Organización Sanitaria Integrada Ezkerraldea-Enkarterri-Cruces
Organización de Osakidetza
University of Chicago
Chicago, Estados UnidosPublikationen in Zusammenarbeit mit Forschern von University of Chicago (18)
2024
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Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study
Brain, Vol. 147, Núm. 8, pp. 2652-2667
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The prognostic value of blood cellular indices in pulmonary embolism
American Journal of Hematology, Vol. 99, Núm. 9, pp. 1704-1711
2022
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Development of a core outcome set for lateral elbow tendinopathy (COS-LET) using best available evidence and an international consensus process
British Journal of Sports Medicine, Vol. 56, Núm. 12, pp. 657-666
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Gluten-induced RNA methylation changes regulate intestinal inflammation via allele-specific XPO1 translation in epithelial cells
Gut, Vol. 71, Núm. 1, pp. 68-77
2021
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Timing and characteristics of venous thromboembolism after noncancer surgery
Journal of Vascular Surgery: Venous and Lymphatic Disorders, Vol. 9, Núm. 4, pp. 859-867.e2
2020
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Real-Time Dissemination of Aggregate Data on Presentation and Outcomes of Patients With Venous Thromboembolism: The RIETE Infographics Project
Clinical and Applied Thrombosis/Hemostasis, Vol. 26
2018
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Biomarkers of carcinogenesis and tumour growth in patients with cutaneous melanoma and obstructive sleep apnoea
European Respiratory Journal, Vol. 51, Núm. 3
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Sleep-Disordered Breathing Is Independently Associated With Increased Aggressiveness of Cutaneous Melanoma: A Multicenter Observational Study in 443 Patients
Chest, Vol. 154, Núm. 6, pp. 1348-1358
2017
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Nature Genetics, Vol. 49, Núm. 12, pp. 1767-1778
2015
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Exploring genetic factors involved in huntington disease age of onset: E2F2 as a new potential modifier gene
PLoS ONE, Vol. 10, Núm. 7
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High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation
Human Mutation, Vol. 36, Núm. 11, pp. 1052-1063
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Inflammation: A possible mechanism for a causative role of hyperuricemia/gout in cardiovascular disease
Current Medical Research and Opinion
2014
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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nature Genetics, Vol. 46, Núm. 9, pp. 989-993
2012
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Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Cancer Epidemiology Biomarkers and Prevention, Vol. 21, Núm. 4, pp. 645-657
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Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: A systematic analysis for the Global Burden of Disease Study 2010
The Lancet, Vol. 380, Núm. 9859, pp. 2197-2223
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Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: A systematic analysis for the Global Burden of Disease Study 2010
The Lancet, Vol. 380, Núm. 9859, pp. 2095-2128
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Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: A systematic analysis for the Global Burden of Disease Study 2010
The Lancet, Vol. 380, Núm. 9859, pp. 2163-2196
2005
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Outcome measures for acute and chronic gout
Journal of Rheumatology