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Torres-Esquius S, Beas F, Chen-Liang TH, Pomares H, Santiago M, Varela ND, Liquori A, Hernandez F, Xicoy B, Hermosin L, Arnan M, Tazon-Vega B, Blanco A, Cervera J, Diez-Campelo M, Lozano ML, Valcarcel D, Bosch F, Montoro MJ, Jerez A; GESMD centres. Germline assessment for alloHSCT candidates over 50 years: A 'Fast-Track' screening in myeloid neoplasms. Br J Haematol. 2024 Aug;205(2):503-509. doi: 10.1111/bjh.19460. Epub 2024 Apr 19. PubMed PMID: 38639421.
AÑO: 2024; IF: 5.1
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Teruel-Montoya R, Rivera J, Lozano ML. The importance of genetic variant cleaners: From patient to wet lab and back to clinical practice. Br J Haematol. 2024 Dec;205(6):2122-2124. doi: 10.1111/bjh.19818. Epub 2024 Oct 7. PubMed PMID: 39375956.
AÑO: 2024; IF: 5.1
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Cuenca-Zamora EJ, Martinez C, Morales ML, Guijarro-Carrillo PJ, Lopez-Poveda MJ, Alcolea-Guardiola C, Vidal-Garrido N, Lozano ML, Gonzalez-Conejero R, Teruel-Montoya R, Ferrer-Marin F. Pacritinib prevents inflammation-driven myelofibrosis-like phenotype in a miR-146a-/- murine model. Biomed Pharmacother. 2024 Dec;181:117712. doi: 10.1016/j.biopha.2024.117712. Epub 2024 Nov 26. PubMed PMID: 39603040.
AÑO: 2024; IF: 6.9
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Bravo-Perez C, Cifuentes-Riquelme R, Padilla J, de la Morena-Barrio ME, Ortuno FJ, Garrido-Rodriguez P, Amigo ML, Heras I, Vicente V, Lozano ML, Teruel-Montoya R, de la Morena-Barrio B, Corral J. The whole is greater than the sum of its parts: Long-read sequencing for solving clinical problems in haematology. J Cell Mol Med. 2024 Feb;28(3):e17961. doi: 10.1111/jcmm.17961. Epub 2024 Jan 23. No abstract available. PubMed PMID: 38260950; PubMed Central PMCID: PMC10844759.
AÑO: 2024; IF: 4.3
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Palma-Barqueros V, Bastida JM, Lopez Andreo MJ, Zamora-Canovas A, Zaninetti C, Ruiz-Pividal JF, Bohdan N, Padilla J, Teruel-Montoya R, Marin-Quilez A, Revilla N, Sanchez-Fuentes A, Rodriguez-Alen A, Benito R, Vicente V, Iturbe T, Greinacher A, Lozano ML, Rivera J; Grupo Espanol de Alteraciones Plaquetarias Congenitas (GEAPC); Spanish Society of Thrombosis and Haemostasis (SETH). Platelet transcriptome analysis in patients with germline RUNX1 mutations. J Thromb Haemost. 2023 May;21(5):1352-1365. doi: 10.1016/j.jtha.2023.01.023. Epub 2023 Feb 1. PubMed PMID: 36736831.
AÑO: 2023; IF: 5.5
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