Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Hautakangas H, Winsvold BS, Ruotsalainen SE, Bjornsdottir G, Harder AVE, …, Ripatti S, Zwart JA, Palotie A, Pirinen M (2022), Nature Genetics 54: 152-160.
Bayesian mixture model for clustering rare-variant effects in human genetic studies. Venkataraman GR, DeBoever C, Tanigawa Y, Aguirre M, Ioannidis AG, Mostafavi H, Spencer CCA, Poterba T, Bustamante CD, Daly MJ, Pirinen M, Rivas MA (2021), The American Journal of Human Genetics 108: 2354-2367.
Changes in the fine-scale genetic structure of Finland through the 20th century. Kerminen S, Cerioli N, Pacauskas D, Havulinna AS, Perola M, Jousilahti P, Salomaa V, Daly MJ, Vyas R, Ripatti S, Pirinen M (2021), PLoS Genetics.
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland. Kerminen S, Martin AR, Koskela J, Ruotsalainen S, Havulinna AS, Surakka I, Palotie A, Perola M, Salomaa V, Daly MJ, Ripatti S, Pirinen M (2019), The American Journal of Human Genetics 10.1016/j.ajhg.2019.05.001.
Bayesian meta-analysis across genome-wide association studies of diverse phenotypes. Trochet H*, Pirinen M*, Band G, Jostins L, McVean G, Spencer CCA (2019), Genetic Epidemiology, 43: 532-547.