Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Neurogenetics

Volumn 13, Issue 1, 2012, Pages 97-101

  Maher, B H ^a   Kerr, M ^a   Cox, H C ^a   MacMillan, J C ^b   Brimage, P J ^c   Esposito, T ^d   Gianfrancesco, F ^d   Haupt, L M ^a   Nyholt, D R ^e   Lea, R A ^a   Griffiths, L R ^a  

^a GRIFFITH UNIVERSITY   (Australia)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

^c PRINCE OF WALES HOSPITAL   (Australia)

^d INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

^e QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

Author keywords

MA; Migraine; MO; X linked

Indexed keywords

ALLELE; ARTICLE; CASE CONTROL STUDY; CHROMOSOME XQ; CHROMOSOME XQ27; CHROMOSOME XQ28; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE PREDISPOSITION; FEMALE; GENE LOCUS; HAPLOTYPE; HUMAN; MALE; MICROSATELLITE MARKER; MIGRAINE; PEDIGREE; PRIORITY JOURNAL; AUSTRALIA; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; X CHROMOSOME;

MICROSATELLITE DNA;

AUSTRALIA; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, X; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MICROSATELLITE REPEATS; MIGRAINE DISORDERS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84861305425     PISSN: 13646745     EISSN: 13646753     Source Type: Journal    
DOI: 10.1007/s10048-011-0312-7     Document Type: Article

References (20)

1. Mulder EJ, Van Baal C, Gaist D, Kallela M, Kaprio J, Svensson DA, Nyholt DR, Martin NG, MacGregor AJ, Cherkas LF, Boomsma DI, Palotie A (2003) Genetic and environmental influences on migraine: a twin study across six countries. Twin Res 6 (5):422-431 (Pubitemid 38019780)
2. Lipton RB, Bigal ME, Diamond M, Freitag F, Reed ML, Stewart WF (2007) Migraine prevalence, disease burden, and the need for preventive therapy. Neurology 68(5):343-349
3. Stovner LJ, Zwart JA, Hagen K, Terwindt GM, Pascual J (2006) Epidemiology of headache in Europe. Eur J Neurol 13 (4):333-345
4. Stewart WF, Bigal ME, Kolodner K, Dowson A, Liberman JN, Lipton RB (2006) Familial risk of migraine: variation by proband age at onset and headache severity. Neurology 66(3):344-348 (Pubitemid 43739934)
5. Nyholt DR, Curtain RP, Griffiths LR (2000) Familial typical migraine: significant linkage and localization of a gene to Xq24-28. Hum Genet 107(1):18-23 (Pubitemid 30598941)
6. Nyholt DR, Dawkins JL, Brimage PJ, Goadsby PJ, Nicholson GA, Griffiths LR (1998) Evidence for an X-linked genetic component in familial typical migraine. Hum Mol Genet 7(3):459-463 (Pubitemid 28120636)
7. IHS (2004) The international classification of the headache disorders 2nd ed. Cephalalgia 24(Suppl 1):1-150
8. Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res 16(3):1215
9. Duffy DL (2006) An integrated genetic map for linkage analysis. Behav Genet 36(1):4-6
10. O'Connell JR, Weeks DE (1998) PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63(1):259-266 (Pubitemid 30428342)
11. Kong A, Cox NJ (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61(5):1179-1188 (Pubitemid 27492328)
12. Nyholt DR (2000) All LODs are not created equal. Am J Hum Genet 67(2):282-288
13. Abecasis GR, Cherny SS, Cookson WO, Cardon LR (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30(1):97-101
14. Barrett JC (2009) Haploview: visualization and analysis of SNP genotype data. Cold Spring Harb Protoc 2009 (10):pdb ip71
15. Sham PC, Curtis D (1995) Monte Carlo tests for associations between disease and alleles at highly polymorphic loci. Ann Hum Genet 59(Pt 1):97-105
16. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81(3):559-575 (Pubitemid 47330214)
17. Barrett JC, Fry B, Maller J, Daly MJ (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21 (2):263-265 (Pubitemid 40202029)
18. Odegaard KJ, Greenwood TA, Lunde A, Fasmer OB, Akiskal HS, Kelsoe JR, Consortium NGIBD (2010) 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. J Affect Disord 122(1-2):14-26
19. Wieser T, Pascual J, Oterino A, Soso M, Barmada M, Gardner KL (2010) A novel locus for familial migraine on Xp22. Headache 50 (6):955-962
20. Silberstein SD (2005) Cardiovascular risk factors associated with migraine. Lancet Neurol 4(7):391-392