The genetics of migraine (Q35172431)

6 August 2017

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title

The genetics of migraine. (English)

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Elisabeth Tournier-Lasserve

6 August 2017

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Marie-Germaine Bousser

series ordinal

3

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Anne Ducros

object named as

Anne Ducros

series ordinal

1

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object named as

Elisabeth Tournier-Lasserve

series ordinal

2

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publication date

1 September 2002

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6 August 2017

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6 August 2017

1

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6 August 2017

285-293

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6 August 2017

5

1 reference

A nationwide survey of migraine in France: prevalence and clinical features in adults. GRIM

6 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

An update on the epidemiology of migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Intracranial arteriovenous malformation and migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Antiphospholipid syndrome: clinical and immunologic manifestations and patterns of disease expression in a cohort of 1,000 patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Is familial hemiplegic migraine a hereditary form of basilar migraine?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial migraine coma: a case study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine, nystagmus, and cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Genetic heterogeneity of familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

The genetics of migraine without aura and migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Headache in a non-clinic twin population

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

1 reference

7 January 2021

Migraine and concomitant symptoms among 8167 adult twin pairs.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Genetic influence in headaches: a Swedish twin study.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Migraine in twins raised together and apart

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Migraine without aura: A population-based twin study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

The relative role of genetic and environmental factors in migraine without aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Evidence of a genetic factor in migraine with aura: a population-based Danish twin study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Migraine: Intelligence, Social Class, and Familial Prevalence

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Migraine in patients attending a migraine clinic: an analysis by computer of age, sex and family history

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Genetics of migraine and migraine accompagneé: a study of eighty-one children and their families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Testing Models for Genetic Determination in Migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

A 40-year follow-up of school children with migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Increased familial risk and evidence of genetic factor in migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial risk of migraine: A population-based study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Inheritance of migraine investigated by complex segregation analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Analysis of 31 families with an apparently autosomal-dominant transmission of migraine with aura in the nuclear family.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Association studies of genetic polymorphisms and complex disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

A new locus for hemiplegic migraine maps to chromosome 1q31

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Molecular and functional diversity of voltage-gated calcium channels

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Three for T: molecular analysis of the low voltage-activated calcium channel family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca(2+) channel mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Splicing of alpha 1A subunit gene generates phenotypic variants of P- and Q-type calcium channels.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Genetic heterogeneity in Italian families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

A nosographic analysis of the migraine aura in a general population.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Impairment of neuromuscular transmission in a subgroup of migraine patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Neuromuscular transmission in migraine: a single-fiber EMG study in clinical subgroups.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Searching for migraine genes: exclusion of 290 cM out of the whole human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Investigation of theCACNA1A gene as a candidate for typical migraine susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

A typical migraine susceptibility region localizes to chromosome 1q31

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Molecular genetics of migraine headaches: a review

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Association between dopamine receptor genes and migraine without aura in a Sardinian sample

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Significance of serotonin transporter gene polymorphism in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Significance of the catechol-O-methyltransferase gene polymorphism in migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

Association between migraine and endothelin type A receptor (ETA -231 A/G) gene polymorphism.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900134-5

7 January 2021

10.1016/S1474-4422(02)00134-5

Identifiers

DOI

1 reference

6 August 2017

1 reference

PubMed ID

12849426