Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
- Resource Type
- Authors
- Yin, Xianyong; Chan, Lap Sum; Bose, Debraj; Jackson, Anne U; VandeHaar, Peter; Locke, Adam E; Fuchsberger, Christian; Stringham, Heather M; Welch, Ryan; Yu, Ketian; Fernandes Silva, Lilian; Service, Susan K; Zhang, Daiwei; Hector, Emily C; Young, Erica; Ganel, Liron; Das, Indraniel; Abel, Haley; Erdos, Michael R; Bonnycastle, Lori L; Kuusisto, Johanna; Stitziel, Nathan O; Hall, Ira M; Wagner, Gregory R; FinnGen; Kang, Jian; Morrison, Jean; Burant, Charles F; Collins, Francis S; Ripatti, Samuli; Palotie, Aarno; Freimer, Nelson B; Mohlke, Karen L; Scott, Laura J; Wen, Xiaoquan; Fauman, Eric B; Laakso, Markku; Boehnke, Michael
- Source
- Nature communications, vol 13, iss 1
- Subject
- Male
Human Genome
Single Nucleotide
FinnGen
Phenotype
Gene Frequency
Clinical Research
Genetics
Humans
2.1 Biological and endogenous factors
Genetic Predisposition to Disease
Polymorphism
Aetiology
Alleles
Finland
Genome-Wide Association Study
- Language
Few studies have explored the impact of rare variants (minor allele frequency