Migraine genes and the relation to gender (Q37883448)

24 August 2017

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title

Migraine genes and the relation to gender (English)

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24 August 2017

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2

Boukje de Vries

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author name string

Reinald Shyti

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1

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PubMed ID

21631474

24 August 2017

Boukje de Vries

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2

1 reference

PubMed ID

21631474

24 August 2017

Arn van den Maagdenberg

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3

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24 August 2017

1 June 2011

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24 August 2017

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24 August 2017

51

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24 August 2017

6

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24 August 2017

880-890

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Migraine--current understanding and treatment

24 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The influence of estrogen on migraine: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Prevalence and burden of migraine in the United States: data from the American Migraine Study II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Pathophysiology of the migraine aura. The spreading depression theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Mechanisms of migraine aura revealed by functional MRI in human visual cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Activation of meningeal nociceptors by cortical spreading depression: implications for migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The effect of estrogen and progesterone on spreading depression in rat neocortical tissues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Effects of ovarian hormones on human cortical excitability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Reduced threshold for cortical spreading depression in female mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Molecular genetics of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A susceptibility locus for migraine with aura, on chromosome 4q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Localization of a gene for migraine without aura to chromosome 4q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Trait components provide tools to dissect the genetic susceptibility of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Consistently replicating locus linked to migraine on 10q22-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Evidence for an X-linked genetic component in familial typical migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Familial typical migraine: significant linkage and localization of a gene to Xq24-28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A novel locus for familial migraine on Xp22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Single nucleotide polymorphisms of the serotonin transporter gene in migraine--an association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

MTHFR T677 homozygosis influences the presence of aura in migraineurs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Thymidylate synthase promoter tandem repeat and MTHFD1 R653Q polymorphisms modulate the risk for migraine conferred by the MTHFR T677 allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Analysis of the MTHFR C677T variant with migraine phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Multilocus analyses reveal involvement of the ESR1, ESR2, and FSHR genes in migraine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Migraine: gene mutations and functional consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Sodium channel mutations in epilepsy and other neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Is brain estradiol a hormone or a neurotransmitter?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Transcription of estrogen receptor alpha and beta in mouse cerebral cortex: effect of age, sex, 17beta-estradiol and testosterone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Sensitization of calcitonin gene-related peptide receptors by receptor activity-modifying protein-1 in the trigeminal ganglion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

RAMPs regulate the transport and ligand specificity of the calcitonin-receptor-like receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Vasoactive peptide release in the extracerebral circulation of humans during migraine headache

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

NO-induced migraine attack: strong increase in plasma calcitonin gene-related peptide (CGRP) concentration and negative correlation with platelet serotonin release

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Calcitonin gene-related peptide receptor antagonist BIBN 4096 BS for the acute treatment of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Randomized controlled trial of an oral CGRP receptor antagonist, MK-0974, in acute treatment of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

The development of cutaneous allodynia during a migraine attack clinical evidence for the sequential recruitment of spinal and supraspinal nociceptive neurons in migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Genetic enhancement of calcitonin gene-related Peptide-induced central sensitization to mechanical stimuli in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Role of calcitonin gene-related peptide in light-aversive behavior: implications for migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Induction of multiple photophobic behaviors in a transgenic mouse sensitized to CGRP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

A genome-wide association study of bipolar disorder and comorbid migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Exome sequencing: the sweet spot before whole genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Familial Hemiplegic Migraine Type 1 Shows no Hypersensitivity to Nitric Oxide

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

Calcitonin gene-related peptide does not cause the familial hemiplegic migraine phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2011.01913.X

10.1111/J.1526-4610.2011.01913.X

21 January 2018

Identifiers

DOI

1 reference

24 August 2017

1 reference

PubMed ID

21631474