These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
269 related articles for article (PubMed ID: 16080125)
1. Genomewide significant linkage to migrainous headache on chromosome 5q21. Nyholt DR; Morley KI; Ferreira MA; Medland SE; Boomsma DI; Heath AC; Merikangas KR; Montgomery GW; Martin NG Am J Hum Genet; 2005 Sep; 77(3):500-12. PubMed ID: 16080125 [TBL] [Abstract][Full Text] [Related]
2. 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; 147B(7):1186-95. PubMed ID: 18361423 [TBL] [Abstract][Full Text] [Related]
3. Recent findings in headache genetics. Kors EE; Vanmolkot KR; Haan J; Frants RR; van den Maagdenberg AM; Ferrari MD Curr Opin Neurol; 2004 Jun; 17(3):283-8. PubMed ID: 15167062 [TBL] [Abstract][Full Text] [Related]
4. A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11. Oedegaard KJ; Greenwood TA; Lunde A; Fasmer OB; Akiskal HS; Kelsoe JR; J Affect Disord; 2010 Apr; 122(1-2):14-26. PubMed ID: 19819557 [TBL] [Abstract][Full Text] [Related]
5. Trait components provide tools to dissect the genetic susceptibility of migraine. Anttila V; Kallela M; Oswell G; Kaunisto MA; Nyholt DR; Hamalainen E; Havanka H; Ilmavirta M; Terwilliger J; Sobel E; Peltonen L; Kaprio J; Farkkila M; Wessman M; Palotie A Am J Hum Genet; 2006 Jul; 79(1):85-99. PubMed ID: 16773568 [TBL] [Abstract][Full Text] [Related]
6. Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees. Curtain RP; Lea RA; Tajouri L; Haupt LM; Ovcaric M; MacMillan J; Griffiths LR Neurol Res; 2005 Sep; 27(6):647-52. PubMed ID: 16157018 [TBL] [Abstract][Full Text] [Related]
7. A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. Kaunisto MA; Harno H; Vanmolkot KR; Gargus JJ; Sun G; Hämäläinen E; Liukkonen E; Kallela M; van den Maagdenberg AM; Frants RR; Färkkilä M; Palotie A; Wessman M Neurogenetics; 2004 Jun; 5(2):141-6. PubMed ID: 15133718 [TBL] [Abstract][Full Text] [Related]
8. [Genetics of migraine]. Freilinger T; Dichgans M Nervenarzt; 2006 Oct; 77(10):1186, 1188-95. PubMed ID: 16915377 [TBL] [Abstract][Full Text] [Related]
9. Clinical characteristics of migraine concordant monozygotic twin pairs. Kallela M; Wessman M; Färkkilä M; Palotie A; Koskenvuo M; Honkasalo ML; Kaprio J Acta Neurol Scand; 1999 Oct; 100(4):254-9. PubMed ID: 10510686 [TBL] [Abstract][Full Text] [Related]
10. The molecular genetics of migraine. Wessman M; Kaunisto MA; Kallela M; Palotie A Ann Med; 2004; 36(6):462-73. PubMed ID: 15513297 [TBL] [Abstract][Full Text] [Related]
12. The genetic spectrum of a population-based sample of familial hemiplegic migraine. Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831 [TBL] [Abstract][Full Text] [Related]
13. Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p. Hovatta I; Kallela M; Färkkilä M; Peltonen L Genomics; 1994 Oct; 23(3):707-9. PubMed ID: 7851903 [TBL] [Abstract][Full Text] [Related]
14. A new locus for hemiplegic migraine maps to chromosome 1q31. Gardner K; Barmada MM; Ptacek LJ; Hoffman EP Neurology; 1997 Nov; 49(5):1231-8. PubMed ID: 9371899 [TBL] [Abstract][Full Text] [Related]
15. Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families. Ahmed MA; Reid E; Cooke A; Arngrímsson R; Tolmie JL; Stephenson JB J Neurol Neurosurg Psychiatry; 1996 Dec; 61(6):616-20. PubMed ID: 8971111 [TBL] [Abstract][Full Text] [Related]
16. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ducros A; Joutel A; Vahedi K; Cecillon M; Ferreira A; Bernard E; Verier A; Echenne B; Lopez de Munain A; Bousser MG; Tournier-Lasserve E Ann Neurol; 1997 Dec; 42(6):885-90. PubMed ID: 9403481 [TBL] [Abstract][Full Text] [Related]
17. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Addis L; Chiang T; Clarke T; Hardison H; Kugler S; Mandelbaum DE; Novotny E; Wolf S; Strug LJ; Pal DK Genes Brain Behav; 2014 Mar; 13(3):333-40. PubMed ID: 24286483 [TBL] [Abstract][Full Text] [Related]
18. A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. Costa C; Prontera P; Sarchielli P; Tonelli A; Bassi MT; Cupini LM; Caproni S; Siliquini S; Donti E; Calabresi P Cephalalgia; 2014 Jan; 34(1):68-72. PubMed ID: 23918834 [TBL] [Abstract][Full Text] [Related]
19. A typical migraine susceptibility region localizes to chromosome 1q31. Lea RA; Shepherd AG; Curtain RP; Nyholt DR; Quinlan S; Brimage PJ; Griffiths LR Neurogenetics; 2002 Mar; 4(1):17-22. PubMed ID: 12030327 [TBL] [Abstract][Full Text] [Related]
20. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred. Fernandez DM; Hand CK; Sweeney BJ; Parfrey NA Headache; 2008 Jan; 48(1):101-8. PubMed ID: 18184292 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]