Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 49

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.
3.

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.

Dichgans M, Freilinger T, Eckstein G, Babini E, Lorenz-Depiereux B, Biskup S, Ferrari MD, Herzog J, van den Maagdenberg AM, Pusch M, Strom TM.

Lancet. 2005 Jul 30-Aug 5;366(9483):371-7.

PMID:
16054936
4.

Schizophrenia: genes at last?

Owen MJ, Craddock N, O'Donovan MC.

Trends Genet. 2005 Sep;21(9):518-25. Review.

PMID:
16009449
5.

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
6.

Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension.

Hamet P, Merlo E, Seda O, Broeckel U, Tremblay J, Kaldunski M, Gaudet D, Bouchard G, Deslauriers B, Gagnon F, Antoniol G, Pausová Z, Labuda M, Jomphe M, Gossard F, Tremblay G, Kirova R, Tonellato P, Orlov SN, Pintos J, Platko J, Hudson TJ, Rioux JD, Kotchen TA, Cowley AW Jr.

Am J Hum Genet. 2005 May;76(5):815-32. Epub 2005 Mar 30.

7.

Complement factor H polymorphism and age-related macular degeneration.

Edwards AO, Ritter R 3rd, Abel KJ, Manning A, Panhuysen C, Farrer LA.

Science. 2005 Apr 15;308(5720):421-4. Epub 2005 Mar 10.

8.

A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes.

Russo L, Mariotti P, Sangiorgi E, Giordano T, Ricci I, Lupi F, Chiera R, Guzzetta F, Neri G, Gurrieri F.

Am J Hum Genet. 2005 Feb;76(2):327-33. Epub 2004 Dec 7.

9.

Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families.

Bouzigon E, Dizier MH, Krähenbühl C, Lemainque A, Annesi-Maesano I, Betard C, Bousquet J, Charpin D, Gormand F, Guilloud-Bataille M, Just J, Le Moual N, Maccario J, Matran R, Neukirch F, Oryszczyn MP, Paty E, Pin I, Rosenberg-Bourgin M, Vervloet D, Kauffmann F, Lathrop M, Demenais F.

Hum Mol Genet. 2004 Dec 15;13(24):3103-13. Epub 2004 Oct 27.

10.

Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.

Paunio T, Tuulio-Henriksson A, Hiekkalinna T, Perola M, Varilo T, Partonen T, Cannon TD, Lönnqvist J, Peltonen L.

Hum Mol Genet. 2004 Aug 15;13(16):1693-702. Epub 2004 Jun 15.

11.

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities.

Nyholt DR, Gillespie NG, Heath AC, Merikangas KR, Duffy DL, Martin NG.

Genet Epidemiol. 2004 Apr;26(3):231-44.

PMID:
15022209
12.

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes.

Bottini N, Musumeci L, Alonso A, Rahmouni S, Nika K, Rostamkhani M, MacMurray J, Meloni GF, Lucarelli P, Pellecchia M, Eisenbarth GS, Comings D, Mustelin T.

Nat Genet. 2004 Apr;36(4):337-8. Epub 2004 Mar 7.

PMID:
15004560
13.
14.

The International Classification of Headache Disorders: 2nd edition.

Headache Classification Subcommittee of the International Headache Society.

Cephalalgia. 2004;24 Suppl 1:9-160. No abstract available.

PMID:
14979299
15.

Genetics of familial combined hyperlipidemia and risk of coronary heart disease.

Shoulders CC, Jones EL, Naoumova RP.

Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R149-60. Epub 2004 Feb 5. Review.

16.

Localization of a gene for migraine without aura to chromosome 4q21.

Björnsson A, Gudmundsson G, Gudfinnsson E, Hrafnsdóttir M, Benedikz J, Skúladóttir S, Kristjánsson K, Frigge ML, Kong A, Stefánsson K, Gulcher JR.

Am J Hum Genet. 2003 Nov;73(5):986-93. Epub 2003 Sep 25. Erratum in: Am J Hum Genet. 2005 Apr;76(4):715.

17.

Significant linkage to migraine with aura on chromosome 11q24.

Cader ZM, Noble-Topham S, Dyment DA, Cherny SS, Brown JD, Rice GP, Ebers GC.

Hum Mol Genet. 2003 Oct 1;12(19):2511-7. Epub 2003 Jul 29.

18.

The endophenotype concept in psychiatry: etymology and strategic intentions.

Gottesman II, Gould TD.

Am J Psychiatry. 2003 Apr;160(4):636-45. Review.

PMID:
12668349
19.

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

De Fusco M, Marconi R, Silvestri L, Atorino L, Rampoldi L, Morgante L, Ballabio A, Aridon P, Casari G.

Nat Genet. 2003 Feb;33(2):192-6. Epub 2003 Jan 21.

PMID:
12539047
20.

A locus for migraine without aura maps on chromosome 14q21.2-q22.3.

Soragna D, Vettori A, Carraro G, Marchioni E, Vazza G, Bellini S, Tupler R, Savoldi F, Mostacciuolo ML.

Am J Hum Genet. 2003 Jan;72(1):161-7. Epub 2002 Dec 9.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk