(Q38106687)

29 August 2017

title

Pearls and pitfalls in genetic studies of migraine (English)

1 reference

29 August 2017

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Arn van den Maagdenberg

5

object named as

Arn M J M van den Maagdenberg

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Boukje de Vries

2

object named as

Boukje de Vries

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Gisela M Terwindt

4

object named as

Gisela M Terwindt

1 reference

29 August 2017

3

Michel D Ferrari

1 reference

29 August 2017

Else Eising

1

1 reference

29 August 2017

Boukje de Vries

2

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29 August 2017

language of work or name

English

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publication date

1 June 2013

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29 August 2017

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29 August 2017

volume

33

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29 August 2017

issue

8

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29 August 2017

page(s)

614-625

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

29 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

The prevalence and characteristics of migraine in a population-based cohort: the GEM study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Pathophysiology of the migraine aura. The spreading depression theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Clinical relevance of cortical spreading depression in neurological disorders: migraine, malignant stroke, subarachnoid and intracranial hemorrhage, and traumatic brain injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Activation of central trigeminovascular neurons by cortical spreading depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Increased familial risk and evidence of genetic factor in migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

The Prevalence and Characteristics of Migraine in Twins From the General Population

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Genetic and environmental influences on migraine: a twin study across six countries

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Migraine: gene mutations and functional consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Clinical spectrum of SCN1A mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

A high-density association screen of 155 ion transport genes for involvement with common migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Insights into migraine mechanisms and CaV2.1 calcium channel function from mouse models of familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Effects of familial hemiplegic migraine type 1 mutation T666M on voltage-gated calcium channel activities in trigeminal ganglion neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Divergent sodium channel defects in familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

Coding of facial expressions of pain in the laboratory mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Identification of a specific role for the Na,K-ATPase alpha 2 isoform as a regulator of calcium in the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Hypoxia suppresses glutamate transport in astrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Molecular basis of nuclear factor-kappaB activation by astrocyte elevated gene-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Cloning and characterization of HIV-1-inducible astrocyte elevated gene-1, AEG-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Differential involvement of TNF alpha in hypoxic suppression of astrocyte glutamate transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

A TRP channel that senses cold stimuli and menthol

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Analgesia mediated by the TRPM8 cold receptor in chronic neuropathic pain

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Neuropathic pain: emerging treatments

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Glutamate controls tPA recycling by astrocytes, which in turn influences glutamatergic signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

PRDM16 controls a brown fat/skeletal muscle switch

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Prdm proto-oncogene transcription factor family expression and interaction with the Notch-Hes pathway in mouse neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Chromatin modification of Notch targets in olfactory receptor neuron diversification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Genome-wide analysis of MEF2 transcriptional program reveals synaptic target genes and neuronal activity-dependent polyadenylation site selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

PACAP38 induces migraine-like attacks in patients with migraine without aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Depletion of the novel protein PHACTR-1 from human endothelial cells abolishes tube formation and induces cell death receptor apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Analysing biological pathways in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Model organisms--A historical perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Concise review: the promise of human induced pluripotent stem cell-based studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Molecular genetics of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Genomewide significant linkage to migrainous headache on chromosome 5q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Trait components provide tools to dissect the genetic susceptibility of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Consistently replicating locus linked to migraine on 10q22-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Neuropsychological measures probably facilitate heritability research of ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

MTHFR 677C>T and ACE D/I polymorphisms in migraine: a systematic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

The relationship between homocysteine and genes of folate-related enzymes in migraine patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Defective membrane expression of the Na + -HCO 3 − cotransporter NBCe1 is associated with familial migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Functional analysis of missense variants in the TRESK (KCNK18) K channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Exome sequencing as a tool for Mendelian disease gene discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Migraine: Role of the TRESK two-pore potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

TRESK channel contribution to nociceptive sensory neurons excitability: modulation by nerve injury.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Novel genomic techniques open new avenues in the analysis of monogenic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Exome sequencing identifies the cause of a mendelian disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Nitric oxide in primary headaches

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

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/10.1177%2F0333102413484988

The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0333102413484988

21 January 2018

Identifiers

DOI

10.1177/0333102413484988

1 reference

29 August 2017

1 reference