Localization of a gene for migraine without aura to chromosome 4q21. - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q33905673

about

Investigating the genetic role of aquaporin4 gene in migraine Genetics of migraine in the age of genome-wide association studies Current issues in migraine genetics.A visual migraine aura locus maps to 9q21-q22 Genomewide significant linkage to migrainous headache on chromosome 5q21.Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26 Trait components provide tools to dissect the genetic susceptibility of migraine.Studies on the pathophysiology and genetic basis of migraine.Migraine genetics.Meta-analysis of genome-wide association for migraine in six population-based European cohorts.The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology.Complex trait mapping in isolated populations: Are specific statistical methods required?Migraine: new treatment options from molecular biology.The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.Genetic biomarkers for migraine.Selected confirmed, probable, and exploratory migraine biomarkers.Genetics of migraine: an update.Consistently replicating locus linked to migraine on 10q22-q23 A pharmacogenomic evaluation of migraine therapy.Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island.Identification of molecular genetic factors that influence migraine.Migraine genes and the relation to gender.Human studies in the pathophysiology of migraine: genetics and functional neuroimaging.Pearls and pitfalls in genetic studies of migraine.Population-based approaches to genetics of migraine.Migraine genetics: current findings and future lines of research.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 The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine.Family-based association study of chromosome 6p12.2-p21.1 migraine locus.

P2860

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P2860

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

http://www.wikidata.org/entity/Q33905673

description

2003 nî lūn-bûn

@nan

2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

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

@ast

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

@en

type

label

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

@ast

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

@en

prefLabel

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

@ast

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

@en

P1433

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P1433

American Journal of Human Genetics

P1476

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

@en

P2093

Asgeir Björnsson

http://www.w3.org/2001/XMLSchema#string

Augustine Kong

http://www.w3.org/2001/XMLSchema#string

Einar Gudfinnsson

http://www.w3.org/2001/XMLSchema#string

Grétar Gudmundsson

http://www.w3.org/2001/XMLSchema#string

Jeffrey R Gulcher

http://www.w3.org/2001/XMLSchema#string

John Benedikz

http://www.w3.org/2001/XMLSchema#string

Kristleifur Kristjánsson

http://www.w3.org/2001/XMLSchema#string

Kári Stefánsson

http://www.w3.org/2001/XMLSchema#string

María Hrafnsdóttir

http://www.w3.org/2001/XMLSchema#string

Michael L Frigge

http://www.w3.org/2001/XMLSchema#string

P2860

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

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

A new locus for hemiplegic migraine maps to chromosome 1q31

A gene for familial hemiplegic migraine maps to chromosome 19

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

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

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

Parametric and nonparametric linkage analysis: a unified multipoint approach

A high-resolution recombination map of the human genome

Allegro, a new computer program for multipoint linkage analysis

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986-993

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10.1086/378417

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P433

5

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73

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9077882

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14513409

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P921

migraine disorder

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1180504

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