BIO Investigación vasca en salud
Centro
Catholic University of the Sacred Heart
Milán, ItaliaPublicaciones en colaboración con investigadores/as de Catholic University of the Sacred Heart (70)
2024
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At-admission prediction of mortality and pulmonary embolism in an international cohort of hospitalised patients with COVID-19 using statistical and machine learning methods
Scientific Reports, Vol. 14, Núm. 1
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Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
Brain : a journal of neurology, Vol. 147, Núm. 5, pp. 1887-1898
2023
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A patient-driven registry on Behçet’s disease: the AIDA for patients pilot project
Frontiers in Medicine, Vol. 10
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Circular and Circulating DNA in Inflammatory Bowel Disease: From Pathogenesis to Potential Molecular Therapies
Cells, Vol. 12, Núm. 15
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Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer” (eBioMedicine (2023) 92, (S2352396423001810), (10.1016/j.ebiom.2023.104616))
eBioMedicine
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Dissecting the genetic heterogeneity of gastric cancer
eBioMedicine, Vol. 92
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Efficacy and Safety of Adalimumab in Pediatric Non-infectious Non-anterior Uveitis: Real-life Experience From the International AIDA Network Uveitis Registry
Ophthalmology and Therapy, Vol. 12, Núm. 4, pp. 1957-1971
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Empirical rescue treatment of Helicobacter pylori infection in third and subsequent lines: 8-year experience in 2144 patients from the European Registry on H. pylori management (Hp-EuReg)
Gut, Vol. 72, Núm. 6, pp. 1054-1072
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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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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
The Lancet. Oncology, Vol. 24, Núm. 1, pp. 91-106
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Impact of lymph node ratio and number of lymph node metastases on survival and recurrence in laryngeal squamous cell carcinoma
Head and Neck, Vol. 45, Núm. 9, pp. 2274-2293
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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
2022
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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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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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ISARIC-COVID-19 dataset: A Prospective, Standardized, Global Dataset of Patients Hospitalized with COVID-19
Scientific Data, Vol. 9, Núm. 1
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New insights into the genetic etiology of Alzheimer's disease and related dementias
Nature genetics, Vol. 54, Núm. 4, pp. 412-436
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Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study
Nephrology Dialysis Transplantation, Vol. 37, Núm. 12, pp. 2474-2486
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Presentations of children to emergency departments across Europe and the COVID-19 pandemic: A multinational observational study
PLoS medicine, Vol. 19, Núm. 8, pp. e1003974
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SUCCOR quality: validation of ESGO quality indicators for surgical treatment of cervical cancer
International Journal of Gynecological Cancer, Vol. 32, Núm. 10, pp. 1236-1243