Research output per year
Research output per year
Personal profile
Fields of Science
- 1184 Genetics, developmental biology, physiology
International and National Collaboration
Publications and projects within past five years.
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Identification of DHX40 as a candidate susceptibility gene for colorectal and hematological neoplasia
Olkinuora, A., Nieminen, T. T., Douglas, S., Kauppinen, A., Kontro, M., Väänänen, J., Kankainen, M., Ristimäki, A., Mäkinen, M., Lahermo, P., Heckman, C., Saarela, J., Salonen, M., Lepistö, A., Järvinen, H., Mecklin, J.-P., Kilpivaara, O., Wartiovaara-Kautto, U., Porkka, K. & Peltomäki, P., 11 Sept 2023, In: Leukemia. 37, 11, p. 2301–2305 5 p.Research output: Contribution to journal › Letter › Scientific
Open AccessFile -
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene
Hackman, P., Rusanen, S. M., Johari, M., Vihola, A., Jonson, P. H., Sarparanta, J., Donner, K., Lahermo, P., Koivunen, S., Luque, H., Soininen, M., Mahjneh, I., Auranen, M., Arumilli, M., Savarese, M. & Udd, B., Dec 2021, In: Neurology Genetics. 7, 6, 10 p., 632.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions
Johari, M., Sarparanta, J., Vihola, A., Jonson, P. H., Savarese, M., Jokela, M., Torella, A., Piluso, G., Said, E., Vella, N., Cauchi, M., Magot, A., Magri, F., Mauri, E., Kornblum, C., Reimann, J., Stojkovic, T., Romero, N. B., Luque, H. & Huovinen, S. & 6 others, , Aug 2021, In: Acta Neuropathologica. 142, p. 375-393 19 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
Genetic background of ataxia in children younger than 5 years in Finland
Ignatius, E., Isohanni, P., Pohjanpelto, M., Lahermo, P., Ojanen, S., Brilhante, V., Palin, E., Suomalainen, A., Lönnqvist, T. & Carroll, C. J., Aug 2020, In: Neurology Genetics. 6, 4, 9 p., 444.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes
Luukkonen, T. M., Mehrjouy, M. M., Pöyhönen, M., Anttonen, A.-K., Lahermo, P., Ellonen, P., Paulin, L., Tommerup, N., Palotie, A. & Varilo, T., Jan 2018, In: Molecular Genetics & Genomic Medicine. 6, 1, p. 56-68 13 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile
Activities
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FIMM Scientific Direction Discussion
Lahermo, P. (Attendee)
15 Aug 2016Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars
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FIMM Scientific Retreat 2016
Lahermo, P. (Attendee)
2 May 2016 → 3 May 2016Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars
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SPR Veripalvelu
Lahermo, P. (Visiting researcher)
2 Dec 2016Activity: Visiting an external institution types › Academic visit to other institution
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Genotyping Unit Data and Quality management day
Lahermo, P. (Attendee)
7 Jun 2016Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars
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Janika Sirjalan insinöörityön ohjaus, Metropolia
Lahermo, P. (Supervisor)
1 Dec 2016 → 31 Mar 2017Activity: Examination types › Supervision of other thesis (Master's, Licentiate)