(Q24653482)

33

0 references

Jaakko Kaprio

8

0 references

Aarno Palotie

34

0 references

Martin Dichgans

28

0 references

Mikko Kallela

3

Mikko Kallela

0 references

Arn van den Maagdenberg

29

Arn M J M van den Maagdenberg

0 references

Maija Wessman

32

Maija Wessman

0 references

Boukje de Vries

18

Boukje de Vries

0 references

Christian Kubisch

30

Christian Kubisch

0 references

Kirsi Alakurtti

4

Kirsi Alakurtti

0 references

Verneri Anttila

5

Verneri Anttila

0 references

Mari Anneli Kaunisto

Mari A Kaunisto

9

0 references

Grant W. Montgomery

Grant W Montgomery

11

0 references

Nick Martin

Nicholas G Martin

31

0 references

Dale R Nyholt

Dale R Nyholt

1

0 references

Lenore J Launer

15

Lenore J Launer

0 references

Mark Joseph Daly

26

Mark J Daly

0 references

David R. Cox

27

David R Cox

0 references

Gisela M Terwindt

17

Gisela M Terwindt

0 references

Michel Ferrari

14

Michel D Ferrari

0 references

Andrew C. Heath

10

Andrew C Heath

0 references

Hartmut Göbel

12

Hartmut Göbel

0 references

Rune Frants

16

Rune R Frants

0 references

Andreas Straube

23

Andreas Straube

0 references

author name string

K Steven LaForge

2

0 references

Mikko Kallela

3

0 references

Kirsi Alakurtti

4

0 references

Markus Färkkilä

6

0 references

Eija Hämaläinen

7

0 references

Unda Todt

13

0 references

Boukje de Vries

18

0 references

W M Monique Verschuren

19

0 references

Jan Brand

20

0 references

Tobias Freilinger

21

0 references

Volker Pfaffenrath

22

0 references

Dennis G Ballinger

24

0 references

Yiping Zhan

25

0 references

Maija Wessman

A second generation human haplotype map of over 3.1 million SNPs

32

0 references

language of work or name

English

0 references

publication date

1 November 2008

0 references

published in

Human Molecular Genetics

0 references

volume

17

0 references

issue

21

0 references

page(s)

3318-31

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Statistical significance for genomewide studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

M-type KCNQ2-KCNQ3 potassium channels are modulated by the KCNE2 subunit

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

More powerful procedures for multiple significance testing

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

The International Classification of Headache Disorders: 2nd edition

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

New models of collaboration in genome-wide association studies: the Genetic Association Information Network

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Whole-genome patterns of common DNA variation in three human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Pathway-based approaches for analysis of genomewide association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Migraine: gene mutations and functional consequences

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

A tutorial on statistical methods for population association studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Genomewide significant linkage to migrainous headache on chromosome 5q21.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Genome-wide association studies: theoretical and practical concerns

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Neurobiology of migraine.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Genetic and environmental factors in complex diseases: the older Finnish Twin Cohort

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Migraine--current understanding and treatment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Familial migraine with and without aura: clinical characteristics and co-occurrence

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Quantitative trait locus mapping using human pedigrees.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Genetic heterogeneity of familial hemiplegic migraine

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Power and sample size calculations. A review and computer program

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2566523

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

28 September 2017

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

Validation of a migraine-specific questionnaire for use in family studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

Cardiovascular risk factors and migraine: the GEM population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

Migraine and MTHFR C677T genotype in a population-based sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

The impact of migraine on quality of life in the general population: the GEM study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

Predictors of non-response to a questionnaire survey of a volunteer twin panel: findings from the Australian 1989 twin cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

A direct approach to false discovery rates

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

Testing Models for Genetic Determination in Migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

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/10.1093%2FHMG%2FDDN227

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/10.1093%2FHMG%2FDDN227

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN227

First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine

21 January 2018

1 reference

12 December 2020

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

1 reference

12 December 2020

Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with aura

1 reference

12 December 2020

GRR: graphical representation of relationship errors

1 reference

12 December 2020

Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Headache Classification Committee of the International Headache Society

1 reference

12 December 2020

Genetic heterogeneity of familial hemiplegic migraine

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDN227

1 reference

1 reference

1 reference

PubMed publication ID

18676988

1 reference