José Rivera Pozo

Marin-Quilez A, Vuelta E, Diaz-Ajenjo L, Fernandez-Infante C, Garcia-Tunon I, Benito R, Palma-Barqueros V, Hernandez-Rivas JM, Gonzalez-Porras JR, Rivera J, Bastida JM. A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling. J Thromb Haemost. 2022 May;20(5):1248-1255. doi: 10.1111/jth.15672. Epub 2022 Feb 28. PubMed PMID: 35170221; PubMed Central PMCID: PMC9306899.

AÑO: 2022; IF: 10.4

35170221

Balduini C, Freson K, Greinacher A, Gresele P, Kuhne T, Scully M, Bakchoul T, Coppo P, Dovc Drnovsek T, Godeau B, Gruel Y, Rao AK, Kremer Hovinga JA, Makris M, Matzdorff A, Mumford A, Pecci A, Raslova H, Rivera J, Roberts I, Scharf RE, Semple JW, Van Geet C. The EHA Research Roadmap: Platelet Disorders. Hemasphere. 2021 Jun 30;5(7):e601. doi: 10.1097/HS9.0000000000000601. eCollection 2021 Jul. No abstract available. PubMed PMID: 34476343; PubMed Central PMCID: PMC8386910.

AÑO: 2021; IF: 8.3

34476343

Frelinger AL 3rd, Rivera J, Connor DE, Freson K, Greinacher A, Harrison P, Kunishima S, Lordkipanidze M, Michelson AD, Ramstrom S, Gresele P. Consensus recommendations on flow cytometry for the assessment of inherited and acquired disorders of platelet number and function: Communication from the ISTH SSC Subcommittee on Platelet Physiology. J Thromb Haemost. 2021 Dec;19(12):3193-3202. doi: 10.1111/jth.15526. Epub 2021 Sep 27. PubMed PMID: 34580997.

AÑO: 2021; IF: 16.036

34580997

Palma-Barqueros V, Crescente M, de la Morena ME, Chan MV, Almarza E, Revilla N, Bohdan N, Minano A, Padilla J, Allan HE, Maffucci T, Edin ML, Zeldin DC, Mesa-Nunez C, Damian C, Marin-Quilez A, Benito R, Martinez-Martinez I, Bermejo N, Casas-Aviles I, Rodriguez-Alen A, Gonzalez-Porras JR, Hernandez-Rivas JM, Vicente V, Corral J, Lozano ML, Warner TD, Bastida JM, Rivera J. A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis. Am J Hematol. 2021 Mar 1;96(3):E83-E88. doi: 10.1002/ajh.26076. Epub 2021 Jan 5. No abstract available. PubMed PMID: 33326144; PubMed Central PMCID: PMC10938055.

AÑO: 2021; IF: 13.265

33326144

Megy K, Downes K, Morel-Kopp MC, Bastida JM, Brooks S, Bury L, Leinoe E, Gomez K, Morgan NV, Othman M, Ouwehand WH, Perez Botero J, Rivera J, Schulze H, Tregouet DA, Freson K. 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. doi: 10.1111/jth.15459. Epub 2021 Aug 5. Erratum In: J Thromb Haemost. 2023 Apr;21(4):1067. PubMed PMID: 34355501; PubMed Central PMCID: PMC9291976.

AÑO: 2021; IF: 16.036

34355501