Grupo de genetica y epigenetica de enfermedades complejas
Instituto de Investigación Sanitaria Biocruces Bizkaia
Barakaldo, EspañaPublicaciones en colaboración con investigadoras/es de Instituto de Investigación Sanitaria Biocruces Bizkaia (83)
2024
2023
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Analysis of germline variants in pediatric patients diagnosed with desmoid tumors and nuchal-type fibromas
Translational Pediatrics, Vol. 12, Núm. 9, pp. 1715-1724
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Decoding the molecular heterogeneity of pediatric monomorphic post–solid organ transplant lymphoproliferative disorders
Blood, Vol. 142, Núm. 5, pp. 434-445
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Genetics and Epigenetics in Complex Diseases
International Journal of Molecular Sciences
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How do hospitalised children die? The context of death and end-of-life decision-making
Journal of Paediatrics and Child Health, Vol. 59, Núm. 4, pp. 625-630
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Identification of germline cancer predisposition variants in pediatric sarcoma patients from somatic tumor testing
Scientific Reports, Vol. 13, Núm. 1
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Molecular characterisation defines clinically-actionable heterogeneity within Group 4 medulloblastoma and improves disease risk-stratification
Acta Neuropathologica, Vol. 145, Núm. 5, pp. 651-666
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The Role of the Dysregulation of Long Non-Coding and Circular RNA Expression in Medulloblastoma: A Systematic Review
Cancers, Vol. 15, Núm. 19
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microRNA sequencing for biomarker detection in the diagnosis, classification and prognosis of Diffuse Large B Cell Lymphoma
Scientific reports, Vol. 13, Núm. 1, pp. 12159
2022
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A Three-Protein Panel to Support the Diagnosis of Sepsis in Children
Journal of Clinical Medicine, Vol. 11, Núm. 6
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Characteristics of white blood cell count in acute lymphoblastic leukemia: A COST LEGEND phenotype–genotype study
Pediatric Blood and Cancer, Vol. 69, Núm. 6
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Clinical management of the acute complications of sickle cell anemia: 11 years of experience in a tertiary hospital
Anales de Pediatria, Vol. 97, Núm. 1, pp. 4-11
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Clinical spectrum of COVID-19 and risk factors associated with severity in Spanish children
European journal of pediatrics, Vol. 181, Núm. 3, pp. 1105-1115
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Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma
Pediatric Blood and Cancer, Vol. 69, Núm. 11
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Identification and Functional Analysis of a Novel CTNNB1 Mutation in Pediatric Medulloblastoma
Cancers, Vol. 14, Núm. 2
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Langerhans cell histiocytosis. Advances in pathogenesis and clinical practice
Anales de Pediatria, Vol. 97, Núm. 2, pp. 130.e1-130.e7
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Methionine adenosyltransferase 1a antisense oligonucleotides activate the liver-brown adipose tissue axis preventing obesity and associated hepatosteatosis
Nature Communications, Vol. 13, Núm. 1
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MicroRNA-based therapeutic strategies for cancer
MicroRNA: From Bench to Bedside (Elsevier), pp. 503-520
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Neutropenia en la infancia. De la teoría a la práctica clínica, a propósito de dos casos clínicos
Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 123, pp. 129-136
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Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma
New England Journal of Medicine, Vol. 386, Núm. 26, pp. 2471-2481