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Best matches for migraine disorders AND single nucleotide polymorphism:

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Items: 1 to 20 of 210

1.

The NRP1 migraine risk variant shows evidence of association with menstrual migraine.

Pollock CE, Sutherland HG, Maher BH, Lea RA, Haupt LM, Frith A, Anne MacGregor E, Griffiths LR.

J Headache Pain. 2018 Apr 18;19(1):31. doi: 10.1186/s10194-018-0857-z.

2.

Migrainomics - identifying brain and genetic markers of migraine.

Nyholt DR, Borsook D, Griffiths LR.

Nat Rev Neurol. 2017 Dec;13(12):725-741. doi: 10.1038/nrneurol.2017.151. Epub 2017 Nov 17. Review.

PMID:
29146952
3.

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.

Winsvold BS, Bettella F, Witoelar A, Anttila V, Gormley P, Kurth T, Terwindt GM, Freilinger TM, Frei O, Shadrin A, Wang Y, Dale AM, van den Maagdenberg AMJM, Chasman DI, Nyholt DR, Palotie A, Andreassen OA, Zwart JA; International Headache Genetics Consortium.

PLoS One. 2017 Sep 28;12(9):e0185663. doi: 10.1371/journal.pone.0185663. eCollection 2017.

4.

A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression.

Gupta RM, Hadaya J, Trehan A, Zekavat SM, Roselli C, Klarin D, Emdin CA, Hilvering CRE, Bianchi V, Mueller C, Khera AV, Ryan RJH, Engreitz JM, Issner R, Shoresh N, Epstein CB, de Laat W, Brown JD, Schnabel RB, Bernstein BE, Kathiresan S.

Cell. 2017 Jul 27;170(3):522-533.e15. doi: 10.1016/j.cell.2017.06.049.

5.

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.

García-Martín E, Martínez C, Serrador M, Alonso-Navarro H, Navacerrada F, Esguevillas G, García-Albea E, Agúndez JAG, Jiménez-Jiménez FJ.

Headache. 2017 Jul;57(7):1118-1135. doi: 10.1111/head.13122. Epub 2017 Jun 14.

PMID:
28699326
6.

A genetic risk score is differentially associated with migraine with and without aura.

Pisanu C, Preisig M, Castelao E, Glaus J, Pistis G, Squassina A, Del Zompo M, Merikangas KR, Waeber G, Vollenweider P, Mwinyi J, Schiöth HB.

Hum Genet. 2017 Aug;136(8):999-1008. doi: 10.1007/s00439-017-1816-5. Epub 2017 Jun 27.

7.

Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes.

Ambrosini A, D'Onofrio M, Buzzi MG, Arisi I, Grieco GS, Pierelli F, Santorelli FM, Schoenen J.

Headache. 2017 Jul;57(7):1136-1144. doi: 10.1111/head.13107. Epub 2017 Jun 1.

PMID:
28573794
8.

Cannabinoid Receptor Type 1 and mu-Opioid Receptor Polymorphisms Are Associated With Cyclic Vomiting Syndrome.

Wasilewski A, Lewandowska U, Mosinska P, Watala C, Storr M, Fichna J, Venkatesan T.

Am J Gastroenterol. 2017 Jun;112(6):933-939. doi: 10.1038/ajg.2017.73. Epub 2017 Mar 28.

PMID:
28349993
9.

Investigation of polymorphisms in genes involved in estrogen metabolism in menstrual migraine.

Sutherland HG, Champion M, Plays A, Stuart S, Haupt LM, Frith A, MacGregor EA, Griffiths LR.

Gene. 2017 Apr 5;607:36-40. doi: 10.1016/j.gene.2017.01.008. Epub 2017 Jan 13.

PMID:
28089731
10.

Multilocus analysis reveals three candidate genes for Chinese migraine susceptibility.

An XK, Fang J, Yu ZZ, Lin Q, Lu CX, Qu HL, Ma QL.

Clin Genet. 2017 Aug;92(2):143-149. doi: 10.1111/cge.12962. Epub 2017 Feb 22.

PMID:
28058730
11.

Association of ATP6V1B2 rs1106634 with lifetime risk of depression and hippocampal neurocognitive deficits: possible novel mechanisms in the etiopathology of depression.

Gonda X, Eszlari N, Anderson IM, Deakin JF, Bagdy G, Juhasz G.

Transl Psychiatry. 2016 Nov 8;6(11):e945. doi: 10.1038/tp.2016.221.

12.

New evidence for involvement of ESR1 gene in susceptibility to Chinese migraine.

An X, Fang J, Lin Q, Lu C, Ma Q, Qu H.

J Neurol. 2017 Jan;264(1):81-87. doi: 10.1007/s00415-016-8321-y. Epub 2016 Oct 24.

PMID:
27778160
13.

Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress.

Juhasz G, Csepany E, Magyar M, Edes AE, Eszlari N, Hullam G, Antal P, Kokonyei G, Anderson IM, Deakin JF, Bagdy G.

Genes Brain Behav. 2017 Mar;16(3):384-393. doi: 10.1111/gbb.12352. Epub 2016 Nov 23.

14.

Nicotinamide-N-Methyltransferase gene rs694539 variant and migraine risk.

Sazci A, Sazci G, Sazci B, Ergul E, Idrisoglu HA.

J Headache Pain. 2016 Dec;17(1):93. Epub 2016 Oct 10.

15.

Leveraging electronic health records to study pleiotropic effects on bipolar disorder and medical comorbidities.

Prieto ML, Ryu E, Jenkins GD, Batzler A, Nassan MM, Cuellar-Barboza AB, Pathak J, McElroy SL, Frye MA, Biernacka JM.

Transl Psychiatry. 2016 Aug 16;6:e870. doi: 10.1038/tp.2016.138.

16.

Association of Polymorphisms within the Serotonin Receptor Genes 5-HTR1A, 5-HTR1B, 5-HTR2A and 5-HTR2C and Migraine Susceptibility in a Turkish Population.

Yücel Y, Coşkun S, Cengiz B, Özdemir HH, Uzar E, Çim A, Camkurt MA, Aluclu MU.

Clin Psychopharmacol Neurosci. 2016 Aug 31;14(3):250-5. doi: 10.9758/cpn.2016.14.3.250.

17.

MTHFR and ACE Polymorphisms Do Not Increase Susceptibility to Migraine Neither Alone Nor in Combination.

Essmeister R, Kress HG, Zierz S, Griffith L, Lea R, Wieser T.

Headache. 2016 Sep;56(8):1267-73. doi: 10.1111/head.12893. Epub 2016 Aug 2.

PMID:
27483173
18.

The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine.

Van der Auwera S, Teumer A, Hertel J, Homuth G, Völker U, Lucht MJ, Degenhardt F, Schulze T, Rietschel M, Nöthen MM, John U, Nauck M, Grabe HJ.

Eur Neuropsychopharmacol. 2016 Sep;26(9):1507-1515. doi: 10.1016/j.euroneuro.2016.03.019. Epub 2016 Jul 6.

PMID:
27394076
19.

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.

Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH, Lehtimäki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schürks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Färkkilä M, Artto V, Kaunisto M, Vepsäläinen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Mägi R, Pärn K, Hämäläinen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkilä K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Männikkö M, Mihailov E, Milani L, Göbel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium, Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson N, Daly MJ, Neale BM, Olesen J, Chasman DI, Nyholt DR, Palotie A.

Nat Genet. 2016 Aug;48(8):856-66. doi: 10.1038/ng.3598. Epub 2016 Jun 20. Erratum in: Nat Genet. 2016 Sep 28;48(10 ):1296.

20.

The association between COMT Val158Met polymorphism and migraine risk: A meta-analysis.

Liao YJ, Jiang JR, Jin SQ.

Cephalalgia. 2017 May;37(6):592-598. doi: 10.1177/0333102416649758. Epub 2016 May 6.

PMID:
27154995

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