-
1
-
-
4944267513
-
Migraine
-
King R.J., and Motulsky A.G. (Eds), Oxford Univ. Press, Oxford
-
Palotie B.R., and Wessman M. Migraine. In: King R.J., and Motulsky A.G. (Eds). The Genetic Basis of Common Diseases (2002), Oxford Univ. Press, Oxford 935-947
-
(2002)
The Genetic Basis of Common Diseases
, pp. 935-947
-
-
Palotie, B.R.1
Wessman, M.2
-
2
-
-
1442265540
-
Headache Classification Subcommittee of the International Headache Society
-
The international classification of headache disorders. 2nd ed.
-
Headache Classification Subcommittee of the International Headache Society. The international classification of headache disorders. 2nd ed. Cephalalgia 24 Suppl. 1 (2004) 9-160
-
(2004)
Cephalalgia
, vol.24 SUPPL. 1
, pp. 9-160
-
-
-
3
-
-
0029119352
-
Increased familial risk and evidence of genetic factor in migraine
-
Russell M.B., and Olesen J. Increased familial risk and evidence of genetic factor in migraine. BMJ 311 (1995) 541-544
-
(1995)
BMJ
, vol.311
, pp. 541-544
-
-
Russell, M.B.1
Olesen, J.2
-
4
-
-
18244378312
-
Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine
-
McCarthy L.C., Hosford D.A., Riley J.H., Bird M.I., White N.J., Hewett D.R., Peroutka S.J., Griffiths L.R., Boyd P.R., Lea R.A., Bhatti S.M., Hosking L.K., Hood C.M., Jones K.W., Handley A.R., Rallan R., Lewis K.F., Yeo A.J., Williams P.M., Priest R.C., Khan P., Donnelly C., Lumsden S.M., O J., 'Sullivan, See C.G., Smart D.H., Shaw-Hawkins S., Patel J., Langrish T.C., Feniuk W., Knowles R.G., Thomas M., Libri V., Montgomery D.S., Manasco P.K., Xu C.F., Dykes C., Humphrey P.P., Roses A.D., and Purvis I.J. Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. Genomics 78 (2001) 135-149
-
(2001)
Genomics
, vol.78
, pp. 135-149
-
-
McCarthy, L.C.1
Hosford, D.A.2
Riley, J.H.3
Bird, M.I.4
White, N.J.5
Hewett, D.R.6
Peroutka, S.J.7
Griffiths, L.R.8
Boyd, P.R.9
Lea, R.A.10
Bhatti, S.M.11
Hosking, L.K.12
Hood, C.M.13
Jones, K.W.14
Handley, A.R.15
Rallan, R.16
Lewis, K.F.17
Yeo, A.J.18
Williams, P.M.19
Priest, R.C.20
Khan, P.21
Donnelly, C.22
Lumsden, S.M.23
O'Sullivan, J.24
See, C.G.25
Smart, D.H.26
Shaw-Hawkins, S.27
Patel, J.28
Langrish, T.C.29
Feniuk, W.30
Knowles, R.G.31
Thomas, M.32
Libri, V.33
Montgomery, D.S.34
Manasco, P.K.35
Xu, C.F.36
Dykes, C.37
Humphrey, P.P.38
Roses, A.D.39
Purvis, I.J.40
more..
-
5
-
-
16044370232
-
2+ channel gene CACNL1A4
-
2+ channel gene CACNL1A4. Cell 87 (1996) 543-552
-
(1996)
Cell
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
Terwindt, G.M.2
Vergouwe, M.N.3
van Eijk, R.4
Oefner, P.J.5
Hoffman, S.M.6
Lamerdin, J.E.7
Mohrenweiser, H.W.8
Bulman, D.E.9
Ferrari, M.10
Haan, J.11
Lindhout, D.12
van Ommen, G.J.13
Hofker, M.H.14
Ferrari, M.D.15
Frants, R.R.16
-
6
-
-
0035885854
-
Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus
-
Jones K.W., Ehm M.G., Pericak-Vance M.A., Haines J.L., Boyd P.R., and Peroutka S.J. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus. Genomics 78 (2001) 150-154
-
(2001)
Genomics
, vol.78
, pp. 150-154
-
-
Jones, K.W.1
Ehm, M.G.2
Pericak-Vance, M.A.3
Haines, J.L.4
Boyd, P.R.5
Peroutka, S.J.6
-
7
-
-
19944429551
-
Chromosome 19p13 loci in Finnish migraine with aura families
-
Kaunisto M.A., Tikka P.J., Kallela M., Leal S.M., Papp J.C., Korhonen A., Hamalainen E., Harno H., Havanka H., Nissila M., Sako E., Ilmavirta M., Kaprio J., Farkkila M., Ophoff R.A., Palotie A., and Wessman M. Chromosome 19p13 loci in Finnish migraine with aura families. Am. J. Med. Genet. B Neuropsychiatr. Genet. 132 (2005) 85-89
-
(2005)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.132
, pp. 85-89
-
-
Kaunisto, M.A.1
Tikka, P.J.2
Kallela, M.3
Leal, S.M.4
Papp, J.C.5
Korhonen, A.6
Hamalainen, E.7
Harno, H.8
Havanka, H.9
Nissila, M.10
Sako, E.11
Ilmavirta, M.12
Kaprio, J.13
Farkkila, M.14
Ophoff, R.A.15
Palotie, A.16
Wessman, M.17
-
8
-
-
32244444320
-
No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree
-
Curtain R., Tajouri L., Lea R., MacMillan J., and Griffiths L. No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree. Eur. J. Med. Genet. 49 (2006) 57-62
-
(2006)
Eur. J. Med. Genet.
, vol.49
, pp. 57-62
-
-
Curtain, R.1
Tajouri, L.2
Lea, R.3
MacMillan, J.4
Griffiths, L.5
-
9
-
-
0035829979
-
Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility
-
Lea R.A., Curtain R.P., Hutchins C., Brimage P.J., and Griffiths L.R. Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility. Am. J. Med. Genet. 105 (2001) 707-712
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 707-712
-
-
Lea, R.A.1
Curtain, R.P.2
Hutchins, C.3
Brimage, P.J.4
Griffiths, L.R.5
-
10
-
-
0031433317
-
Headaches in non insulin-dependent diabetes mellitus
-
Split W., and Szydlowska M. Headaches in non insulin-dependent diabetes mellitus. Funct. Neurol. 12 (1997) 327-332
-
(1997)
Funct. Neurol.
, vol.12
, pp. 327-332
-
-
Split, W.1
Szydlowska, M.2
-
11
-
-
4243062602
-
Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action
-
Barroso I., Luan J., Middelberg R.P., Harding A.H., Franks P.W., Jakes R.W., Clayton D., Schafer A.J., O S., 'Rahilly, and Wareham N.J. Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action. PLoS Biol. 1 (2003) E20
-
(2003)
PLoS Biol.
, vol.1
-
-
Barroso, I.1
Luan, J.2
Middelberg, R.P.3
Harding, A.H.4
Franks, P.W.5
Jakes, R.W.6
Clayton, D.7
Schafer, A.J.8
O'Rahilly, S.9
Wareham, N.J.10
-
12
-
-
0023028209
-
Glucose and diet in the fasting migraineur
-
Marsters J.B., Mortimer M.J., and Hay K.M. Glucose and diet in the fasting migraineur. Headache 26 (1986) 243-247
-
(1986)
Headache
, vol.26
, pp. 243-247
-
-
Marsters, J.B.1
Mortimer, M.J.2
Hay, K.M.3
-
13
-
-
0034922937
-
Toward a rational understanding of migraine trigger factors
-
Martin V.T., and Behbehani M.M. Toward a rational understanding of migraine trigger factors. Med. Clin. North Am. 85 (2001) 911-941
-
(2001)
Med. Clin. North Am.
, vol.85
, pp. 911-941
-
-
Martin, V.T.1
Behbehani, M.M.2
-
14
-
-
0037231174
-
The diet factor in pediatric and adolescent migraine
-
Millichap J.G., and Yee M.M. The diet factor in pediatric and adolescent migraine. Pediatr. Neurol. 28 (2003) 9-15
-
(2003)
Pediatr. Neurol.
, vol.28
, pp. 9-15
-
-
Millichap, J.G.1
Yee, M.M.2
-
15
-
-
0028328627
-
Precipitating factors in migraine: a retrospective review of 494 patients
-
Robbins L. Precipitating factors in migraine: a retrospective review of 494 patients. Headache 34 (1994) 214-216
-
(1994)
Headache
, vol.34
, pp. 214-216
-
-
Robbins, L.1
-
16
-
-
36749021694
-
Insulin metabolism is altered in migraineurs: a new pathogenic mechanism for migraine?
-
Cavestro C., Rosatello A., Micca G., Ravotto M., Marino M.P., Asteggiano G., and Beghi E. Insulin metabolism is altered in migraineurs: a new pathogenic mechanism for migraine?. Headache 47 (2007) 1436-1442
-
(2007)
Headache
, vol.47
, pp. 1436-1442
-
-
Cavestro, C.1
Rosatello, A.2
Micca, G.3
Ravotto, M.4
Marino, M.P.5
Asteggiano, G.6
Beghi, E.7
-
17
-
-
33645963747
-
Haplotype-based systematic association studies of ATP1A2 in migraine with aura
-
Netzer C., Todt U., Heinze A., Freudenberg J., Zumbroich V., Becker T., Goebel I., Ohlraun S., Goebel H., and Kubisch C. Haplotype-based systematic association studies of ATP1A2 in migraine with aura. Am. J. Med. Genet. B Neuropsychiatr. Genet. 141 (2006) 257-260
-
(2006)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.141
, pp. 257-260
-
-
Netzer, C.1
Todt, U.2
Heinze, A.3
Freudenberg, J.4
Zumbroich, V.5
Becker, T.6
Goebel, I.7
Ohlraun, S.8
Goebel, H.9
Kubisch, C.10
-
18
-
-
25444479378
-
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine
-
Todt U., Dichgans M., Jurkat-Rott K., Heinze A., Zifarelli G., Koenderink J.B., Goebel I., Zumbroich V., Stiller A., Ramirez A., Friedrich T., Gobel H., and Kubisch C. Rare missense variants in ATP1A2 in families with clustering of common forms of migraine. Hum. Mutat. 26 (2005) 315-321
-
(2005)
Hum. Mutat.
, vol.26
, pp. 315-321
-
-
Todt, U.1
Dichgans, M.2
Jurkat-Rott, K.3
Heinze, A.4
Zifarelli, G.5
Koenderink, J.B.6
Goebel, I.7
Zumbroich, V.8
Stiller, A.9
Ramirez, A.10
Friedrich, T.11
Gobel, H.12
Kubisch, C.13
-
19
-
-
33750977566
-
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura
-
Todt U., Freudenberg J., Goebel I., Heinze A., Heinze-Kuhn K., Rietschel M., Gobel H., and Kubisch C. Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura. Neurology 67 (2006) 1707-1709
-
(2006)
Neurology
, vol.67
, pp. 1707-1709
-
-
Todt, U.1
Freudenberg, J.2
Goebel, I.3
Heinze, A.4
Heinze-Kuhn, K.5
Rietschel, M.6
Gobel, H.7
Kubisch, C.8
-
20
-
-
2442658957
-
Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies
-
Zhang K., Qin Z.S., Liu J.S., Chen T., Waterman M.S., and Sun F. Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies. Genome Res. 14 (2004) 908-916
-
(2004)
Genome Res.
, vol.14
, pp. 908-916
-
-
Zhang, K.1
Qin, Z.S.2
Liu, J.S.3
Chen, T.4
Waterman, M.S.5
Sun, F.6
-
21
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet. Epidemiol. 25 (2003) 115-121
-
(2003)
Genet. Epidemiol.
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
22
-
-
12244264435
-
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits
-
Purcell S., Cherny S.S., and Sham P.C. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19 (2003) 149-150
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
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