Publicaciones (15) Publicaciones de Susana Riesco Riesco

2023

  1. Immune stress suppresses innate immune signaling in preleukemic precursor B-cells to provoke leukemia in predisposed mice

    Nature Communications, Vol. 14, Núm. 1

  2. Lessons from mouse models in the impact of risk factors on the genesis of childhood B-cell leukemia

    Frontiers in Immunology

2022

  1. Childhood B-Cell Preleukemia Mouse Modeling

    International Journal of Molecular Sciences, Vol. 23, Núm. 14

  2. Transient Inhibition of the JAK/STAT Pathway Prevents B-ALL Development in Genetically Predisposed Mice

    Cancer research, Vol. 82, Núm. 6, pp. 1098-1109

2021

  1. Cribado neonatal de drepanocitosis en Castilla y León: Estudio descriptivo

    Boletin de pediatria, Vol. 61, Núm. 257, pp. 160-165

  2. Cáncer de tiroides en pediatría

    Revista ORL, Vol. 12, Vol. 4, pp. 303-312

  3. Juvenile myelomonocytic leukemia in CBL syndrome associated with germline splice-site mutations: Two case reports and a literature review

    Clinical Case Reports, Vol. 9, Núm. 5

2020

  1. Helpful criteria when implementing ngs panels in childhood lymphoblastic leukemia

    Journal of Personalized Medicine, Vol. 10, Núm. 4, pp. 1-15

2019

  1. Hipoxemia como única manifestación de hemoglobinopatía estructural

    Revista Pediatría de Atención Primaria, Vol. 21, Núm. 83, pp. 10

2018

  1. Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders

    Haematologica, Vol. 103, Núm. 1, pp. 148-162

2017

  1. Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes

    Thrombosis and Haemostasis, Vol. 117, Núm. 1, pp. 66-74

  2. Mutations in TP53 and JAK2 are independent prognostic biomarkers in B-cell precursor acute lymphoblastic leukaemia

    British Journal of Cancer, Vol. 117, Núm. 2, pp. 256-265

  3. Wiskott–Aldrich syndrome in a child presenting with macrothrombocytopenia

    Platelets, Vol. 28, Núm. 4, pp. 417-420

2016

  1. Design and application of a 23-gene panel by next-generation sequencing for inherited coagulation bleeding disorders

    Haemophilia, Vol. 22, Núm. 4, pp. 590-597

  2. Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome

    PloS one, Vol. 11, Núm. 2, pp. e0148972