Biobizkaia
Centro de investigación
University of Liverpool
Liverpool, Reino UnidoPublicaciones en colaboración con investigadores/as de University of Liverpool (36)
2024
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Type 1 Autoimmune Pancreatitis in Europe: Clinical Profile and Response to Treatment
Clinical Gastroenterology and Hepatology, Vol. 22, Núm. 5, pp. 994-1004.e10
2023
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Disruption of Dcp1 leads to a Dcp2-dependent aberrant ribosome profiles in Aspergillus nidulans
Molecular Microbiology, Vol. 119, Núm. 5, pp. 630-639
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Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x)
Nature
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Global Incidence and Risk Factors Associated with Postoperative Urinary Retention Following Elective Inguinal Hernia Repair: The Retention of Urine after Inguinal Hernia Elective Repair (RETAINER I) Study
JAMA Surgery, Vol. 158, Núm. 8, pp. 865-873
2022
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CT or Invasive Coronary Angiography in Stable Chest Pain
New England Journal of Medicine, Vol. 386, Núm. 17, pp. 1591-1602
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Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
Human Genetics, Vol. 141, Núm. 1, pp. 147-173
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Factors associated with clinical progression to severe COVID-19 in people with cystic fibrosis: A global observational study
Journal of Cystic Fibrosis, Vol. 21, Núm. 4, pp. e221-e231
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Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (Nature, (2022), 611, 7934, (115-123), 10.1038/s41586-022-05165-3)
Nature
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Stroke genetics informs drug discovery and risk prediction across ancestries
Nature, Vol. 611, Núm. 7934, pp. 115-123
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Validation of the OAKS prognostic model for acute kidney injury after gastrointestinal surgery
BJS Open, Vol. 6, Núm. 1
2021
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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Nature Communications, Vol. 12, Núm. 1
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Genetic mechanisms of critical illness in COVID-19
Nature, Vol. 591, Núm. 7848, pp. 92-98
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Histone mRNA is subject to 3′ uridylation and re-adenylation in Aspergillus nidulans
Molecular Microbiology, Vol. 115, Núm. 2, pp. 238-254
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Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage
Nature Communications, Vol. 12, Núm. 1
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Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
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The ethics of preconception expanded carrier screening in patients seeking assisted reproduction
Human Reproduction Open, Vol. 2021, Núm. 1
2020
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Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Nature Communications, Vol. 11, Núm. 1
2019
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Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
npj Parkinson's Disease, Vol. 5, Núm. 1
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Molecular epidemiology of G12 rotavirus strains during eight consecutive epidemic seasons in the Basque Country (North of Spain), 2010–2018
Infection, Genetics and Evolution, Vol. 71, pp. 67-75
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Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
npj Parkinson's Disease, Vol. 5, Núm. 1