Projects per year
Organization profile
The Ripatti group studies genome-wide variation and its relation to complex traits and diseases, with a particular focus, but not limited to, on cardiovascular diseases and metabolism. We build on our understanding of genome-wide variation, Finnish genetically and epidemiologically well-profiled cohorts and knowledge and development of statistical and computational tools, and aim at identifying variants, genes and genetic loci modifying complex disease risks. We also study ways to translate the findings into potential intervention targets and comprehensive disease risk assessments.
International and National Collaboration
Publications and projects within past five years.
Profiles
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Paavo Häppölä
- Institute for Molecular Medicine Finland - Bioinformatician
- Complex Disease Genetics
- Genomics of Neurological and Neuropsychiatric Disorders
Person: M5 Teaching and research support staff
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Aki Havulinna
- Medicum - Title of Docent
- Institute for Molecular Medicine Finland - Senior Researcher
- Complex Disease Genetics
Person: U3 Research and teaching staff
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Finngen: FinnGen
Palotie, A., Pitkänen, K., Jalanko, A., Lyhs, U., Donner, K. M., Kaunisto, M., Kurki, M. I., Kristiansson, K., Laiho, P., Laivuori, H., Loukola, A., Palta, P., Perola, M., Kajanne, R., Harju, J. J. & Havulinna, A.
15/08/2017 → …
Project: Research project
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Department of Public Health, University of Helsinki
Wedenoja, J., Kaprio, J., Loukola, A., Korhonen, T., Hällfors, J., Heikkilä, K., Ripatti, S. & Tikkanen, E.
01/04/2011 → …
Project: Research project
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Persinalized disease risk assessment platform
Palta, P., Häppölä, P. & Koskela, J.
01/06/2018 → 31/12/2019
Project: Research project
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ePerMed: Rise of scientific excellence and collaboratio for implementing personalised medicine in Estonia
01/01/2016 → 31/12/2018
Project: Other project
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FinnGen provides genetic insights from a well-phenotyped isolated population
Kurki, M., Karjalainen, J. M., Palta, P., Sipilä, T., Kristiansson, K., Donner, K. M., Reeve, M. P., Laivuori, H., Aavikko, M., Kaunisto, M., Loukola, A., Lahtela, L. E., Mattsson, H. & Laiho, P., 18 Jan 2023, In: Nature.Research output: Contribution to journal › Article › Scientific › peer-review
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Psoriatic arthritis, axial spondyloarthritis and rheumatoid arthritis in Norway: nationwide prevalence and use of biologic agents
Kerola, A. M., Rollefstad, S., Kazemi, A., Wibetoe, G., Sexton, J., Mars, N., Kauppi, M., Kvien, T. K., Haavardsholm, E. A. & Semb, A. G., 2 Jan 2023, In: Scandinavian Journal of Rheumatology. 52, 1, p. 42-50 9 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
The validity of rheumatoid arthritis diagnoses in Finnish biobanks
FinnGen Investigators, Paltta, J., Heikkilä, H-K., Pirilä, L., Eklund, K. K., Huhtakangas, J., Isomäki, P., Kaipiainen-Seppänen, O., Kristiansson, K., Havulinna, A. S., Sokka-Isler, T. & Palomäki, A., 2 Jan 2023, In: Scandinavian Journal of Rheumatology. 52, 1, p. 1-9 9 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
A genome-wide association study of outcome from traumatic brain injury
Genetic Assoc Neurotrauma Gain Con, CENTER-TBI, CABI, MGB, TBIcare Studies, Kals, M., Kunzmann, K., Parodi, L., Palotie, A., Ripatti, S. & Menon, D. K., Mar 2022, In: EBioMedicine. 77, 12 p., 103933.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
Million Veterans Program, Global Lipids Genetics Consortium, Ramdas, S., Judd, J., Graham, S. E., Surakka, I., Havulinna, A. S., Weir, D. R., Ruotsalainen, S. E., Loukola, A., Bollepalli, S., Kaprio, J., Koistinen, H. A., Kivimäki, M., Ripatti, S., Widén, E., Tuomilehto, J., Jousilahti, P. & Sun, Y. V., 4 Aug 2022, In: American Journal of Human Genetics. 109, 8, p. 1366-1387 23 p.Research output: Contribution to journal › Article › Scientific › peer-review
Activities
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Finnish examples of good practice: Clinical genomics
Samuli Ripatti (Speaker)
1 Feb 2023Activity: Talk or presentation types › Invited talk
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ERC Consolidator Grant 2022 Step 1 (Event)
Samuli Ripatti (Board member)
14 Jun 2022 → 16 Jun 2022Activity: Membership types › Membership or other role in review committee
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Biostatistiikka ja laskennalliset menetelmät väitöskirjatyössä
Samuli Ripatti (Speaker)
31 May 2022Activity: Talk or presentation types › Oral presentation
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Genomics-based personalised medicine – experience from Finland
Samuli Ripatti (Speaker)
1 Jun 2022Activity: Talk or presentation types › Oral presentation
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Polygenic Risk Score: From Research Towards Clinics
Samuli Ripatti (Speaker)
28 Mar 2022Activity: Talk or presentation types › Invited talk
Prizes
Press / Media
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Haastattelu Tiedeykkösessä: Vaihdetaanko labrojen poistogeeniset hiiret suomalaisiin, joilla on vastaavat sammuneet geenit?
14/09/2021
1 Media contribution
Press/Media: Press / Media
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Genes and sleep apnea associated with risk for severe COVID-19
01/06/2021
1 item of Media coverage
Press/Media: Press / Media
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Lähes joka toinen 50–70-vuotiaan koronatartunta oireeton: geenit vaikuttavat taudin vakavuuteen
30/05/2021
1 item of Media coverage
Press/Media: Press / Media
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Suomessa selvitettiin: Lähes joka toinen 50–70-vuotiaiden koronatartunta oireeton, perimä vaikuttaa tautimuotoon
30/05/2021
1 item of Media coverage
Press/Media: Press / Media