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Publication date
2016 08
Authors
Gormley, P Anttila, V Winsvold, BS Palta, P Esko, T Pers, TH Farh, KH Cuenca-Leon, E Muona, M Furlotte, NA Kurth, T Ingason, A McMahon, G Ligthart, L Terwindt, GM Kallela, M Freilinger, TM Ran, C Gordon, SG Stam, AH Steinberg, S Borck, G Koiranen, M Quaye, L Adams, HHH Lehtimaki, T Sarin, AP Wedenoja, J Hinds, DA Buring, JE Schurks, M Ridker, PM Hrafnsdottir, MG Stefansson, H Ring, SM Hottenga, JJ Penninx, BWJH Farkkila, M Artto, V Kaunisto, M Vepsalainen, S Malik, R Heath, AC Madden, PAF Martin, NG Montgomery, GW Kurki, MI Kals, M Magi, R Parn, K Hamalainen, E Huang, HL Byrnes, AE Franke, L Huang, J Stergiakouli, E Lee, PH Sandor, C Webber, C Cader, Z Muller-Myhsok, B Schreiber, S Meitinger, T Eriksson, JG Salomaa, V Heikkila, K Loehrer, E Uitterlinden, AG Hofman, A van Duijn, CM Cherkas, L Pedersen, LM Stubhaug, A Nielsen, CS Mannikko, M Mihailov, E Milani, L Gobel, H Esserlind, AL Christensen, AF Hansen, TF Werge, T Kaprio, J Aromaa, AJ Raitakari, O Ikram, MA Spector, T Jarvelin, MR Metspalu, A Kubisch, C Strachan, DP Ferrari, MD Belin, AC Dichgans, M Wessman, M van den Maagdenberg, AMJM Zwart, JA Boomsma, DI Smith, GD Stefansson, K Eriksson, N Daly, MJ Neale, BM Olesen, J Chasman, DI Nyholt, DR Palotie, A
Group authors
Int Headache Genetics Consortium
Author KI Usernames
Belin, AC|ancarm Ran, C|carran
Pubmed ID
27322543
Journal
Nature genetics
Doctype
Article
KI Connection
Låg
Mesh SV
Fall-kontrollstudier Genetiska loci Genetiska markörer Genetiska sjukdomsanlag Genome-Wide Association Study Genomik Glatt muskulatur Kärlsjukdomar Migränsjukdomar Människa Polymorfism, enkelnukleotid
Mesh EN
Case-Control Studies Genetic Loci Genetic Markers Genetic Predisposition to Disease Genome-Wide Association Study Genomics Migraine Disorders Muscle, Smooth Polymorphism, Single Nucleotide Vascular Diseases
First date
2016-09-11T10:48:50.595Z