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 | 1122 | 2023 |
Mapping the human genetic architecture of COVID-19 MEK Niemi, J Karjalainen, RG Liao, BM Neale, M Daly, A Ganna, ... Nature 600 (7889), 472-477, 2021 | 752* | 2021 |
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets TM Delorey, CGK Ziegler, G Heimberg, R Normand, Y Yang, ... Nature, 1-32, 2021 | 635 | 2021 |
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 | 397 | 2022 |
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders MEK Niemi, HC Martin, DL Rice, G Gallone, S Gordon, M Kelemen, ... Nature 562 (7726), 268-271, 2018 | 306 | 2018 |
Quantifying the contribution of recessive coding variation to developmental disorders HC Martin, WD Jones, R McIntyre, G Sanchez-Andrade, M Sanderson, ... Science 362 (6419), 1161-1164, 2018 | 176 | 2018 |
Cognitive impairment and health-related quality of life following traumatic brain injury N Gorgoraptis, J Zaw-Linn, C Feeney, C Tenorio-Jimenez, M Niemi, ... NeuroRehabilitation 44 (3), 321-331, 2019 | 122 | 2019 |
The human genetic epidemiology of COVID-19 MEK Niemi, MJ Daly, A Ganna Nature Reviews Genetics 23 (9), 533-546, 2022 | 113 | 2022 |
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality T Nakanishi, S Pigazzini, F Degenhardt, M Cordioli, G Butler-Laporte, ... MedRxiv, 2021 | 104 | 2021 |
Mapping the human genetic architecture of COVID-19 by worldwide meta-analysis COVID-19 Host Genetics Initiative MedRxiv, 2021 | 72* | 2021 |
Detailed stratified GWAS analysis for severe COVID-19 in four European populations F Degenhardt, D Ellinghaus, S Juzenas, J Lerga-Jaso, M Wendorff, ... Human molecular genetics 31 (23), 3945-3966, 2022 | 59 | 2022 |
Prevalence and correlates of vitamin D deficiency in adults after traumatic brain injury OA Jamall, C Feeney, J Zaw‐Linn, A Malik, MEK Niemi, ... Clinical endocrinology 85 (4), 636-644, 2016 | 45 | 2016 |
Reduced reproductive success is associated with selective constraint on human genes EJ Gardner, MDC Neville, KE Samocha, K Barclay, M Kolk, MEK Niemi, ... Nature, 1-6, 2022 | 44 | 2022 |
A single-cell and spatial atlas of autopsy tissues reveals pathology and cellular targets of SARS-CoV-2 TM Delorey, CGK Ziegler, G Heimberg, R Normand, Y Yang, ... bioRxiv, 2021 | 41 | 2021 |
The contribution of X-linked coding variation to severe developmental disorders HC Martin, EJ Gardner, KE Samocha, J Kaplanis, N Akawi, A Sifrim, ... Nature communications 12 (1), 1-13, 2021 | 40 | 2021 |
New susceptibility loci for severe COVID-19 by detailed GWAS analysis in European populations F Degenhardt, D Ellinghaus, S Juzenas, J Lerga-Jaso, M Wendorff, ... medRxiv, 2021 | 13 | 2021 |
Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19 M Hultström, R Frithiof, J Grip, L Lindelöf, O Rooijackers, S Pigazzini, ... Nature Immunology 23 (6), 861-864, 2022 | 9 | 2022 |
Sex-biased reduction in reproductive success drives selective constraint on human genes EJ Gardner, MDC Neville, KE Samocha, K Barclay, M Kolk, MEK Niemi, ... bioRxiv, 2020 | 6 | 2020 |
Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen RS Rodosthenous, MEK Niemi, L Kallio, M Perala, P Terho, T Knopp, ... BMJ open 12 (10), e064695, 2022 | 4 | 2022 |
Autosomal recessive coding variants explain only a small proportion of undiagnosed developmental disorders in the British Isles HC Martin, WD Jones, J Stephenson, J Handsaker, G Gallone, JF McRae, ... bioRxiv, 201533, 2017 | 2 | 2017 |