FAC MEDICINA
Centro
University College London
Londres, Reino UnidoPublicaciones en colaboración con investigadores/as de University College London (51)
2024
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Visualization and Identification of Silicone Oil Emulsification Using Dynamic Infrared Confocal Scanning Laser Ophthalmoscopy
Case Reports in Ophthalmology, pp. 36-40
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What can we learn from general practitioners who left Spain? A mixed methods international study
Human Resources for Health, Vol. 22, Núm. 1
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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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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Quantitative aortography for assessment of aortic regurgitation in the era of percutaneous aortic valve replacement
Frontiers in Cardiovascular Medicine, Vol. 10
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Use of aequorin-based indicators for monitoring Ca2+ in acidic organelles
Biochimica et Biophysica Acta - Molecular Cell Research, Vol. 1870, Núm. 6
2022
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Whole-genome sequencing reveals host factors underlying critical COVID-19
Nature, Vol. 607, Núm. 7917, pp. 97-103
2021
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Elective Cancer Surgery in COVID-19-Free Surgical Pathways during the SARS-CoV-2 Pandemic: An International, Multicenter, Comparative Cohort Study
Journal of Clinical Oncology, Vol. 39, Núm. 1, pp. 66-78
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Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
Molecular Psychiatry, Vol. 26, Núm. 9, pp. 5307-5319
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Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)
European Journal of Immunology, Vol. 51, Núm. 12, pp. 2708-3145
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Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
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Smart Nanoparticles as Advanced Anti-Akt Kinase Delivery Systems for Pancreatic Cancer Therapy
ACS Applied Materials and Interfaces, Vol. 13, Núm. 47, pp. 55790-55805
2020
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Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy
Clinical Genetics, Vol. 98, Núm. 1, pp. 86-90
2019
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Corrigendum to Supplemental Material: ‘D242N, a K V 7.1 LQTS mutation uncovers a key residue for I Ks voltage dependence’ [Journal of Molecular and Cellular Cardiology, Volume 110, September 2017, Pages 61–69](S0022282817301633)(10.1016/j.yjmcc.2017.07.009)
Journal of Molecular and Cellular Cardiology
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Prospective observational cohort study on grading the severity of postoperative complications in global surgery research
British Journal of Surgery, Vol. 106, Núm. 2, pp. e73-e80
2018
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A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 177, Núm. 1, pp. 21-34
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Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains
Psychological Medicine, Vol. 48, Núm. 8, pp. 1325-1340
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Effectiveness of the physical activity intervention program in the PREDIMED-Plus study: A randomized controlled trial 11 Medical and Health Sciences 1117 Public Health and Health Services
International Journal of Behavioral Nutrition and Physical Activity, Vol. 15, Núm. 1
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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy
Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2457-2467
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Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: data from the E-HOD registry
Journal of Inherited Metabolic Disease