Leveraging nationwide health care records in Estonia to identify the genetic background of understudied disease phenotypes
Anastasiia Alekseienko(University of Tartu), Erik Abner(University of Tartu), Teele Palumaa(East Tallinn Central Hospital), Anu Reigo(University of Tartu), Kanwal Batool(University of Tartu), Urmo Võsa(University Medical Center Groningen), Priit Palta(University of Tartu), Jaanika Kronberg(University of Tartu), Tõnu Esko(Broad Institute), Klavs Jermakovs(University of Cambridge)
Cited by 0
Related Papers
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
|Nature Genetics|2021|2.2k
Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases
|Nature Genetics|2019|1.6k
Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans
|PLoS ONE|2015|1.2k
Gene co-expression analysis for functional classification and gene–disease predictions
|Briefings in Bioinformatics|2016|1.1k