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Page 1
Assessment of the clinical utility of four NGS panels in myeloid malignancies. Suggestions for NGS panel choice or design.
Aguilera-Diaz A, Vazquez I, Ariceta B, Mañú A, Blasco-Iturri Z, Palomino-Echeverría S, Larrayoz MJ, García-Sanz R, Prieto-Conde MI, Del Carmen Chillón M, Alfonso-Pierola A, Prosper F, Fernandez-Mercado M, Calasanz MJ. Aguilera-Diaz A, et al. PLoS One. 2020 Jan 24;15(1):e0227986. doi: 10.1371/journal.pone.0227986. eCollection 2020. PLoS One. 2020. PMID: 31978184 Free PMC article.
The association of increased p14ARF/p16INK4a and p15INK4a gene expression with proliferative activity and the clinical course of multiple myeloma.
Sarasquete ME, García-Sanz R, Armellini A, Fuertes M, Martín-Jiménez P, Sierra M, Del Carmen Chillón M, Alcoceba M, Balanzategui A, Ortega F, Hernández JM, Sureda A, Palomera L, González M, San Miguel JF. Sarasquete ME, et al. Haematologica. 2006 Nov;91(11):1551-4. Epub 2006 Oct 17. Haematologica. 2006. PMID: 17043023
Design and application of a 23-gene panel by next-generation sequencing for inherited coagulation bleeding disorders.
Bastida JM, Del Rey M, Lozano ML, Sarasquete ME, Benito R, Fontecha ME, Fisac R, García-Frade LJ, Aguilar C, Martínez MP, Pardal E, Aguilera C, Pérez B, Ramos R, Cardesa MR, Martin-Antorán JM, Silvestre LA, Cebeira MJ, Bermejo N, Riesco S, Mendoza MC, García-Sanz R, González-Díaz M, Hernández-Rivas JM, González-Porras JR. Bastida JM, et al. Haemophilia. 2016 Jul;22(4):590-7. doi: 10.1111/hae.12908. Epub 2016 Feb 15. Haemophilia. 2016. PMID: 26879396
A Next-Generation Sequencing Strategy for Evaluating the Most Common Genetic Abnormalities in Multiple Myeloma.
Jiménez C, Jara-Acevedo M, Corchete LA, Castillo D, Ordóñez GR, Sarasquete ME, Puig N, Martínez-López J, Prieto-Conde MI, García-Álvarez M, Chillón MC, Balanzategui A, Alcoceba M, Oriol A, Rosiñol L, Palomera L, Teruel AI, Lahuerta JJ, Bladé J, Mateos MV, Orfão A, San Miguel JF, González M, Gutiérrez NC, García-Sanz R. Jiménez C, et al. J Mol Diagn. 2017 Jan;19(1):99-106. doi: 10.1016/j.jmoldx.2016.08.004. Epub 2016 Nov 15. J Mol Diagn. 2017. PMID: 27863261 Free article.
From Waldenström's macroglobulinemia to aggressive diffuse large B-cell lymphoma: a whole-exome analysis of abnormalities leading to transformation.
Jiménez C, Alonso-Álvarez S, Alcoceba M, Ordóñez GR, García-Álvarez M, Prieto-Conde MI, Chillón MC, Balanzategui A, Corral R, Marín LA, Gutiérrez NC, Puig N, Sarasquete ME, González M, García-Sanz R. Jiménez C, et al. Blood Cancer J. 2017 Aug 25;7(8):e591. doi: 10.1038/bcj.2017.72. Blood Cancer J. 2017. PMID: 28841204 Free PMC article.
Unraveling the heterogeneity of IgM monoclonal gammopathies: a gene mutational and gene expression study.
Jiménez C, Prieto-Conde MI, García-Álvarez M, Alcoceba M, Escalante F, Chillón MDC, García de Coca A, Balanzategui A, Cantalapiedra A, Aguilar C, Corral R, González-López T, Marín LA, Bárez A, Puig N, García-Mateo A, Gutiérrez NC, Sarasquete ME, González M, García-Sanz R. Jiménez C, et al. Ann Hematol. 2018 Mar;97(3):475-484. doi: 10.1007/s00277-017-3207-3. Epub 2018 Jan 20. Ann Hematol. 2018. PMID: 29353304
Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder.
Prieto-Conde MI, Labrador J, Hermida G, Alonso S, Jiménez C, García-Álvarez M, Medina A, Balanzategui A, Alcoceba M, Sarasquete ME, Puig N, González V, Gutiérrez NC, García-Sanz R, González-Díaz M, Chillón MDC. Prieto-Conde MI, et al. Leuk Lymphoma. 2020 Jan;61(1):181-184. doi: 10.1080/10428194.2019.1648801. Epub 2019 Aug 6. Leuk Lymphoma. 2020. PMID: 31385734 No abstract available.
A New Next-Generation Sequencing Strategy for the Simultaneous Analysis of Mutations and Chromosomal Rearrangements at DNA Level in Acute Myeloid Leukemia Patients.
Prieto-Conde MI, Corchete LA, García-Álvarez M, Jiménez C, Medina A, Balanzategui A, Hernández-Ruano M, Maldonado R, Sarasquete ME, Alcoceba M, Puig N, González-Calle V, García-Sanz R, Gutiérrez NC, González-Díaz M, Chillón MC. Prieto-Conde MI, et al. J Mol Diagn. 2020 Jan;22(1):60-71. doi: 10.1016/j.jmoldx.2019.08.002. Epub 2019 Oct 9. J Mol Diagn. 2020. PMID: 31605801 Free article.
Reply to Brown et al: 'Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis'.
Prieto-Conde MI, Labrador J, Hermida G, Alonso S, Jiménez C, García-Alvarez M, Medina A, Balanzategui A, Alcoceba M, Sarasquete ME, Puig N, González V, Gutiérrez NC, García-Sanz R, González-Díaz M, Chillón MDC. Prieto-Conde MI, et al. Leuk Lymphoma. 2020 Jan;61(1):248-249. doi: 10.1080/10428194.2019.1680843. Epub 2019 Oct 23. Leuk Lymphoma. 2020. PMID: 31642380 No abstract available.
Identification of relapse-associated gene mutations by next-generation sequencing in low-risk acute myeloid leukaemia patients.
Prieto-Conde MI, Jiménez C, García-Álvarez M, Ramos F, Medina A, Cuello R, Balanzategui A, Alonso JM, Sarasquete ME, Queizán JA, Alcoceba M, Bárez A, Puig N, Cantalapiedra A, Gutiérrez NC, García-Sanz R, González-Díaz M, Chillón MC. Prieto-Conde MI, et al. Br J Haematol. 2020 May;189(4):718-730. doi: 10.1111/bjh.16420. Epub 2020 Mar 2. Br J Haematol. 2020. PMID: 32124426 Free article.
368 results