Genome-wide association analysis identifies susceptibility loci for migraine without aura

Tobias Freilinger, Verneri Anttila, Boukje de Vries, +39

Nature Genetics

Genome-wide Association StudyCluster HeadacheNeurogenomicsGeneticsGenetic Epidemiology +3

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

Katherine M. Siewert, Derek Klarin, Scott M. Damrauer, +129

International Journal of Epidemiology

Biallelic SZT2 Mutations Cause Infantile Encephalopathy with Epilepsy and Dysmorphic Corpus Callosum

Lina Basel‐Vanagaite, Tova Hershkovitz, Eli Heyman, +18

The American Journal of Human Genetics

Neurological DisorderGenetic DisorderGeneticsNeuroscienceNeurology +5

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik, +277

Neurology Genetics

Divergent influences of the locus coeruleus on migraine pathophysiology

Marta Vila‐Pueyo, Lauren C. Strother, Malak Kefel, +2

Pain

Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia

Cèlia Sintas, Oriel Carreño, Noèlia Fernàndez‐Castillo, +9

Scientific Reports

A loss-of-function CACNA1A mutation causing benign paroxysmal torticollis of infancy

Marta Vila‐Pueyo, Gemma G. Gené, Marina Flotats-Bastardes, +6

European Journal of Paediatric Neurology

BiologyGeneticsLoss-of-function Cacna1a Mutation

Screening of <scp><i>CACNA1A</i></scp> and <scp><i>ATP1A2</i></scp> genes in hemiplegic migraine: clinical, genetic, and functional studies

Oriel Carreño, Roser Corominas, Selma A. Serra, +13

Molecular Genetics & Genomic Medicine

Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura

Cèlia Sintas, Jessica Fernández‐Morales, Marta Vila‐Pueyo, +5

Cephalalgia

Elucidating the relationship between migraine risk and brain structure using genetic data

Brittany L. Mitchell, Santiago Díaz‐Torres, Svetlana Bivol, +131

Brain

NeurogenomicsBrain DevelopmentGeneticsGenetic EpidemiologyGenetic Foundation +22