A Iglesias, B Sobrino, M Brion, ... PloS one 10 (7), e0133037, 2015 | 62 | 2015 |
| Tetra-allelic SNPs: informative forensic markers compiled from public whole-genome sequence data C Phillips, J Amigo, Á Carracedo, MV Lareu Forensic Science International: Genetics 19, 100-106, 2015 | 60 | 2015 |
| Building a custom large-scale panel of novel microhaplotypes for forensic identification using MiSeq and Ion S5 massively parallel sequencing systems M de la Puente, C Phillips, C Xavier, J Amigo, A Carracedo, W Parson, ... Forensic Science International: Genetics 45, 102213, 2020 | 59 | 2020 |
| Completion of a worldwide reference panel of samples for an ancestry informative Indel assay C Santos, C Phillips, F Oldoni, J Amigo, M Fondevila, R Pereira, ... Forensic Science International: Genetics 17, 75-80, 2015 | 57 | 2015 |
| A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease E Balboa-Beltran, MJ Fernández-Seara, A Pérez-Muñuzuri, R Lago, ... Journal of Medical Genetics 51 (7), 475-478, 2014 | 56 | 2014 |
| Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders A Fernández-Marmiesse, M Morey, M Pineda, J Eiris, ML Couce, ... Orphanet journal of rare diseases 9 (1), 59, 2014 | 56 | 2014 |
| ENGINES: exploring single nucleotide variation in entire human genomes J Amigo, A Salas, C Phillips BMC bioinformatics 12 (1), 105, 2011 | 47 | 2011 |
| pop. STR—an online population frequency browser for established and new forensic STRs J Amigo, C Phillips, T Salas, LF Formoso, Á Carracedo, M Lareu Forensic Science International: Genetics Supplement Series 2 (1), 361-362, 2009 | 47 | 2009 |
| A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel C Phillips, J Amigo, AO Tillmar, MA Peck, M de la Puente, J Ruiz-Ramírez, ... Forensic Science International: Genetics 46, 102232, 2020 | 46 | 2020 |
| CSVS, a crowdsourcing database of the Spanish population genetic variability M Peña-Chilet, G Roldán, J Perez-Florido, FM Ortuño, R Carmona, ... Nucleic Acids Research 49 (D1), D1130-D1137, 2021 | 44 | 2021 |
| Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders M Brion, A Blanco‐Verea, B Sobrino, M Santori, R Gil, E Ramos‐Luis, ... Electrophoresis 35 (21-22), 3111-3116, 2014 | 44 | 2014 |
| Comprehensive molecular testing in patients with high functioning autism spectrum disorder MI Alvarez-Mora, RC Escalona, OP Navarro, I Madrigal, I Quintela, ... Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 784, 46-52, 2016 | 38 | 2016 |
Angel CarracedoGrupo de Medicina Xenomica. Instituto Ciencias Forenses. Universidad de Santiago de CompostelaVerified email at usc.es
