Biogipuzkoa
Centro de investigación
Queen Mary University of London
Londres, Reino UnidoPublicaciones en colaboración con investigadores/as de Queen Mary University of London (50)
2024
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Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches
Journal of Extracellular Vesicles, Vol. 13, Núm. 2
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Neuronal alpha-Synuclein Disease integrated staging system performance in PPMI, PASADENA, and SPARK baseline cohorts
npj Parkinson's Disease, Vol. 10, Núm. 1
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Achilles tendon forces and pain during common rehabilitation exercises in male runners with Achilles tendinopathy. A laboratory study
Physical Therapy in Sport, Vol. 60, pp. 26-33
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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
2022
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Association between use of enhanced recovery after surgery protocols and postoperative complications in colorectal surgery in Europe: The EuroPOWER international observational study
Journal of Clinical Anesthesia, Vol. 80
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Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization
The Journal of clinical endocrinology and metabolism, Vol. 107, Núm. 7, pp. e2952-e2961
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Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses
Circulation, Vol. 146, Núm. 20, pp. 1507-1517
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Recreational runners with Achilles tendinopathy have clinically detectable impairments: A case-control study
Physical Therapy in Sport, Vol. 55, pp. 241-247
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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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Blood Metal Levels and Amyotrophic Lateral Sclerosis Risk: A Prospective Cohort
Annals of Neurology, Vol. 89, Núm. 1, pp. 125-133
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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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Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
Nature Genetics, Vol. 53, Núm. 11, pp. 1543-1552
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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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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Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
Annals of Neurology, Vol. 90, Núm. 1, pp. 35-42
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Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
2020
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Alcohol Consumption and Risk of Parkinson's Disease: Data From a Large Prospective European Cohort
Movement Disorders, Vol. 35, Núm. 7, pp. 1258-1263
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Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study
Scientific Data
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Identification of recurrent mutations in the microrna‐binding sites of b‐cell lymphoma‐ associated genes in follicular lymphoma
International Journal of Molecular Sciences, Vol. 21, Núm. 22, pp. 1-12