Publicacións en colaboración con investigadores/as de University of Leicester (21)

2023

  1. Diminishing benefits of urban living for children and adolescents’ growth and development

    Nature, Vol. 615, Núm. 7954, pp. 874-883

2022

  1. A genome-wide association study of survival in patients with sepsis

    Critical Care, Vol. 26, Núm. 1

  2. Efficacy of empagliflozin in heart failure with preserved versus mid-range ejection fraction: a pre-specified analysis of EMPEROR-Preserved

    Nature Medicine, Vol. 28, Núm. 12, pp. 2512-2520

2021

  1. Empagliflozin in heart failure with a preserved ejection fraction

    New England Journal of Medicine, Vol. 385, Núm. 16, pp. 1451-1461

  2. The Role of Digital Technologies in Responding to the Grand Challenges of the Natural Environment: The Windermere Accord

    Patterns, Vol. 2, Núm. 1

2020

  1. Corrigendum to “Recommendations from the United European Gastroenterology evidence-based guidelines for the diagnosis and therapy of chronic pancreatitis” (Pancreatology (2018) 18(8) (847–854), (S1424390318306938), (10.1016/j.pan.2018.09.016))

    Pancreatology

2018

  1. Recommendations from the United European Gastroenterology evidence-based guidelines for the diagnosis and therapy of chronic pancreatitis

    Pancreatology, Vol. 18, Núm. 8, pp. 847-854

2017

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

    Nature Communications, Vol. 8

  2. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases

    American Journal of Human Genetics

2016

  1. Distinct phosphorylation sites on the ghrelin receptor, GHSR1a, establish a code that determines the functions of ß-arrestins

    Scientific Reports, Vol. 6

  2. Oxaliplatin and 5-FU/folinic acid (modified FOLFOX6) with or without aflibercept in first-line treatment of patients with metastatic colorectal cancer: The AFFIRM study

    Annals of Oncology, Vol. 27, Núm. 7, pp. 1273-1279

  3. Prognostic significance of anaemia in patients with heart failure with preserved and reduced ejection fraction: Results from the MAGGIC individual patient data meta-analysis

    QJM, Vol. 109, Núm. 6, pp. 377-382

2014

  1. A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

    Forensic Science International: Genetics, Vol. 12, pp. 12-23

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

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

2010

  1. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

    Nature Genetics, Vol. 42, Núm. 2, pp. 132-136

2008

  1. The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula

    American Journal of Human Genetics, Vol. 83, Núm. 6, pp. 725-736

2005

  1. Migration and mental health in Europe (The state of the mental health in Europe working group: Appendix I)

    Clinical Practice and Epidemiology in Mental Health, Vol. 1

2001

  1. DNA Commission of the International Society of Forensic Genetics: Recommendations on forensic analysis using Y-chromosome STRs

    Forensic Science International, Vol. 124, Núm. 1, pp. 5-10

  2. DNA commission of the International Society of Forensic Genetics: Recommendations on forensic analysis using Y-chromosome STRs

    International Journal of Legal Medicine, Vol. 114, Núm. 6, pp. 305-309

  3. DNA commission of the International Society of Forensic Genetics: Recommendations on forensic analysis using Y-chromosome short tandem repeats

    Legal Medicine, Vol. 3, Núm. 4, pp. 252-257