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Items: 1 to 20 of 101

1.

Genome-wide association analysis identifies susceptibility loci for migraine without aura.

Freilinger T, Anttila V, de Vries B, Malik R, Kallela M, Terwindt GM, Pozo-Rosich P, Winsvold B, Nyholt DR, van Oosterhout WP, Artto V, Todt U, Hämäläinen E, Fernández-Morales J, Louter MA, Kaunisto MA, Schoenen J, Raitakari O, Lehtimäki T, Vila-Pueyo M, Göbel H, Wichmann E, Sintas C, Uitterlinden AG, Hofman A, Rivadeneira F, Heinze A, Tronvik E, van Duijn CM, Kaprio J, Cormand B, Wessman M, Frants RR, Meitinger T, Müller-Myhsok B, Zwart JA, Färkkilä M, Macaya A, Ferrari MD, Kubisch C, Palotie A, Dichgans M, van den Maagdenberg AM; International Headache Genetics Consortium.

Nat Genet. 2012 Jun 10;44(7):777-82. doi: 10.1038/ng.2307.

2.

Replication of migraine GWAS susceptibility loci in Chinese Han population.

Fan X, Wang J, Fan W, Chen L, Gui B, Tan G, Zhou J.

Headache. 2014 Apr;54(4):709-15. doi: 10.1111/head.12329. Epub 2014 Mar 25.

PMID:
24666033
3.

Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine.

Esserlind AL, Christensen AF, Le H, Kirchmann M, Hauge AW, Toyserkani NM, Hansen T, Grarup N, Werge T, Steinberg S, Bettella F, Stefansson H, Olesen J.

Eur J Neurol. 2013 May;20(5):765-72. doi: 10.1111/ene.12055. Epub 2013 Jan 7.

PMID:
23294458
4.

Genome-wide association study reveals three susceptibility loci for common migraine in the general population.

Chasman DI, Schürks M, Anttila V, de Vries B, Schminke U, Launer LJ, Terwindt GM, van den Maagdenberg AM, Fendrich K, Völzke H, Ernst F, Griffiths LR, Buring JE, Kallela M, Freilinger T, Kubisch C, Ridker PM, Palotie A, Ferrari MD, Hoffmann W, Zee RY, Kurth T.

Nat Genet. 2011 Jun 12;43(7):695-8. doi: 10.1038/ng.856.

5.

Genetics of migraine in the age of genome-wide association studies.

Schürks M.

J Headache Pain. 2012 Jan;13(1):1-9. doi: 10.1007/s10194-011-0399-0. Epub 2011 Nov 11. Review.

6.

Genome-wide-associated variants in migraine susceptibility: a replication study from North India.

Ghosh J, Pradhan S, Mittal B.

Headache. 2013 Nov-Dec;53(10):1583-94. doi: 10.1111/head.12240. Epub 2013 Oct 29.

PMID:
24266335
7.

A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample.

Sintas C, Carreño O, Fernández-Morales J, Cacheiro P, Sobrido MJ, Narberhaus B, Pozo-Rosich P, Macaya A, Cormand B.

Cephalalgia. 2012 Oct;32(14):1076-80. doi: 10.1177/0333102412457090. Epub 2012 Aug 20.

PMID:
22908361
8.

Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura.

Sintas C, Fernández-Morales J, Vila-Pueyo M, Narberhaus B, Arenas C, Pozo-Rosich P, Macaya A, Cormand B.

Cephalalgia. 2015 Aug;35(9):776-82. doi: 10.1177/0333102414557841. Epub 2014 Nov 11.

PMID:
25388962
9.

Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.

Schürks M, Buring JE, Ridker PM, Chasman DI, Kurth T.

PLoS One. 2011;6(7):e22106. doi: 10.1371/journal.pone.0022106. Epub 2011 Jul 14.

10.

A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine.

Ligthart L, Nyholt DR, Hottenga JJ, Distel MA, Willemsen G, Boomsma DI.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1186-95. doi: 10.1002/ajmg.b.30749.

PMID:
18361423
11.

SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population.

Carreño O, Corominas R, Fernández-Morales J, Camiña M, Sobrido MJ, Fernández-Fernández JM, Pozo-Rosich P, Cormand B, Macaya A.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):94-103. doi: 10.1002/ajmg.b.32007. Epub 2011 Dec 7.

PMID:
22162417
12.

Haplotypes in candidate genes related to nitric oxide pathway and vascular permeability associated with migraine and aura.

Gonçalves FM, Luizon MR, Speciali JG.

J Headache Pain. 2012 Jun;13(4):335-6; author reply 337-8. doi: 10.1007/s10194-012-0438-5. Epub 2012 Mar 25. No abstract available.

13.

Investigation of TNFA 308G > A and TNFB 252G > A polymorphisms in genetic susceptibility to migraine.

Ghosh J, Joshi G, Pradhan S, Mittal B.

J Neurol. 2010 Jun;257(6):898-904. doi: 10.1007/s00415-009-5430-x. Epub 2009 Dec 25.

PMID:
20035431
14.

Investigation of gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility.

Fernandez F, Esposito T, Lea RA, Colson NJ, Ciccodicola A, Gianfrancesco F, Griffiths LR.

BMC Med Genet. 2008 Dec 16;9:109. doi: 10.1186/1471-2350-9-109.

15.

A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample.

Ran C, Graae L, Magnusson PK, Pedersen NL, Olson L, Belin AC.

BMC Med Genet. 2014 Mar 28;15:38. doi: 10.1186/1471-2350-15-38.

16.

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

Lea RA, Nyholt DR, Curtain RP, Ovcaric M, Sciascia R, Bellis C, Macmillan J, Quinlan S, Gibson RA, McCarthy LC, Riley JH, Smithies YJ, Kinrade S, Griffiths LR.

Neurogenetics. 2005 May;6(2):67-72. Epub 2005 Apr 14.

PMID:
15830246
17.

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.

Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Gretarsdottir S, Badger SA, Bradley DT, Burnand K, Child AH, Clough RE, Cockerill G, Hafez H, Scott DJ, Futers S, Johnson A, Sohrabi S, Smith A, Thompson MM, van Bockxmeer FM, Waltham M, Matthiasson SE, Thorleifsson G, Thorsteinsdottir U, Blankensteijn JD, Teijink JA, Wijmenga C, de Graaf J, Kiemeney LA, Assimes TL, McPherson R; CARDIoGRAM Consortium; Global BPgen Consortium; DIAGRAM Consortium; VRCNZ Consortium, Folkersen L, Franco-Cereceda A, Palmen J, Smith AJ, Sylvius N, Wild JB, Refstrup M, Edkins S, Gwilliam R, Hunt SE, Potter S, Lindholt JS, Frikke-Schmidt R, Tybjærg-Hansen A, Hughes AE, Golledge J, Norman PE, van Rij A, Powell JT, Eriksson P, Stefansson K, Thompson JR, Humphries SE, Sayers RD, Deloukas P, Samani NJ.

Am J Hum Genet. 2011 Nov 11;89(5):619-27. doi: 10.1016/j.ajhg.2011.10.002. Epub 2011 Nov 4.

18.

Role of the oestrogen receptor (ESR1 PvuII and ESR1 325 C->G) and progesterone receptor (PROGINS) polymorphisms in genetic susceptibility to migraine in a North Indian population.

Joshi G, Pradhan S, Mittal B.

Cephalalgia. 2010 Mar;30(3):311-20. doi: 10.1111/j.1468-2982.2009.01967.x. Epub 2010 Feb 11.

PMID:
19673915
19.

The transforming growth factor-β receptor genes and the risk of intracranial aneurysms.

Ruigrok YM, Baas AF, Medic J, Wijmenga C, Rinkel GJ.

Int J Stroke. 2012 Dec;7(8):645-8. doi: 10.1111/j.1747-4949.2011.00615.x. Epub 2011 Oct 6.

PMID:
21978186
20.

A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.

Yamazaki K, Umeno J, Takahashi A, Hirano A, Johnson TA, Kumasaka N, Morizono T, Hosono N, Kawaguchi T, Takazoe M, Yamada T, Suzuki Y, Tanaka H, Motoya S, Hosokawa M, Arimura Y, Shinomura Y, Matsui T, Matsumoto T, Iida M, Tsunoda T, Nakamura Y, Kamatani N, Kubo M.

Gastroenterology. 2013 Apr;144(4):781-8. doi: 10.1053/j.gastro.2012.12.021. Epub 2012 Dec 22.

PMID:
23266558
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