Impact of CHEK2 germline variants on haematological malignancy risk and outcomes of allogeneic HSCT

dc.contributor.authorLahtinen, Atte K.
dc.contributor.authorKaru, Maarja
dc.contributor.authorKoski, Jessica R.
dc.contributor.authorRitari, Jarmo
dc.contributor.authorHyvärinen, Kati
dc.contributor.authorKoskela, Satu
dc.contributor.authorNihtilä, Julia
dc.contributor.authorPartanen, Jukka
dc.contributor.authorVettenranta, Kim
dc.contributor.authorKoskenvuo, Minna
dc.contributor.authorNiittyvuopio, Riitta
dc.contributor.authorSalmenniemi, Urpu
dc.contributor.authorItälä‐Remes, Maija
dc.contributor.authorJahnukainen, Kirsi
dc.contributor.authorKilpivaara, Outi
dc.contributor.authorWartiovaara‐Kautto, Ulla
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.converis.publication-id499131612
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/499131612
dc.date.accessioned2025-08-27T21:57:20Z
dc.date.available2025-08-27T21:57:20Z
dc.description.abstract<p><br></p>
dc.format.pagerange636
dc.format.pagerange641
dc.identifier.eissn1365-2141
dc.identifier.jour-issn0007-1048
dc.identifier.olddbid201479
dc.identifier.oldhandle10024/184506
dc.identifier.urihttps://www.utupub.fi/handle/11111/48373
dc.identifier.urlhttps://doi.org/10.1111/bjh.20196
dc.identifier.urnURN:NBN:fi-fe2025082785391
dc.language.isoen
dc.okm.affiliatedauthorItälä-Remes, Maija
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeB1 Other Article
dc.publisherWiley-Blackwell
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumberbjh.20196
dc.relation.doi10.1111/bjh.20196
dc.relation.ispartofjournalBritish Journal of Haematology
dc.relation.issue2
dc.relation.volume207
dc.source.identifierhttps://www.utupub.fi/handle/10024/184506
dc.titleImpact of CHEK2 germline variants on haematological malignancy risk and outcomes of allogeneic HSCT
dc.year.issued2025

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