Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Bjornsdottir, G; Chalmer, MA; Stefansdottir, L; Skuladottir, AT; Einarsson, G; Andresdottir, M; Beyter, D; Ferkingstad, E; Gretarsdottir, S; Halldorsson, BV; Halldorsson, GH; Helgadottir, A; Helgason, H; Eldjarn, GH; Jonasdottir, A; Jonasdottir, A; Jonsdottir, I; Knowlton, KU; Nadauld, LD; Lund, SH; Magnusson, OT; Melsted, P; Moore, KHS; Oddsson, A; Olason, PI; Sigurdsson, A; Stefansson, OA; Saemundsdottir, J; Sveinbjornsson, G; Tragante, V; Unnsteinsdottir, U; Walters, GB; Zink, F; Rodevand, L; Andreassen, OA; Igland, J; Lie, RT; Haavik, J; Banasik, K; Brunak, S; Didriksen, M; Bruun, MT; Erikstrup, C; Kogelman, LJA; Nielsen, KR; Sorensen, E; Pedersen, OB; Ullum, H; Masson, G; Thorsteinsdottir, U; Olesen, J; Ludvigsson, P; Thorarensen, O; Bjornsdottir, A; Sigurdardottir, GR; Sveinsson, OA; Ostrowski, SR; Holm, H; Gudbjartsson, DF; Thorleifsson, G; Sulem, P; Stefansson, H; Thorgeirsson, TE; Hansen, TF; Stefansson, K

Bjornsdottir, G; Stefansson, K (通讯作者),Amgen Inc, deCODE Genet, Reykjavik, Iceland.;Stefansson, K (通讯作者),Univ Iceland, Sch Hlth Sci, Fac Med, Reykjavik, Iceland.

NATURE GENETICS, 2023; ():

Abstract

Migraine is a complex neurovascular disease with a range of severity and symptoms, yet mostly studied as one phenotype in genome-wide association stud......

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