Mitja Kurki
Mitja Kurki
Unknown affiliation
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Cited by
Cited by
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
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Hypertension predisposes to the formation of saccular intracranial aneurysms in 467 unruptured and 1053 ruptured patients in Eastern Finland
AE Lindgren, MI Kurki, A Riihinen, T Koivisto, A Ronkainen, J Rinne, ...
Annals of medicine 46 (3), 169-176, 2014
Haplotype sharing provides insights into fine-scale population history and disease in Finland
AR Martin, KJ Karczewski, S Kerminen, MI Kurki, AP Sarin, M Artomov, ...
The American Journal of Human Genetics 102 (5), 760-775, 2018
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms
MI Kurki, EI Gaal, J Kettunen, T Lappalainen, A Menelaou, V Anttila, ...
PLoS genetics 10 (1), e1004134, 2014
Trans-biobank analysis with 676,000 individuals elucidates the association of polygenic risk scores of complex traits with human lifespan
S Sakaue, M Kanai, J Karjalainen, M Akiyama, M Kurki, N Matoba, ...
Nature medicine 26 (4), 542-548, 2020
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