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Megy K, Downes K, Morel-Kopp MC, Bastida JM, Brooks S, Bury L, Leinoe E, Gomez K, Morgan NV, Othman M, Ouwehand WH, Botero JP, Rivera J, Schulze H, Tregouet DA, Freson K. Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021 Oct;19(10):2612-2617]. J Thromb Haemost. 2023 Apr;21(4):1067. doi: 10.1016/j.jtha.2023.01.021. Epub 2023 Feb 1. No abstract available. PubMed PMID: 36737374; PubMed Central PMCID: PMC10501975.
AÑO: 2023; IF: 5.5
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36737374
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Marin-Quilez A, Diaz-Ajenjo L, Di Buduo CA, Zamora-Canovas A, Lozano ML, Benito R, Gonzalez-Porras JR, Balduini A, Rivera J, Bastida JM. Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation. Int J Mol Sci. 2023 Mar 7;24(6):5109. doi: 10.3390/ijms24065109. PubMed PMID: 36982178; PubMed Central PMCID: PMC10049517.
AÑO: 2023; IF: 4.9
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Marin-Quilez A, Di Buduo CA, Diaz-Ajenjo L, Abbonante V, Vuelta E, Soprano PM, Miguel-Garcia C, Santos-Minguez S, Serramito-Gomez I, Ruiz-Sala P, Penarrubia MJ, Pardal E, Hernandez-Rivas JM, Gonzalez-Porras JR, Garcia-Tunon I, Benito R, Rivera J, Balduini A, Bastida JM. Novel variants in GALE cause syndromic macrothrombocytopenia by disrupting glycosylation and thrombopoiesis. Blood. 2023 Jan 26;141(4):406-421. doi: 10.1182/blood.2022016995. PubMed PMID: 36395340; PubMed Central PMCID: PMC10644051.
AÑO: 2023; IF: 21.0
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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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Zaninetti C, Leinoe E, Lozano ML, Rossing M, Bastida JM, Zetterberg E, Rivera J, Greinacher A. Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders. J Thromb Haemost. 2023 Apr;21(4):1010-1019. doi: 10.1016/j.jtha.2022.12.031. Epub 2023 Jan 10. PubMed PMID: 36732160.
AÑO: 2023; IF: 5.5
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