(Q48335894)

10 February 2018

title

Identification of novel genes involved in migraine (English)

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10 February 2018

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2

Guy A Rouleau

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10 February 2018

Ronald G Lafrenière

1

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10 February 2018

publication date

1 October 2012

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10 February 2018

published in

Headache

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10 February 2018

volume

52 Suppl 2

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10 February 2018

page(s)

107-110

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10 February 2018

Migraine prevalence, disease burden, and the need for preventive therapy

cites work

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https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Is migraine a genetic illness? The various forms of migraine share a common genetic cause

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.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.1526-4610.2012.02237.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.1526-4610.2012.02237.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.1526-4610.2012.02237.X

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/10.1111%2FJ.1526-4610.2012.02237.X

Significant linkage to migraine with aura on chromosome 11q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

SIFT: Predicting amino acid changes that affect protein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Human non-synonymous SNPs: server and survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

PANTHER: a library of protein families and subfamilies indexed by function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

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/10.1111%2FJ.1526-4610.2012.02237.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Medical sequencing at the extremes of human body mass

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Migraine: Role of the TRESK two-pore potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

TRESK two-pore-domain K+ channels constitute a significant component of background potassium currents in murine dorsal root ganglion neurones.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

Familial Clustering of Migraine: Further Evidence From a Portuguese Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1526-4610.2012.02237.X

10.1111/J.1526-4610.2012.02237.X

21 January 2018

Identifiers

DOI

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10 February 2018

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10 February 2018