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Cephalalgia : an International Journal of Headache|May 15, 2014
A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhoodClaudia M Weller, Wilhelmina G Leen, Brian G R Neville, et al.Plos Genetics|January 9, 2015
Insight in genome-wide association of metabolite quantitative traits by exome sequence analysesAyşe Demirkan, Peter Henneman, Aswin Verhoeven, et al.Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.European Journal of Human Genetics : EJHG|May 3, 2007
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraineKaate R J Vanmolkot, Anine H Stam, Ashok Raman, et al.Nature Genetics|June 14, 2011
Genome-wide association study reveals three susceptibility loci for common migraine in the general populationDaniel I Chasman, Markus Schürks, Verneri Anttila, et al.Orphanet Journal of Rare Diseases|September 28, 2015
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patientsEleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, et al.Human Genetics|February 23, 2016
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain AtlasElse Eising, Sjoerd M H Huisman, Ahmed Mahfouz, et al.European Journal of Human Genetics : EJHG|March 31, 2011
Meta-analysis of genome-wide association for migraine in six population-based European cohortsLannie Ligthart, Boukje de Vries, Albert V Smith, et al.Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.Pageof 4