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Publication date
2019 03
Authors
Jansen, PR Watanabe, K Stringer, S Skene, N Bryois, J Hammerschlag, AR de Leeuw, CA Benjamins, JS Munoz-Manchado, AB Nagel, M Savage, JE Tiemeier, H White, T Tung, JY Hinds, DA Vacic, V Wang, X Sullivan, PF van der Sluis, S Polderman, TJC Smit, AB Hjerling-Leffler, J Van Someren, EJW Posthuma, D Agee, M Alipanahi, B Auton, A Bell, RK Bryc, K Elson, SL Fontanillas, P Furlotte, NA Huber, KE Kleinman, A Litterman, NK McCreight, JC McIntyre, MH Mountain, JL Noblin, ES Northover, CAM Pitts, SJ Sathirapongsasuti, JF Sazonova, OV Shelton, JF Shringarpure, S Tian, C Wilson, CH
Group authors
23andMe Res Team
Author KI Usernames
Bryois, J|julbry Hjerling-Leffler, J|jenhje Munoz-Manchado, AB|anamun Muñoz-Manchado, AB|anamun Sullivan, PF|patrsu
Pubmed ID
30804565
Journal
Nature genetics
Doctype
Article
KI Connection
Låg
Mesh SV
Fenotyp Genetiska sjukdomsanlag Genome-Wide Association Study Insomningsproblem och tidigt uppvaknande Kromatin Kvinnlig Manlig Medelålders personer Människa Polymorfism, enkelnukleotid QTL Sömn
Mesh EN
Chromatin Genetic Predisposition to Disease Genome-Wide Association Study Phenotype Polymorphism, Single Nucleotide Quantitative Trait Loci Sleep Sleep Initiation and Maintenance Disorders
First date
2019-03-24T03:34:54.14Z