Localization of a Gene for Migraine without Aura to Chromosome 4q21
Tài liệu tham khảo
Carlsson, 2002, Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1, Neurology, 59, 1804, 10.1212/01.WNL.0000036617.04943.96
De Fusco, 2003, Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2, Nat Genet, 33, 192, 10.1038/ng1081
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
Fjalldal, 2001, Automated genotyping: combining neural networks and decision trees to perform robust allele calling, Proc Int Joint Conf Neural Networks, A1
Gardner, 1997, A new locus for hemiplegic migraine maps to chromosome 1q31, Neurology, 49, 1231, 10.1212/WNL.49.5.1231
Gervil, 1999, The relative role of genetic and environmental factors in migraine without aura, 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
Gudbjartsson, 2000, Allegro, a new computer program for multipoint linkage analysis, Nat Genet, 25, 12, 10.1038/75514
Gulcher, 1998, Population genomics: laying the groundwork for genetic disease modeling and targeting, Clin Chem Lab Med, 36, 523, 10.1515/CCLM.1998.089
Gulcher, 2000, Protection of privacy by third-party encryption in genetic research in Iceland, Eur J Hum Genet, 8, 739, 10.1038/sj.ejhg.5200530
Headache Classification Committee of the International Headache Society, 1988, Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain, Cephalalgia, 1
Hodge, 1984, The information contained in multiple sibling pairs, Genet Epidemiol, 1, 109, 10.1002/gepi.1370010203
Honkasalo, 1995, Migraine and concomitant symptoms among 8167 adult twin pairs, Headache, 35, 70, 10.1111/j.1526-4610.1995.hed3502070.x
Jones, 2001, Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus, Genomics, 78, 150, 10.1006/geno.2001.6665
Joutel, 1993, A gene for familial hemiplegic migraine maps to chromosome 19, Nat Genet, 5, 40, 10.1038/ng0993-40
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
Kallela, 1999, Clinical characteristics of migraine in a population-based twin sample: similarities and differences between migraine with and without aura, Cephalalgia, 19, 151, 10.1046/j.1468-2982.1999.1903151.x
Kallela, 2001, Familial migraine with and without aura: clinical characteristics and co-occurrence, Eur J Neurol, 8, 441, 10.1046/j.1468-1331.2001.00260.x
Kong, 1997, Allele-sharing models: LOD scores and accurate linkage tests, Am J Hum Genet, 61, 1179, 10.1086/301592
Kong, 2002, A high-resolution recombination map of the human genome, Nat Genet, 31, 241, 10.1038/ng917
Kruglyak, 1996, Parametric and nonparametric linkage analysis: a unified multipoint approach, Am J Hum Genet, 58, 1347
Larsson, 1995, Genetic influence in headaches: a Swedish twin study, Headache, 35, 513, 10.1111/j.1526-4610.1995.hed3509513.x
Launer, 1999, The prevalence and characteristics of migraine in a population-based cohort: the GEM study, Neurology, 53, 537, 10.1212/WNL.53.3.537
Lea, 2002, A typical migraine susceptibility region localizes to chromosome 1q31, Neurogenetics, 4, 17, 10.1007/s10048-001-0125-1
McCarthy, 2001, Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine, Genomics, 78, 135, 10.1006/geno.2001.6647
Mochi, 1993, Testing models for genetic determination in migraine, Cephalalgia, 13, 389, 10.1046/j.1468-2982.1993.1306389.x
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
Ophoff, 1996, Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca(2+) channel gene CACNL1A4, Cell, 87, 543, 10.1016/S0092-8674(00)81373-2
Pálsson, 1999, Using quality measures to facilitate allele calling in high-throughput genotyping, Genome Res, 9, 1002, 10.1101/gr.9.10.1002
Rasmussen, 1992, Migraine with aura and migraine without aura: an epidemiological study, Cephalalgia, 12, 221, 10.1046/j.1468-2982.1992.1204221.x
Russell, 1995, Inheritance of migraine investigated by complex segregation analysis, Hum Genet, 96, 726, 10.1007/BF00210307
Russell, 1996, Migraine without aura and migraine with aura are inherited disorders, Cephalalgia, 16, 305, 10.1046/j.1468-2982.1996.1605305.x
Russell, 1995, Increased familial risk and evidence of genetic factor in migraine, Brit Med J, 311, 541, 10.1136/bmj.311.7004.541
Russell, 1995, Prevalence and sex-ratio of the subtypes of migraine, Int J Epidemiol, 24, 612, 10.1093/ije/24.3.612
Russell, 2002, Migraine without aura and migraine with aura are distinct disorders: a population-based twin survey, Headache, 42, 332, 10.1046/j.1526-4610.2002.02102.x
Soragna, 2003, A locus for migraine without aura maps on chromosome 14q21.2-q22.3, Am J Hum Genet, 72, 161, 10.1086/345298
Stewart, 1992, Prevalence of migraine headache in the United States: relation to age, income, race, and other sociodemographic factors, JAMA, 267, 64, 10.1001/jama.1992.03480010072027
Stewart, 1997, Familial risk of migraine: a population-based study, Ann Neurol, 41, 166, 10.1002/ana.410410207
Svensson, 2002, Lifetime prevalence and characteristics of recurrent primary headaches in a population-based sample of Swedish twins, Headache, 42, 754, 10.1046/j.1526-4610.2002.02177.x
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
Ulrich, 2000, Twin studies of migraine with and without aura, 27
Ulrich, 1999, The prevalence and characteristics of migraine in twins from the 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
Weeks, 1988, The affected-pedigree-member method of linkage analysis, Am J Hum Genet, 42, 315
Wessman, 2002, A susceptibility locus for migraine with aura, on chromosome 4q24, Am J Hum Genet, 70, 652, 10.1086/339078
Whittemore, 1994, A class of tests for linkage using affected pedigree members, Biometrics, 50, 118, 10.2307/2533202
Zhuchenko, 1997, Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α 1A-voltage-dependent calcium channel, Nat Genet, 15, 62, 10.1038/ng0197-62