Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

Author:

Ganna Andrea,Satterstrom F. Kyle,Zekavat Seyedeh M.,Das Indraniel,Kurki Mitja I.,Churchhouse Claire,Alfoldi Jessica,Martin Alicia R.,Havulinna Aki S.,Byrnes Andrea,Thompson Wesley K.,Nielsen Philip R.,Karczewski Konrad J.,Saarentaus Elmo,Rivas Manuel A.,Gupta Namrata,Pietiläinen Olli,Emdin Connor A.,Lescai Francesco,Bybjerg-Grauholm Jonas,Flannick Jason,Mercader Josep M.,Udler Miriam,Laakso Markku,Salomaa Veikko,Hultman Christina,Ripatti Samuli,Hämäläinen Eija,Moilanen Jukka S.,Körkkö Jarmo,Kuismin Outi,Nordentoft Merete,Hougaard David M.,Mors Ole,Werge Thomas,Mortensen Preben Bo,MacArthur Daniel,Daly Mark J.,Sullivan Patrick F.,Locke Adam E.,Palotie Aarno,Børglum Anders D.,Kathiresan Sekar,Neale Benjamin M.

Funder

Knut and Alice Wallenberg Foundation

Swedish Research Council

National Human Genome Research Institute

National Institute of Mental Health

National Institute of Diabetes and Digestive and Kidney Disease

Stanley Center for Psychiatric Research

Alexander and Margaret Stewart Trust

Sylvan C. Herman Foundation

Finnish Foundation for Cardiovascular Research

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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