Genomewide significant linkage to migrainous headache on chromosome 5q21. (Q34021170)

30 July 2017

0 references

Genomewide significant linkage to migrainous headache on chromosome 5q21. (English)

1 reference

30 July 2017

1 reference

Katherine I Morley

2

0 references

Sarah E. Medland

Sarah E Medland

4

0 references

Grant W. Montgomery

Grant W Montgomery

8

0 references

Nick Martin

Nicholas G Martin

9

0 references

Dale R Nyholt

Dale R Nyholt

1

0 references

Dorret Boomsma

5

Dorret I Boomsma

1 reference

30 July 2017

6

Andrew C Heath

1 reference

30 July 2017

Manuel A R Ferreira

3

1 reference

PubMed ID

16080125

30 July 2017

Kathleen R Merikangas

7

1 reference

PubMed ID

16080125

30 July 2017

language of work or name

English

0 references

publication date

28 July 2005

1 reference

American Journal of Human Genetics

30 July 2017

1 reference

30 July 2017

77

1 reference

30 July 2017

3

1 reference

30 July 2017

500-512

1 reference

A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A combined linkage-physical map of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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=1226215

A locus for migraine without aura maps on chromosome 14q21.2-q22.3.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Evaluating the results of genomewide linkage scans of complex traits by locus counting

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Powerful regression-based quantitative-trait linkage analysis of general pedigrees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical 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=1226215

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Improved inference of relationship for pairs of individuals

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Familial typical migraine: significant linkage and localization of a gene to Xq24-28.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

All LODs are not created equal

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Multipoint quantitative-trait linkage analysis in general pedigrees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Linkage thresholds for two-stage genome scans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Evidence for an X-linked genetic component in familial typical 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=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A new locus for hemiplegic migraine maps to chromosome 1q31

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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=1226215

Parametric and nonparametric linkage analysis: a unified multipoint approach

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A gene for familial hemiplegic migraine maps to chromosome 19

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Twin studies of psychiatric illness. Current status and future directions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Genetic heterogeneity of 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=1226215

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A simple method to detect linkage for rare recessive diseases: An application to juvenile 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=1226215

Investigation of hormone receptor genes 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=1226215

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Significant linkage to migraine with aura on chromosome 11q24.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Glutathione S-Transferase Polymorphisms: Susceptibility to Migraine without Aura

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

A simple correction for multiple comparisons in interval mapping genome scans.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Significance of serotonin transporter gene polymorphism in migraine.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Is there an association between migraine headache and open-angle glaucoma? Findings from the Blue Mountains Eye Study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Empirical genomewide significance levels established by whole genome simulations.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Validation of diagnostic criteria for migraine in the Zürich longitudinal cohort study.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Testing Models for Genetic Determination in Migraine

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226215

Angiotensin-converting enzyme gene deletion polymorphism determines an increase in frequency of migraine attacks in patients suffering from migraine without aura

29 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

GRR: graphical representation of relationship errors

1 reference

12 December 2020

A typical migraine susceptibility region localizes to chromosome 1q31

1 reference

12 December 2020

A polymorphism in the interleukin-1alpha gene influences the clinical features of migraine

1 reference

12 December 2020

Tumor necrosis factor gene polymorphism in migraine

1 reference

12 December 2020

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

1 reference

12 December 2020

The investigation of linkage between a quantitative trait and a marker locus

1 reference

12 December 2020

The value of latent class analysis in medical diagnosis

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

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

12 December 2020

Diagnostic criteria for migraine. A validity study

1 reference

12 December 2020

Genetic heterogeneity of familial hemiplegic migraine

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic markers: association study in migraine

1 reference

12 December 2020

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

1 reference

12 December 2020

A variance component approach to dichotomous trait linkage analysis using a threshold model

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1086/444510

1 reference

30 July 2017

1 reference

30 July 2017

1 reference

PubMed ID

16080125