| 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 | 742 | 2016 |
| 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 | 333 | 2022 |
| The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis T Fall, S Hägg, R Maegi, A Ploner, K Fischer, M Horikoshi, AP Sarin, ... PLoS medicine 10 (6), e1001474, 2013 | 251 | 2013 |
| 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 | 208 | 2017 |
| Adiposity as a cause of cardiovascular disease: a Mendelian randomization study S Hägg, T Fall, A Ploner, R Mägi, K Fischer, HHM Draisma, M Kals, ... International journal of epidemiology 44 (2), 578-586, 2015 | 167 | 2015 |
| Genetic and epigenetic regulation of gene expression in fetal and adult human livers MJ Bonder, S Kasela, M Kals, R Tamm, K Lokk, I Barragan, WA Buurman, ... BMC genomics 15, 1-13, 2014 | 140 | 2014 |
| Clear differences in adiponectin level and glutathione redox status revealed in obese and normal‐weight patients with psoriasis S Kaur, K Zilmer, C Kairane, M Kals, M Zilmer British Journal of Dermatology 159 (6), 1364-1367, 2008 | 120 | 2008 |
| Evidence of inbreeding depression on human height R McQuillan, N Eklund, N Pirastu, M Kuningas, BP McEvoy, T Esko, ... PLoS genetics 8 (7), e1002655, 2012 | 119 | 2012 |
| 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 | 111 | 2016 |
| Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions S Reisberg, K Krebs, M Lepamets, M Kals, R Mägi, K Metsalu, ... Genetics in Medicine 21 (6), 1345-1354, 2019 | 98 | 2019 |
| Age-and sex-specific causal effects of adiposity on cardiovascular risk factors T Fall, S Hägg, A Ploner, R Mägi, K Fischer, HHM Draisma, AP Sarin, ... Diabetes 64 (5), 1841-1852, 2015 | 90 | 2015 |
| A Missense Mutation in DUSP6 is Associated with Class III Malocclusion T Nikopensius, M Saag, T Jagomägi, T Annilo, M Kals, PA Kivistik, ... Journal of dental research 92 (10), 893-898, 2013 | 86 | 2013 |
| De NovoSCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and … U Vaher, M Nõukas, T Nikopensius, M Kals, T Annilo, M Nelis, K Õunap, ... Journal of child neurology 29 (12), NP202-NP206, 2014 | 83 | 2014 |
| Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function M Ivanov, M Kals, M Kacevska, I Barragan, K Kasuga, A Rane, A Metspalu, ... Genome biology 14, 1-15, 2013 | 74 | 2013 |
| Inflammation and oxidative stress are associated differently with endothelial function and arterial stiffness in healthy subjects and in patients with atherosclerosis J Kals, P Kampus, M Kals, A Pulges, R Teesalu, K Zilmer, T Kullisaar, ... Scandinavian Journal of Clinical and Laboratory Investigation 68 (7), 594-601, 2008 | 73 | 2008 |
| Impact of oxidative stress on arterial elasticity in patients with atherosclerosis J Kals, P Kampus, M Kals, K Zilmer, T Kullisaar, R Teesalu, A Pulges, ... American journal of hypertension 19 (9), 902-908, 2006 | 72 | 2006 |
| High-prevalence and high-estimated incidence of HIV infection among new injecting drug users in Estonia: need for large scale prevention programs A Uusküla, M Kals, K Rajaleid, K Abel, A Talu, K Rüütel, L Platt, T Rhodes, ... Journal of Public Health 30 (2), 119-125, 2008 | 69 | 2008 |
| Whole-exome sequencing identifies loci associated with blood cell traits and reveals a role for alternative GFI1B splice variants in human hematopoiesis LM Polfus, RK Khajuria, UM Schick, N Pankratz, R Pazoki, JA Brody, ... The American Journal of Human Genetics 99 (2), 481-488, 2016 | 63 | 2016 |
| Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases O Tšuiko, M Noukas, O Žilina, K Hensen, JS Tapanainen, R Mägi, M Kals, ... Human reproduction 31 (8), 1913-1925, 2016 | 60 | 2016 |
| Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia M Alver, M Palover, A Saar, K Läll, SM Zekavat, N Tõnisson, L Leitsalu, ... Genetics in Medicine 21 (5), 1173-1180, 2019 | 54 | 2019 |
