| 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 | 1508* | 2023 |
| Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ... Nature genetics 54 (5), 560-572, 2022 | 355 | 2022 |
| Attention decay in science P della Briotta Parolo, RK Pan, R Ghosh, BA Huberman, K Kaski, ... Journal of Informetrics 9 (4), 734-745, 2015 | 204 | 2015 |
| Genetic analyses identify widespread sex-differential participation bias N Pirastu, M Cordioli, P Nandakumar, G Mignogna, A Abdellaoui, B Hollis, ... Nature Genetics 53 (5), 663-671, 2021 | 189 | 2021 |
| 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 | 148 | 2019 |
| 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 | 112 | 2020 |
| Systematic comparison of family history and polygenic risk across 24 common diseases N Mars, JV Lindbohm, P della Briotta Parolo, E Widén, J Kaprio, A Palotie, ... The American Journal of Human Genetics 109 (12), 2152-2162, 2022 | 76 | 2022 |
| Genome-wide risk prediction of common diseases across ancestries in one million people N Mars, S Kerminen, YCA Feng, M Kanai, K Läll, LF Thomas, AH Skogholt, ... Cell Genomics 2 (4), 2022 | 58 | 2022 |
| Growing time lag threatens Nobels S Fortunato, A Chatterjee, M Mitrovic, R Pan, P della Briotta Parolo, ... Nature 508 (7495), 186, 2014 | 48* | 2014 |
| Genetic risk factors associated with preeclampsia and hypertensive disorders of pregnancy JS Tyrmi, T Kaartokallio, AI Lokki, T Jääskeläinen, E Kortelainen, ... JAMA cardiology 8 (7), 674-683, 2023 | 31 | 2023 |
| Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices P Natarajan, A Pampana, SE Graham, SE Ruotsalainen, JA Perry, ... Nature communications 12 (1), 2182, 2021 | 17 | 2021 |
| The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections SE Jones, FI Maisha, SJ Strausz, V Lammi, BE Cade, A Tervi, ... Ebiomedicine 93, 2023 | 13 | 2023 |
| Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis SE Ruotsalainen, I Surakka, N Mars, J Karjalainen, M Kurki, M Kanai, ... Communications biology 5 (1), 802, 2022 | 11 | 2022 |
| Prediction and impact of personalized donation intervals J Toivonen, Y Koski, E Turkulainen, F Prinsze, P della Briotta Parolo, ... Vox Sanguinis 117 (4), 504-512, 2022 | 11 | 2022 |
| Association of the MYOC p.(Gln368Ter) Variant with Glaucoma in a Finnish Population PJ Liuska, S Lemmelä, AS Havulinna, K Kaarniranta, H Uusitalo, ... JAMA ophthalmology 139 (7), 762-768, 2021 | 9 | 2021 |
| Tracking the cumulative knowledge spreading in a comprehensive citation network P della Briotta Parolo, R Kujala, K Kaski, M Kivelä Physical Review Research 2 (1), 013181, 2020 | 9* | 2020 |
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| Comprehensive inherited risk estimation for risk-based breast cancer screening in women N Mars, S Kerminen, M Tamlander, M Pirinen, E Jakkula, K Aaltonen, ... Journal of Clinical Oncology 42 (13), 1477-1487, 2024 | 5 | 2024 |
| Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals R Ågren, S Patil, X Zhou, K Sahlholm, S Pääbo, H Zeberg Molecular biology and evolution 40 (6), msad130, 2023 | 3 | 2023 |
| High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases O Youssef, A Loukola, YHS Zidi-Mouaffak, M Tamlander, S Ruotsalainen, ... Laboratory Investigation 104 (4), 100325, 2024 | | 2024 |
