{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,2]],"date-time":"2025-11-02T16:45:00Z","timestamp":1762101900769,"version":"3.40.5"},"reference-count":140,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2016,10,1]],"date-time":"2016-10-01T00:00:00Z","timestamp":1475280000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","jns-journal.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of the Neurological Sciences"],"published-print":{"date-parts":[[2016,10]]},"DOI":"10.1016\/j.jns.2016.08.008","type":"journal-article","created":{"date-parts":[[2016,8,4]],"date-time":"2016-08-04T18:04:22Z","timestamp":1470333862000},"page":"63-76","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":20,"special_numbering":"C","title":["Biomarkers of migraine: Part 1 \u2013 Genetic markers"],"prefix":"10.1016","volume":"369","author":[{"given":"Natalia","family":"Kondratieva","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julia","family":"Azimova","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kirill","family":"Skorobogatykh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexey","family":"Sergeev","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elena","family":"Naumova","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zarema","family":"Kokaeva","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Arina","family":"Anuchina","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Olga","family":"Rudko","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gyuzyal","family":"Tabeeva","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2674-5783","authenticated-orcid":false,"given":"Eugene","family":"Klimov","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0005","doi-asserted-by":"crossref","first-page":"650","DOI":"10.1212\/01.wnl.0000342517.97178.f6","article-title":"ACE D\/I polymorphism, migraine, and cardiovascular disease in women","volume":"72","author":"Schurks","year":"2009","journal-title":"Neurology"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0010","doi-asserted-by":"crossref","first-page":"147","DOI":"10.2217\/pgs.13.186","article-title":"Association between migraine and ACE gene (insertion\/deletion) polymorphism: the BioBIM study","volume":"15","author":"Palmirotta","year":"2014","journal-title":"Pharmacogenomics"},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0015","first-page":"120","article-title":"Homozygous deletion genotype of angiotensin converting enzyme confers protection against migraine in man","volume":"14","author":"Lin","year":"2005","journal-title":"Acta Neurol. Taiwanica"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0020","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1111\/head.12008","article-title":"Angiotensin I-converting enzyme gene (I\/D) polymorphism in patients with migraine","volume":"53","author":"Horasanli","year":"2013","journal-title":"Headache"},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0025","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1159\/000008151","article-title":"Angiotensin-converting enzyme gene deletion polymorphism determines an increase in frequency of migraine attacks in patients suffering from migraine without aura","volume":"43","author":"Paterna","year":"2000","journal-title":"Eur. Neurol."},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0030","doi-asserted-by":"crossref","first-page":"588","DOI":"10.1111\/j.1526-4610.2009.01570.x","article-title":"MTHFR 677C>T and ACE D\/I polymorphisms in migraine: a systematic review and meta-analysis","volume":"50","author":"Schurks","year":"2010","journal-title":"Headache"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0035","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1016\/j.neulet.2004.10.041","article-title":"Association of the insertion\/deletion polymorphism of the angiotensin I-converting enzyme gene in patients of migraine with aura","volume":"374","author":"Kowa","year":"2005","journal-title":"Neurosci. Lett."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0040","doi-asserted-by":"crossref","first-page":"357","DOI":"10.1007\/s11010-011-1188-4","article-title":"MAOA, MTHFR, and TNF-beta genes polymorphisms and personality traits in the pathogenesis of migraine","volume":"363","author":"Ishii","year":"2012","journal-title":"Mol. Cell. Biochem."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0045","doi-asserted-by":"crossref","first-page":"91","DOI":"10.2174\/187152410791196404","article-title":"Migraine and coronary artery disease: an open study on the genetic polymorphism of the 5, 10 methylenetetrahydrofolate (MTHFR) and angiotensin I-converting enzyme (ACE) genes","volume":"10","author":"Pizza","year":"2010","journal-title":"Cent. Nerv. Syst. Agents Med. Chem."},{"issue":"9","key":"10.1016\/j.jns.2016.08.008_bb0050","doi-asserted-by":"crossref","first-page":"960","DOI":"10.1111\/j.1468-2982.2008.01824.x","article-title":"Association of von Willebrand factor activity with ACE I\/D and MTHFR C677T polymorphisms in migraine","volume":"29","author":"Tietjen","year":"2009","journal-title":"Cephalalgia"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0055","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1016\/j.jns.2008.11.002","article-title":"Role of the ACE ID and MTHFR C677T polymorphisms in genetic susceptibility of migraine in a north Indian population","volume":"277","author":"Joshi","year":"2009","journal-title":"J. Neurol. Sci."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0060","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1016\/j.molbrainres.2005.01.006","article-title":"Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility","volume":"136","author":"Lea","year":"2005","journal-title":"Brain Res. Mol. Brain Res."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0065","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1111\/j.1468-2982.2006.01269.x","article-title":"Combined effects of ACE and MMP-3 polymorphisms on migraine development","volume":"27","author":"Kara","year":"2007","journal-title":"Cephalalgia"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0070","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1111\/j.1526-4610.2009.01396.x","article-title":"Alcohol dehydrogenase 2 genotype and risk for migraine","volume":"50","author":"Garcia-Martin","year":"2010","journal-title":"Headache"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0075","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1007\/s12017-012-8195-9","article-title":"Identification of a novel ANKK1 and other dopaminergic (DRD2 and DBH) gene variants in migraine susceptibility","volume":"15","author":"Ghosh","year":"2013","journal-title":"Neruomol. Med."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0080","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1111\/head.12493","article-title":"Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine","volume":"55","author":"Garcia-Martin","year":"2015","journal-title":"Headache"},{"issue":"8","key":"10.1016\/j.jns.2016.08.008_bb0085","doi-asserted-by":"crossref","first-page":"568","DOI":"10.1089\/gtmb.2014.0037","article-title":"DNA repair gene variants in migraine","volume":"18","author":"Cetinkaya","year":"2014","journal-title":"Genet. Test. Mol. Biomarkers."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0090","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1016\/S0304-3940(01)02432-6","article-title":"Apolipoprotein E gene polymorphisms in patients with migraine","volume":"317","author":"Rainero","year":"2002","journal-title":"Neurosci. Lett."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0095","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1007\/s10194-008-0094-y","article-title":"Polymorphism in apolipoprotein E among migraineurs and tension-type headache subjects","volume":"10","author":"Gupta","year":"2009","journal-title":"J. Headache Pain."},{"issue":"8","key":"10.1016\/j.jns.2016.08.008_bb0100","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1089\/dna.2010.1197","article-title":"Vascular gene polymorphisms (EDNRA-231 G>A and APOE HhaI) and risk for migraine","volume":"30","author":"Joshi","year":"2011","journal-title":"DNA Cell Biol."},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0105","doi-asserted-by":"crossref","first-page":"777","DOI":"10.1038\/ng.2307","article-title":"Genome-wide association analysis identifies susceptibility loci for migraine without aura","volume":"44","author":"Freilinger","year":"2012","journal-title":"Nat. Genet."},{"issue":"11","key":"10.1016\/j.jns.2016.08.008_bb0110","doi-asserted-by":"crossref","first-page":"1375","DOI":"10.1177\/0333102410368443","article-title":"BDNF and CGRP interaction: implications in migraine susceptibility","volume":"30","author":"Lemos","year":"2010","journal-title":"Cephalalgia"},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0115","doi-asserted-by":"crossref","first-page":"1184","DOI":"10.1111\/head.12351","article-title":"Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraine","volume":"54","author":"Sutherland","year":"2014","journal-title":"Headache"},{"issue":"21","key":"10.1016\/j.jns.2016.08.008_bb0120","doi-asserted-by":"crossref","first-page":"3318","DOI":"10.1093\/hmg\/ddn227","article-title":"A high-density association screen of 155 ion transport genes for involvement with common migraine","volume":"17","author":"Nyholt","year":"2008","journal-title":"Hum. Mol. Genet."},{"issue":"12","key":"10.1016\/j.jns.2016.08.008_bb0125","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0029337","article-title":"Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory","volume":"6","author":"Heck","year":"2011","journal-title":"PLoS One"},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0130","doi-asserted-by":"crossref","first-page":"1136","DOI":"10.1111\/j.1526-4610.2006.00504.x","article-title":"Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4","volume":"46","author":"von Brevern","year":"2006","journal-title":"Headache"},{"issue":"Suppl.1","key":"10.1016\/j.jns.2016.08.008_bb0135","article-title":"Association of cholecystokinin receptor 1 gene polymorphism and migraine","volume":"333","author":"Kondratyeva","year":"2013","journal-title":"J. Neurol. Sci."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0140","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1016\/j.neulet.2009.06.021","article-title":"Variations in the cannabinoid receptor 1 gene predispose to migraine","volume":"461","author":"Juhasz","year":"2009","journal-title":"Neurosci. Lett."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0145","doi-asserted-by":"crossref","first-page":"1097","DOI":"10.1016\/j.jpain.2013.04.006","article-title":"An opposite-direction modulation of the COMT Val158Met polymorphism on the clinical response to intrathecal morphine and triptans","volume":"14","author":"Cargnin","year":"2013","journal-title":"J. Pain"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0150","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1016\/S0169-328X(01)00219-4","article-title":"Significance of the catechol-O-methyltransferase gene polymorphism in migraine","volume":"94","author":"Emin Erdal","year":"2001","journal-title":"Brain Res. Mol. Brain Res."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0155","doi-asserted-by":"crossref","first-page":"24","DOI":"10.3988\/jcn.2007.3.1.24","article-title":"Genetic contribution of catechol-O-methyltransferase polymorphism in patients with migraine without Aura","volume":"3","author":"Park","year":"2007","journal-title":"J. Clin. Neurol."},{"issue":"183","key":"10.1016\/j.jns.2016.08.008_bb0160","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1126\/scitranslmed.3005784","article-title":"Casein kinase idelta mutations in familial migraine and advanced sleep phase","volume":"5","author":"Brennan","year":"2013","journal-title":"Sci. Transl. Med."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0165","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1007\/s10194-010-0202-7","article-title":"Frequencies of genetic polymorphisms related to triptans metabolism in chronic migraine","volume":"11","author":"Gentile","year":"2010","journal-title":"J. Headache Pain."},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0170","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0034828","article-title":"Potential role of aromatase over estrogen receptor gene polymorphisms in migraine susceptibility: a case control study from North India","volume":"7","author":"Ghosh","year":"2012","journal-title":"PLoS One"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0175","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1007\/PL00022977","article-title":"Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine","volume":"3","author":"Lea","year":"2000","journal-title":"Neurogenetics"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0180","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1016\/j.jns.2006.09.013","article-title":"Association between a 19bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura","volume":"251","author":"Fernandez","year":"2006","journal-title":"J. Neurol. Sci."},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0185","doi-asserted-by":"crossref","first-page":"1109","DOI":"10.1111\/j.1526-4637.2011.01153.x","article-title":"Role of dopaminergic gene polymorphisms (DBH 19bp indel and DRD2 Nco I) in genetic susceptibility to migraine in North Indian population","volume":"12","author":"Ghosh","year":"2011","journal-title":"Pain Med."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0190","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1007\/s00439-009-0623-z","article-title":"New genetic evidence for involvement of the dopamine system in migraine with aura","volume":"125","author":"Todt","year":"2009","journal-title":"Hum. Genet."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0195","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1007\/s10048-009-0176-2","article-title":"Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus","volume":"10","author":"Fernandez","year":"2009","journal-title":"Neurogenetics"},{"issue":"9","key":"10.1016\/j.jns.2016.08.008_bb0200","doi-asserted-by":"crossref","first-page":"1220","DOI":"10.1111\/j.1468-1331.2010.02988.x","article-title":"Dopamine receptor 3 (DRD3) polymorphism and risk for migraine","volume":"17","author":"Garcia-Martin","year":"2010","journal-title":"Eur. J. Neurol."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0205","doi-asserted-by":"crossref","first-page":"574","DOI":"10.1002\/ana.21140","article-title":"A dopamine D4 receptor exon 3 VNTR allele protecting against migraine without aura","volume":"61","author":"de Sousa","year":"2007","journal-title":"Ann. Neurol."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0210","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1007\/s100720300005","article-title":"A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes","volume":"23","author":"Mochi","year":"2003","journal-title":"Neurol. Sci."},{"issue":"9","key":"10.1016\/j.jns.2016.08.008_bb0215","doi-asserted-by":"crossref","first-page":"1009","DOI":"10.1111\/j.1468-1331.2006.01415.x","article-title":"A genetic association study of dopamine metabolism-related genes and chronic headache with drug abuse","volume":"13","author":"Cevoli","year":"2006","journal-title":"Eur. J. Neurol."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0220","doi-asserted-by":"crossref","first-page":"e550","DOI":"10.1161\/STROKEAHA.109.557462","article-title":"Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study","volume":"40","author":"MacClellan","year":"2009","journal-title":"Stroke"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0225","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1016\/j.jns.2012.09.027","article-title":"Association of 231G>A polymorphism of endothelin type A receptor gene with migraine: a meta-analysis","volume":"323","author":"Miao","year":"2012","journal-title":"J. Neurol. Sci."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0230","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1111\/j.1468-2982.2009.01967.x","article-title":"Role of the oestrogen receptor (ESR1 PvuII and ESR1 325C->G) and progesterone receptor (PROGINS) polymorphisms in genetic susceptibility to migraine in a North Indian population","volume":"30","author":"Joshi","year":"2010","journal-title":"Cephalalgia"},{"issue":"12","key":"10.1016\/j.jns.2016.08.008_bb0235","doi-asserted-by":"crossref","first-page":"1462","DOI":"10.1111\/j.1468-2982.2006.01228.x","article-title":"Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura","volume":"26","author":"Kaunisto","year":"2006","journal-title":"Cephalalgia"},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0240","doi-asserted-by":"crossref","first-page":"1438","DOI":"10.1111\/j.1526-4610.2008.01294.x","article-title":"Multilocus analyses reveal involvement of the ESR1, ESR2, and FSHR genes in migraine","volume":"48","author":"Oterino","year":"2008","journal-title":"Headache"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0245","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1007\/s10048-004-0181-4","article-title":"The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case\/control groups","volume":"5","author":"Colson","year":"2004","journal-title":"Neurogenetics"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0250","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1097\/01.wnr.0000192735.85287.f4","article-title":"Association of migraine and ESR1 G325C polymorphism","volume":"17","author":"Oterino","year":"2006","journal-title":"Neuroreport"},{"issue":"5","key":"10.1016\/j.jns.2016.08.008_bb0255","doi-asserted-by":"crossref","first-page":"714","DOI":"10.1016\/j.thromres.2014.01.025","article-title":"Should women suffering from migraine with aura be screened for biological thrombophilia?: results from a cross-sectional French study","volume":"133","author":"Maitrot-Mantelet","year":"2014","journal-title":"Thromb. Res."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0260","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1179\/102453312X13221316478010","article-title":"Thrombophilic gene mutations in children with migraine","volume":"17","author":"Ferrara","year":"2012","journal-title":"Hematology"},{"key":"10.1016\/j.jns.2016.08.008_bb0265","article-title":"Gene-based pleiotropy across migraine with aura and migraine without aura patient groups","author":"Zhao","year":"2015","journal-title":"Cephalalgia"},{"issue":"9","key":"10.1016\/j.jns.2016.08.008_bb0270","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0074087","article-title":"Interaction between gamma-aminobutyric acid A receptor genes: new evidence in migraine susceptibility","volume":"8","author":"Quintas","year":"2013","journal-title":"PLoS One"},{"key":"10.1016\/j.jns.2016.08.008_bb0275","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1186\/1471-2350-11-103","article-title":"Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility","volume":"11","author":"Formicola","year":"2010","journal-title":"BMC Med. Genet."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0280","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1186\/s10194-016-0592-2","article-title":"Case-control study of GRIA1 and GRIA3 gene variants in migraine","volume":"17","author":"Fang","year":"2015","journal-title":"J. Headache Pain."},{"issue":"8","key":"10.1016\/j.jns.2016.08.008_bb0285","doi-asserted-by":"crossref","first-page":"1245","DOI":"10.1111\/head.12151","article-title":"Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort","volume":"53","author":"Maher","year":"2013","journal-title":"Headache"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0290","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1007\/s10194-011-0314-8","article-title":"Evidence for an association between migraine and the hypocretin receptor 1 gene","volume":"12","author":"Rainero","year":"2011","journal-title":"J. Headache Pain."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0295","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1111\/j.1468-2982.2006.01231.x","article-title":"Haemochromatosis gene (HFE) polymorphisms and migraine: an association study","volume":"27","author":"Rainero","year":"2007","journal-title":"Cephalalgia"},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0300","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1007\/s10194-005-0180-3","article-title":"Association between migraine and HLA-DRB1 gene polymorphisms","volume":"6","author":"Rainero","year":"2005","journal-title":"J. Headache Pain"},{"issue":"2\u20133","key":"10.1016\/j.jns.2016.08.008_bb0305","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1016\/j.neulet.2005.08.071","article-title":"HLA-DRB1 genotyping in Italian migraine patients","volume":"393","author":"Rainero","year":"2006","journal-title":"Neurosci. Lett."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0310","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1016\/j.arcmed.2011.01.009","article-title":"A280V polymorphism in the histamine H3 receptor as a risk factor for migraine","volume":"42","author":"Millan-Guerrero","year":"2011","journal-title":"Arch. Med. Res."},{"issue":"9","key":"10.1016\/j.jns.2016.08.008_bb0315","doi-asserted-by":"crossref","first-page":"1227","DOI":"10.1007\/s00702-007-0713-9","article-title":"Functional polymorphisms of the 5-HT1A and 5-HT1B receptor are associated with clinical symptoms in migraineurs","volume":"114","author":"Marziniak","year":"2007","journal-title":"J. Neural Transm."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0320","doi-asserted-by":"crossref","first-page":"1751","DOI":"10.1248\/bpb.33.1751","article-title":"Association of the A-1438G polymorphism in serotonin 2A receptor in migraine with aura among Japanese patients","volume":"33","author":"Naito","year":"2010","journal-title":"Biol. Pharm. Bull."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0325","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1016\/S0022-510X(01)00556-1","article-title":"Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine","volume":"188","author":"Erdal","year":"2001","journal-title":"J. Neurol. Sci."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0330","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1016\/j.jns.2014.07.030","article-title":"Associations of a polymorphism in the intercellular adhesion molecule-1 (ICAM1) gene and ICAM1 serum levels with migraine in a Chinese Han population","volume":"345","author":"He","year":"2014","journal-title":"J. Neurol. Sci."},{"issue":"5","key":"10.1016\/j.jns.2016.08.008_bb0335","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1046\/j.1526-4610.2002.02103.x","article-title":"A polymorphism in the interleukin-1alpha gene influences the clinical features of migraine","volume":"42","author":"Rainero","year":"2002","journal-title":"Headache"},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0340","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1111\/j.1526-4637.2009.00791.x","article-title":"Cytokine polymorphism in patients with migraine: some suggestive clues of migraine and inflammation","volume":"11","author":"Yilmaz","year":"2010","journal-title":"Pain Med."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0345","doi-asserted-by":"crossref","first-page":"135","DOI":"10.1006\/geno.2001.6647","article-title":"Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine","volume":"78","author":"McCarthy","year":"2001","journal-title":"Genomics"},{"issue":"Suppl. 2","key":"10.1016\/j.jns.2016.08.008_bb0350","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1111\/j.1526-4610.2012.02237.x","article-title":"Identification of novel genes involved in migraine","volume":"52","author":"Lafreniere","year":"2012","journal-title":"Headache"},{"key":"10.1016\/j.jns.2016.08.008_bb0355","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1186\/1471-2350-8-57","article-title":"Association analysis of chromosome 1 migraine candidate genes","volume":"8","author":"Fernandez","year":"2007","journal-title":"BMC Med. Genet."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0360","doi-asserted-by":"crossref","first-page":"1157","DOI":"10.1038\/nm.2216","article-title":"A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura","volume":"16","author":"Lafreniere","year":"2010","journal-title":"Nat. Med."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0365","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1007\/s10194-011-0392-7","article-title":"Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate","volume":"12","author":"Cox","year":"2011","journal-title":"J. Headache Pain"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0370","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1111\/j.1526-4610.2005.05027.x","article-title":"A highly polymorphic poly-glutamine stretch in the potassium channel KCNN3 in migraine","volume":"45","author":"Mossner","year":"2005","journal-title":"Headache"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0375","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/S0022-510X(03)00124-2","article-title":"Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura","volume":"213","author":"Mochi","year":"2003","journal-title":"J. Neurol. Sci."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0380","doi-asserted-by":"crossref","first-page":"1583","DOI":"10.1111\/head.12240","article-title":"Genome-wide-associated variants in migraine susceptibility: a replication study from North India","volume":"53","author":"Ghosh","year":"2013","journal-title":"Headache"},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0385","doi-asserted-by":"crossref","first-page":"695","DOI":"10.1038\/ng.856","article-title":"Genome-wide association study reveals three susceptibility loci for common migraine in the general population","volume":"43","author":"Chasman","year":"2011","journal-title":"Nat. Genet."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0390","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1016\/j.jns.2013.12.022","article-title":"SLC1A2 rs3794087 variant and risk for migraine","volume":"338","author":"Garcia-Martin","year":"2014","journal-title":"J. Neurol. Sci."},{"issue":"5","key":"10.1016\/j.jns.2016.08.008_bb0395","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1046\/j.1526-4610.2002.02104.x","article-title":"Tumor necrosis factor gene polymorphism in migraine","volume":"42","author":"Trabace","year":"2002","journal-title":"Headache"},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0400","doi-asserted-by":"crossref","first-page":"1056","DOI":"10.1111\/j.1526-4610.2007.00847.x","article-title":"Association between a polymorphism in the lymphotoxin-a promoter region and migraine","volume":"47","author":"Lee","year":"2007","journal-title":"Headache"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0405","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/j.jns.2004.11.045","article-title":"Monoamine oxidases A and B gene polymorphisms in migraine patients","volume":"228","author":"Filic","year":"2005","journal-title":"J. Neurol. Sci."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0410","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1016\/j.neulet.2005.11.039","article-title":"Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG","volume":"396","author":"Norberg","year":"2006","journal-title":"Neurosci. Lett."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0415","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1016\/j.gene.2012.09.109","article-title":"Matrix metalloproteinase (MMP)-2 gene polymorphisms affect circulating MMP-2 levels in patients with migraine with aura","volume":"512","author":"Goncalves","year":"2013","journal-title":"Gene"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0420","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1016\/j.jneuroim.2012.07.016","article-title":"Specific matrix metalloproteinase 9 (MMP-9) haplotype affect the circulating MMP-9 levels in women with migraine","volume":"252","author":"Martins-Oliveira","year":"2012","journal-title":"J. Neuroimmunol."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0425","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1038\/ng.652","article-title":"Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1","volume":"42","author":"Anttila","year":"2010","journal-title":"Nat. Genet."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0430","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1016\/j.molbrainres.2005.05.015","article-title":"Thymidylate synthase promoter tandem repeat and MTHFD1 R653Q polymorphisms modulate the risk for migraine conferred by the MTHFR T677 allele","volume":"139","author":"Oterino","year":"2005","journal-title":"Brain Res. Mol. Brain Res."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0435","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1016\/j.jns.2013.10.008","article-title":"MTHFR C677T polymorphism and migraine risk: a meta-analysis","volume":"336","author":"Liu","year":"2014","journal-title":"J. Neurol. Sci."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0440","doi-asserted-by":"crossref","first-page":"762","DOI":"10.1002\/1096-8628(20001204)96:6<762::AID-AJMG12>3.0.CO;2-X","article-title":"The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine","volume":"96","author":"Kowa","year":"2000","journal-title":"Am. J. Med. Genet."},{"issue":"12","key":"10.1016\/j.jns.2016.08.008_bb0445","doi-asserted-by":"crossref","first-page":"3145","DOI":"10.1161\/STROKEAHA.107.491506","article-title":"Migraine mediates the influence of C677T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect","volume":"38","author":"Pezzini","year":"2007","journal-title":"Stroke"},{"key":"10.1016\/j.jns.2016.08.008_bb0450","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1186\/1756-0500-3-213","article-title":"Analysis of the MTHFR C677T variant with migraine phenotypes","volume":"3","author":"Liu","year":"2010","journal-title":"BMC Res. Notes"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0455","doi-asserted-by":"crossref","first-page":"372","DOI":"10.1002\/ana.20755","article-title":"Migraine and MTHFR C677T genotype in a population-based sample","volume":"59","author":"Scher","year":"2006","journal-title":"Ann. Neurol."},{"issue":"8","key":"10.1016\/j.jns.2016.08.008_bb0460","doi-asserted-by":"crossref","first-page":"818","DOI":"10.1111\/j.1468-2982.2007.01400.x","article-title":"Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis","volume":"29","author":"Rubino","year":"2009","journal-title":"Cephalalgia"},{"key":"10.1016\/j.jns.2016.08.008_bb0465","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1186\/1741-7015-2-3","article-title":"The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura","volume":"2","author":"Lea","year":"2004","journal-title":"BMC Med."},{"key":"10.1016\/j.jns.2016.08.008_bb0470","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1016\/j.neulet.2013.06.028","article-title":"Association of MTHFR C677T polymorphism with susceptibility to migraine in the Chinese population","volume":"549","author":"An","year":"2013","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.jns.2016.08.008_bb0475","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1186\/1471-2377-13-103","article-title":"Effects of MTHFR gene polymorphism on the clinical and electrophysiological characteristics of migraine","volume":"13","author":"Azimova","year":"2013","journal-title":"BMC Neurol."},{"key":"10.1016\/j.jns.2016.08.008_bb0480","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1186\/1471-2377-11-66","article-title":"Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis","volume":"11","author":"Samaan","year":"2011","journal-title":"BMC Neurol."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0485","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1111\/j.1468-2982.2004.00692.x","article-title":"MTHFR T677 homozygosis influences the presence of aura in migraineurs","volume":"24","author":"Oterino","year":"2004","journal-title":"Cephalalgia"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0490","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1016\/S0169-328X(02)00672-1","article-title":"Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk","volume":"111","author":"Kara","year":"2003","journal-title":"Brain Res. Mol. Brain Res."},{"issue":"8","key":"10.1016\/j.jns.2016.08.008_bb0495","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1038\/ejhg.2011.48","article-title":"Meta-analysis of genome-wide association for migraine in six population-based European cohorts","volume":"19","author":"Ligthart","year":"2011","journal-title":"Eur. J. Hum. Genet."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0500","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1089\/dna.2010.1102","article-title":"Association of the pentanucleotide repeat polymorphism in NOS2 promoter region with susceptibility to migraine in a Chinese population","volume":"30","author":"Jia","year":"2011","journal-title":"DNA Cell Biol."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0505","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1007\/s11010-012-1231-0","article-title":"Inducible nitric oxide synthase haplotype associated with migraine and aura","volume":"364","author":"de OS","year":"2012","journal-title":"Mol. Cell. Biochem."},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0510","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1007\/s11010-012-1409-5","article-title":"Interaction among nitric oxide (NO)-related genes in migraine susceptibility","volume":"370","author":"Goncalves","year":"2012","journal-title":"Mol. Cell. Biochem."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0515","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1089\/dna.2010.1152","article-title":"Endothelial nitric oxide synthase haplotypes associated with aura in patients with migraine","volume":"30","author":"Goncalves","year":"2011","journal-title":"DNA Cell Biol."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0520","doi-asserted-by":"crossref","first-page":"1575","DOI":"10.1111\/j.1526-4610.2006.00614.x","article-title":"Endothelial nitric oxide synthase (Glu298Asp) polymorphism is an independent risk factor for migraine with aura","volume":"46","author":"Borroni","year":"2006","journal-title":"Headache"},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0525","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1177\/0333102410381143","article-title":"Association of a Notch 3 gene polymorphism with migraine susceptibility","volume":"31","author":"Menon","year":"2011","journal-title":"Cephalalgia"},{"key":"10.1016\/j.jns.2016.08.008_bb0530","doi-asserted-by":"crossref","first-page":"28","DOI":"10.1186\/1129-2377-14-28","article-title":"Genetic variants in the NOTCH4 gene influence the clinical features of migraine","volume":"14","author":"Rubino","year":"2013","journal-title":"J. Headache Pain"},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0535","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1007\/s10194-012-0468-z","article-title":"The human mu-opioid receptor gene polymorphism (A118G) is associated with head pain severity in a clinical cohort of female migraine with aura patients","volume":"13","author":"Menon","year":"2012","journal-title":"J. Headache Pain"},{"key":"10.1016\/j.jns.2016.08.008_bb0540","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/j.clineuro.2014.02.003","article-title":"Association between promoter region of the uPAR (rs344781) gene polymorphism in genetic susceptibility to migraine without aura in three Iranian hospitals","volume":"120","author":"Zandifar","year":"2014","journal-title":"Clin. Neurol. Neurosurg."},{"issue":"9","key":"10.1016\/j.jns.2016.08.008_bb0545","doi-asserted-by":"crossref","first-page":"1482","DOI":"10.1007\/s00415-010-5551-2","article-title":"Paraoxonase 1 (PON1) polymorphisms and risk for migraine","volume":"257","author":"Garcia-Martin","year":"2010","journal-title":"J. Neurol."},{"issue":"10\u221211","key":"10.1016\/j.jns.2016.08.008_bb0550","doi-asserted-by":"crossref","first-page":"832","DOI":"10.1016\/j.clinbiochem.2011.04.015","article-title":"Increased levels of total oxidant status and decreased activity of arylesterase in migraineurs","volume":"44","author":"Yilmaz","year":"2011","journal-title":"Clin. Biochem."},{"key":"10.1016\/j.jns.2016.08.008_bb0555","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1186\/1471-2350-15-38","article-title":"A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample","volume":"15","author":"Ran","year":"2014","journal-title":"BMC Med. Genet."},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0560","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1016\/j.gene.2012.12.110","article-title":"Cox-2 gene variants in migraine","volume":"518","author":"Dasdemir","year":"2013","journal-title":"Gene"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0565","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1016\/j.gene.2012.11.053","article-title":"Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine","volume":"515","author":"Sutherland","year":"2013","journal-title":"Gene"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0570","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1016\/j.jns.2015.01.015","article-title":"Association of the long pentraxin PTX3 gene polymorphism (rs3816527) with migraine in an Iranian population","volume":"349","author":"Zandifar","year":"2015","journal-title":"J. Neurol. Sci."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0575","doi-asserted-by":"crossref","first-page":"143","DOI":"10.3988\/jcn.2011.7.3.143","article-title":"Polymorphism of the glutamate transporter protein EAAT2 and migraine transformation into chronic daily headache","volume":"7","author":"Shin","year":"2011","journal-title":"J. Clin. Neurol."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0580","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1111\/j.1526-4610.2006.00379.x","article-title":"Contribution of serotonin transporter gene polymorphisms to pediatric migraine","volume":"46","author":"Szilagyi","year":"2006","journal-title":"Headache"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0585","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/S0022-510X(01)00491-9","article-title":"Significance of serotonin transporter gene polymorphism in migraine","volume":"186","author":"Yilmaz","year":"2001","journal-title":"J. Neurol. Sci."},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0590","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1007\/s10194-010-0230-3","article-title":"STin2 VNTR polymorphism in the serotonin transporter gene and migraine: pooled and meta-analyses","volume":"11","author":"Schurks","year":"2010","journal-title":"J. Headache Pain"},{"issue":"1\u20132","key":"10.1016\/j.jns.2016.08.008_bb0595","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1016\/j.jns.2011.03.016","article-title":"Association of 5-HTT gene polymorphisms with migraine: a systematic review and meta-analysis","volume":"305","author":"Liu","year":"2011","journal-title":"J. Neurol. Sci."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0600","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1046\/j.1468-2982.1998.1801023.x","article-title":"Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura","volume":"18","author":"Ogilvie","year":"1998","journal-title":"Cephalalgia"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0605","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1111\/j.1526-4610.2009.01553.x","article-title":"Single nucleotide polymorphisms of the serotonin transporter gene in migraine\u2013an association study","volume":"50","author":"Bayerer","year":"2010","journal-title":"Headache"},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0610","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1212\/01.WNL.0000148597.52312.9E","article-title":"A functional serotonin transporter gene polymorphism is associated with migraine with aura","volume":"64","author":"Marziniak","year":"2005","journal-title":"Neurology"},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0615","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1007\/s10194-005-0179-9","article-title":"Functional serotonin 5-HTTLPR polymorphism is a risk factor for migraine with aura","volume":"6","author":"Borroni","year":"2005","journal-title":"J. Headache Pain"},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0620","doi-asserted-by":"crossref","first-page":"2019","DOI":"10.1007\/s00415-014-7475-8","article-title":"Novel mutation of SLC20A2 in an Italian patient presenting with migraine","volume":"261","author":"Rubino","year":"2014","journal-title":"J. Neurol."},{"issue":"4","key":"10.1016\/j.jns.2016.08.008_bb0625","doi-asserted-by":"crossref","first-page":"422","DOI":"10.1001\/archneurol.2010.37","article-title":"Evidence of syntaxin 1A involvement in migraine susceptibility: a Portuguese study","volume":"67","author":"Lemos","year":"2010","journal-title":"Arch. Neurol."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0630","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1177\/0333102411433300","article-title":"Association analysis of STX1A gene variants in common forms of migraine","volume":"32","author":"Tropeano","year":"2012","journal-title":"Cephalalgia"},{"issue":"2","key":"10.1016\/j.jns.2016.08.008_bb0635","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1016\/j.neulet.2009.03.011","article-title":"Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population","volume":"455","author":"Corominas","year":"2009","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.jns.2016.08.008_bb0640","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1186\/1129-2377-15-62","article-title":"Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine","volume":"15","author":"Rodriguez-Acevedo","year":"2014","journal-title":"J. Headache Pain."},{"issue":"11","key":"10.1016\/j.jns.2016.08.008_bb0645","doi-asserted-by":"crossref","first-page":"1253","DOI":"10.1007\/s00702-010-0468-6","article-title":"Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura","volume":"117","author":"Jung","year":"2010","journal-title":"J. Neural Transm."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0650","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1177\/0883073814527163","article-title":"TGF-beta1 genotype in pediatric migraine patients","volume":"30","author":"Saygi","year":"2015","journal-title":"J. Child Neurol."},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0655","first-page":"159","article-title":"Toll like receptor-4 896A\/G gene variation, a risk factor for migraine headaches","volume":"9","author":"Rafiei","year":"2012","journal-title":"Iran. J. Immunol."},{"issue":"10","key":"10.1016\/j.jns.2016.08.008_bb0660","doi-asserted-by":"crossref","first-page":"1464","DOI":"10.1111\/j.1526-4637.2011.01200.x","article-title":"Genetic variations in tumor necrosis factor alpha, interleukin-10 genes, and migraine susceptibility","volume":"12","author":"Ates","year":"2011","journal-title":"Pain Med."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0665","doi-asserted-by":"crossref","first-page":"1082","DOI":"10.3892\/etm.2012.533","article-title":"The TNF-alpha-308G\/A polymorphism is associated with migraine risk: a meta-analysis","volume":"3","author":"Gu","year":"2012","journal-title":"Exp. Ther. Med."},{"issue":"6","key":"10.1016\/j.jns.2016.08.008_bb0670","doi-asserted-by":"crossref","first-page":"898","DOI":"10.1007\/s00415-009-5430-x","article-title":"Investigation of TNFA 308G>A and TNFB 252G>A polymorphisms in genetic susceptibility to migraine","volume":"257","author":"Ghosh","year":"2010","journal-title":"J. Neurol."},{"issue":"12","key":"10.1016\/j.jns.2016.08.008_bb0675","doi-asserted-by":"crossref","first-page":"1589","DOI":"10.1007\/s00415-006-0270-4","article-title":"The G-308A promoter variant of the tumor necrosis factor-alpha gene is associated with migraine without aura","volume":"253","author":"Mazaheri","year":"2006","journal-title":"J. Neurol."},{"issue":"1","key":"10.1016\/j.jns.2016.08.008_bb0680","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1212\/01.WNL.0000101717.16799.8F","article-title":"Association between the tumor necrosis factor-alpha -308G\/A gene polymorphism and migraine","volume":"62","author":"Rainero","year":"2004","journal-title":"Neurology"},{"issue":"5","key":"10.1016\/j.jns.2016.08.008_bb0685","doi-asserted-by":"crossref","first-page":"750","DOI":"10.1016\/j.jocn.2011.08.033","article-title":"Association analysis of TNFRSF1B polymorphism with susceptibility for migraine in the Chinese Han population","volume":"19","author":"Dong","year":"2012","journal-title":"J. Clin. Neuroscience"},{"issue":"3","key":"10.1016\/j.jns.2016.08.008_bb0690","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1016\/j.jocn.2006.04.018","article-title":"The A218C polymorphism of tryptophan hydroxylase gene and migraine","volume":"14","author":"Erdal","year":"2007","journal-title":"J. Clin. Neurosci."},{"key":"10.1016\/j.jns.2016.08.008_bb0695","doi-asserted-by":"crossref","first-page":"351942","DOI":"10.1155\/2013\/351942","article-title":"Relationship between vitamin D receptor gene polymorphisms and migraine without aura in an Iranian population","volume":"2013","author":"Motaghi","year":"2013","journal-title":"BioMed Res. Int."},{"issue":"7","key":"10.1016\/j.jns.2016.08.008_bb0700","doi-asserted-by":"crossref","first-page":"357","DOI":"10.1089\/dna.2010.1025","article-title":"Vascular endothelial growth factor genetic polymorphisms and haplotypes in women with migraine","volume":"29","author":"Goncalves","year":"2010","journal-title":"DNA Cell Biol."}],"container-title":["Journal of the Neurological Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X16304877?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X16304877?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2023,8,19]],"date-time":"2023-08-19T14:03:33Z","timestamp":1692453813000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022510X16304877"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,10]]},"references-count":140,"alternative-id":["S0022510X16304877"],"URL":"https:\/\/doi.org\/10.1016\/j.jns.2016.08.008","relation":{},"ISSN":["0022-510X"],"issn-type":[{"type":"print","value":"0022-510X"}],"subject":[],"published":{"date-parts":[[2016,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Biomarkers of migraine: Part 1 \u2013 Genetic markers","name":"articletitle","label":"Article Title"},{"value":"Journal of the Neurological Sciences","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jns.2016.08.008","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}