Research output per year
Research output per year
International and National Collaboration
Publications and projects within past five years.
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Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Int Headache Genetics Consortium, HUNT All-in Headache & Danish Blood Donor Study Genomic C, Feb 2022, In: Nature Genetics. 54, 2, p. 152-+ 16 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
Nuottamo, M. E., Häppölä, P., Artto, V., Hautakangas, H., Pirinen, M., Hiekkalinna, T., Ellonen, P., Lepistö, M., Hämäläinen, E., Siren, A., Lehesjoki, A-E., Kallela, M., Palotie, A., Kaunisto, M. A. & Wessman, M., Jun 2022, In: Cephalalgia. 42, 7, p. 631-644 14 p., 03331024211068065.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families
IHGC, Häppölä, P., Gormley, P., Nuottamo, M. E., Artto, V., Sumelahti, M-L., Nissilä, M., Keski-Santti, P., Ilmavirta, M., Kaunisto, M. A., Hämäläinen, E. I., Ripatti, S., Pirinen, M., Wessman, M., Palotie, A. & Kallela, M., Apr 2022, In: Cephalalgia. 42, 4-5, p. 345-356 12 p., 03331024211045651.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
Translating genetic epidemiology to health applications with large-scale biobank data
Häppölä, P., 2022, Helsinki: Helsingin yliopisto. 95 p.Research output: Thesis › Doctoral Thesis › Collection of Articles
Open Access -
Familial hypercholesterolaemia and LDL-C polygenic risk in patients with severe carotid artery stenosis
Ijäs, P., Kemppainen, K., Häppölä, P., Eriksson, H., Sebastian, R., Palta, P., Nuotio, K., Vikatmaa, P., Soinne, L., Lindsberg, P. J. & Kovanen, P. T., 1 Aug 2021, In: Atherosclerosis. 331, 1 p., e48.Research output: Contribution to journal › Meeting Abstract › peer-review
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CoECDG: Center of Excellence in Complex Disease Genetics-from Discovery to Precision Medicine
Suomen Akatemia Projektilaskutus
01/01/2023 → 31/12/2025
Project: Academy of Finland: Centres of Exellence funding
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Persinalized disease risk assessment platform
Palta, P., Häppölä, P. & Koskela, J.
01/06/2018 → 31/12/2019
Project: Research project