User profiles for Mari Nelis

Mari Nelis

University of Tartu
Verified email at ut.ee
Cited by 54337

FinnGen: Unique genetic insights from combining isolated population and national health register data

…, J Waring, D Waterworth, R Yang, M Nelis - MedRxiv, 2022 - medrxiv.org
Population isolates such as Finland provide benefits in genetic studies because the allelic
spectrum of damaging alleles in any gene is often concentrated on a small number of low-…

Systematic identification of trans eQTLs as putative drivers of known disease associations

…, PAC 't Hoen, E Reinmaa, K Fischer, M Nelis… - Nature …, 2013 - nature.com
Identifying the downstream effects of disease-associated SNPs is challenging. To help
overcome this problem, we performed expression quantitative trait locus (eQTL) meta-analysis in …

Sequence variants at CHRNB3CHRNA6 and CYP2A6 affect smoking behavior

…, H Stefansson, JR Thompson, YS Aulchenko, M Nelis… - Nature …, 2010 - nature.com
Smoking is a common risk factor for many diseases 1 . We conducted genome-wide
association meta-analyses for the number of cigarettes smoked per day (CPD) in smokers (n = …

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

…, JC Murray, SS Murray, MA Nalls, P Navarro, M Nelis… - Nature …, 2010 - nature.com
To identify loci for age at menarche, we performed a meta-analysis of 32 genome-wide
association studies in 87,802 women of European descent, with replication in up to 14,731 …

[PDF][PDF] A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

…, C Bouchard, A Metsapalu, T Vooder, M Nelis… - The american journal of …, 2009 - cell.com
Three genetic loci for lung cancer risk have been identified by genome-wide association
studies (GWAS), but inherited susceptibility to specific histologic types of lung cancer is not well …

[HTML][HTML] Genetic structure of Europeans: a view from the North–East

M Nelis, T Esko, R Mägi, F Zimprich, A Zimprich… - PloS one, 2009 - journals.plos.org
Using principal component (PC) analysis, we studied the genetic constitution of 3,112
individuals from Europe as portrayed by more than 270,000 single nucleotide polymorphisms (…

Common variants in KCNN3 are associated with lone atrial fibrillation

…, AV Smith, LJ Launer, TB Harris, S Makino, M Nelis… - Nature …, 2010 - nature.com
Atrial fibrillation (AF) is the most common sustained arrhythmia. Previous studies have
identified several genetic loci associated with typical AF. We sought to identify common genetic …

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

…, G Goodman, S Benhamou, T Vooder, K Välk, M Nelis… - Nature …, 2014 - nature.com
We conducted imputation to the 1000 Genomes Project of four genome-wide association
studies of lung cancer in populations of European ancestry (11,348 cases and 15,861 controls) …

Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders

…, AC Morrison, M Müller-Nurasyid, P Navarro, M Nelis… - Nature …, 2013 - nature.com
Elevated resting heart rate is associated with greater risk of cardiovascular disease and
mortality. In a 2-stage meta-analysis of genome-wide association studies in up to 181,171 …

[PDF][PDF] A cross-disorder dosage sensitivity map of the human genome

…, M Trinh, F Ullah, U Võsa, A Metspalu, R Mägi, M Nelis… - Cell, 2022 - cell.com
Rare copy-number variants (rCNVs) include deletions and duplications that occur infrequently
in the global human population and can confer substantial risk for disease. In this study, …