Publicacións en colaboración con investigadores/as de Hospital Universitario de Valladolid (29)

2024

  1. Evaluation of Genetic Variants Associated with the Risk of Thiopurine-Related Pancreatitis: A Case Control Study from ENEIDA Registry

    Digestive Diseases, Vol. 42, Núm. 3, pp. 257-264

  2. Novel risk loci for COVID-19 hospitalization among admixed American populations

    eLife, Vol. 13

2023

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

    Nature

  2. Addressing influenza’s underestimated burden – Iberian experts call to action

    BMC Infectious Diseases

  3. Excess hospitalizations and mortality associated with seasonal influenza in Spain, 2008–2018

    BMC Infectious Diseases, Vol. 23, Núm. 1

2022

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

    Critical Care, Vol. 26, Núm. 1

  2. Clinical and economic burden of physician-diagnosed influenza in adults during the 2017/2018 epidemic season in Spain

    BMC Public Health, Vol. 22, Núm. 1

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

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

  4. Risk factors and bronchopulmonary dysplasia severity: data from the Spanish Bronchopulmonary Dysplasia Research Network

    European Journal of Pediatrics, Vol. 181, Núm. 2, pp. 789-799

2021

  1. Chemotherapy or allogeneic transplantation in high-risk Philadelphia chromosome–negative adult lymphoblastic leukemia

    Blood, Vol. 137, Núm. 14, pp. 1879-1894

2020

  1. From trivalent to quadrivalent influenza vaccines: Public health and economic burden for different immunization strategies in Spain

    PLoS ONE, Vol. 15, Núm. 5

2018

  1. Spanish collaborative study: Description of usual clinical practice in infant obesity

    Anales de Pediatria, Vol. 88, Núm. 6, pp. 340-349

2017

  1. Incremento de peso en pacientes con fibrosis quística: ¿Es siempre beneficioso?

    Nutricion Hospitalaria, Vol. 34, Núm. 3, pp. 578-583

  2. The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study

    Journal of Molecular and Cellular Cardiology, Vol. 102, pp. 3-9

2016

  1. ESPGHAN 2012 guidelines for Coeliac disease diagnosis: Validation through a retrospective Spanish multicentric study

    Journal of Pediatric Gastroenterology and Nutrition, Vol. 62, Núm. 2, pp. 284-291

  2. Vertically transmitted cytomegalovirus infection in newborn preterm infants

    Journal of Perinatal Medicine, Vol. 44, Núm. 5, pp. 485-490

2015

  1. Association between SNPs of metalloproteinases and prostaglandin f2α receptor genes and latanoprost response in open-angle glaucoma

    Ophthalmology, Vol. 122, Núm. 5, pp. 1040-1048.e4

  2. Predicting proliferative vitreoretinopathy: Temporal and external validation of models based on genetic and clinical variables

    British Journal of Ophthalmology, Vol. 99, Núm. 1, pp. 41-48

2013

  1. A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy

    Investigative Ophthalmology and Visual Science, Vol. 54, Núm. 3, pp. 1665-1678

2011

  1. Consensus on paediatric enteral nutrition access: A document approved by SENPE/SEGHNP/ANECIPN/SECP

    Nutricion Hospitalaria, Vol. 26, Núm. 1, pp. 1-15