Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine

LC McCarthy, DA Hosford, JH Riley, MI Bird, NJ White… - Genomics, 2001 - Elsevier
We have identified a migraine locus on chromosome 19p13. 3/2 using linkage and
association analysis. We isolated 48 single-nucleotide polymorphisms within the locus, of …

[HTML][HTML] Meta-analysis of genome-wide association for migraine in six population-based European cohorts

L Ligthart, B De Vries, AV Smith, MA Ikram… - European Journal of …, 2011 - nature.com
Migraine is a common neurological disorder with a genetically complex background. This
paper describes a meta-analysis of genome-wide association (GWA) studies on migraine …

Genetic epidemiology of migraine and depression

Y Yang, L Ligthart, GM Terwindt, DI Boomsma… - …, 2016 - journals.sagepub.com
Background Migraine and major depressive disorder (commonly referred to as depression)
are both common disorders with a significant impact on society. Studies in both clinical and …

Migraine and psychiatric comorbidity: from theory and hypotheses to clinical application

FD Sheftell, SJ Atlas - Headache: The Journal of Head and …, 2002 - Wiley Online Library
Objective.—To review psychiatric issues that accompany migraine and means of addressing
these issues. Background.—Psychiatric factors and migraine may interact in three general …

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups

NJ Colson, RA Lea, S Quinlan, J MacMillan… - Neurogenetics, 2004 - Springer
Migraine is a painful and debilitating disorder with a significant genetic component. Steroid
hormones, in particular estrogen, have long been considered to play a role in migraine, as …

The genetics of migraine

A Ducros, E Tournier-Lasserve, MG Bousser - The Lancet Neurology, 2002 - thelancet.com
The search for genes involved in the pathophysiology of migraine poses major difficulties.
First, there is no objective diagnostic method to assess the status of the individuals studied …

[HTML][HTML] Genomewide significant linkage to migrainous headache on chromosome 5q21

DR Nyholt, KI Morley, MAR Ferreira… - The American Journal of …, 2005 - cell.com
Familial typical migraine is a common, complex disorder that shows strong familial
aggregation. Using latent-class analysis (LCA), we identified subgroups of people with …

Significant linkage to migraine with aura on chromosome 11q24

ZM Cader, S Noble-Topham, DA Dyment… - Human molecular …, 2003 - academic.oup.com
Migraine with aura (MA) is a prevalent neurological condition with strong evidence for a
genetic basis. Familial hemiplegic migraine, a rare Mendelian form of MA, can be caused by …

Investigation of hormone receptor genes in migraine

NJ Colson, RA Lea, S Quinlan, J MacMillan… - Neurogenetics, 2005 - Springer
Migraine is a common neurological condition with a complex mode of inheritance. Steroid
hormones have long been implicated in migraine, although their role remains unclear. Our …

[HTML][HTML] A locus for migraine without aura maps on chromosome 14q21. 2-q22. 3

D Soragna, A Vettori, G Carraro, E Marchioni… - The American Journal of …, 2003 - cell.com
Migraine is a common and disabling neurological disease of unknown origin characterized
by a remarkable clinical variability. It shows strong familial aggregation, suggesting that …