María Isabel Prieto-Conde (Isabel Prieto-Conde)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 5

Top Venues

Leukemia & lymphoma

Blood cancer journal

British journal of haematology

This page only lists publications with an associated author ORCID identifier.

Publications

María García-Álvarez, Sara Alonso-Álvarez, María Isabel Prieto-Conde, Cristina Jiménez, María Eugenia Sarasquete, M Carmen Chillón, Alejandro Medina Herrera, Ana Balanzategui, Rebeca Maldonado, Alicia Antón, Marta Rodríguez, Oscar Blanco, Luis G Díaz, Pilar Tamayo, Pedro Blanco, Carmen Esteban, Verónica González-Calle, Noemí Puig, Norma Gutiérrez, Alejandro Martín, Miriam Santero, Marcos González, M Dolores Caballero, Miguel Alcoceba
Genetic complexity impacts the clinical outcome of follicular lymphoma patients. Blood cancer journal 11 (1) (2021)
María Isabel Prieto-Conde, Cristina Jiménez, María García-Álvarez, Fernando Ramos, Alejandro Medina, Rebeca Cuello, Ana Balanzategui, José M Alonso, Maria Eugenia Sarasquete, José Antonio Queizán, Miguel Alcoceba, Abelardo Bárez, Noemi Puig, Alberto Cantalapiedra, Norma C Gutiérrez, Ramón García-Sanz, Marcos González-Díaz, María Carmen Chillón
Identification of relapse-associated gene mutations by next-generation sequencing in low-risk acute myeloid leukaemia patients. British journal of haematology 189 (4) (2020)
Alejandro Medina Herrera, Cristina Jiménez, M Eugenia Sarasquete, Marcos González, M Carmen Chillón, Ana Balanzategui, María Isabel Prieto-Conde, María García-Álvarez, Noemí Puig, Verónica González-Calle, Miguel Alcoceba, Isabel Cuenca, Santiago Barrio, Fernando Escalante, Norma C Gutiérrez, Mercedes Gironella, Miguel T Hernández, Anna Sureda, Albert Oriol, Joan Bladé, Juan-José Lahuerta, Jesús F San Miguel, Maria-Victoria Mateos-Manteca, Joaquín Martínez-López, María-José Calasanz, Miriam Santero
Molecular profiling of immunoglobulin heavy-chain gene rearrangements unveils new potential prognostic markers for multiple myeloma patients. Blood cancer journal 10 (2) (2020)
María Isabel Prieto-Conde, Jorge Labrador, Gerardo Hermida, Sara Alonso, Cristina Jiménez, María García-Alvarez, Alejandro Medina, Ana Balanzategui, Miguel Alcoceba, María Eugenia Sarasquete, Noemí Puig, Verónica González, Norma C Gutiérrez, Ramón García-Sanz, Marcos González-Díaz, María Del Carmen Chillón
Reply to Brown et al: 'Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis'. Leukemia & lymphoma 61 (1) (2019)
María Isabel Prieto-Conde, Jorge Labrador, Gerardo Hermida, Sara Alonso, Cristina Jiménez, María García-Álvarez, Alejandro Medina, Ana Balanzategui, Miguel Alcoceba, María Eugenia Sarasquete, Noemí Puig, Verónica González, Norma C Gutiérrez, Ramón García-Sanz, Marcos González-Díaz, María Del Carmen Chillón
Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder. Leukemia & lymphoma 61 (1) (2019)

María Isabel Prieto-Conde.css-eqlu8i{font-size:small;padding-left:4px;} (Isabel Prieto-Conde)

Publication Activity (10 Years)

Top Topics

Top Venues

María Isabel Prieto-Conde (Isabel Prieto-Conde)