Research output per year
Research output per year
Personal profile
Fields of Science
- 1184 Genetics, developmental biology, physiology
- 3111 Biomedicine
- 3142 Public health care science, environmental and occupational health
International and National Collaboration
Publications and projects within past five years.
Publications
- 6 Article
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Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA
FinnGen, Tervi, A., Junna, N., Broberg, M., Jones, S. E., Strausz, S., Kreivi, H-R., Heckman, C. A. & Ollila, H. M., 1 Jan 2023, In: Human Molecular Genetics. 32, 1, p. 161–171 11 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open Access -
How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study
Widen, E., Junna, N., Ruotsalainen, S., Surakka, I., Mars, N., Ripatti, P., Partanen, J. J., Aro, J., Mustonen, P., Tuomi, T., Palotie, A., Salomaa, V., Kaprio, J., Partanen, J., Hotakainen, K., Pöllänen, P. & Ripatti, S., Apr 2022, In: Circulation-Genomic and precision medicine. 15, 2, p. 91-99 9 p., 003459.Research output: Contribution to journal › Article › Scientific › peer-review
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LIN28B affects gene expression at the hypothalamic-pituitary axis and serum testosterone levels
Leinonen, J. T., Chen, Y-C., Pennonen, J., Lehtonen, L., Junna, N., Tukiainen, T., Panula, P. & Widen, E., 2 Dec 2019, In: Scientific Reports. 9, 13 p., 18060.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?
Leinonen, J. T., Crotti, L., Djupsjobacka, A., Castelletti, S., Junna, N., Ghidoni, A., Tuiskula, A. M., Spazzolini, C., Dagradi, F., Viitasalo, M., Kontula, K., Kotta, M-C., Widen, E., Swan, H. & Schwartz, P. J., 1 Jan 2018, In: International Journal of Cardiology. 250, p. 139-145 7 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy
Lee, J-R., Srour, M., Kim, D., Hamdan, F. F., Lim, S-H., Brunel-Guitton, C., Decarie, J-C., Rossignol, E., Mitchell, G. A., Schreiber, A., Moran, R., Van Haren, K., Richardson, R., Nicolai, J., Oberndorff, K. M. E. J., Wagner, J. D., Boycott, K. M., Rahikkala, E., Junna, N., Tyynismaa, H., & 10 others, Jan 2015, In: Human Mutation. 36, 1, p. 69-78 10 p.Research output: Contribution to journal › Article › Scientific › peer-review
Projects
- 1 Active
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CoECDG: Center of Excellence in Complex Disease Genetics-from Discovery to Precision Medicine
Junna, N., Ranta, A. K. & Widen, E.
Suomen Akatemia Projektilaskutus
01/01/2023 → 31/12/2025
Project: Academy of Finland: Centres of Exellence funding
Activities
- 4 Organisation and participation in conferences, workshops, courses, seminars
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87th Congress of the European-Atherosclerosis-Society (EAS)
Nella Junna (Attendee)
26 May 2019 → 29 May 2019Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars
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The European Human Genetics Conference 2018
Nella Junna (Attendee)
16 Jun 2018 → 19 Jun 2018Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars
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The European Human Genetics Conference 2017
Nella Junna (Attendee)
27 May 2017 → 30 May 2017Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars
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American Society of Human Genetics Meeting 2017
Nella Junna (Attendee)
17 Oct 2017 → 21 Oct 2017Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars