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

Ganna, A (author)

Satterstrom, FK (author)

Zekavat, SM (author)

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Das, I (author)

Kurki, MI (author)

Churchhouse, C (author)

Alfoldi, J (author)

Martin, AR (author)

Havulinna, AS (author)

Byrnes, A (author)

Thompson, WK (author)

Nielsen, PR (author)

Karczewski, KJ (author)

Saarentaus, E (author)

Rivas, MA (author)

Gupta, N (author)

Pietilainen, O (author)

Emdin, CA (author)

Lescai, F (author)

Bybjerg-Grauholm, J (author)

Flannick, J (author)

Mercader, JM (author)

Udler, M (author)

Laakso, M (author)

Salomaa, V (author)

Hultman, C (author)

Karolinska Institutet

Ripatti, S (author)

Hamalainen, E (author)

Moilanen, JS (author)

Korkko, J (author)

Kuismin, O (author)

Nordentoft, M (author)

Hougaard, DM (author)

Mors, O (author)

Werge, T (author)

Mortensen, PB (author)

MacArthur, D (author)

Daly, MJ (author)

Sullivan, PF (author)

Karolinska Institutet

Locke, AE (author)

Palotie, A (author)

Borglum, AD (author)

Kathiresan, S (author)

Neale, BM (author)

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 (creator_code:org_t)

Elsevier BV, 2018

2018

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 102:6, s. 1204-1211

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• Journal article (peer-reviewed)