-
1
-
-
0030927625
-
A 40-year follow-up of school children with migraine
-
(1997)
Cephalalgia
, vol.17
, pp. 488-491
-
-
Bille, B.1
-
7
-
-
0035811775
-
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
-
(2001)
N Engl J Med
, vol.345
, pp. 17-24
-
-
Ducros, A.1
Denier, C.2
Joutel, A.3
Cecillon, M.4
Lescoat, C.5
Vahedi, K.6
Darcel, F.7
Vicaut, E.8
Bousser, M.G.9
Tournier-Lasserve, E.10
-
8
-
-
0031470730
-
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
-
(1997)
Ann Neurol
, vol.42
, pp. 885-890
-
-
Ducros, A.1
Joutel, A.2
Vahedi, K.3
Cecillon, M.4
Ferreira, A.5
Bernard, E.6
Verier, A.7
Echenne, B.8
Lopez de Manain, A.9
Boussier, M.G.10
Tournier-Lasserve, E.11
-
9
-
-
18144434579
-
Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1049-1057
-
-
Ekelund, J.1
Lichtermann, D.2
Hovatta, I.3
Ellonen, P.4
Suvisaari, J.5
Terwilliger, J.D.6
Juvonen, H.7
Varilo, T.8
Arajarvi, R.9
Kokko-Sahin, M.L.10
Lönnqvist, J.11
Peltonen, L.12
-
15
-
-
0000874908
-
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
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1310-1327
-
-
-
18
-
-
0346031709
-
Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain
-
(1988)
Cephalalgia
, vol.8
, pp. 1-96
-
-
-
22
-
-
0033364825
-
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1114-1124
-
-
Hovatta, I.1
Varilo, T.2
Suvisaari, J.3
Terwilliger, J.4
Ollikainen, V.5
Arajärvi, R.6
Juvonen, H.7
Kokko-Sahin, M.8
Väisänen, L.9
Mannila, H.10
Lönnqvist, J.11
Peltonen, L.12
-
23
-
-
9844263366
-
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1973-1978
-
-
Jodice, C.1
Mantuano, E.2
Veneziano, L.3
Trettel, F.4
Sabbadini, G.5
Calandriello, L.6
Francia, A.7
Spadaro, M.8
Pierelli, F.9
Salvi, F.10
Ophoff, R.A.11
Frants, R.R.12
Frontali, M.13
-
24
-
-
0027306090
-
A gene for familial hemiplegic migraine maps to chromosome 19
-
(1993)
Nat Genet
, vol.5
, pp. 40-45
-
-
Joutel, A.1
Bousser, M.-G.2
Biousse, V.3
Labauge, P.4
Chabriat, H.5
Nibbio, A.6
Maciazek, J.7
Meyer, B.8
Bach, M.-A.9
Weissenbach, J.10
Lathrop, G.M.11
Tournier-Lasserve, E.12
-
29
-
-
17344367913
-
Genomewide scan of multiple sclerosis in Finnish multiplex families
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1379-1387
-
-
Kuokkanen, S.1
Gschwend, M.2
Rioux, J.3
Daly, M.4
Terwilligr, J.5
Tienari, P.6
Wikstrom, J.7
Palo, J.8
Stein, L.9
Hudson, T.10
Lander, E.11
Peltonen, L.12
-
30
-
-
0035030767
-
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population
-
(2001)
Nat Genet
, vol.28
, pp. 87-91
-
-
Laitinen, T.1
Daly, M.J.2
Rioux, J.D.3
Kauppi, P.4
Laprise, C.5
Petays, T.6
Green, T.7
Cargill, M.8
Haahtela, T.9
Lander, E.S.10
Laitinen, L.A.11
Hudson, T.J.12
Kere, J.13
-
31
-
-
0028877463
-
Genetic dissection of complex traits: Guideline for interpreting and reporting linkage results
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
36
-
-
2142854406
-
Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: Evidence for a locus on 2q
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1060-1067
-
-
Leppävuori, J.1
Kujala, U.2
Kinnunen, J.3
Kaprio, J.4
Nissila, M.5
Heliovaara, M.6
Klinger, N.7
Partanen, J.8
Terwilliger, J.D.9
Peltonen, L.10
-
39
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families
-
(1996)
Nat Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
Thomas, J.4
McCarthy, M.5
Brayer, J.6
Bryant, B.7
Chan, G.8
Daly, M.9
Forsblom, C.10
Kanninen, T.11
Kirby, A.12
Kruglyak, L.13
Munnelly, K.14
Parkkonen, M.15
Reeve-Daly, M.P.16
Weaver, A.17
Brettin, T.18
Duyk, G.19
Lander, E.S.20
Groop, L.C.21
more..
-
40
-
-
0028806580
-
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
-
(1995)
Hum Genet
, vol.96
, pp. 604-608
-
-
May, A.1
Ophoff, R.A.2
Terwindt, G.M.3
Urban, C.4
Van Eijk, R.5
Haan, J.6
Diener, H.C.7
Lindhout, D.8
Frants, R.R.9
Sandkuijl, L.A.10
Ferrari, M.D.11
Van Eijk, R.12
-
41
-
-
0027755143
-
Testing models for genetic determination in migraine
-
(1993)
Cephalalgia
, vol.13
, pp. 389-394
-
-
Mochi, M.1
Sangiorgi, S.2
Cortelli, P.3
Carelli, V.4
Scapoli, C.5
Crisci, M.6
Monari, L.7
Pierangeli, G.8
Montagna, P.9
-
48
-
-
0031931027
-
Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura
-
(1998)
Cephalalgia
, vol.18
, pp. 23-26
-
-
Ogilvie, A.D.1
Russell, M.B.2
Dhall, P.3
Battersby, S.4
Ulrich, V.5
Smith, C.A.6
Goodwin, G.M.7
Harmar, A.J.8
Olesen, J.9
-
50
-
-
16044370232
-
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutation in the Ca2+ channel gene CACNL1A4
-
(1996)
Cell
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
Terwindt, G.M.2
Vergouve, 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
-
52
-
-
0021064786
-
Linkage analysis and family classification under heterogeneity
-
(1983)
Ann Hum Genet
, vol.47
, pp. 311-320
-
-
Ott, J.1
-
53
-
-
0033362160
-
Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1453-1463
-
-
Pajukanta, P.1
Terwilliger, J.D.2
Perola, M.3
Hiekkalinna, T.4
Nuotio, I.5
Ellonen, P.6
Parkkonen, M.7
Hartiala, J.8
Ylitalo, K.9
Pihlajamaki, J.10
Porkka, K.11
Laakso, M.12
Viikari, J.13
Ehnholm, C.14
Taskinen, M.R.15
Peltonen, L.16
-
61
-
-
0029119352
-
Increased familial risk and evidence of genetic factor in migraine
-
(1995)
BMJ
, vol.311
, pp. 541-544
-
-
-
64
-
-
0029945706
-
Descent graphs in pedigree analysis: Application to haplotyping, location scores, and marker sharing statistics
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
66
-
-
0035942343
-
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
-
(2001)
Neurology
, vol.56
, pp. 1028-1032
-
-
Terwindt, G.M.1
Ophoff, R.A.2
Van Eijk, R.3
Vergouwe, M.N.4
Haan, J.5
Frants, R.R.6
Sandkuijl, L.A.7
Ferrari, M.D.8
-
70
-
-
0000112531
-
Single nucleotide polymorphism (SNP) alleles in the insulin receptor (INSR) gene are associated with migraine
-
(2001)
Cephalalgia
, vol.21
, pp. 280
-
-
White, N.J.1
Hosford, D.A.2
Humprey, P.P.3
Boyd, P.R.4
Griffits, L.R.5
Peroutka, S.6
Roses, A.D.7
Purvis, I.J.8
McCarthy, L.C.9
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