{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,29]],"date-time":"2022-03-29T20:18:29Z","timestamp":1648585109374},"reference-count":56,"publisher":"Springer Science and Business Media LLC","issue":"8","license":[{"start":{"date-parts":[[2014,7,11]],"date-time":"2014-07-11T00:00:00Z","timestamp":1405036800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Bundesgesundheitsbl."],"published-print":{"date-parts":[[2014,8]]},"DOI":"10.1007\/s00103-014-1998-0","type":"journal-article","created":{"date-parts":[[2014,7,10]],"date-time":"2014-07-10T14:19:38Z","timestamp":1405001978000},"page":"919-927","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Genetik prim\u00e4rer Kopfschmerzen"],"prefix":"10.1007","volume":"57","author":[{"given":"T.","family":"Freilinger","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2014,7,11]]},"reference":[{"issue":"4","key":"1998_CR1","doi-asserted-by":"crossref","first-page":"606","DOI":"10.1002\/1531-8249(199910)46:4<606::AID-ANA8>3.0.CO;2-O","volume":"46","author":"M Gervil","year":"1999","unstructured":"Gervil M, Ulrich V, Kyvik KO, Olesen J, Russell MBR (1999) Migraine without aura: a population-based twin study. Ann Neurol 46(4):606\u2013611","journal-title":"Ann Neurol"},{"issue":"2","key":"1998_CR2","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1002\/1531-8249(199902)45:2<242::AID-ANA15>3.0.CO;2-1","volume":"45","author":"VV Ulrich","year":"1999","unstructured":"Ulrich VV, Gervil MM, Kyvik KOK, Olesen JJ, Russell MBM (1999) Evidence of a genetic factor in migraine with aura: a population-based Danish twin study. Ann Neurol 45(2):242\u2013246","journal-title":"Ann Neurol"},{"issue":"7004","key":"1998_CR3","doi-asserted-by":"crossref","first-page":"541","DOI":"10.1136\/bmj.311.7004.541","volume":"311","author":"MB Russell","year":"1995","unstructured":"Russell MB, Olesen J (1995) Increased familial risk and evidence of genetic factor in migraine. BMJ 311(7004):541\u2013544","journal-title":"BMJ"},{"issue":"5","key":"1998_CR4","doi-asserted-by":"crossref","first-page":"422","DOI":"10.1375\/136905203770326420","volume":"6","author":"EJE Mulder","year":"2003","unstructured":"Mulder EJE, Van Baal CC, Gaist DD et al (2003) Genetic and environmental influences on migraine: a twin study across six countries. Twin Res 6(5):422\u2013431","journal-title":"Twin Res"},{"issue":"9","key":"1998_CR5","doi-asserted-by":"crossref","first-page":"629","DOI":"10.1177\/0333102413485658","volume":"33","author":"Headache Classification Committee of the International Headache Society (IHS)","year":"2013","unstructured":"Headache Classification Committee of the International Headache Society (IHS) (2013) The international classification of headache disorders, 3rd edition (beta version). Cephalalgia 33(9):629\u2013808","journal-title":"Cephalalgia"},{"issue":"1","key":"1998_CR6","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1056\/NEJM200107053450103","volume":"345","author":"A Ducros","year":"2001","unstructured":"Ducros A, Denier C, Joutel A et al (2001) The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med 345(1):17\u201324","journal-title":"N Engl J Med"},{"issue":"5","key":"1998_CR7","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1016\/S1474-4422(11)70048-5","volume":"10","author":"MB Russell","year":"2011","unstructured":"Russell MB, Ducros A (2011) Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management. Lancet Neurol 10(5):14\u201344","journal-title":"Lancet Neurol"},{"issue":"6","key":"1998_CR8","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1046\/j.1468-2982.1995.1506477.x","volume":"15","author":"JJ Haan","year":"1995","unstructured":"Haan JJ, Terwindt GMG, Ophoff RAR et al (1995) Is familial hemiplegic migraine a hereditary form of basilar migraine? Cephalalgia 15(6):477\u2013481","journal-title":"Cephalalgia"},{"issue":"4","key":"1998_CR9","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1111\/j.1468-2982.2008.01540.x","volume":"28","author":"T Freilinger","year":"2008","unstructured":"Freilinger T, Bohe M, Wegener B, Muller-Myhsok B, Dichgans M, Knoblauch H (2008) Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. Cephalalgia 28(4):403\u2013407","journal-title":"Cephalalgia"},{"issue":"1\u20132","key":"1998_CR10","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1016\/j.jns.2010.09.032","volume":"300","author":"T Freilinger","year":"2011","unstructured":"Freilinger T, Ackl N, Ebert A et al (2011) A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline. J Neurol Sci 300(1\u20132):160\u2013163","journal-title":"J Neurol Sci"},{"issue":"4","key":"1998_CR11","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1046\/j.1468-1331.2003.00621.x","volume":"10","author":"LL Thomsen","year":"2003","unstructured":"Thomsen LL, Olesen J, Russell MB (2003) Increased risk of migraine with typical aura in probands with familial hemiplegic migraine and their relatives. Eur J Neurol 10(4):421\u2013427","journal-title":"Eur J Neurol"},{"issue":"3","key":"1998_CR12","doi-asserted-by":"crossref","first-page":"543","DOI":"10.1016\/S0092-8674(00)81373-2","volume":"87","author":"RAR Ophoff","year":"1996","unstructured":"Ophoff RAR, Terwindt GMG, Vergouwe MNM et al (1996) Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87(3):543\u2013552","journal-title":"Cell"},{"issue":"2","key":"1998_CR13","doi-asserted-by":"crossref","first-page":"192","DOI":"10.1038\/ng1081","volume":"33","author":"MD Fusco","year":"2003","unstructured":"Fusco MD, Marconi R, Silvestri L et al (2003) Haploinsufficiency of ATP1A2 encoding the Na+\/K+ pump \u03b12 subunit associated with familial hemiplegic migraine type 2. Nat Genet 33(2):192\u2013196","journal-title":"Nat Genet"},{"issue":"45","key":"1998_CR14","doi-asserted-by":"crossref","first-page":"31097","DOI":"10.1074\/jbc.M802771200","volume":"283","author":"NN Tavraz","year":"2008","unstructured":"Tavraz NN, Friedrich T, Durr KL et al (2008) Diverse functional consequences of mutations in the Na+\/K+-ATPase 2-subunit causing familial hemiplegic migraine type 2. J Biol Chem 283(45):31097\u201331106","journal-title":"J Biol Chem"},{"issue":"9483","key":"1998_CR15","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1016\/S0140-6736(05)66786-4","volume":"366","author":"M Dichgans","year":"2005","unstructured":"Dichgans M, Freilinger T, Eckstein G et al (2005) Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet 366(9483):371\u2013377","journal-title":"Lancet"},{"issue":"28","key":"1998_CR16","doi-asserted-by":"crossref","first-page":"9799","DOI":"10.1073\/pnas.0711717105","volume":"105","author":"KM Kahlig","year":"2008","unstructured":"Kahlig KM, Rhodes TH, Pusch M et al (2008) Divergent sodium channel defects in familial hemiplegic migraine. Proc Natl Acad Sci U S A 105(28):9799\u20139804","journal-title":"Proc Natl Acad Sci U S A"},{"key":"1998_CR17","doi-asserted-by":"crossref","unstructured":"Cest\u00e8le S, Schiavon E, Rusconi R et al (2013) Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects. Proc Natl Acad Sci U S A 110(43):17546\u201317551. doi:10.1073\/pnas.1309827110","DOI":"10.1073\/pnas.1309827110"},{"issue":"2","key":"1998_CR18","doi-asserted-by":"crossref","first-page":"346","DOI":"10.1093\/brain\/awl334","volume":"130","author":"LL Thomsen","year":"2007","unstructured":"Thomsen LL, Kirchmann M, Bjornsson A et al (2007) The genetic spectrum of a population-based sample of familial hemiplegic migraine. Brain 130(2):346\u2013356","journal-title":"Brain"},{"issue":"3","key":"1998_CR19","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1007\/s10048-004-0183-2","volume":"5","author":"M Spadaro","year":"2004","unstructured":"Spadaro M, Ursu S, Lehmann-Horn F et al (2004) A G301R Na+\/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. Neurogenetics 5(3):177\u2013185","journal-title":"Neurogenetics"},{"issue":"6","key":"1998_CR20","doi-asserted-by":"crossref","first-page":"753","DOI":"10.1002\/ana.1031","volume":"49","author":"EEE Kors","year":"2001","unstructured":"Kors EEE, Terwindt GMG, Vermeulen FLF et al (2001) Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Ann Neurol 49(6):753\u2013760","journal-title":"Ann Neurol"},{"issue":"1\u20132","key":"1998_CR21","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1016\/j.jns.2009.08.050","volume":"287","author":"T Freilinger","year":"2009","unstructured":"Freilinger T, Peters N, R\u00e9mi J et al (2009) A case of Sturge-Weber syndrome with symptomatic hemiplegic migraine: clinical and multimodality imaging data during a prolonged attack. J Neurol Sci 287(1\u20132):271\u2013274","journal-title":"J Neurol Sci"},{"issue":"23","key":"1998_CR22","doi-asserted-by":"crossref","first-page":"2170","DOI":"10.1212\/01.wnl.0000295670.01629.5a","volume":"69","author":"B, Freilinger Vries de","year":"2007","unstructured":"de Vries B, Freilinger, Vanmolkot KRJ et al (2007) Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine. Neurology 69(23):2170\u20132176","journal-title":"Neurology"},{"issue":"11","key":"1998_CR23","doi-asserted-by":"crossref","first-page":"967","DOI":"10.1212\/WNL.0b013e3181f25e8f","volume":"75","author":"F Riant","year":"2010","unstructured":"Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E (2010) De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. Neurology 75(11):967\u2013972","journal-title":"Neurology"},{"issue":"2","key":"1998_CR24","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1177\/0333102410375629","volume":"31","author":"AH Stam","year":"2011","unstructured":"Stam AH, Louter MA, Haan J et al (2011) A long-term follow-up study of 18 patients with sporadic hemiplegic migraine. Cephalalgia 31(2):199\u2013205","journal-title":"Cephalalgia"},{"issue":"36","key":"1998_CR25","doi-asserted-by":"crossref","first-page":"15963","DOI":"10.1073\/pnas.1008705107","volume":"107","author":"M Suzuki","year":"2010","unstructured":"Suzuki M, Van Paesschen W, Stalmans I et al (2010) Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine. Proc Natl Acad Sci U S A 107(36):15963\u201315968","journal-title":"Proc Natl Acad Sci U S A"},{"issue":"21","key":"1998_CR26","doi-asserted-by":"crossref","first-page":"2122","DOI":"10.1212\/WNL.0b013e3182752cb8","volume":"79","author":"F Riant","year":"2012","unstructured":"Riant F, Roze E, Barbance C et al (2012) PRRT2 mutations cause hemiplegic migraine. Neurology 79(21):2122\u20132124","journal-title":"Neurology"},{"issue":"2","key":"1998_CR27","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1002\/ana.20035","volume":"55","author":"MAM Moskowitz","year":"2004","unstructured":"Moskowitz MAM, Bolay HH, Dalkara TT (2004) Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes. Ann Neurol 55(2):276\u2013280","journal-title":"Ann Neurol"},{"issue":"5","key":"1998_CR28","doi-asserted-by":"crossref","first-page":"701","DOI":"10.1016\/S0896-6273(04)00085-6","volume":"41","author":"AMJM Maagdenberg van den","year":"2004","unstructured":"van den Maagdenberg AMJM, Pietrobon D, Pizzorusso T et al (2004) A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression. Neuron 41(5):701\u2013710","journal-title":"Neuron"},{"issue":"1","key":"1998_CR29","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1002\/ana.21815","volume":"67","author":"AMJM Maagdenberg van den","year":"2010","unstructured":"van den Maagdenberg AMJM, Pizzorusso T, Kaja S et al (2010) High cortical spreading depression susceptibility and migraine-associated symptoms in Ca v2.1 S218L mice. Ann Neurol 67(1):85\u201398","journal-title":"Ann Neurol"},{"issue":"5","key":"1998_CR30","doi-asserted-by":"crossref","first-page":"762","DOI":"10.1016\/j.neuron.2009.01.027","volume":"61","author":"A Tottene","year":"2009","unstructured":"Tottene A, Conti R, Fabbro A et al (2009) Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in CaV2.1 knockin migraine mice. Neuron 61(5):762\u2013773","journal-title":"Neuron"},{"issue":"15","key":"1998_CR31","doi-asserted-by":"crossref","first-page":"5755","DOI":"10.1523\/JNEUROSCI.5346-10.2011","volume":"31","author":"K Eikermann-Haerter","year":"2011","unstructured":"Eikermann-Haerter K, Yuzawa I, Qin T et al (2011) Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice. J Neurosci 31(15):5755\u20135763","journal-title":"J Neurosci"},{"issue":"2","key":"1998_CR32","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1161\/CIRCULATIONAHA.111.045096","volume":"125","author":"K Eikermann-Haerter","year":"2012","unstructured":"Eikermann-Haerter K, Lee JH, Yuzawa I et al (2012) Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizations. Circulation 125(2):335\u2013345","journal-title":"Circulation"},{"issue":"6","key":"1998_CR33","doi-asserted-by":"crossref","first-page":"e1002129","DOI":"10.1371\/journal.pgen.1002129","volume":"7","author":"L Leo","year":"2011","unstructured":"Leo L, Gherardini L, Barone V et al (2011) Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2. PLoS Genet 7(6):e1002129\u20139","journal-title":"PLoS Genet"},{"issue":"13","key":"1998_CR34","doi-asserted-by":"crossref","first-page":"9823","DOI":"10.1074\/jbc.M109.078568","volume":"285","author":"MS Martin","year":"2010","unstructured":"Martin MS, Dutt K, Papale LA et al (2010) Altered function of the SCN1A voltage-gated sodium channel leads to -aminobutyric acid-ergic (GABAergic) interneuron abnormalities. J Biol Chem 285(13):9823\u20139834","journal-title":"J Biol Chem"},{"issue":"1","key":"1998_CR35","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1038\/ng0197-62","volume":"15","author":"O Zhuchenko","year":"1997","unstructured":"Zhuchenko O, Bailey J, Bonnen P et al (1997) Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the \u03b11A-voltage-dependent calcium channel. Nat Genet 15(1):62\u201369","journal-title":"Nat Genet"},{"issue":"6","key":"1998_CR36","doi-asserted-by":"crossref","first-page":"884","DOI":"10.1002\/ana.20134","volume":"55","author":"KJ Swoboda","year":"2004","unstructured":"Swoboda KJ, Kanavakis E, Xaidara A et al (2004) Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novelATP1A2 mutation. Ann Neurol 55(6):884\u2013887","journal-title":"Ann Neurol"},{"issue":"3","key":"1998_CR37","doi-asserted-by":"crossref","first-page":"360","DOI":"10.1002\/ana.10674","volume":"54","author":"K Vanmolkot","year":"2003","unstructured":"Vanmolkot K, Kors EE, Hottenga JJ et al (2003) Novel mutations in the Na+, K+ ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Ann Neurol 54(3):360\u2013366","journal-title":"Ann Neurol"},{"issue":"4","key":"1998_CR38","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1038\/74159","volume":"24","author":"AA Escayg","year":"2000","unstructured":"Escayg AA, MacDonald BTB, Meisler MHM et al (2000) Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nat Genet 24(4):343\u2013345","journal-title":"Nat Genet"},{"issue":"6","key":"1998_CR39","doi-asserted-by":"crossref","first-page":"1327","DOI":"10.1086\/320609","volume":"68","author":"L Claes","year":"2001","unstructured":"Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (2001) De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet 68(6):1327\u20131332","journal-title":"Am J Hum Genet"},{"issue":"13","key":"1998_CR40","doi-asserted-by":"crossref","first-page":"1178","DOI":"10.1212\/01.wnl.0000345393.53132.8c","volume":"72","author":"K Vahedi","year":"2009","unstructured":"Vahedi K, Depienne C, Le Fort D et al (2009) Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. Neurology 72(13):1178\u20131183","journal-title":"Neurology"},{"issue":"4","key":"1998_CR41","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1002\/humu.20229","volume":"26","author":"U Todt","year":"2005","unstructured":"Todt U, Dichgans M, Jurkat-Rott K et al (2005) Rare missense variants in ATP1A2 in families with clustering of common forms of migraine. Hum Mutat 26(4):315\u2013321","journal-title":"Hum Mutat"},{"issue":"10","key":"1998_CR42","doi-asserted-by":"crossref","first-page":"1157","DOI":"10.1038\/nm.2216","volume":"16","author":"RGR Lafreni\u00e8re","year":"2010","unstructured":"Lafreni\u00e8re RGR, Cader MZM, Poulin J-FJ et al (2010) A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. Nat Med 16(10):1157\u20131160","journal-title":"Nat Med"},{"issue":"8","key":"1998_CR43","doi-asserted-by":"crossref","first-page":"1237","DOI":"10.1001\/archneur.61.8.1237","volume":"61","author":"K Vahedi","year":"2004","unstructured":"Vahedi K, Chabriat H, Levy C, Joutel A, Tournier-Lasserve E, Bousser M-G (2004) Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL. Arch Neurol 61(8):1237\u20131240","journal-title":"Arch Neurol"},{"issue":"9","key":"1998_CR44","doi-asserted-by":"crossref","first-page":"1068","DOI":"10.1038\/ng2082","volume":"39","author":"A Richards","year":"2007","unstructured":"Richards A, van den Maagdenberg AMJM, Jen JC et al (2007) C-terminal truncations in human 3\u2032\u20135\u2032 DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Nat Genet 39(9):1068\u20131070","journal-title":"Nat Genet"},{"issue":"10","key":"1998_CR45","doi-asserted-by":"crossref","first-page":"1186","DOI":"10.1007\/s00115-006-2134-7","volume":"77","author":"T Freilinger","year":"2006","unstructured":"Freilinger T, Dichgans M (2006) Genetik der Migr\u00e4ne. Nervenarzt 77(10):1186\u20131195","journal-title":"Nervenarzt"},{"issue":"3","key":"1998_CR46","doi-asserted-by":"crossref","first-page":"202","DOI":"10.1212\/WNL.0b013e31823fcd87","volume":"78","author":"A Polvi","year":"2012","unstructured":"Polvi A, Siren A, Kallela M et al (2012) Shared loci for migraine and epilepsy on chromosomes 14q12\u2013q23 and 12q24.2\u2013q24.3. Neurology 78(3):202\u2013209","journal-title":"Neurology"},{"issue":"5","key":"1998_CR47","doi-asserted-by":"crossref","first-page":"613","DOI":"10.2217\/fnl.12.56","volume":"7","author":"TM Freilinger","year":"2012","unstructured":"Freilinger TM (2012) Genetics of migraine: an update. Future Neurol 7(5):613\u2013626","journal-title":"Future Neurol"},{"issue":"21","key":"1998_CR48","doi-asserted-by":"crossref","first-page":"3318","DOI":"10.1093\/hmg\/ddn227","volume":"17","author":"DR Nyholt","year":"2008","unstructured":"Nyholt DR, LaForge KS, Kallela M et al (2008) A high-density association screen of 155 ion transport genes for involvement with common migraine. Hum Mol Genet 17(21):3318\u20133331","journal-title":"Hum Mol Genet"},{"issue":"10","key":"1998_CR49","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1038\/ng.652","volume":"42","author":"V Anttila","year":"2010","unstructured":"Anttila V, Stefansson H, Kallela M et al (2010) Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat Genet 42(10):869\u2013873","journal-title":"Nat Genet"},{"issue":"7","key":"1998_CR50","doi-asserted-by":"crossref","first-page":"695","DOI":"10.1038\/ng.856","volume":"43","author":"DI Chasman","year":"2011","unstructured":"Chasman DI, Sch\u00fcrks M, Anttila V et al (2011) Genome-wide association study reveals three susceptibility loci for common migraine in the general population. Nat Genet 43(7):695\u2013698","journal-title":"Nat Genet"},{"issue":"7","key":"1998_CR51","doi-asserted-by":"crossref","first-page":"777","DOI":"10.1038\/ng.2307","volume":"44","author":"T Freilinger","year":"2012","unstructured":"Freilinger T, Anttila V, de Vries B et al (2012) Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat Genet 44(7):777\u2013782","journal-title":"Nat Genet"},{"issue":"8","key":"1998_CR52","doi-asserted-by":"crossref","first-page":"912","DOI":"10.1038\/ng.2676","volume":"45","author":"V Anttila","year":"2013","unstructured":"Anttila V, Winsvold BS, Gormley P et al (2013) Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat Genet 45(8):912\u2013917","journal-title":"Nat Genet"},{"issue":"5","key":"1998_CR53","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1016\/S1474-4422(04)00735-5","volume":"3","author":"M Bj\u00f8rn Russell","year":"2004","unstructured":"Bj\u00f8rn Russell M (2004) Epidemiology and genetics of cluster headache. Lancet Neurol 3(5):279\u2013283","journal-title":"Lancet Neurol"},{"issue":"2","key":"1998_CR54","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1007\/s11916-010-0096-8","volume":"14","author":"M Sch\u00fcrks","year":"2010","unstructured":"Sch\u00fcrks M (2010) Genetics of cluster headache. Curr Pain Headache Rep 14(2):132\u2013139","journal-title":"Curr Pain Headache Rep"},{"issue":"3","key":"1998_CR55","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1007\/s10194-007-0383-x","volume":"8","author":"I Rainero","year":"2007","unstructured":"Rainero I, Rubino E, Valfr\u00e8 W et al (2007) Association between the G1246A polymorphism of the hypocretin receptor 2 gene and cluster headache: a meta-analysis. J Headache Pain 8(3):152\u2013156","journal-title":"J Headache Pain"},{"issue":"2","key":"1998_CR56","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1007\/s10194-007-0366-y","volume":"8","author":"MB Russell","year":"2007","unstructured":"Russell MB (2007) Genetics of tension-type headache. J Headache Pain 8(2):71\u201376","journal-title":"J Headache Pain"}],"container-title":["Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00103-014-1998-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00103-014-1998-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00103-014-1998-0","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,23]],"date-time":"2019-05-23T03:17:03Z","timestamp":1558581423000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00103-014-1998-0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,7,11]]},"references-count":56,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2014,8]]}},"alternative-id":["1998"],"URL":"https:\/\/doi.org\/10.1007\/s00103-014-1998-0","relation":{},"ISSN":["1436-9990","1437-1588"],"issn-type":[{"value":"1436-9990","type":"print"},{"value":"1437-1588","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,7,11]]}}}