Articles 2025

Boilard E, Burger D, Buzas E, Gresele P, Machlus KR, Mackman N, Siljander P, Nieuwland R. Deciphering Platelets: Are They Cells or an Evolved Form of Extracellular Vesicles? Circ Res. 2025 Feb 14;136(4):442-452. doi: 10.1161/CIRCRESAHA.124.324721. Epub 2025 Feb 13. PMID: 39946441.

Ilvonen P, Susila S, Impola U, Pusa R, Helin T, Joutsi-Korhonen L, Laitinen S, Lauronen J, Ilmakunnas M. Extracellular vesicles in ageing cold-stored whole blood may not compensate for the decreasing haemostatic function in vitro. Transfus Med. 2025 Jan 24. doi: 10.1111/tme.13122. Epub ahead of print. PMID: 39865366.

Pitkänen HH, Helin T, Khawaja T, Pietilä JP, Kajova M, Välimaa H, Vahlberg T, Ihalainen J, Vierikko A, Vapalahti O, Kantele A, Lassila R. Coagulation Profile of Convalescent Plasma Donors and Recipients. Clin Appl Thromb Hemost. 2025 Jan-Dec;31:10760296251317522. doi: 10.1177/10760296251317522. PMID: 39886886.

Susila S, Helin T, Joutsi-Korhonen L, Lauronen J, Ilmakunnas M. Quality of whole blood stored in room temperature for up to 5 days. Transfusion. 2025 Feb 5. doi: 10.1111/trf.18133. Epub ahead of print. PMID: 39908257.

Consortium publications

Räsänen J, Helisalmi S, Heikkinen S, Raivo J, Korhonen VE, Martiskainen H, Junkkari A, Grenier-Boley B, Bellenguez C, Oinas M, Avellan C, Frantzen J, Kotkansalo A, Rinne J, Ronkainen A, Kauppinen M, von Und Zu Fraunberg M, Lönnrot K, Satopää J, Perola M, Koivisto AM, Julkunen V, Portaankorva AM, Mannermaa A, Soininen H, Jääskeläinen JE, Lambert JC, Eide PK; FinnGen; Palotie A, Kurki MI, Hiltunen M, Leinonen V, Lipponen A. Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study. Fluids Barriers CNS. 2025 Feb 13;22(1):17. doi: 10.1186/s12987-025-00625-0. PMID: 39948543.

Weng LC, Rämö JT, Jurgens SJ, Khurshid S, Chaffin M, Hall AW, Morrill VN, Wang X, Nauffal V, Sun YV, Beer D, Lee S, Nadkarni GN, Duong T, Wang B, Czuba T, Austin TR, Yoneda ZT, Friedman DJ, Clayton A, Hyman MC, Judy RL, Skanes AC, Orland KM, Treu TM, Oetjens MT, Alonso A, Soliman EZ, Lin H, Lunetta KL, van der Pals J, Issa TZ, Nafissi NA, May HT, Leong-Sit P, Roselli C, Choi SH; FinnGen; Million Veteran Program; Regeneron Genetics Center; Khan HR, Knight S, Karlsson Linnér R, Bezzina CR, Ripatti S, Heckbert SR, Gaziano JM, Loos RJF, Psaty BM, Smith JG, Benjamin EJ, Arking DE, Rader DJ, Shah SH, Roden DM, Damrauer SM, Eckhardt LL, Roberts JD, Cutler MJ, Shoemaker MB, Haggerty CM, Cho K, Palotie A, Wilson PWF, Ellinor PT, Lubitz SA. The impact of common and rare genetic variants on bradyarrhythmia development. Nat Genet. 2025 Jan 2. doi: 10.1038/s41588-024-01978-2. Epub ahead of print. PMID: 39747593.