A Susceptibility Locus for Migraine with Aura, on Chromosome 4q24
Tài liệu tham khảo
Bille, 1997, A 40-year follow-up of school children with migraine, Cephalalgia, 17, 488, 10.1046/j.1468-2982.1997.1704488.x
Broman, 1998, Comprehensive human genetic maps: individual and sex-specific variation in recombination, Am J Hum Genet, 63, 861, 10.1086/302011
Brzustowicz, 2000, Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22, Science, 288, 678, 10.1126/science.288.5466.678
Chiano, 1995, Linkage detection under heterogeneity and the mixture problem, Ann Hum Genet, 59, 83, 10.1111/j.1469-1809.1995.tb01607.x
de la Chapelle, 1993, Disease gene mapping in isolated human populations: the example of Finland, J Med Genet, 30, 857, 10.1136/jmg.30.10.857
Del Zompo, 1998, Association between dopamine receptor genes and migraine without aura in a Sardinian sample, Neurology, 51, 781, 10.1212/WNL.51.3.781
Ducros, 2001, The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel, N Engl J Med, 345, 17, 10.1056/NEJM200107053450103
Ducros, 1997, Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity, Ann Neurol, 42, 885, 10.1002/ana.410420610
Ekelund, 2000, Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22, Hum Mol Genet, 9, 1049, 10.1093/hmg/9.7.1049
Färkkilä, 1992, Raised plasma endothelin during acute migraine attack, Cephalalgia, 12, 383, 10.1111/j.1468-2982.1992.00383.x
Gardner, 1997, A new locus for hemiplegic migraine maps to chromosome 1q31, Neurology, 49, 1231, 10.1212/WNL.49.5.1231
Gervil, 1999, Genetic and environmental factors in migraine, Neurology, 53, 995, 10.1212/WNL.53.5.995
Gervil, 1999, Migraine without aura: a population-based twin study, Ann Neurol, 46, 606, 10.1002/1531-8249(199910)46:4<606::AID-ANA8>3.0.CO;2-O
Göring, 2000, Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters, Am J Hum Genet, 66, 1298, 10.1086/302846
Göring, 2000, Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified, Am J Hum Genet, 66, 1310, 10.1086/302845
Hagen, 2000, Prevalence of migraine and non-migrainous headache--head-HUNT, a large population-based study, Cephalalgia, 20, 900, 10.1046/j.1468-2982.2000.00145.x
Hasselblatt, 1999, Simultaneous monitoring of endothelin-1 and vasopressin plasma levels in migraine, Neuroreport, 10, 423, 10.1097/00001756-199902050-00039
Headache Classification Committee of the International Headache Society, 1988, Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain, Cephalalgia, 8, 1
Henry, 1992, A nationwide survey of migraine in France: prevalence and clinical features in adults. GRIM, Cephalalgia, 12, 229, 10.1046/j.1468-2982.1992.1204229.x
Honkasalo, 1995, Migraine and concomitant symptoms among 8167 adult twin pairs, Headache, 35, 70, 10.1111/j.1526-4610.1995.hed3502070.x
Hovatta, 1994, Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p, Genomics, 23, 707, 10.1006/geno.1994.1563
Hovatta, 1999, A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci, Am J Hum Genet, 65, 1114, 10.1086/302567
Jodice, 1997, Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p, Hum Mol Genet, 6, 1973, 10.1093/hmg/6.11.1973
Joutel, 1993, A gene for familial hemiplegic migraine maps to chromosome 19, Nat Genet, 5, 40, 10.1038/ng0993-40
Kallela, 1998, Endothelin in migraine patients, Cephalalgia, 18, 329, 10.1046/j.1468-2982.1998.1806329.x
Kallela, 2001, Validation of a migraine specific questionnaire for use in family studies, Eur J Neurol, 8, 61, 10.1046/j.1468-1331.2001.00165.x
Kowa, 2000, The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine, Am J Med Genet, 96, 762, 10.1002/1096-8628(20001204)96:6<762::AID-AJMG12>3.0.CO;2-X
Kruglyak, 1996, Parametric and nonparametric linkage analysis: a unified multipoint approach, Am J Hum Genet, 58, 1347
Kuokkanen, 1997, Genomewide scan of multiple sclerosis in Finnish multiplex families, Am J Hum Genet, 61, 1379, 10.1086/301637
Laitinen, 2001, A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population, Nat Genet, 28, 87, 10.1038/ng0501-87
Lander, 1995, Genetic dissection of complex traits: guideline for interpreting and reporting linkage results, Nat Genet, 11, 241, 10.1038/ng1195-241
Lander, 1994, Genetic dissection of complex traits, Science, 265, 2037, 10.1126/science.8091226
Larsson, 1995, Genetic influence in headaches: a Swedish twin study, Headache, 35, 513, 10.1111/j.1526-4610.1995.hed3509513.x
Lathrop, 1984, Easy calculations of lod scores and genetic risks on small computers, Am J Hum Genet, 36, 460
Lea, 2000, Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine, Neurogenetics, 3, 35, 10.1007/PL00022977
Leppävuori, 1999, Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q, Am J Hum Genet, 65, 1060, 10.1086/302569
Lipton, 1994, An update on the epidemiology of migraine, Headache, 34, 319, 10.1111/j.1526-4610.1994.hed3406319.x
Lipton, 2001, Prevalence and burden of migraine in the United States: data from the American Migraine Study II, Headache, 41, 646, 10.1046/j.1526-4610.2001.041007646.x
Mahtani, 1996, Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families, Nat Genet, 14, 90, 10.1038/ng0996-90
May, 1995, Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura, Hum Genet, 96, 604, 10.1007/BF00197420
Mochi, 1993, Testing models for genetic determination in migraine, Cephalalgia, 13, 389, 10.1046/j.1468-2982.1993.1306389.x
Nyholt, 2000, All LODs are not created equal, Am J Hum Genet, 67, 282, 10.1086/303029
Nyholt, 2000, Familial typical migraine: significant linkage and localization of a gene to Xq24-28, Hum Genet, 107, 18
Nyholt, 1998, Evidence for an X-linked genetic component in familial typical migraine, Hum Mol Genet, 7, 459, 10.1093/hmg/7.3.459
Nyholt, 1998, Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity, Neurology, 50, 1428, 10.1212/WNL.50.5.1428
O'Brien, 1994, Prevalence of migraine headache in Canada: a population-based survey, Int J Epidemiol, 23, 1020, 10.1093/ije/23.5.1020
O'Connell, 1998, PedCheck: a program for identification of genotype incompatibilities in linkage analysis, Am J Hum Genet, 63, 259, 10.1086/301904
Ogilvie, 1998, Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura, Cephalalgia, 18, 23, 10.1046/j.1468-2982.1998.1801023.x
Ophoff, 1997, Involvement of a Ca2+channel gene in familial hemiplegic migraine and migraine with and without aura, Headache, 37, 479, 10.1046/j.1526-4610.1997.3708479.x
Ophoff, 1996, Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutation in the Ca2+ channel gene CACNL1A4, Cell, 87, 543, 10.1016/S0092-8674(00)81373-2
Oterino, 2001, A new locus for migraine with aura on Xq13, Cephalalgia, 21, 346
Ott, 1983, Linkage analysis and family classification under heterogeneity, Ann Hum Genet, 47, 311, 10.1111/j.1469-1809.1983.tb01001.x
Pajukanta, 1999, Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels, Am J Hum Genet, 64, 1453, 10.1086/302365
Pardo, 1995, Genetic markers: association study in migraine, Cephalalgia, 15, 200, 10.1046/j.1468-2982.1995.015003200.x
Peltonen, 2000, Use of population isolates for mapping complex traits, Nat Rev Genet, 1, 182, 10.1038/35042049
Peroutka, 1997, Clinical susceptibility to migraine with aura is modified by dopamine D2-receptor (DRD2) Nco I alleles, Neurology, 49, 201, 10.1212/WNL.49.1.201
Rasmussen, 1992, Migraine with aura and migraine without aura: an epidemiological study, Cephalalgia, 12, 221, 10.1046/j.1468-2982.1992.1204221.x
Risch, 1992, Model misspecification and multipoint linkage analysis, Hum Hered, 42, 77, 10.1159/000154047
Russell, 1995, Inheritance of migraine investigated by complex segregation analysis, Hum Genet, 96, 726, 10.1007/BF00210307
Russell, 1993, The genetics of migraine without aura and migraine with aura, Cephalalgia, 13, 245, 10.1046/j.1468-2982.1993.1304245.x
Russell, 1995, Increased familial risk and evidence of genetic factor in migraine, BMJ, 311, 541, 10.1136/bmj.311.7004.541
Russell, 1996, Migraine without aura and migraine with aura are distinct clinical entities: a study of four hundred and eighty-four male and female migraineurs from the general population, Cephalalgia, 16, 239, 10.1046/j.1468-2982.1996.1604239.x
Russell, 2001, Migraine without aura and migraine with aura are distinct disorders: a population-based twin survey, Cephalalgia, 21, 346
Sobel, 1996, Descent graphs in pedigree analysis: application to haplotyping, location scores, and marker sharing statistics, Am J Hum Genet, 58, 1323
Stewart, 1992, Prevalence of migraine headache in the United States, JAMA, 267, 64, 10.1001/jama.1992.03480010072027
Terwindt, 2001, Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura, Neurology, 56, 1028, 10.1212/WNL.56.8.1028
Tzourio, 2001, Association between migraine and endothelin type A receptor (ETA −231 A/G) gene polymorphism, Neurology, 56, 1273, 10.1212/WNL.56.10.1273
Ulrich, 1999, The prevalence and characteristics of migraine in twins from general population, Headache, 39, 173, 10.1046/j.1526-4610.1999.3903173.x
Ulrich, 1999, Evidence of a genetic factor in migraine with aura: a population-based Danish twin study, Ann Neurol, 45, 242, 10.1002/1531-8249(199902)45:2<242::AID-ANA15>3.0.CO;2-1
White, 2001, Single nucleotide polymorphism (SNP) alleles in the insulin receptor (INSR) gene are associated with migraine, Cephalalgia, 21, 280
Wieser, 2001, Genetic analysis of the X-chromosome in migraine families, Cephalalgia, 21, 280
Ziegler, 1998, Migraine in twins raised together and apart, Headache, 38, 417, 10.1046/j.1526-4610.1998.3806417.x