Publicaciones en colaboración con investigadores/as de University of Michigan–Ann Arbor (22)

2024

  1. International Society for Heart and Lung Transplantation Guidelines for the Evaluation and Care of Cardiac Transplant Candidates—2024

    Journal of Heart and Lung Transplantation, Vol. 43, Núm. 10, pp. 1529-1628.e54

2023

  1. 2022 Year in Review: Countdown of the Best Manuscripts in 2022

    JACC: Case Reports

  2. Donor heart selection: Evidence-based guidelines for providers

    Journal of Heart and Lung Transplantation, Vol. 42, Núm. 1, pp. 7-29

  3. Health-related quality of life following valoctocogene roxaparvovec gene therapy for severe hemophilia A in the phase 3 trial GENEr8-1

    Journal of Thrombosis and Haemostasis

2022

  1. Extended anticoagulation for venous thromboembolism: A survey of the American Venous Forum and the European Venous Forum

    Journal of Vascular Surgery: Venous and Lymphatic Disorders, Vol. 10, Núm. 5, pp. 1012-1020.e3

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2020

  1. Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial

    The Lancet, Vol. 396, Núm. 10253, pp. 759-769

2019

  1. 2019 update of the WSES guidelines for management of Clostridioides (Clostridium) difficile infection in surgical patients

    World Journal of Emergency Surgery, Vol. 14, Núm. 1

  2. Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients

    Journal of Cellular and Molecular Medicine, Vol. 23, Núm. 3, pp. 2125-2135

2018

  1. The management of antibodies in heart transplantation: An ISHLT consensus document

    Journal of Heart and Lung Transplantation, Vol. 37, Núm. 5, pp. 537-547

2017

  1. The GH/IGF-1 axis in a critical period early in life determines cellular DNA repair capacity by altering transcriptional regulation of DNA repair-related genes: implications for the developmental origins of cancer

    GeroScience, Vol. 39, Núm. 2, pp. 147-160

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Genome-wide associations for birth weight and correlations with adult disease

    Nature, Vol. 538, Núm. 7624, pp. 248-252

  3. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

2015

  1. A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data

    BMC Genomics, Vol. 16, Núm. 1

  2. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

    Nature Genetics, Vol. 47, Núm. 6, pp. 579-581

  3. WSES guidelines for management of Clostridium difficile infection in surgical patients

    World Journal of Emergency Surgery, Vol. 10, Núm. 1

2014

  1. Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Núm. 36, pp. 13127-13132

  2. The alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles

    American Journal of Human Genetics, Vol. 95, Núm. 2, pp. 143-161

2013

  1. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

    Neurogenetics, Vol. 14, Núm. 1, pp. 11-22