Migraine: a complex genetic disorder (Q36825299)

16 August 2017

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title

Migraine: a complex genetic disorder (English)

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16 August 2017

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1

Maija Wessman

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Mari Anneli Kaunisto

series ordinal

3

object named as

Mari A Kaunisto

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16 August 2017

4

Aarno Palotie

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16 August 2017

2

Gisela M Terwindt

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16 August 2017

Maija Wessman

1

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PubMed ID

17509487

16 August 2017

Roel A Ophoff

series ordinal

5

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16 August 2017

1 June 2007

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16 August 2017

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16 August 2017

6

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16 August 2017

521-532

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16 August 2017

6

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Neurobiology of migraine.

16 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Epidemiology of headache in Europe

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine as a risk factor for subclinical brain lesions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine--current understanding and treatment

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The global burden of disease study: implications for neurology

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Cost of disorders of the brain in Europe

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine: theories of pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine with aura and migraine without aura are not different entities

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine without aura and migraine with aura are distinct disorders. A population-based twin survey.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Epilepsy and migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine with aura is a risk factor for unprovoked seizures in children

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Comorbidity of migraine and depression: investigating potential etiology and prognosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Increased familial risk and evidence of genetic factor in migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Inheritance of migraine investigated by complex segregation analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine and concomitant symptoms among 8167 adult twin pairs.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Genetic influence in headaches: a Swedish twin study.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The relative role of genetic and environmental factors in migraine without aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Evidence of a genetic factor in migraine with aura: a population-based Danish twin study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Genetic and environmental influences on migraine: a twin study across six countries.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine in twins raised together and apart

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Shared rearing environment in migraine: results from twins reared apart and twins reared together

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Genetic heterogeneity in Italian families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Gating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Genetic heterogeneity of familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A new locus for hemiplegic migraine maps to chromosome 1q31

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

ATP1A2 mutations in 11 families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A novel ATP1A2 mutation in a family with FHM type II

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Degeneration of the amygdala/piriform cortex and enhanced fear/anxiety behaviors in sodium pump alpha2 subunit (Atp1a2)-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Functional roles of the alpha isoforms of the Na,K-ATPase

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Sodium channel mutations in epilepsy and other neurological disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Investigation of theCACNA1A gene as a candidate for typical migraine susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Is the CACNA1A gene involved in familial migraine with aura?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Haplotype-based systematic association studies of ATP1A2 in migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Association of migraine and ESR1 G325C polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Investigation of hormone receptor genes in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Migraine and MTHFR C677T genotype in a population-based sample.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Association between the tumor necrosis factor-alpha -308 G/A gene polymorphism and migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Association between migraine and HLA-DRB1 gene polymorphisms.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Update on the genetics of migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Recent findings in headache genetics

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

MTHFR T677 homozygosis influences the presence of aura in migraineurs

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

MTHFR C677T polymorphism and migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Association studies of genetic polymorphisms and complex disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Replication validity of genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Testing for population subdivision and association in four case-control studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Assessing the impact of population stratification on genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The effects of human population structure on large genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

An Icelandic example of the impact of population structure on association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A genome-wide search for human type 1 diabetes susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Significant linkage to migraine with aura on chromosome 11q24.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Prevalence and sex-ratio of the subtypes of migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Genomewide significant linkage to migrainous headache on chromosome 5q21.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Trait components provide tools to dissect the genetic susceptibility of migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

A typical migraine susceptibility region localizes to chromosome 1q31

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Genomewide scans of complex human diseases: true linkage is hard to find

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

The endophenotype concept in psychiatry: etymology and strategic intentions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Sexual morality, pro-life values, and attitudes toward abortion: a simultaneous latent structure analysis for 1978-1983.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Alternative phenotypes for the complex genetics of schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

Molecular mechanisms of human hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970126-6

7 January 2021

10.1016/S1474-4422(07)70126-6

Identifiers

DOI

1 reference

16 August 2017

1 reference

PubMed ID

17509487