| P50 | author | Aarno Palotie | Q29840663 |
| | Mari Anneli Kaunisto | Q42088784 |
| | Maija Wessman | Q42539403 |
| | Gisela M Terwindt | Q78712524 |
| P2093 | author name string | Roel A Ophoff | |
| | Maija Wessman | |
| P2860 | cites work | Genomewide scans of complex human diseases: true linkage is hard to find | Q22337170 |
| | The effects of human population structure on large genetic association studies | Q22337233 |
| | Assessing the impact of population stratification on genetic association studies | Q22337235 |
| | Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2 | Q24293004 |
| | Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2 | Q24531852 |
| | Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons | Q24538702 |
| | Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia | Q24540027 |
| | Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission | Q24556684 |
| | Mechanisms of migraine aura revealed by functional MRI in human visual cortex | Q24635174 |
| | 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 | Q24657270 |
| | A haplotype map of the human genome | Q24679827 |
| | The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura | Q24803265 |
| | MTHFR C677T polymorphism and migraine with aura | Q79788302 |
| | Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation | Q80795910 |
| | Association of migraine and ESR1 G325C polymorphism | Q81639868 |
| | Haplotype-based systematic association studies of ATP1A2 in migraine with aura | Q82690942 |
| | The global burden of disease study: implications for neurology | Q28138436 |
| | Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM | Q28138735 |
| | Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics | Q28139662 |
| | Genetic heterogeneity in Italian families with familial hemiplegic migraine | Q28139759 |
| | A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia | Q28139793 |
| | CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy | Q28142853 |
| | The endophenotype concept in psychiatry: etymology and strategic intentions | Q28187744 |
| | Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family | Q28198668 |
| | Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine | Q28202137 |
| | Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine | Q28203682 |
| | Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions | Q28204791 |
| | The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel | Q28204946 |
| | Functional roles of the alpha isoforms of the Na,K-ATPase | Q28206096 |
| | 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 | Q28237739 |
| | Gating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channel | Q28241997 |
| | A genome-wide search for human type 1 diabetes susceptibility genes | Q28247197 |
| | A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression | Q28248603 |
| | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | Q28251354 |
| | 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 | Q28251552 |
| | A new locus for hemiplegic migraine maps to chromosome 1q31 | Q28254832 |
| | A gene for familial hemiplegic migraine maps to chromosome 19 | Q28255425 |
| | Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity | Q28256929 |
| | A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2 | Q28260868 |
| | Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants | Q28263111 |
| | Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics | Q28263620 |
| | Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine | Q28264653 |
| | ATP1A2 mutations in 11 families with familial hemiplegic migraine | Q28266414 |
| | Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23 | Q28267263 |
| | Rare missense variants in ATP1A2 in families with clustering of common forms of migraine | Q28268080 |
| | Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures | Q28268524 |
| | New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus | Q28270794 |
| | Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects | Q28284668 |
| | A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs | Q28285675 |
| | Familial basilar migraine associated with a new mutation in the ATP1A2 gene | Q28286457 |
| | Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation | Q28293829 |
| | Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 | Q28295213 |
| | A novel ATP1A2 mutation in a family with FHM type II | Q28296728 |
| | Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel | Q28300848 |
| | The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice | Q28589473 |
| | Degeneration of the amygdala/piriform cortex and enhanced fear/anxiety behaviors in sodium pump alpha2 subunit (Atp1a2)-deficient mice | Q28593844 |
| | Replication validity of genetic association studies | Q29615456 |
| | Molecular mechanisms of human hypertension | Q32138445 |
| | Neurobiology of migraine. | Q33186891 |
| | Alternative phenotypes for the complex genetics of schizophrenia | Q33544013 |
| | Association studies of genetic polymorphisms and complex disease | Q33838028 |
| | Localization of a gene for migraine without aura to chromosome 4q21. | Q33905673 |
| | A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes | Q33938560 |
| | Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension | Q33942295 |
| | Epidemiology of headache in Europe | Q33995405 |
| | Genomewide significant linkage to migrainous headache on chromosome 5q21. | Q34021170 |
| | Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine | Q34179270 |
| | Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura | Q34469365 |
| | Migraine with aura is a risk factor for unprovoked seizures in children | Q34479239 |
| | Migraine--current understanding and treatment | Q34504002 |
| | The relative role of genetic and environmental factors in migraine without aura | Q34505089 |
| | Trait components provide tools to dissect the genetic susceptibility of migraine | Q34658426 |
| | Prevalence and sex-ratio of the subtypes of migraine. | Q34721342 |
| | Ion channel diseases | Q34915275 |
| | Epilepsy and migraine | Q35550769 |
| | Update on the genetics of migraine | Q35587401 |
| | Recent findings in headache genetics | Q35786716 |
| | Cost of disorders of the brain in Europe | Q36118614 |
| | Sodium channel mutations in epilepsy and other neurological disorders | Q36216288 |
| | Association between migraine and HLA-DRB1 gene polymorphisms. | Q36260391 |
| | Increased familial risk and evidence of genetic factor in migraine | Q36904792 |
| | A locus for migraine without aura maps on chromosome 14q21.2-q22.3. | Q37205369 |
| | Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families | Q37360470 |
| | A susceptibility locus for migraine with aura, on chromosome 4q24. | Q37361279 |
| | Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. | Q38294179 |
| | Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q. | Q38421457 |
| | Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura | Q39416650 |
| | The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura | Q40346824 |
| | Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy | Q40528552 |
| | Familial migraine with and without aura: clinical characteristics and co-occurrence | Q40686682 |
| | Testing for population subdivision and association in four case-control studies | Q40725291 |
| | The prevalence and characteristics of migraine in a population-based cohort: the GEM study | Q40801339 |
| | Migraine: theories of pathogenesis | Q42030542 |
| | Shared rearing environment in migraine: results from twins reared apart and twins reared together | Q42695344 |
| | Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene | Q43070130 |
| | Evidence of a genetic factor in migraine with aura: a population-based Danish twin study | Q43798765 |
| | Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder | Q43857315 |
| | Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model | Q43873034 |
| | Migraine prevalence, disease burden, and the need for preventive therapy | Q43983035 |
| | Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk | Q44374190 |
| | Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine | Q44447061 |
| | Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura | Q44520847 |
| | MTHFR T677 homozygosis influences the presence of aura in migraineurs | Q44904193 |
| | Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families | Q45127817 |
| | Sporadic hemiplegic migraine | Q45164389 |
| | Investigation of hormone receptor genes in migraine. | Q45227254 |
| | Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus | Q46190178 |
| | No mutations in CACNA1A and ATP1A2 in probands with common types of migraine | Q46776240 |
| | Migraine and MTHFR C677T genotype in a population-based sample | Q46859904 |
| | Association between the tumor necrosis factor-alpha -308 G/A gene polymorphism and migraine | Q47270009 |
| | The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups | Q47631295 |
| | Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing. | Q47962832 |
| | Genetic and environmental influences on migraine: a twin study across six countries | Q48141800 |
| | Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group | Q48480301 |
| | Is the CACNA1A gene involved in familial migraine with aura? | Q48553911 |
| | Migraine and concomitant symptoms among 8167 adult twin pairs | Q49163682 |
| | Inheritance of migraine investigated by complex segregation analysis. | Q51049481 |
| | Significant linkage to migraine with aura on chromosome 11q24. | Q52010989 |
| | Genetic influence in headaches: a Swedish twin study. | Q52328632 |
| | Sexual morality, pro-life values, and attitudes toward abortion: a simultaneous latent structure analysis for 1978-1983. | Q52585032 |
| | Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity. | Q53151351 |
| | A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. | Q53275072 |
| | Migraine without aura and migraine with aura are distinct disorders. A population-based twin survey. | Q53314169 |
| | An Icelandic example of the impact of population structure on association studies | Q56681114 |
| | Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura | Q57256979 |
| | Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities | Q57268943 |
| | Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia | Q57557338 |
| | A typical migraine susceptibility region localizes to chromosome 1q31 | Q59590792 |
| | Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p | Q61819951 |
| | Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma | Q61982612 |
| | No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree | Q61982613 |
| | Investigation of theCACNA1A gene as a candidate for typical migraine susceptibility | Q61982638 |
| | Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23 | Q63383621 |
| | Migraine with aura and migraine without aura are not different entities | Q71729569 |
| | Genetic heterogeneity of familial hemiplegic migraine | Q72803020 |
| | Comorbidity of migraine and depression: investigating potential etiology and prognosis | Q73299949 |
| | The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine | Q73307591 |
| | Angiotensin-converting enzyme gene deletion polymorphism determines an increase in frequency of migraine attacks in patients suffering from migraine without aura | Q73676409 |
| | Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura | Q73800890 |
| | Migraine in twins raised together and apart | Q74778828 |
| | Migraine as a risk factor for subclinical brain lesions | Q75347052 |
| | Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13 | Q78347038 |
| | Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1. | Q78633416 |
| P433 | issue | 6 | |
| P921 | main subject | migraine | Q133823 |
| P304 | page(s) | 521-532 | |
| P577 | publication date | 2007-06-01 | |
| P1433 | published in | Lancet Neurology | Q15755067 |
| P1476 | title | Migraine: a complex genetic disorder | |
| P478 | volume | 6 | |