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Publication date
2016 08 18
Authors
Lek, M Karczewski, KJ Minikel, EV Samocha, KE Banks, E Fennell, T O'Donnell-Luria, AH Ware, JS Hill, AJ Cummings, BB Tukiainen, T Birnbaum, DP Kosmicki, JA Duncan, LE Estrada, K Zhao, FM Zou, J Pierce-Hollman, E Berghout, J Cooper, DN Deflaux, N DePristo, M Do, R Flannick, J Fromer, M Gauthier, L Goldstein, J Gupta, N Howrigan, D Kiezun, A Kurki, MI Moonshine, AL Natarajan, P Orozeo, L Peloso, GM Poplin, R Rivas, MA Ruano-Rubio, V Rose, SA Ruderfer, DM Shakir, K Stenson, PD Stevens, C Thomas, BP Tiao, G Tusie-Luna, MT Weisburd, B Won, HH Yu, DM Altshuler, DM Ardissino, D Boehnke, M Danesh, J Donnelly, S Elosua, R Florez, JC Gabriel, SB Getz, G Glatt, SJ Hultman, CM Kathiresan, S Laakso, M NcCarroll, S McCarthy, MI McGovern, D McPherson, R Neale, BM Palotie, A Purcell, SM Saleheen, D Scharf, JM Sklar, P Sullivan, PF Tuomilehto, J Tsuang, MT Watkins, HC Wilson, JG Daly, MJ MacArthur, DG
Group authors
Exome Aggregation Consortium
Author KI Usernames
Hultman, CM|chrhul Sullivan, PF|patrsu
Pubmed ID
27535533
Journal
Nature
Doctype
Article
KI Connection
Låg
Mesh SV
Dataset som ämne DNA-mutationsanalys Exom Fenotyp Genetisk variation Människa Proteom Stickprovsstorlek Sällsynta sjukdomar
Mesh EN
Datasets as Topic DNA Mutational Analysis Exome Genetic Variation Phenotype Proteome Rare Diseases Sample Size
First date
2016-10-02T10:57:34.342Z