Organización Sanitaria Integrada Ezkerraldea-Enkarterri-Cruces
Organización de Osakidetza
VU University Medical Center
Ámsterdam, HolandaPublications en collaboration avec des chercheurs de VU University Medical Center (21)
2023
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Evaluating the Construct of Damage in Systemic Lupus Erythematosus
Arthritis Care and Research, Vol. 75, Núm. 5, pp. 998-1006
2020
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Systematic review of educational interventions to improve contouring in radiotherapy
Radiotherapy and Oncology, Vol. 144, pp. 86-92
2018
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Prognosis of sporadic resected small (≤2 cm) nonfunctional pancreatic neuroendocrine tumors – a multi-institutional study
HPB, Vol. 20, Núm. 3, pp. 251-259
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
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Sunitinib-induced hypertension in CYP3A4 rs4646437 A-allele carriers with metastatic renal cell carcinoma
Pharmacogenomics Journal, Vol. 17, Núm. 1, pp. 42-46
2016
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Off-label use of rituximab for systemic lupus erythematosus in Europe
Lupus Science and Medicine, Vol. 3, Núm. 1
2015
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Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
JAMA - Journal of the American Medical Association, Vol. 313, Núm. 13, pp. 1347-1361
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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 2, pp. 296-312
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Information Flow between Resting-State Networks
Brain Connectivity, Vol. 5, Núm. 9, pp. 554-564
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Pharmacogenomic study in patients with multiple sclerosis Responders and nonresponders to IFN-β
Neurology: Neuroimmunology and NeuroInflammation, Vol. 2, Núm. 5, pp. e154
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
2013
2012
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A European multicentre photopatch test study
British Journal of Dermatology, Vol. 166, Núm. 5, pp. 1002-1009
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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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Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
Human Mutation, Vol. 33, Núm. 4, pp. 690-702
2011
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Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
Journal of the National Cancer Institute, Vol. 103, Núm. 2, pp. 105-116
2010
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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction
Cancer Research, Vol. 70, Núm. 23, pp. 9742-9754
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Deferasirox in iron-overloaded patients with transfusion-dependent myelodysplastic syndromes: Results from the large 1-year EPIC study
Leukemia Research, Vol. 34, Núm. 9, pp. 1143-1150
2009
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Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
Nature Genetics, Vol. 41, Núm. 7, pp. 829-832
2007
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Clinical and molecular phenotype of Aicardi-Goutières syndrome
American Journal of Human Genetics, Vol. 81, Núm. 4, pp. 713-725