-
2
-
-
0033624575
-
The common PPAR Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
(2000)
Nat Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.5
Nemesh, J.6
Lane, C.R.7
Schaffner, S.F.8
Bolk, S.9
Brewer, C.10
Tuomi, T.11
Gaudet, D.12
Hudson, T.J.13
Daly, M.14
Groop, L.15
Lander, E.S.16
-
4
-
-
17544398904
-
Schizophrenia susceptibility and chromosome 6p24-22
-
(1995)
Nat Genet
, vol.11
, pp. 235-236
-
-
Antonarakis, S.E.1
Blouin, J.L.2
Pulver, A.E.3
Wolyniec, P.4
Lasseter, V.K.5
Nestadt, G.6
Kasch, L.7
Babb, R.8
Kazazian, H.H.9
Dombroski, B.10
Kimberland, M.11
Ott, J.12
Housman, D.13
Karayiorgou, M.14
MacLean, C.J.15
-
5
-
-
0029819112
-
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease
-
(1996)
Am J Med Genet
, vol.67
, pp. 564-579
-
-
Arolt, V.1
Lencer, R.2
Nolte, A.3
Müller-Myhsok, B.4
Purmann, S.5
Schürmann, M.6
Leutelt, J.7
Pinnow, M.8
Schwinger, E.9
-
6
-
-
0033663062
-
Genome scan for susceptibility loci for schizophrenia
-
(2000)
Neuropsychobiology
, vol.42
, pp. 175-182
-
-
Bailer, U.1
Leisch, F.2
Meszaros, K.3
Lenzinger, E.4
Willinger, U.5
Strobl, R.6
Gebhardt, C.7
Gerhard, E.8
Fuchs, K.9
Sieghart, W.10
Kasper, S.11
Hornik, K.12
Aschauer, H.N.13
-
7
-
-
0035121790
-
Genetics of schizophrenia and the new millennium: Progress and pitfalls
-
(2001)
Am J Hum Genet
, vol.68
, pp. 299-312
-
-
Baron, M.1
-
16
-
-
0033007317
-
Homogeneous genotyping assays for single nucleotide polymorphisms with fluorescence resonance energy transfer detection
-
(1999)
Genet Anal
, vol.14
, pp. 157-163
-
-
Chen, X.1
Kwok, P.Y.2
-
18
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
20
-
-
0035475967
-
Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: Examples from studies of the calpain-10 gene
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2301-2305
-
-
Cox, N.J.1
-
21
-
-
0032547356
-
Untangling the genetics of a complex disease
-
(1998)
JAMA
, vol.280
, pp. 652-653
-
-
Daly, M.J.1
-
32
-
-
0031718093
-
Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p, and 22q in a population-based sampled Finnish family set
-
(1998)
Mol Psychiatry
, vol.3
, pp. 452-457
-
-
Hovatta, I.1
Lichtermann, D.2
Juvonen, H.3
Suvisaari, J.4
Terwilliger, J.D.5
Arajarvi, R.6
Kokko-Sahin, M.-L.7
Ekelund, J.8
Lonnqvist, J.9
Peltonen, L.10
-
35
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.19
Clayton, D.G.20
Todd, J.A.21
more..
-
41
-
-
0027272195
-
The Roscommon family study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 527-540
-
-
Kendler, K.S.1
McGuire, M.2
Gruenberg, A.M.3
O'Hare, A.4
Spellman, M.5
Walsh, D.6
-
42
-
-
0027328215
-
The Roscommon Family Study. II. The risk of nonschizophrenic nonaffective psychoses in relatives
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 645-652
-
-
-
43
-
-
0027383067
-
The Roscommon family study. III. Schizophrenia-related personality disorders in relatives
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 781-788
-
-
-
45
-
-
0029983060
-
Irish study of high-density schizophrenia families: Field methods and power to detect linkage
-
(1996)
Am J Med Genet
, vol.67
, pp. 179-190
-
-
Kendler, K.S.1
O'Neill, F.A.2
Burke, J.3
Murphy, B.4
Duke, F.5
Straub, R.E.6
Shinkwin, R.7
Nuallain, M.N.8
MacLean, C.J.9
Walsh, D.10
-
48
-
-
0033588260
-
Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23
-
(1999)
Am J Med Genet
, vol.88
, pp. 369-377
-
-
Lindholm, E.1
Ekholm, B.2
Balciuniene, J.3
Johansson, G.4
Castensson, A.5
Koisti, M.6
Nylander, P.O.7
Pettersson, U.8
Adolfsson, R.9
Jazin, E.10
-
50
-
-
0033863391
-
SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
-
(2000)
Am J Hum Genet
, vol.67
, pp. 383-394
-
-
Martin, E.R.1
Lai, E.H.2
Gilbert, J.R.3
Rogala, A.R.4
Afshari, A.J.5
Riley, J.6
Finch, K.L.7
Stevens, J.F.8
Livak, K.J.9
Slotterbeck, B.D.10
Slifer, S.H.11
Warren, L.L.12
Conneally, P.M.13
Schmechel, D.E.14
Purvis, I.15
Pericak-Vance, M.A.16
Roses, A.D.17
Vance, J.M.18
-
51
-
-
0030913474
-
6p24-22 region and major psychoses in the eastern Quebec population: Le Groupe IREP
-
(1997)
Am J Med Genet
, vol.74
, pp. 311-318
-
-
Maziade, M.1
Bissonnette, L.2
Rouillard, E.3
Martinez, M.4
Turgeon, M.5
Charron, L.6
Pouliot, V.7
Boutin, P.8
Cliche, D.9
Dion, C.10
Fournier, J.P.11
Garneau, Y.12
Lavallee, J.C.13
Montgrain, N.14
Nicole, L.15
Pires, A.16
Ponton, A.M.17
Potvin, A.18
Wallot, H.19
Roy, M.A.20
Merette, C.21
more..
-
52
-
-
0034748350
-
A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: A linkage study in 13 target chromosomes
-
(2001)
Mol Psychiatry
, vol.6
, pp. 684-693
-
-
Maziade, M.1
Roy, M.A.2
Rouillard, E.3
Bissonnette, L.4
Fournier, J.P.5
Roy, A.6
Garneau, Y.7
Montgrain, N.8
Potvin, A.9
Cliche, D.10
Dion, C.11
Wallot, H.12
Fournier, A.13
Nicole, L.14
Lavallee, J.C.15
Merette, C.16
-
53
-
-
0034977822
-
Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland
-
(2001)
Nat Genet
, vol.28
, pp. 128-129
-
-
McGinnis, R.E.1
Fox, H.2
Yates, P.3
Cameron, L.A.4
Barnes, M.R.5
Gray, I.C.6
Spurr, N.K.7
Hurko, O.8
St Clair, D.9
-
62
-
-
0033787023
-
Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene
-
(2000)
Genome Res
, vol.10
, pp. 1532-1545
-
-
Nickerson, D.A.1
Taylor, S.2
Fullerton, S.M.3
Weiss, K.M.4
Clark, A.5
Stengard, J.6
Salomaa, V.7
Boerwinkle, E.8
Sing, C.F.9
-
65
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
68
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
70
-
-
0029845435
-
Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study
-
(1996)
Am J Med Genet
, vol.67
, pp. 580-594
-
-
-
71
-
-
0028862998
-
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis
-
(1995)
Nat Genet
, vol.11
, pp. 325-327
-
-
Schwab, S.G.1
Albus, M.2
Hallmayer, J.3
Hönig, S.4
Borrmann, M.5
Lichtermann, D.6
Ebstein, R.P.7
Ackenheil, M.8
Lerer, B.9
Risch, N.10
Maier, W.11
Wildenauer, D.B.12
-
72
-
-
0033647377
-
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: Support for loci on chromosome 10p and 6
-
(2000)
Mol Psychiatry
, vol.5
, pp. 638-649
-
-
Schwab, S.G.1
Hallmayer, J.2
Albus, M.3
Lerer, B.4
Eckstein, G.N.5
Borrmann, M.6
Segman, R.H.7
Hanses, C.8
Freymann, J.9
Yakir, A.10
Trixler, M.11
Falkai, P.12
Rietschel, M.13
Maier, W.14
Wildenauer, D.B.15
-
73
-
-
0034975491
-
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls
-
(2001)
Nat Genet
, vol.28
, pp. 126-128
-
-
Sklar, P.1
Schwab, S.G.2
Williams, N.M.3
Daly, M.4
Schaffner, S.5
Maier, W.6
Albus, M.7
Trixler, M.8
Eichhammer, P.9
Lerer, B.10
Hallmayer, J.11
Norton, N.12
Williams, H.13
Zammit, S.14
Cardno, A.G.15
Jones, S.16
McCarthy, G.17
Milanova, V.18
Kirov, G.19
O'Donovan, M.C.20
Lander, E.S.21
Owen, M.J.22
Wildenauer, D.B.23
more..
-
74
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
77
-
-
0036024256
-
Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and followup of selected regions in all families provides evidence for multiple susceptibility genes
-
(2002)
Mol Psychiatry
, vol.7
, pp. 542-559
-
-
Straub, R.E.1
MacLean, C.J.2
Ma, Y.3
Webb, B.T.4
Myakishev, M.V.5
Harris-Kerr, C.6
Wormley, B.7
Sadek, H.8
Kadambi, B.9
O'Neill, F.A.10
Walsh, D.11
Kendler, K.S.12
-
78
-
-
0028820161
-
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: Evidence for genetic heterogeneity
-
(1995)
Nat Genet
, vol.11
, pp. 287-293
-
-
Straub, R.E.1
MacLean, C.J.2
O'Neill, F.A.3
Burke, J.4
Murphy, B.5
Duke, F.6
Shinkwin, R.7
Webb, B.T.8
Zhang, J.9
Walsh, D.10
Kendler, K.S.11
-
82
-
-
0035937646
-
NOTCH4 gene polymorphism and susceptibility to schizophrenia and schizoaffective disorder
-
(2001)
Neurosci Lett
, vol.301
, pp. 41-44
-
-
Ujike, H.1
Takehisa, Y.2
Takaki, M.3
Tanaka, Y.4
Nakata, K.5
Takeda, T.6
Kodama, M.7
Fujiwara, Y.8
Yamamoto, A.9
Kuroda, S.10
-
84
-
-
0029767674
-
Evidence of linkage disequilibrium between schizophrenia and the SCA1 CAG repeat on chromosome 6p23
-
(1996)
Am J Hum Genet
, vol.59
, pp. 731-736
-
-
Wang, S.1
Detera-Wadleigh, S.D.2
Coon, H.3
Sun, C.4
Goldin, L.R.5
Duffy, D.L.6
Byerley, W.F.7
Gershon, E.S.8
Diehl, S.R.9
-
92
-
-
0027537081
-
Cosegregation of schizophrenia with Becker muscular dystrophy: Susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain
-
(1993)
J Med Genet
, vol.30
, pp. 131-134
-
-
Zatz, M.1
Vallada, H.2
Melo, M.S.3
Passos-Bueno, M.R.4
Vieira, A.H.G.5
Vainzof, M.6
Gill, M.7
Gentil, V.8
|