Publicaciones en colaboración con investigadores/as de Queen Mary University of London (43)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. Erratum: Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 (Nature (2023) 617 7962 (764-768))

    Nature

  3. GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

    Nature, Vol. 617, Núm. 7962, pp. 764-768

  4. Genomic investigations of unexplained acute hepatitis in children

    Nature, Vol. 617, Núm. 7961, pp. 564-573

  5. Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study

    The Lancet Rheumatology, Vol. 5, Núm. 4, pp. e184-e199

2019

  1. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

    Nature Communications, Vol. 10, Núm. 1

  2. 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

  3. 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

2016

  1. Comprehensive Analysis of Pan-African Mitochondrial DNA Variation Provides New Insights into Continental Variation and Demography

    Journal of Genetics and Genomics, Vol. 43, Núm. 3, pp. 133-143

2014

  1. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    Nature Genetics, Vol. 46, Núm. 8, pp. 826-836

2013

  1. RNA/DNA co-analysis from human saliva and semen stains-Results of a third collaborative EDNAP exercise

    Forensic Science International: Genetics, Vol. 7, Núm. 2, pp. 230-239

2012

  1. The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data

    Forensic Science International: Genetics, Vol. 6, Núm. 3, pp. 354-365

2008

  1. Forensic typing of autosomal SNPs with a 29 SNP-multiplex-Results of a collaborative EDNAP exercise

    Forensic Science International: Genetics, Vol. 2, Núm. 3, pp. 176-183

  2. Forensic validation of the Genplex SNP typing system-Results of an inter-laboratory study

    Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 389-393

2007

  1. Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel

    Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 180-185

  2. Forensic validation of the SNPforID 52-plex assay

    Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 186-190

  3. Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs

    Forensic Science International: Genetics, Vol. 1, Núm. 3-4, pp. 273-280

2006

  1. A compact population analysis test using 32 SNPs with highly diverse allele frequency distributions

    International Congress Series, Vol. 1288, pp. 58-60