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Publication date
2018 06 07
Authors
Ganna, A Satterstrom, FK Zekavat, SM Das, I Kurki, MI Churchhouse, C Alfoldi, J Martin, AR Havulinna, AS Byrnes, A Thompson, WK Nielsen, PR Karczewski, KJ Saarentaus, E Rivas, MA Gupta, N Pietilainen, O Emdin, CA Lescai, F Bybjerg-Grauholm, J Flannick, J Mercader, JM Udler, M Laakso, M Salomaa, V Hultman, C Ripatti, S Hamalainen, E Moilanen, JS Korkko, J Kuismin, O Nordentoft, M Hougaard, DM Mors, O Werge, T Mortensen, PB MacArthur, D Daly, MJ Sullivan, PF Locke, AE Palotie, A Borglum, AD Kathiresan, S Neale, BM
Group authors
iPSYCH-Broad Consortium FinMetSeq Consortium SIGMA Consortium Helmsley IBD Exom GoT2D T2D-GENES Consortium
Author KI Usernames
Hultman, C|chrhul
Pubmed ID
29861106
Journal
American journal of human genetics
Doctype
Article
KI Connection
Hög
Mesh SV
Etniska grupper Fenotyp Genetiska databaser Genetiska sjukdomsanlag Genome-Wide Association Study Mutation Människa Proteiner Öppen läsram
Mesh EN
Databases, Genetic Ethnic Groups Genetic Predisposition to Disease Genome-Wide Association Study Mutation Open Reading Frames Phenotype Proteins
First date
2018-07-09T03:20:02.142Z