María Isabel Prieto-Conde

5PUBLICATIONS
8CO-AUTHORS
Cancer geneticsEpigenetics (incl. genome methylation and epigenomics)Immunogenetics (incl. genetic immunology)Gene expression (incl. microarray and other genome-wide approaches)Cardiovascular medicine and haematology not elsewhere classified
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Publications (5)

|Jan 12, 2021
Genetic complexity impacts the clinical outcome of follicular lymphoma patients.

María García-Álvarez, Sara Alonso-Álvarez, Isabel Prieto-Conde

|Mar 04, 2020
Identification of relapse-associated gene mutations by next-generation sequencing in low-risk acute myeloid leukaemia patients.

María Isabel Prieto-Conde, Cristina Jiménez, María García-Álvarez

|Feb 08, 2020
Molecular profiling of immunoglobulin heavy-chain gene rearrangements unveils new potential prognostic markers for multiple myeloma patients.

Alejandro Medina, Cristina Jiménez, M Eugenia Sarasquete

|Oct 24, 2019
Reply to Brown et al: 'Correct application of variant classification guidelines in germline <i>RUNX1</i> mutated disorders to assist clinical diagnosis'.

María Isabel Prieto-Conde, Jorge Labrador, Gerardo Hermida

|Aug 07, 2019
Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited <i>RUNX1</i> mutations without a pre-existing platelet disorder.

María Isabel Prieto-Conde, Jorge Labrador, Gerardo Hermida

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Frequent Collaborators

3 joint publications

Miguel Alcoceba

2 joint publications

Alejandro Medina

2 joint publications

Ramón García-Sanz

1 joint publications

María-Victoria Mateos