| Analysis of protein-coding genetic variation in 60,706 humans M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ... Nature 536 (7616), 285-291, 2016 | 10261 | 2016 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1365 | 2018 |
| FinnGen provides genetic insights from a well-phenotyped isolated population MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ... Nature 613 (7944), 508-518, 2023 | 737 | 2023 |
| Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ... Nature genetics 48 (8), 856-866, 2016 | 721 | 2016 |
| A cross-population atlas of genetic associations for 220 human phenotypes S Sakaue, M Kanai, Y Tanigawa, J Karjalainen, M Kurki, S Koshiba, ... Nature genetics 53 (10), 1415-1424, 2021 | 650 | 2021 |
| Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders T Singh, MI Kurki, D Curtis, SM Purcell, L Crooks, J McRae, J Suvisaari, ... Nature neuroscience 19 (4), 571-577, 2016 | 430 | 2016 |
| FinnGen: Unique genetic insights from combining isolated population and national health register data MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ... MedRxiv, 2022.03. 03.22271360, 2022 | 348 | 2022 |
| Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers N Mars, JT Koskela, P Ripatti, TTJ Kiiskinen, AS Havulinna, JV Lindbohm, ... Nature medicine 26 (4), 549-557, 2020 | 315 | 2020 |
| Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ... Molecular psychiatry 25 (8), 1859-1875, 2020 | 234 | 2020 |
| Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ... Cell Genomics 2 (10), 2022 | 182 | 2022 |
| Upregulated signaling pathways in ruptured human saccular intracranial aneurysm wall: an emerging regulative role of Toll-like receptor signaling and nuclear factor-κB, hypoxia … MI Kurki, SK Häkkinen, J Frösen, R Tulamo, M von Und Zu Fraunberg, ... Neurosurgery 68 (6), 1667-1676, 2011 | 141 | 2011 |
| Genetic architecture of human plasma lipidome and its link to cardiovascular disease R Tabassum, JT Rämö, P Ripatti, JT Koskela, M Kurki, J Karjalainen, ... Nature communications 10 (1), 4329, 2019 | 139 | 2019 |
| Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum A Ganna, FK Satterstrom, SM Zekavat, I Das, MI Kurki, C Churchhouse, ... The American Journal of Human Genetics 102 (6), 1204-1211, 2018 | 111 | 2018 |
| Ultra-rare disruptive and damaging mutations influence educational attainment in the general population A Ganna, G Genovese, DP Howrigan, A Byrnes, MI Kurki, SM Zekavat, ... Nature neuroscience 19 (12), 1563-1565, 2016 | 108 | 2016 |
| Poor cognitive outcome in shunt-responsive idiopathic normal pressure hydrocephalus AM Koivisto, I Alafuzoff, S Savolainen, A Sutela, J Rummukainen, M Kurki, ... Neurosurgery 72 (1), 1-8, 2013 | 108 | 2013 |
| GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer W Zhou, B Brumpton, O Kabil, J Gudmundsson, G Thorleifsson, ... Nature communications 11 (1), 3981, 2020 | 100 | 2020 |
| Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health S Strausz, S Ruotsalainen, HM Ollila, J Karjalainen, T Kiiskinen, M Reeve, ... European Respiratory Journal 57 (5), 2021 | 97 | 2021 |
| Common variant burden contributes to the familial aggregation of migraine in 1,589 families P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ... Neuron 98 (4), 743-753. e4, 2018 | 97 | 2018 |
| Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population MA Rivas, BE Avila, J Koskela, H Huang, C Stevens, M Pirinen, ... PLoS genetics 14 (5), e1007329, 2018 | 92 | 2018 |
| Epilepsy after aneurysmal subarachnoid hemorrhage: a population-based, long-term follow-up study J Huttunen, MI Kurki, M von und zu Fraunberg, T Koivisto, A Ronkainen, ... Neurology 84 (22), 2229-2237, 2015 | 92 | 2015 |
