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Items: 1 to 20 of 126

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. Epub 2005 Jul 28.

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 5;147B(7):1186-95. doi: 10.1002/ajmg.b.30749.

PMID:
18361423
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. Review.

PMID:
15167062
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; NIMH Genetics Initiative Bipolar Disorder Consortium.

J Affect Disord. 2010 Apr;122(1-2):14-26. doi: 10.1016/j.jad.2009.06.014. Epub 2009 Oct 12.

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. Epub 2006 May 10.

6.

Bayesian latent trait modeling of migraine symptom data.

Chen CC, Keith JM, Nyholt DR, Martin NG, Mengersen KL.

Hum Genet. 2009 Aug;126(2):277-88. doi: 10.1007/s00439-009-0671-4. Epub 2009 Apr 24.

PMID:
19390863
7.

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.

PMID:
10510686
8.

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.

PMID:
16157018
9.

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. Epub 2006 Dec 2.

PMID:
17142831
10.

The molecular genetics of migraine.

Wessman M, Kaunisto MA, Kallela M, Palotie A.

Ann Med. 2004;36(6):462-73. Review.

PMID:
15513297
11.

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.

PMID:
9371899
12.

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H.

Genet Med. 2005 Jul-Aug;7(6):397-405.

PMID:
16024971
13.

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. Epub 2004 May 7.

PMID:
15133718
14.

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.

PMID:
7851903
15.

Consistently replicating locus linked to migraine on 10q22-q23.

Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A.

Am J Hum Genet. 2008 May;82(5):1051-63. doi: 10.1016/j.ajhg.2008.03.003.

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.

PMID:
9403481
17.

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.

PMID:
12030327
18.

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. doi: 10.1111/gbb.12110. Epub 2013 Dec 26.

19.

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.

20.

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.

Jones KW, Ehm MG, Pericak-Vance MA, Haines JL, Boyd PR, Peroutka SJ.

Genomics. 2001 Dec;78(3):150-4.

PMID:
11735221

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