Persones / Equip Humà

Veronica Celis Passini

Buscador de publicacions

Publicacions

  • CastilloSD, Perosanz X, Ressler AK, Ivars M, Rodriguez J, Rovira-Zurriaga C, Nola EM, Llena J, Grego-Bessa J, Roldan-Molina M, Arnau R, Martínez-Romero A, Barber-Martínez de la Torre I, Miguel Bejarano Serrano, Vicente-Villa MA, Celis-Passini V, Salvador-Hernandez H, Mora J, Marchuk DA, Baselga E and Graupera M.

    Somatic Uniparental Disomy of PTEN in Endothelial Cells Causes Vascular Malformations in Patients with PTEN Hamartoma Tumor Syndrome

    CANCER DISCOVERY . 15(7): 1350-1362. Nº de cites: 2

    [doi:10.1158/2159-8290.CD-24-0807]

  • Mato S, Carità L, Colmenero A, Andrés M, Balagué O, Andión M, Astigarraga I, Celis-Passini V, Mendoza C, Guerra-García P, Valero L, Galera A, Tallón M, Pol M, Castrejón-de-Anta N, Frauenfeld L, Garcia N, Campo E, Salaverria I and Verdú-Amorós J.

    Comprehensive analysis of relapsed-refractory mature B-cell non-Hodgkin lymphoma in children and adolescents

    BRITISH JOURNAL OF HAEMATOLOGY . 206(5): 1390-1396.

    [doi:10.1111/bjh.20012]

  • Mato S, Castrejón-de-Anta N, Colmenero A, Carità L, Salmerón-Villalobos J, Ramis-Zaldivar JE, Nadeu F, Garcia N, Wang L, Verdú-Amorós J, Andrés M, Conde N, Celis-Passini V, Ortega MJ, Galera A, Astigarraga I, Perez-Alonso V, Quiroga E, Jiang A, Scott DW, Campo E, Balagué O and Salaverria I.

    MYC-rearranged mature B-cell lymphomas in children and young adults are molecularly Burkitt Lymphoma

    BLOOD CANCER JOURNAL . 14(1): 171-171. Nº de cites: 1

    [doi:10.1038/s41408-024-01153-0]

  • Sánchez-Espino LF, Ivars M, Prat-Torres CS, Lavarino C, Gene-Olaciregui N, Rovira-Zurriaga C, Celis-Passini V, Miguel Bejarano Serrano and Baselga E.

    Single dominant lesion in capillary malformation-arteriovenous malformation (CM-AVM) RASA1 syndrome

    PEDIATRIC DERMATOLOGY . 41(5): 861-865. Nº de cites: 1

    [doi:10.1111/pde.15598]

  • Salmerón-Villalobos J, Castrejon-de-Anta N, Guerra-Garcia P, Ramis-Zaldivar JE, López-Guerra M, Mato S, Colomer D, Diaz Crespo FJ, Menarguez J, Garrido-Pontnou M, Andres M, Garcia-Fernandez E, Llavador M, Frigola G, Garcia N, Gonzalez-Farre B, Martin-Guerrero I, Garrido-Colino C, Astigarraga I, Fernandez A, Verdu-Amorós J, Gonzalez Muñiz S, González-Martínez B, Celis-Passini V, Campo E, Balagué O and Salaverria I.

    Decoding the molecular heterogeneity of pediatric monomorphic post-solid organ transplant lymphoproliferative disorders

    Blood . 142(5): 434-445. Nº de cites: 10

    [doi:10.1182/blood.2022019543]

  • Salmerón-Villalobos J, Ramis-Zaldivar JE, Balagué O, Verdú-Amorós J, Celis-Passini V, Sábado C, Garrido M, Mato S, Uriz J, Ortega MJ, Gutierrez-Camino A, Sinnett D, Illarregi U, Carron M, Regueiro A, Galera A, Gonzalez-Farré B, Campo E, Garcia N, Colomer D, Astigarraga I, Andrés M, Llavador M, Martin-Guerrero I and Salaverria I.

    Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma

    PEDIATRIC BLOOD & CANCER . 69(11): . Nº de cites: 7

    [doi:10.1002/pbc.29926]

  • Kobialka P, Sabata H, Vilalta O, Gouveia L, Angulo-Urarte A, Muixí L, Zanoncello J, Muñoz-Aznar O, Gene-Olaciregui N, Fanlo L, Esteve-Codina A, Lavarino C, Javierre BM, Celis-Passini V, Rovira-Zurriaga C, López-Fernández S, Baselga E, Mora J, CastilloSD and Graupera M.

    The onset of PI3K-related vascular malformations occurs during angiogenesis and is prevented by the AKT inhibitor miransertib

    EMBO Molecular Medicine . 14(7): . Nº de cites: 37

    [doi:10.15252/emmm.202115619]

  • Viñas-Giménez L, Rincón R, Colobran R, de la Cruz X, Celis-Passini V, Dapena JL, Alsina L, Sayós J and Martínez-Gallo M.

    Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient With Hemophagocytic Syndrome and Langerhans Cell Histiocytosis

    FRONTIERS IN IMMUNOLOGY . 12: 723836-723836. Nº de cites: 3

    [doi:10.3389/fimmu.2021.723836]

  • Carrere X, Pinto N, Gene-Olaciregui N, Galluzzo L, Rossetti E, Celis-Passini V, Salvador-Marcos N, Chantada G, Braier J, Lavarino C and Felizzia G.

    High prevalence of BRAF(V600E) in patients with cholestasis, sclerosing cholangitis or liver fibrosis secondary to Langerhans cell histiocytosis

    PEDIATRIC BLOOD & CANCER . 68(7): 29115. Nº de cites: 4

    [doi:10.1002/pbc.29115]

  • Castillo H, Pascual-Pastó G, Pérez-Jaume S, Resa-Parés C, Vilà-Ubach M, Monterrubio C, Jimenez-Cabaco A, Baulenas-Farrés M, Muñoz-Aznar O, Salvador-Marcos N, Cuadrado-Vilanova M, Gene-Olaciregui N, Balaguer-Lluna L, Burgeño-Sandoval V, Vicario FJ, Manzanares-Quintela A, Castañeda-Heredia A, Santa-María López V, Cruz-Martínez O, Celis-Passini V, Morales-La Madrid A, Garraus-Oneca M, Gorostegui M, Vancells M, Carrasco-Torrents R, Krauel L, Torner-Rubies F, Suñol M, Lavarino C, Mora J and Carcaboso AM.

    Prognostic value of patient-derived xenograft engraftment in pediatric sarcomas

    JOURNAL OF PATHOLOGY CLINICAL RESEARCH . 7(4): 338-349. Nº de cites: 21

    [doi:10.1002/cjp2.210]