E
Elina A. M. Hirvonen
Researcher at University of Helsinki
Publications - 8
Citations - 114
Elina A. M. Hirvonen is an academic researcher from University of Helsinki. The author has contributed to research in topics: Germline mutation & Myeloid. The author has an hindex of 4, co-authored 8 publications receiving 80 citations.
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Journal ArticleDOI
Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans.
Eevi Kaasinen,Outi Kuismin,Outi Kuismin,Kristiina Rajamäki,Heikki Ristolainen,Mervi Aavikko,Johanna Kondelin,Silva Saarinen,Davide G. Berta,Riku Katainen,Elina A. M. Hirvonen,Auli Karhu,Aurora Taira,Tomas Tanskanen,Amjad Alkodsi,Minna Taipale,Ekaterina Morgunova,Kaarle Franssila,Rainer Lehtonen,Markus J. Mäkinen,Kristiina Aittomäki,Aarno Palotie,Aarno Palotie,Aarno Palotie,Mitja I. Kurki,Olli Pietilainen,Morgane Hilpert,Elmo Saarentaus,Jaakko Niinimäki,Jaakko Niinimäki,Juhani Junttila,Kari Kaikkonen,Pia Vahteristo,Radek C. Skoda,Mikko Seppänen,Kari K. Eklund,Jussi Taipale,Jussi Taipale,Outi Kilpivaara,Lauri A. Aaltonen,Lauri A. Aaltonen +40 more
TL;DR: Findings provide insight into the interplay between epigenetic modulators and transcription factor activity in hematological neoplasia, but do not confirm the putative role of TET2 in atherosclerosis.
Journal ArticleDOI
Germline alterations in a consecutive series of acute myeloid leukemia.
Ulla Wartiovaara-Kautto,Elina A. M. Hirvonen,Esa Pitkänen,Caroline A. Heckman,Janna Saarela,Kaisa Kettunen,Kimmo Porkka,Outi Kilpivaara +7 more
TL;DR: A systematic analysis of a consecutive series of primary and secondary adult AML patients diagnosed during 2015–2016 in the Helsinki University Hospital (HUH) district found that variant carriers more often had a positive family history of malignancies compared with non-carriers.
Journal ArticleDOI
Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera.
Elina A. M. Hirvonen,Esa Pitkänen,Kari Hemminki,Lauri A. Aaltonen,Lauri A. Aaltonen,Outi Kilpivaara +5 more
TL;DR: This is the first report on Finnish familial PV cases, and exome sequencing provides a powerful tool for the identification of novel variants, and understanding the familial predisposition of diseases.
Journal ArticleDOI
Towards in cellulo virus crystallography
Helen M. E. Duyvesteyn,Helen M. Ginn,Maija K. Pietilä,Armin Wagner,Johan Hattne,Johan Hattne,Jonathan M. Grimes,Elina A. M. Hirvonen,Gwyndaf Evans,Marie-Laure Parsy,Nicholas K. Sauter,Aaron S. Brewster,Juha T. Huiskonen,Juha T. Huiskonen,David I. Stuart,Geoff Sutton,Dennis H. Bamford +16 more
TL;DR: Novel methodology is used to determine a putative space group, unit cell dimensions, particle packing and likely maturation state of the particles in the cells, due to a far from optimal experimental setup.
Journal ArticleDOI
Characterization of an X-chromosome-linked telomere biology disorder in females with DKC1 mutation
Elina A. M. Hirvonen,Saara Peuhkuri,Anna Norberg,Sofie Degerman,Katariina Hannula-Jouppi,Katariina Hannula-Jouppi,Hannamari Välimaa,Outi Kilpivaara,Ulla Wartiovaara-Kautto +8 more
TL;DR: Characterization of an X-chromosome-linked telomere biology disorder in females with DKC1 mutation and its role in apoptosis in young girls is studied.