| De novo mutations in schizophrenia implicate synaptic networks M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ... Nature 506 (7487), 179-184, 2014 | 1787 | 2014 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1366 | 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 | 774 | 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 | 727 | 2016 |
| A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2 RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ... Nature 463 (7281), 671-675, 2010 | 591 | 2010 |
| Genome-wide meta-analysis identifies new susceptibility loci for migraine V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ... Nature genetics 45 (8), 912-917, 2013 | 460 | 2013 |
| Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ... PLoS genetics 6 (2), e1000841, 2010 | 458 | 2010 |
| Distribution and medical impact of loss-of-function variants in the Finnish founder population ET Lim, P Würtz, AS Havulinna, P Palta, T Tukiainen, K Rehnström, ... PLoS genetics 10 (7), e1004494, 2014 | 444 | 2014 |
| 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 | 354 | 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 |
| Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel M Mitt, M Kals, K Pärn, SB Gabriel, ES Lander, A Palotie, S Ripatti, ... European Journal of Human Genetics 25 (7), 869-876, 2017 | 190 | 2017 |
| 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 | 183 | 2022 |
| 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 | 140 | 2019 |
| Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants R Malik, T Freilinger, BS Winsvold, V Anttila, J Vander Heiden, M Traylor, ... Neurology 84 (21), 2132-2145, 2015 | 129 | 2015 |
| A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip® for methylome profiling C Clark, P Palta, CJ Joyce, C Scott, E Grundberg, P Deloukas, A Palotie, ... PloS one 7 (11), e50233, 2012 | 117 | 2012 |
| The role of polygenic risk and susceptibility genes in breast cancer over the course of life N Mars, E Widén, S Kerminen, T Meretoja, M Pirinen, ... Nature communications 11 (1), 6383, 2020 | 103 | 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 | 99 | 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 |
| The GENCODE exome: sequencing the complete human exome AJ Coffey, F Kokocinski, MS Calafato, CE Scott, P Palta, E Drury, ... European journal of human genetics 19 (7), 827-831, 2011 | 85 | 2011 |
| Polygenic hyperlipidemias and coronary artery disease risk P Ripatti, JT Rämö, NJ Mars, Y Fu, J Lin, S Söderlund, C Benner, ... Circulation: Genomic and Precision Medicine 13 (4), e002725, 2020 | 81 | 2020 |
