Publicaciones en colaboración con investigadores/as de University Hospital Bonn (15)

2023

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

    Nature

  2. Animating Clinical Ethics: A Structured Method to Teach Ethical Analysis Through Movies

    HEC Forum, Vol. 35, Núm. 4, pp. 325-335

  3. What Ethics Support for Resolving Ethical Conflicts Do Internists Use in Spanish Hospitals?

    Journal of Bioethical Inquiry

2022

  1. Genetic variants associated with longitudinal changes in brain structure across the lifespan

    Nature neuroscience, Vol. 25, Núm. 4, pp. 421-432

  2. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Nature, Vol. 604, Núm. 7906, pp. 502-508

  3. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

  4. Operation of a triage committee for advanced life support during the COVID-19 pandemic

    Philosophy, Ethics, and Humanities in Medicine, Vol. 17, Núm. 1

2021

  1. MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline elevated serum creatine kinase

    Brain, Vol. 144, Núm. 9, pp. 2722-2731

  2. Psychological well-being of palliative care professionals: Who cares?

    Palliative and Supportive Care, Vol. 19, Núm. 2, pp. 257-261

2020

  1. Glycogenin is Dispensable for Glycogen Synthesis in Human Muscle, and Glycogenin Deficiency Causes Polyglucosan Storage

    Journal of Clinical Endocrinology and Metabolism, Vol. 105, Núm. 2

  2. The Use of Advance Directives in Specialized Care Units: A Focus Group Study With Healthcare Professionals in Madrid

    Journal of Bioethical Inquiry, Vol. 17, Núm. 3, pp. 395-405

2019

  1. Genetic insight into Nigerian population groups using an X-chromosome decaplex system

    Forensic Science International: Genetics Supplement Series, Vol. 7, Núm. 1, pp. 501-503

2014

  1. Common variant at 16p11.2 conferring risk of psychosis

    Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114

2011

  1. Common variants at VRK2 and TCF4 conferring risk of schizophrenia

    Human Molecular Genetics, Vol. 20, Núm. 20, pp. 4076-4081

2009

  1. Common variants conferring risk of schizophrenia

    Nature, Vol. 460, Núm. 7256, pp. 744-747