Publicaciones en colaboración con investigadores/as de King Abdulaziz University (87)

2022

  1. Utility of Circulating Cell-Free DNA in Assessing Microsatellite Instability and Loss of Heterozygosity in Breast Cancer Using Human Identification Approach

    Genes, Vol. 13, Núm. 4

2021

  1. Discovery of a novel and a rare Kristen rat sarcoma viral oncogene homolog (KRAS) gene mutation in colorectal cancer patients

    Bioengineered, Vol. 12, Núm. 1, pp. 5099-5109

2020

  1. Overlapping variants in the blood, tissues and cell lines for patients with intracranial meningiomas are predominant in stem cell-related genes

    Heliyon, Vol. 6, Núm. 11

  2. Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder (Nature Neuroscience, (2017), 20, 9, (1217-1224), 10.1038/nn.4598)

    Nature Neuroscience

2019

  1. Association of GSTP1 and ERCC1 polymorphisms with toxicity in locally advanced head and neck cancer platinum-based chemoradiotherapy treatment

    Head and Neck, Vol. 41, Núm. 8, pp. 2704-2715

  2. Development and validation of the EUROFORGEN NAME (North African and Middle Eastern) ancestry panel

    Forensic Science International: Genetics, Vol. 42, pp. 260-267

  3. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)

    Nature Communications

  4. Genome-wide association study of germline variants and breast cancer-specific mortality

    British Journal of Cancer, Vol. 120, Núm. 6, pp. 647-657

2018

  1. Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

    Nature Communications, Vol. 9, Núm. 1

  2. Germline variation at 8q24 and prostate cancer risk in men of European ancestry

    Nature Communications, Vol. 9, Núm. 1

  3. In situ characterization of stem cells-like biomarkers in meningiomas

    Cancer Cell International, Vol. 18, Núm. 1

  4. Native American gene continuity to the modern admixed population from the Colombian Andes: Implication for biomedical, population and forensic studies

    Forensic Science International: Genetics, Vol. 36, pp. e1-e7

  5. Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

    Forensic Science International: Genetics, Vol. 37, pp. 241-251

2017

  1. A forensic multiplex of nine novel pentameric-repeat STRs

    Forensic Science International: Genetics, Vol. 29, pp. 154-164

  2. Analysis of the R1b-DF27 haplogroup shows that a large fraction of Iberian Y-chromosome lineages originated recently in situ

    Scientific Reports, Vol. 7, Núm. 1

  3. Copy number variation analysis of patients with intellectual disability from North-West Spain

    Gene, Vol. 626, pp. 189-199

  4. Evaluation of the Qiagen 140-SNP forensic identification multiplex for massively parallel sequencing

    Forensic Science International: Genetics, Vol. 28, pp. 35-43

  5. Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia

    Nature Communications, Vol. 8

  6. Making progress in educationThe EUROFORGEN master degree pilot project in forensic genetics

    Forensic Science International: Genetics

  7. Micro and macro geographical analysis of Y-chromosome lineages in South Iberia

    Forensic Science International: Genetics, Vol. 29, pp. e9-e15