Functional gene networks reveal distinct mechanisms segregating in migraine families
Migraine is the most common neurological disorder worldwide and it has been shown to
have complex polygenic origins with a heritability of estimated 40–70%. Both common and …
have complex polygenic origins with a heritability of estimated 40–70%. Both common and …
Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine
Background Familial hemiplegic migraine (FHM) is a rare form of migraine with aura that
often has an autosomal dominant mode of inheritance. Rare mutations in the CACNA1A …
often has an autosomal dominant mode of inheritance. Rare mutations in the CACNA1A …
Familial analysis reveals rare risk variants for migraine in regulatory regions
The most recent genome-wide association study of migraine increased the total number of
known migraine risk loci to 38. Still, most of the heritability of migraine remains unexplained …
known migraine risk loci to 38. Still, most of the heritability of migraine remains unexplained …
Migraine headaches and family planning: what we think we know
Migraine headache is a nearly ubiq-uitous neurological disorder that disproportionately
affects women and has already been identified as the leading cause of years lived with …
affects women and has already been identified as the leading cause of years lived with …
Recognition and clinical implications of high prevalence of migraine in patients with Brugada syndrome and drug‐induced type 1 Brugada pattern
C Hasdemir, F Gokcay, MN Orman… - Journal of …, 2020 - Wiley Online Library
Introduction We have previously reported high 1‐year prevalence of migraine in patients
with atrial arrhythmias associated with DI‐type 1 BrP. The present study was designed to …
with atrial arrhythmias associated with DI‐type 1 BrP. The present study was designed to …