Publicacións en colaboración con investigadores/as de University of Iowa (14)

2023

  1. Applying a muscle fatigue model when optimizing load-sharing between muscles for short-duration high-intensity exercise: A preliminary study

    Frontiers in Physiology, Vol. 14

  2. Proceedings of the 27th Annual Congress of the International Liver Transplantation Society

    Transplantation

2022

  1. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

    Biological Psychiatry, Vol. 91, Núm. 1, pp. 102-117

2021

  1. Deciphering the complex interplay between pancreatic cancer, diabetes mellitus subtypes and obesity/BMI through causal inference and mediation analyses

    Gut, Vol. 70, Núm. 2, pp. 319-329

2017

  1. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

    Nature Genetics, Vol. 49, Núm. 7, pp. 993-1004

  2. New or Progressive Multiple Organ Dysfunction Syndrome in Pediatric Severe Sepsis: A Sepsis Phenotype With Higher Morbidity and Mortality

    Pediatric Critical Care Medicine, Vol. 18, Núm. 1, pp. 8-16

  3. The cellular and molecular bases of leptin and ghrelin resistance in obesity

    Nature Reviews Endocrinology, Vol. 13, Núm. 6, pp. 338-351

  4. Traveling from the hypothalamus to the adipose tissue: The thermogenic pathway

    Redox Biology, Vol. 12, pp. 854-863

2016

  1. Comparison of Pediatric Severe Sepsis Managed in U.S. and European ICUs

    Pediatric Critical Care Medicine, Vol. 17, Núm. 6, pp. 522-530

  2. Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept

    Nature Neuroscience, Vol. 19, Núm. 3, pp. 420-431

2015

  1. Discordant identification of pediatric severe sepsis by research and clinical definitions in the SPROUT international point prevalence study

    Critical Care, Vol. 19, Núm. 1

2013

  1. NANOG-dependent function of TET1 and TET2 in establishment of pluripotency

    Nature, Vol. 495, Núm. 7441, pp. 370-374

2011

  1. Diagnosis and treatment of hyperprolactinemia: An endocrine society clinical practice guideline

    Journal of Clinical Endocrinology and Metabolism, Vol. 96, Núm. 2, pp. 273-288

  2. Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in ménière's disease in a European Caucasian Population

    DNA and Cell Biology, Vol. 30, Núm. 9, pp. 699-708