(Q34023677)

30 July 2017

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

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genome-wide association study

30 July 2017

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36

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40

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51

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Bertram Müller-Myhsok

10

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André Uitterlinden

42

Andre G Uitterlinden

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Cornelia M. van Duijn

44

Cornelia M van Duijn

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John-Anker Zwart

55

John-Anker Zwart

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International Headache Genetics Consortium

30 July 2017

66

International Headache Genetics Consortium

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3

Mikko Kallela

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30 July 2017

Arn van den Maagdenberg

60

Arn M J M van den Maagdenberg

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Maija Wessman

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Maija Wessman

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Eija Hämäläinen

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Boukje de Vries

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Christian Kubisch

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Kirsi Alakurtti

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Kirsi Alakurtti

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45

Päivi Tikka-Kleemola

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57

Jes Olesen

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Thomas Werge

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Thomas Werge

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1

Verneri Anttila

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Federica Tozzi

Federica Tozzi

48

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Mari Anneli Kaunisto

Mari A Kaunisto

14

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Hreinn Stefansson

Hreinn Stefansson

2

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Johan G. Eriksson

Johan G Eriksson

32

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Dale R Nyholt

Dale R Nyholt

7

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Lars Jacob Stovner

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Lars Stovner

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Knut Hagen

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Aarno Palotie

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Albert Hofman

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Mark Daly

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Leena Peltonen-Palotie

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Leena Peltonen

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Martin Dichgans

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Kari Stefansson

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Gisela M Terwindt

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Jean Schoenen

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Michel D Ferrari

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Susanne Moebus

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H-Erich Wichmann

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Michael Inouye

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Monique M B Breteler

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Stefan Schreiber

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Antigone S Dimas

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Emmanouil Dermitzakis

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Emmanouil T Dermitzakis

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Anine H Stam

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Tobias Freilinger

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Jeffrey Barrett

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Stacy Steinberg

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Susanne Lucae

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Pierandrea Muglia

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Asgeir Björnsson

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Katja Heinze-Kuhn

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Ville Artto

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Hartmut Göbel

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Christiane Wolf

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Guntram Borck

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Rune R Frants

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Markus Färkkilä

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Unda Todt

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Axel Heinze

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M Stella Calafato

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Claudia M Weller

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Ingrid Goebel

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Gretar Gudmundsson

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Malene Kirchmann

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Anne Hauge

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Michael Alexander

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Salli Vepsäläinen

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30 July 2017

language of work or name

English

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publication date

29 August 2010

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30 July 2017

5

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published in

Nature Genetics

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30 July 2017

42

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10

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30 July 2017

869-873

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describes a project that uses

30 July 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

exact match

https://scigraph.springernature.com/pub.10.1038/ng.652

0 references

cites work

Astrocyte elevated gene-1 (AEG-1) functions as an oncogene and regulates angiogenesis

1 reference

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Exon expression in lymphoblastoid cell lines from subjects with schizophrenia before and after glucose deprivation.

5 July 2018

1 reference

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Molecular mechanisms of necrosis in glioblastoma: the role of glutamate excitotoxicity

5 July 2018

1 reference

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Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats

5 July 2018

1 reference

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Common regulatory variation impacts gene expression in a cell type-dependent manner

5 July 2018

1 reference

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Molecular genetics of migraine

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.

5 July 2018

1 reference

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Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake

5 July 2018

1 reference

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

5 July 2018

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

5 July 2018

1 reference

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Population genomics of human gene expression

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

A genotype calling algorithm for the Illumina BeadArray platform

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

PLINK: a tool set for whole-genome association and population-based linkage analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Familial hemiplegic migraine

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

The global burden of headache: a documentation of headache prevalence and disability worldwide

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Genetic neurological channelopathies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Epidemiology of headache in Europe

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

The International Classification of Headache Disorders: 2nd edition

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Migraine--current understanding and treatment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Searching for genetic determinants in the new millennium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

Pathophysiology of the migraine aura. The spreading depression theory

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2948563

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

5 July 2018

1 reference

Hypoxia suppresses glutamate transport in astrocytes.

21 January 2018

1 reference

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

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.

21 January 2018

1 reference

21 January 2018

Neurobiology of migraine

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20802479

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.652

1 reference

30 July 2017

1 reference

30 July 2017

1 reference