Articles with public access mandates - Tõnu Esko - Business FinlandLearn more
Available based on mandate: 14
Review
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
Review
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
Review
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
Review
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
J Fadista, L Skotte, J Karjalainen, E Abner, E Sørensen, H Ullum, T Werge, ...
Nature Communications 13 (1), 3200, 2022
Review
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes
A Elliott, RK Walters, M Pirinen, M Kurki, N Junna, JI Goldstein, MP Reeve, ...
Nature Genetics 56 (3), 377-382, 2024
Review
Overlap of genetic loci for central serous chorioretinopathy with age-related macular degeneration
JT Rämö, E Abner, EHC van Dijk, X Wang, J Brinks, T Nikopensius, ...
JAMA ophthalmology 141 (5), 449-457, 2023
Review
Genome-wide screen of otosclerosis in population biobanks: 18 loci and shared heritability with skeletal structure
JT Rämö, T Kiiskinen, J Karjalainen, K Krebs, M Kurki, AS Havulinna, ...
medRxiv, 2020.11. 15.20227868, 2020
Review
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure
JT Rämö, T Kiiskinen, R Seist, K Krebs, M Kanai, J Karjalainen, M Kurki, ...
Nature Communications 14 (1), 157, 2023
Review
SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease
S Strausz, E Abner, G Blacker, S Galloway, P Hansen, Q Feng, BT Lee, ...
Nature Communications 15 (1), 2041, 2024
Review
The α2A-adrenergic receptor (ADRA2A) modulates susceptibility to Raynaud’s syndrome
A Tervi, M Ramste, E Abner, P Cheng, JM Lane, M Maher, V Lammi, ...
Medrxiv, 2023.10. 04.23296526, 2023
Review
Genetic study of psoriasis highlights its close link with socio-economic status and affective symptoms
A Heikkilä, E Sliz, L Huilaja, K Reis, P Palta, AG Elnahas, A Reigo, T Esko, ...
Journal of Investigative Dermatology, 2024
Review
High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6
F Rahimov, P Nieminen, P Kumari, E Juuri, T Nikopensius, K Paraiso, ...
medRxiv, 2024.07. 09.24310146, 2024
Review
Genome-wide association study of anterior uveitis
F Koskimaki, O Ahokas, FinnGen, Estonian Biobank Research Team, ...
medRxiv, 2024.06. 03.24308116, 2024
Review
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
V Salo, J Maatta, E Sliz, FinnGen, E Reimann, R Magi, ...
medRxiv, 2023.10. 15.23296916, 2023
Publication and funding information is determined automatically by a computer program