BIO Investigación vasca en salud
Centro
Essen University Hospital
Essen, AlemaniaPublicaciones en colaboración con investigadores/as de Essen University Hospital (56)
2024
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Longitudinal cerebral perfusion in presymptomatic genetic frontotemporal dementia: GENFI results
Alzheimer's and Dementia, Vol. 20, Núm. 5, pp. 3525-3542
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Metabolic Acidosis Is Associated With an Accelerated Decline of Allograft Function in Pediatric Kidney Transplantation
Kidney International Reports, Vol. 9, Núm. 6, pp. 1684-1693
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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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Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Clinical Epigenetics, Vol. 16, Núm. 1
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Outcomes after surgical revascularization in diabetic patients
Interdisciplinary cardiovascular and thoracic surgery, Vol. 38, Núm. 2
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The “Woundosome” Concept and Its Impact on Procedural Outcomes in Patients With Chronic Limb-Threatening Ischemia
Journal of Endovascular Therapy
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Thyroid hormone receptor alpha modulates fibrogenesis in hepatic stellate cells
Liver International, Vol. 44, Núm. 1, pp. 125-138
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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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A second update on mapping the human genetic architecture of COVID-19
Nature
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EANM practice guideline for quantitative SPECT-CT
European Journal of Nuclear Medicine and Molecular Imaging, Vol. 50, Núm. 4, pp. 980-995
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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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Genetic Associations between Modifiable Risk Factors and Alzheimer Disease
JAMA Network Open, Vol. 6, Núm. 5
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Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
Proceedings of the National Academy of Sciences of the United States of America, Vol. 120, Núm. 36
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Results from an EANM survey on time estimates and personnel responsible for main tasks in molecular radiotherapy dosimetry
European Journal of Nuclear Medicine and Molecular Imaging
2022
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A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
Brain : a journal of neurology, Vol. 145, Núm. 5, pp. 1805-1817
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Association of Rare APOE Missense Variants V236E and R251G with Risk of Alzheimer Disease
JAMA Neurology, Vol. 79, Núm. 7, pp. 652-663
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Bcl-xL as prognostic marker and potential therapeutic target in cholangiocarcinoma
Liver International, Vol. 42, Núm. 12, pp. 2855-2870
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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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Data-driven staging of genetic frontotemporal dementia using multi-modal MRI
Human Brain Mapping, Vol. 43, Núm. 6, pp. 1821-1835
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Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Human Molecular Genetics, Vol. 31, Núm. 23, pp. 3945-3966