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Page 1
Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans.
Kaasinen E, Kuismin O, Rajamäki K, Ristolainen H, Aavikko M, Kondelin J, Saarinen S, Berta DG, Katainen R, Hirvonen EAM, Karhu A, Taira A, Tanskanen T, Alkodsi A, Taipale M, Morgunova E, Franssila K, Lehtonen R, Mäkinen M, Aittomäki K, Palotie A, Kurki MI, Pietiläinen O, Hilpert M, Saarentaus E, Niinimäki J, Junttila J, Kaikkonen K, Vahteristo P, Skoda RC, Seppänen MRJ, Eklund KK, Taipale J, Kilpivaara O, Aaltonen LA. Kaasinen E, et al. Among authors: franssila k. Nat Commun. 2019 Mar 19;10(1):1252. doi: 10.1038/s41467-019-09198-7. Nat Commun. 2019. PMID: 30890702 Free PMC article.
Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphoma.
Saarinen S, Aavikko M, Aittomäki K, Launonen V, Lehtonen R, Franssila K, Lehtonen HJ, Kaasinen E, Broderick P, Tarkkanen J, Bain BJ, Bauduer F, Ünal A, Swerdlow AJ, Cooke R, Mäkinen MJ, Houlston R, Vahteristo P, Aaltonen LA. Saarinen S, et al. Among authors: franssila k. Blood. 2011 Jul 21;118(3):493-8. doi: 10.1182/blood-2011-03-341560. Epub 2011 May 11. Blood. 2011. PMID: 21562039 Free article.
Analysis of KLHDC8B in familial nodular lymphocyte predominant Hodgkin lymphoma.
Saarinen S, Vahteristo P, Launonen V, Franssila K, Kivirikko S, Lehtonen R, Bain BJ, Bauduer F, Ünal A, Aaltonen LA, Aittomäki K. Saarinen S, et al. Among authors: franssila k. Br J Haematol. 2011 Aug;154(3):413-5. doi: 10.1111/j.1365-2141.2010.08528.x. Epub 2011 Apr 22. Br J Haematol. 2011. PMID: 21517803 Free article. No abstract available.
PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas.
Zhu Y, Loukola A, Monni O, Kuokkanen K, Franssila K, Elonen E, Vilpo J, Joensuu H, Kere J, Aaltonen L, Knuutila S. Zhu Y, et al. Among authors: franssila k. Leuk Lymphoma. 2001 Mar;41(1-2):177-83. doi: 10.3109/10428190109057968. Leuk Lymphoma. 2001. PMID: 11342371
154 results