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2012 1
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Page 1
NEMHESYS-European Perspective on the Implementation of Next-generation Sequencing Into Clinical Diagnostics.
Serramito-Gómez I, Clarke KM, Rodríguez-Vicente AE, McGimpsey JE, Abáigar M, Díez CB, Benito R, Bullinger L, Mills KI, Hernández Rivas JM. Serramito-Gómez I, et al. Among authors: abaigar m. Hemasphere. 2021 Feb 17;5(3):e541. doi: 10.1097/HS9.0000000000000541. eCollection 2021 Mar. Hemasphere. 2021. PMID: 33623883 Free PMC article. No abstract available.
aCGH-MAS: analysis of aCGH by means of multiagent system.
De Paz JF, Benito R, Bajo J, Rodríguez AE, Abáigar M. De Paz JF, et al. Among authors: abaigar m. Biomed Res Int. 2015;2015:194624. doi: 10.1155/2015/194624. Epub 2015 Mar 22. Biomed Res Int. 2015. PMID: 25874203 Free PMC article. Review.
CLL cells cumulate genetic aberrations prior to the first therapy even in outwardly inactive disease phase.
Hernández-Sánchez M, Kotaskova J, Rodríguez AE, Radova L, Tamborero D, Abáigar M, Plevova K, Benito R, Tom N, Quijada-Álamo M, Bikos V, Martín AÁ, Pal K, García de Coca A, Doubek M, López-Bigas N, Hernández-Rivas JM, Pospisilova S. Hernández-Sánchez M, et al. Among authors: abaigar m. Leukemia. 2019 Feb;33(2):518-558. doi: 10.1038/s41375-018-0255-1. Epub 2018 Sep 12. Leukemia. 2019. PMID: 30209402 Free PMC article. No abstract available.
Co-occurrence of cohesin complex and Ras signaling mutations during progression from myelodysplastic syndromes to secondary acute myeloid leukemia.
Martín-Izquierdo M, Abáigar M, Hernández-Sánchez JM, Tamborero D, López-Cadenas F, Ramos F, Lumbreras E, Madinaveitia-Ochoa A, Megido M, Labrador J, Sánchez-Real J, Olivier C, Dávila J, Aguilar C, Rodríguez JN, Martín-Nuñez G, Santos-Mínguez S, Miguel-García C, Benito R, Díez-Campelo M, Hernández-Rivas JM. Martín-Izquierdo M, et al. Among authors: abaigar m. Haematologica. 2021 Aug 1;106(8):2215-2223. doi: 10.3324/haematol.2020.248807. Haematologica. 2021. PMID: 32675227 Free PMC article.
Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia.
Palomo L, Ibáñez M, Abáigar M, Vázquez I, Álvarez S, Cabezón M, Tazón-Vega B, Rapado I, Fuster-Tormo F, Cervera J, Benito R, Larrayoz MJ, Cigudosa JC, Zamora L, Valcárcel D, Cedena MT, Acha P, Hernández-Sánchez JM, Fernández-Mercado M, Sanz G, Hernández-Rivas JM, Calasanz MJ, Solé F, Such E; Spanish Group of MDS (GESMD). Palomo L, et al. Among authors: abaigar m. Br J Haematol. 2020 Mar;188(5):605-622. doi: 10.1111/bjh.16175. Epub 2019 Oct 16. Br J Haematol. 2020. PMID: 31621063 Free PMC article.
Multicenter Next-Generation Sequencing Studies between Theory and Practice: Harmonization of Data Analysis Using Real-World Myelodysplastic Syndrome Data.
Sandmann S, de Graaf AO, Tobiasson M, Kosmider O, Abáigar M, Clappier E, Gallì A, van der Reijden BA, Malcovati L, Fenaux P, Díez-Campelo M, Fontenay M, Hellström-Lindberg E, Jansen JH, Dugas M. Sandmann S, et al. Among authors: abaigar m. J Mol Diagn. 2021 Mar;23(3):347-357. doi: 10.1016/j.jmoldx.2020.12.001. Epub 2020 Dec 23. J Mol Diagn. 2021. PMID: 33359455 Free article.
Genome-wide transcriptomics leads to the identification of deregulated genes after deferasirox therapy in low-risk MDS patients.
Sánchez JMH, Lumbreras E, Díez-Campelo M, González T, López DA, Abáigar M, Del Rey M, Martín AÁ, de Paz R, Erquiaga S, Arrizabalaga B, Hernández-Rivas JM, Vicente AER. Sánchez JMH, et al. Among authors: abaigar m. Pharmacogenomics J. 2020 Oct;20(5):664-671. doi: 10.1038/s41397-020-0154-5. Epub 2020 Feb 4. Pharmacogenomics J. 2020. PMID: 32015457
Clinical, biological, and prognostic implications of SF3B1 co-occurrence mutations in very low/low- and intermediate-risk MDS patients.
Janusz K, Izquierdo MM, Cadenas FL, Ramos F, Sánchez JMH, Lumbreras E, Robledo C, Del Real JS, Caballero JC, Collado R, Bernal T, Pedro C, Insunza A, de Paz R, Xicoy B, Salido E, García JS, Mínguez SS, García CM, Muñoz AMS, Barba MS, Rivas JMH, Abáigar M, Campelo MD. Janusz K, et al. Among authors: abaigar m. Ann Hematol. 2021 Aug;100(8):1995-2004. doi: 10.1007/s00277-020-04360-4. Epub 2021 Jan 6. Ann Hematol. 2021. PMID: 33409621
Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.
Abáigar M, Robledo C, Benito R, Ramos F, Díez-Campelo M, Hermosín L, Sánchez-Del-Real J, Alonso JM, Cuello R, Megido M, Rodríguez JN, Martín-Núñez G, Aguilar C, Vargas M, Martín AA, García JL, Kohlmann A, Del Cañizo MC, Hernández-Rivas JM. Abáigar M, et al. PLoS One. 2016 Oct 14;11(10):e0164370. doi: 10.1371/journal.pone.0164370. eCollection 2016. PLoS One. 2016. PMID: 27741277 Free PMC article.
Outcomes and effect of somatic mutations after erythropoiesis stimulating agents in patients with lower-risk myelodysplastic syndromes.
Caballero JC, Dávila J, López-Pavía M, Such E, Bernal T, Ramos F, Calabuig M, Hernández Sánchez JM, Pomares H, Sánchez Barba M, Abáigar M, González B, Merchán B, Sancho-Tello R, Callejas M, Muñoz-Novas C, Cerveró C, Sanz G, Hernández Rivas JM, Díez Campelo M. Caballero JC, et al. Among authors: abaigar m. Ther Adv Hematol. 2024 Jan 4;15:20406207231218157. doi: 10.1177/20406207231218157. eCollection 2024. Ther Adv Hematol. 2024. PMID: 38186638 Free PMC article.
24 results