A typical migraine susceptibility region localizes to chromosome 1q31

Neurogenetics

Volumn 4, Issue 1, 2002, Pages 17-22

  Lea, Rod A ^a   Shepherd, A Graeme ^b   Curtain, Robert P ^a   Nyholt, Dale R ^d   Quinlan, Sharon ^a   Brimage, Peter J ^c   Griffiths, Lyn R ^a  

^a GRIFFITH UNIVERSITY   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

^c PRINCE OF WALES HOSPITAL   (Australia)

^d NONE

Author keywords

Association; Gene; Linkage; Migraine

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1Q; DISEASE PREDISPOSITION; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY STUDY; FEMALE; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 1; FAMILY HEALTH; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LOD SCORE; MALE; MIGRAINE DISORDERS; PEDIGREE;

EID: 0036524555     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-001-0125-1     Document Type: Article

References (27)

1. Headache Classification Committee of the International Headache Society (1988) Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 8 [Suppl 7]:19-28
2. Launer LJ, Terwindt GM, Ferrari MD (1999) The prevalence and characteristics of migraine in a population- based cohort - The GEM Study. Neurology 53:537-542
3. Honkasalo ML, Kaprio J, Winter T, Heikkila K, Sillanpaa M, Koskenvuo M (1995) Migraine and concomitant symptoms among 8167 adult twin pairs. Headache 35:70-78
4. Larsson B, Bille B, Pedersen NL (1995) Genetic influences in headaches: a Swedish twin study. Headache 35:513-519
5. Russell MB, Olesen J (1992) The genetics of migraine without aura and migraine with aura. Cephalalgia 13:245-248
6. Mochi M, Sangiorgi S, Cortelli P, Carelli V, Scapoli C, Crisci M, et al (1993) Testing models for genetic determination in migraine. Cephalalgia 13:389-394
7. Bille B (1997) A 40 year follow-up of school children with migraine. Cephalalgia 17:488-491
8. Russell MB, Rasmussen BK, Thorvaldsen P, Olesen J (1995) Prevalence and sex-ratio of the subtypes of migraine. Int J Epidemiol 24:612-618
9. Blau JN (1995) Migraine with and without aura are not different entities. Cephalalgia 15:186-189
10. Ophoff RA, Terwindt GM, Vergouwe MN, Van Eijk R, Oefner PJ, Hoffman SM, et al (1996) Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87:543-552
11. Gardner K, Barmada MM, Ptacek LJ, Hoffman EP (1997) A new locus for hemiplegic migraine maps to chromosome 1q31. Neurology 49:1231-1238
12. Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR (1998) Familial typical migraine - linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology 50:1428-1432
13. 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 7:459-463
14. Nyholt DR, Curtain RP, Griffiths LR (2000) Familial typical migraine: significant linkage and localization of a gene to Xq24-28. Hum Genet 107:18-23
15. Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, et al (1997) Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Neurology 42:885-890
16. Diriong S, Lory P, Williams ME, Ellis SB, Harpold MM, Taviaux S (1995) Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits. Genomics 30:605-609
17. Blin N, Stafford DW (1976) Isolation of high molecular-weight DNA. Nucleic Acids Res 3:2303
18. Miller SA, Dykes DD, Plensky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res 16:1215
19. Gudbjartsson DF, Jonasson K, Frigge ML, Kong A (2000) Allegro, a new computer program for multipoint linkage analysis. Nat Genet 25:12-13
20. Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363
21. Kong A, Cox NJ (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61:1179-1188
22. McPeek MS (1999) Optimal allele-sharing statistics for genetic mapping using affected relatives. Genet Epidemiol 16:225-249
23. Lander E, Kruglyak L (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11:241-247
24. Laird N, Horvath S, Xu X (2000) Implementing a unified approach to family-based tests of association. Genet Epidemiol 19 [Suppl]:S36-S42
25. Codignola A, Tarroni P, Clementi F, Pollo A, Lovallo M, Carbone E, et al (1993) Calcium channel subtypes controlling serotonin release from human cell lung carcinoma cell lines. J Biol Chem 268:26240-26247
26. Terwilliger JD, Shannon WD, Lathrop GM, Nolan JP, Goldin LR, Chase GA, et al (1997) True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping. Am J Hum Genet 61:430-438
27. Herr M, Dudbridge F, Zavattari P, Cucca F, Guja C, March R, et al (2000) Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21. Hum Mol Genet 9:1291-1301