-
3
-
-
0027216273
-
The genetics of schizophrenia: A current, genetic - Epidemiologic perspective
-
Kendler KS, Diehl SR. The genetics of schizophrenia: a current, genetic - epidemiologic perspective. Schizophr Bull 1993; 19: 261-285.
-
(1993)
Schizophr Bull
, vol.19
, pp. 261-285
-
-
Kendler, K.S.1
Diehl, S.R.2
-
4
-
-
0035121790
-
Genetics of schizophrenia and the new millennium: Progress and pitfalls
-
Baron M. Genetics of schizophrenia and the new millennium: progress and pitfalls. Am J Hum Genet 2001; 68: 299-312.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 299-312
-
-
Baron, M.1
-
5
-
-
0037108758
-
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia
-
Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H et al. Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci USA 2002; 99: 13675-13680.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 13675-13680
-
-
Chumakov, I.1
Blumenfeld, M.2
Guerassimenko, O.3
Cavarec, L.4
Palicio, M.5
Abderrahim, H.6
-
6
-
-
18544366528
-
PRODH mutations and hyperprolinemia in a subset of schizophrenic patients
-
Jacquet H, Raux G, Thibaut F, Hecketsweller B, Houy E, Demilly C et al. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Hum Mol Genet 2002; 11: 2243-2249.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2243-2249
-
-
Jacquet, H.1
Raux, G.2
Thibaut, F.3
Hecketsweller, B.4
Houy, E.5
Demilly, C.6
-
7
-
-
0842326677
-
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia
-
Liu H, Heath SC, Sobin C, Roos JL, Galke BL, Blundell ML et al. Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci USA 2002; 99: 3717-3722.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 3717-3722
-
-
Liu, H.1
Heath, S.C.2
Sobin, C.3
Roos, J.L.4
Galke, B.L.5
Blundell, M.L.6
-
8
-
-
0037168523
-
Genetic variation in the 22q11 locus and susceptibility to schizophrenia
-
Liu H, Abecasis G, Heath S, Knowles A, Demars S, Chen Y-J et al. Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci USA 2002; 99: 16859-16864.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 16859-16864
-
-
Liu, H.1
Abecasis, G.2
Heath, S.3
Knowles, A.4
Demars, S.5
Chen, Y.-J.6
-
9
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Ghosh S et al. Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 2002; 71: 877-892.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 877-892
-
-
Stefansson, H.1
Sigurdsson, E.2
Steinthorsdottir, V.3
Bjornsdottir, S.4
Sigmundsson, T.5
Ghosh, S.6
-
10
-
-
18444364206
-
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia
-
Straub RE, Jiang Y, MacLean CJ, Ma Y, Webb BT, Myakishev MV et al. Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. Am J Hum Genet 2002; 71: 337-348.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 337-348
-
-
Straub, R.E.1
Jiang, Y.2
MacLean, C.J.3
Ma, Y.4
Webb, B.T.5
Myakishev, M.V.6
-
11
-
-
0026949420
-
Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
-
Hastbacka J, de la Chappelle A, Kaitila I, Sistonen P, Weaver A. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nat Genet 1992; 2: 204-211.
-
(1992)
Nat Genet
, vol.2
, pp. 204-211
-
-
Hastbacka, J.1
De La Chappelle, A.2
Kaitila, I.3
Sistonen, P.4
Weaver, A.5
-
12
-
-
16044365767
-
Gene mapping in gypsies identifies a novel demyelinating neuropathy on chromosome 8q24
-
Kalaydjieva L, Hallmayer J, Chandler D, Savoy A, Nikolova A, Angelicheva D et al. Gene mapping in gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nat Genet 1996; 14: 214-217.
-
(1996)
Nat Genet
, vol.14
, pp. 214-217
-
-
Kalaydjieva, L.1
Hallmayer, J.2
Chandler, D.3
Savoy, A.4
Nikolova, A.5
Angelicheva, D.6
-
13
-
-
0029925102
-
A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands
-
Nystuen A, Benke PJ, Merren J, Stone EM, Sheffield VC. A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands. Hum Mol Genet 1996; 5: 525-531.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 525-531
-
-
Nystuen, A.1
Benke, P.J.2
Merren, J.3
Stone, E.M.4
Sheffield, V.C.5
-
14
-
-
19044365959
-
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCSIL
-
Visapaa I, Fellman V, Vesa J, Dasvarma A, Hutton JL, Kumar V et al. GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCSIL. Am J Hum Genet 2002; 71: 863-876.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 863-876
-
-
Visapaa, I.1
Fellman, V.2
Vesa, J.3
Dasvarma, A.4
Hutton, J.L.5
Kumar, V.6
-
15
-
-
0032514681
-
Linkage disequilibrium mapping in isolated populations: The example of Finland revisited
-
De La Chapelle A, Wright F. Linkage disequilibrium mapping in isolated populations: the example of Finland revisited. Proc Natl Acad Sci USA 1998; 95: 12416-12423.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 12416-12423
-
-
De La Chapelle, A.1
Wright, F.2
-
16
-
-
0031954852
-
The genetics of asthma. Mapping genes for complex traits in founder populations
-
Ober C, Cox N. The genetics of asthma. Mapping genes for complex traits in founder populations. Clin Exp Allergy 1998; 28: 101-105.
-
(1998)
Clin Exp Allergy
, vol.28
, pp. 101-105
-
-
Ober, C.1
Cox, N.2
-
17
-
-
0034574603
-
Use of population isolates for mapping complex traits
-
Peltonen L, Palotie A, Lange K. Use of population isolates for mapping complex traits. Nat Rev Genet 2000; 1: 182-190.
-
(2000)
Nat Rev Genet
, vol.1
, pp. 182-190
-
-
Peltonen, L.1
Palotie, A.2
Lange, K.3
-
18
-
-
0031472342
-
A variance component approach to dichotomous trait linkage analysis using a threshold model
-
Duggirala R, Williams JT, Williams-Blangero S, Blangero J. A variance component approach to dichotomous trait linkage analysis using a threshold model. Genet Epidemiol 1997; 14: 987-992.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 987-992
-
-
Duggirala, R.1
Williams, J.T.2
Williams-Blangero, S.3
Blangero, J.4
-
19
-
-
0031469587
-
Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: Summary of GAW10 contributions
-
Wijsman EM, Amos C. Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions. Genet Epidemiol 1997; 14: 719-735.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 719-735
-
-
Wijsman, E.M.1
Amos, C.2
-
20
-
-
0031472926
-
Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees
-
Williams JT, Duggirala R, Blangero J. Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees. Genet Epidemiol 1997; 14: 1065-1070.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 1065-1070
-
-
Williams, J.T.1
Duggirala, R.2
Blangero, J.3
-
21
-
-
0034798151
-
The effect of pedigree complexity on quantitative trait linkage analysis
-
Dyer T, Blangero J, Williams J, Göring H, Mahaney M. The effect of pedigree complexity on quantitative trait linkage analysis. Genet Epidemiol 2001; 21(Suppl 1): S236-S243.
-
(2001)
Genet Epidemiol
, vol.21
, Issue.1 SUPPL.
-
-
Dyer, T.1
Blangero, J.2
Williams, J.3
Göring, H.4
Mahaney, M.5
-
22
-
-
0033364825
-
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
-
Hovatta I, Varilo T, Suvisaari J, Terwilliger JD, Ollikainen V, Arajarvi R et al. A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. Am J Med Genet 1999; 65: 1114-1124.
-
(1999)
Am J Med Genet
, vol.65
, pp. 1114-1124
-
-
Hovatta, I.1
Varilo, T.2
Suvisaari, J.3
Terwilliger, J.D.4
Ollikainen, V.5
Arajarvi, R.6
-
23
-
-
18144434579
-
Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
-
Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD et al. Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22. Hum Mol Genet 2000; 9: 1049-1057.
-
(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
-
24
-
-
18244400458
-
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q
-
Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA et al. Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q. Hum Mol Genet 2001; 10: 3037-3048.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 3037-3048
-
-
Paunio, T.1
Ekelund, J.2
Varilo, T.3
Parker, A.4
Hovatta, I.5
Turunen, J.A.6
-
25
-
-
0028156726
-
Analysis of chromosome 22 markers in nine schizophrenia pedigrees
-
Coon H, Holik J, Hoff M, Reimherr F, Wender P, Myles-Worsley M et al. Analysis of chromosome 22 markers in nine schizophrenia pedigrees. Am J Med Genet 1994; 54: 72-79.
-
(1994)
Am J Med Genet
, vol.54
, pp. 72-79
-
-
Coon, H.1
Holik, J.2
Hoff, M.3
Reimherr, F.4
Wender, P.5
Myles-Worsley, M.6
-
26
-
-
0035205379
-
Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markovchain Monte Carlo method
-
Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M. Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markovchain Monte Carlo method. Am J Hum Genet 2001; 69: 1278-1289.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1278-1289
-
-
Camp, N.J.1
Neuhausen, S.L.2
Tiobech, J.3
Polloi, A.4
Coon, H.5
Myles-Worsley, M.6
-
27
-
-
0036366996
-
Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau
-
Devlin B, Bacanu SA, Roeder K, Reimherr F, Wender P, Galke B et al. Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau. Mol Psychiatry 2002; 7: 689-694.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 689-694
-
-
Devlin, B.1
Bacanu, S.A.2
Roeder, K.3
Reimherr, F.4
Wender, P.5
Galke, B.6
-
28
-
-
0034972560
-
A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees
-
Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U et al. A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees. Am J Hum Genet 2001; 69: 96-105.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 96-105
-
-
Lindholm, E.1
Ekholm, B.2
Shaw, S.3
Jalonen, P.4
Johansson, G.5
Pettersson, U.6
-
29
-
-
0037043050
-
Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica
-
DeLisi LE, Mesen A, Rodriguez C, Bertheau A, LaPrade B, Llach M et al. Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica. Am J Med Genet 2002; 114: 497-508.
-
(2002)
Am J Med Genet
, vol.114
, pp. 497-508
-
-
DeLisi, L.E.1
Mesen, A.2
Rodriguez, C.3
Bertheau, A.4
LaPrade, B.5
Llach, M.6
-
30
-
-
0028170206
-
Travels with DNA in the Pacific
-
Clegg J. Travels with DNA in the Pacific. Lancet 1994; 34: 1070-1072.
-
(1994)
Lancet
, vol.34
, pp. 1070-1072
-
-
Clegg, J.1
-
31
-
-
0004225754
-
-
University of California Press: Berkeley & Los Angeles
-
Campbell I. A History of the Pacific Islands. University of California Press: Berkeley & Los Angeles, 1989.
-
(1989)
A History of the Pacific Islands
-
-
Campbell, I.1
-
35
-
-
0003716639
-
-
Kosrae Tourist Division, Department of Conservation and Development, Kosrae State Government: Federated States of Micronesia
-
Segal H. Kosrae: The Sleeping Lady Awakens. Kosrae Tourist Division, Department of Conservation and Development, Kosrae State Government: Federated States of Micronesia, 1989.
-
(1989)
Kosrae: The Sleeping Lady Awakens
-
-
Segal, H.1
-
36
-
-
0035213379
-
Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of Micronesia
-
Shmulewitz D, Auerbach SB, Lehner T, Blundell ML, Winick JD, Youngman LD, Skilling V, Heath SC, Ott J, Stoffel M, Breslow JL, Friedman JM. Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of Micronesia. Hum Hered 2001; 51(1-2): 8-19.
-
(2001)
Hum Hered
, vol.51
, Issue.1-2
, pp. 8-19
-
-
Shmulewitz, D.1
Auerbach, S.B.2
Lehner, T.3
Blundell, M.L.4
Winick, J.D.5
Youngman, L.D.6
Skilling, V.7
Heath, S.C.8
Ott, J.9
Stoffel, M.10
Breslow, J.L.11
Friedman, J.M.12
-
37
-
-
18444402178
-
Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia
-
Han Z, Heath SC, Shmulewitz D, Li W, Auerbach SB, Blundell ML et al. Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia. Am J Med Genet 2002; 110: 234-242.
-
(2002)
Am J Med Genet
, vol.110
, pp. 234-242
-
-
Han, Z.1
Heath, S.C.2
Shmulewitz, D.3
Li, W.4
Auerbach, S.B.5
Blundell, M.L.6
-
38
-
-
0028134880
-
Diagnostic interview for genetic studies: Rationale, unique features, and training. NIMH genetics initiative
-
Nurnberger J, Blehar M, Kaufmann C, York-Cooler C, Simpson S, Harkavy-Friedman J et al. Diagnostic interview for genetic studies: rationale, unique features, and training. NIMH genetics initiative. Arch Gen Psychiatry 1994; 51: 840-859.
-
(1994)
Arch Gen Psychiatry
, vol.51
, pp. 840-859
-
-
Nurnberger, J.1
Blehar, M.2
Kaufmann, C.3
York-Cooler, C.4
Simpson, S.5
Harkavy-Friedman, J.6
-
39
-
-
0003401166
-
-
American Psychiatric Association, Washington, DC
-
American Psychiatric Association. Diagnostic and Statistical Manual, 4th edn. American Psychiatric Association, Washington, DC, 1994.
-
(1994)
Diagnostic and Statistical Manual, 4th Edn.
-
-
-
40
-
-
0018245628
-
Schizophrenia in a North Swedish geographical isolate, 1900-1977: Epidemiology, genetics and biochemistry
-
Böök J, Wetterberg L, Modrzeewska K. Schizophrenia in a North Swedish geographical isolate, 1900-1977: epidemiology, genetics and biochemistry. Clin Genet 1978; 14: 373-394.
-
(1978)
Clin Genet
, vol.14
, pp. 373-394
-
-
Böök, J.1
Wetterberg, L.2
Modrzeewska, K.3
-
41
-
-
0034062074
-
Schizophrenia: The fundamental questions
-
Andreasen NC. Schizophrenia: the fundamental questions. Brain Res Rev 2000; 31: 106-112.
-
(2000)
Brain Res Rev
, vol.31
, pp. 106-112
-
-
Andreasen, N.C.1
-
43
-
-
0034020603
-
Heterogeneity in schizophrenia; mixture modelling of age-at-first-admission, gender and diagnosis
-
Welham J, McLachlan G, Davies G, McGrath J. Heterogeneity in schizophrenia; mixture modelling of age-at-first-admission, gender and diagnosis. Acta Psychiatr Scand 2000; 101: 312-317.
-
(2000)
Acta Psychiatr Scand
, vol.101
, pp. 312-317
-
-
Welham, J.1
McLachlan, G.2
Davies, G.3
McGrath, J.4
-
44
-
-
0029928598
-
Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment
-
Levinson DF, Mowry BJ, Sharpe L, Endicott J. Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment. Genet Epidemiol 1996; 13: 11-21.
-
(1996)
Genet Epidemiol
, vol.13
, pp. 11-21
-
-
Levinson, D.F.1
Mowry, B.J.2
Sharpe, L.3
Endicott, J.4
-
45
-
-
0034800186
-
The importance of connections: Joining components of the Hutterite pedigree
-
Chapman N, Leutenegger A-L, Badzioch M, Bogdan M, Conlon E, Daw E et al. The importance of connections: joining components of the Hutterite pedigree. Genet Epidemiol 2001; 21(Suppl 1): S230-S235.
-
(2001)
Genet Epidemiol
, vol.21
, Issue.1 SUPPL.
-
-
Chapman, N.1
Leutenegger, A.-L.2
Badzioch, M.3
Bogdan, M.4
Conlon, E.5
Daw, E.6
-
47
-
-
0031972889
-
Automatic selection of loop breakers for genetic linkage analysis
-
Becker A, Geiger D, Schaffer A. Automatic selection of loop breakers for genetic linkage analysis. Hum Heredity 1998; 48: 49-60.
-
(1998)
Hum Heredity
, vol.48
, pp. 49-60
-
-
Becker, A.1
Geiger, D.2
Schaffer, A.3
-
48
-
-
0026684478
-
Adequacy of single-locus approximations for linkage analyses of oligogenic traits
-
Vieland VJ, Hodge SE, Greenberg DA. Adequacy of single-locus approximations for linkage analyses of oligogenic traits. Genet Epidemiol 1992; 9: 45-59.
-
(1992)
Genet Epidemiol
, vol.9
, pp. 45-59
-
-
Vieland, V.J.1
Hodge, S.E.2
Greenberg, D.A.3
-
49
-
-
0032231937
-
The power to detect linkage in complex disease by means of simple LOD-score analyses
-
Greenberg D, Abreu P, Hodge S. The power to detect linkage in complex disease by means of simple LOD-score analyses. Am J Hum Genet 1998; 63: 870-879.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 870-879
-
-
Greenberg, D.1
Abreu, P.2
Hodge, S.3
-
50
-
-
0033362231
-
Direct power comparison between simple LOD scores and NPL scores for linkage analysis in complex diseases
-
Abreu P, Greenberg D, Hodge S. Direct power comparison between simple LOD scores and NPL scores for linkage analysis in complex diseases. Am J Hum Genet 1999; 65: 847-857.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 847-857
-
-
Abreu, P.1
Greenberg, D.2
Hodge, S.3
-
51
-
-
0026629701
-
Strategies for characterizing highly polymorphic markers in human gene mapping
-
Ott J. Strategies for characterizing highly polymorphic markers in human gene mapping. Am J Hum Genet 1992; 51: 283-290.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 283-290
-
-
Ott, J.1
-
52
-
-
0027730584
-
The effect of misspecifying allele frequencies in incompletely typed families
-
Kapp M, Seuchter SA, Baur MP. The effect of misspecifying allele frequencies in incompletely typed families. Genet Epidemiol 1993; 10: 413-418.
-
(1993)
Genet Epidemiol
, vol.10
, pp. 413-418
-
-
Kapp, M.1
Seuchter, S.A.2
Baur, M.P.3
-
53
-
-
0027770586
-
The impact of some parameters on linkage analysis of Alzheimer's disease
-
Xu J, Taylor E, Lung F, Chung A, Chase G, Maestri N et al. The impact of some parameters on linkage analysis of Alzheimer's disease. Genet Epidemiol 1993; 10: 407-412.
-
(1993)
Genet Epidemiol
, vol.10
, pp. 407-412
-
-
Xu, J.1
Taylor, E.2
Lung, F.3
Chung, A.4
Chase, G.5
Maestri, N.6
-
54
-
-
0033711876
-
Bias in multipoint linkage analysis arising from map misspecification
-
Daw E, Thompson E, Wijsman E. Bias in multipoint linkage analysis arising from map misspecification. Genet Epidemiol 2000; 19: 336-380.
-
(2000)
Genet Epidemiol
, vol.19
, pp. 336-380
-
-
Daw, E.1
Thompson, E.2
Wijsman, E.3
-
55
-
-
0023807680
-
A simple method for DNA purification from peripheral blood
-
Ciulla TA, Sklar RM, Hauser SL. A simple method for DNA purification from peripheral blood. Anal Biochem 1988; 174: 485-488.
-
(1988)
Anal Biochem
, vol.174
, pp. 485-488
-
-
Ciulla, T.A.1
Sklar, R.M.2
Hauser, S.L.3
-
56
-
-
0001506104
-
Modulation of non-templated nucleotide addition by Taq DNA polymerase: Primer modifications that facilitate genotyping
-
Brownstein MJ, Carpten JD, Smith JR. Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping. Biotechniques 1996; 20: 1004-1006, 1008-1010.
-
(1996)
Biotechniques
, vol.20
, pp. 1004-1006
-
-
Brownstein, M.J.1
Carpten, J.D.2
Smith, J.R.3
-
57
-
-
0028577384
-
Automation of genetic linkage analysis using fluorescent microsatellite markers
-
Mansfield DC, Brown AF, Green DK, Carothers AD, Morris SW, Evans HJ et al. Automation of genetic linkage analysis using fluorescent microsatellite markers. Genomics 1994; 24: 225-233.
-
(1994)
Genomics
, vol.24
, pp. 225-233
-
-
Mansfield, D.C.1
Brown, A.F.2
Green, D.K.3
Carothers, A.D.4
Morris, S.W.5
Evans, H.J.6
-
58
-
-
0031456689
-
Improvement of the power to detect complex disease genes by regional inference procedures
-
Goldin LR, Chase GA. Improvement of the power to detect complex disease genes by regional inference procedures. Genet Epidemiol 1997; 14: 785-789.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 785-789
-
-
Goldin, L.R.1
Chase, G.A.2
-
59
-
-
0034724924
-
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
-
Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 2000; 288: 678-682.
-
(2000)
Science
, vol.288
, pp. 678-682
-
-
Brzustowicz, L.M.1
Hodgkinson, K.A.2
Chow, E.W.3
Honer, W.G.4
Bassett, A.S.5
-
60
-
-
0035089756
-
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23
-
Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS et al. Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. Am J Hum Genet 2001; 68: 661-673.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 661-673
-
-
Gurling, H.M.1
Kalsi, G.2
Brynjolfson, J.3
Sigmundsson, T.4
Sherrington, R.5
Mankoo, B.S.6
-
62
-
-
0030903121
-
Optimal strategies for mapping complex diseases in the presence of multiple loci
-
Goldgar DE, Easton DF. Optimal strategies for mapping complex diseases in the presence of multiple loci. Am J Hum Genet 1997; 60: 1222-1232.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1222-1232
-
-
Goldgar, D.E.1
Easton, D.F.2
-
63
-
-
0031815979
-
Sib-pair collection strategies for complex diseases
-
McCarthy M, Kruglyak L, Lander E. Sib-pair collection strategies for complex diseases. Genet Epidemiol 1998; 15: 317-340.
-
(1998)
Genet Epidemiol
, vol.15
, pp. 317-340
-
-
McCarthy, M.1
Kruglyak, L.2
Lander, E.3
-
64
-
-
84933490415
-
Schizophrenia and chronic mental illness in Micronesia: An epidemiological survey
-
Hezel F, Wylie A. Schizophrenia and chronic mental illness in Micronesia: an epidemiological survey. ISLA: J Micronesian Stud 1992; 1: 329-354.
-
(1992)
ISLA: J Micronesian Stud
, vol.1
, pp. 329-354
-
-
Hezel, F.1
Wylie, A.2
-
65
-
-
0032213597
-
The role of gender differences in the reduction of etiologic heterogeneity in schizophrenia
-
Salem JE, Kring AM. The role of gender differences in the reduction of etiologic heterogeneity in schizophrenia. Clin Psychol Rev 1998; 18: 795-819.
-
(1998)
Clin Psychol Rev
, vol.18
, pp. 795-819
-
-
Salem, J.E.1
Kring, A.M.2
-
66
-
-
12444333185
-
Sex differences and psychiatric disorders
-
Dohrenwend B, Dohrenwend B. Sex differences and psychiatric disorders. Ann Rev Psychol 1974; 25: 117-152.
-
(1974)
Ann Rev Psychol
, vol.25
, pp. 117-152
-
-
Dohrenwend, B.1
Dohrenwend, B.2
-
67
-
-
0021365709
-
Effect of diagnostic criteria on the ratio of male to female schizophrenic patients
-
Lewine R, Burbach D, Meltzer HY. Effect of diagnostic criteria on the ratio of male to female schizophrenic patients. Am J Psychiatry 1984; 141: 84-87.
-
(1984)
Am J Psychiatry
, vol.141
, pp. 84-87
-
-
Lewine, R.1
Burbach, D.2
Meltzer, H.Y.3
-
68
-
-
0026806985
-
Where are the women in first-episode studies of schizophrenia?
-
Iacono WG, Beiser M. Where are the women in first-episode studies of schizophrenia? Schizophr Bull 1992; 18: 471-480.
-
(1992)
Schizophr Bull
, vol.18
, pp. 471-480
-
-
Iacono, W.G.1
Beiser, M.2
-
69
-
-
0033525171
-
Genetic epidemiological study of schizophrenia in Palau, Micronesia: Prevalence and familiality
-
Myles-Worsley M, Coon H, Tiobech J, Collier J, Dale P, Wender P et al. Genetic epidemiological study of schizophrenia in Palau, Micronesia: prevalence and familiality. Am J Med Genet 1999; 88: 4-10.
-
(1999)
Am J Med Genet
, vol.88
, pp. 4-10
-
-
Myles-Worsley, M.1
Coon, H.2
Tiobech, J.3
Collier, J.4
Dale, P.5
Wender, P.6
-
70
-
-
0033135862
-
Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive - Compulsive disorder
-
Karayiorgou M, Sobin C, Blundell M, Galke B, Malinova L, Goldberg P et al. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive - compulsive disorder. Biol Psychiatry 1999; 45: 1178-1189.
-
(1999)
Biol Psychiatry
, vol.45
, pp. 1178-1189
-
-
Karayiorgou, M.1
Sobin, C.2
Blundell, M.3
Galke, B.4
Malinova, L.5
Goldberg, P.6
-
71
-
-
0035826463
-
Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive - Compulsive disorder
-
Camarena B, Rinetti G, Cruz C, Gomez A, de La Fuente JR, Nicolini H. Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive - compulsive disorder. Am J Med Genet 2001; 105: 279-282.
-
(2001)
Am J Med Genet
, vol.105
, pp. 279-282
-
-
Camarena, B.1
Rinetti, G.2
Cruz, C.3
Gomez, A.4
De La Fuente, J.R.5
Nicolini, H.6
-
72
-
-
0032544012
-
Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
-
Gogos JA, Morgan M, Luine V, Santha M, Ogawa S, Pfaff D et al. Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. Proc Natl Acad Sci USA 1998; 95: 9991-9996.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 9991-9996
-
-
Gogos, J.A.1
Morgan, M.2
Luine, V.3
Santha, M.4
Ogawa, S.5
Pfaff, D.6
-
73
-
-
0036137946
-
Mice deficient for both corticotropin-releasing factor receptor 1 (CRFR1) and CRFR2 have an impaired stress response and display sexually dichotomous anxiety-like behavior
-
Bale TL, Picetti R, Contarino A, Koob GF, Vale WW, Lee KF. Mice deficient for both corticotropin-releasing factor receptor 1 (CRFR1) and CRFR2 have an impaired stress response and display sexually dichotomous anxiety-like behavior. J Neurosci 2002; 22: 193-199.
-
(2002)
J Neurosci
, vol.22
, pp. 193-199
-
-
Bale, T.L.1
Picetti, R.2
Contarino, A.3
Koob, G.F.4
Vale, W.W.5
Lee, K.F.6
-
74
-
-
0028293134
-
Can estradiol modulate schizophrenic symptomatology?
-
Riecher-Rossler A, Hafner H, Stumbaum M, Maurer K, Schmidt R. Can estradiol modulate schizophrenic symptomatology? Schizophr Bull 1994; 20: 203-214.
-
(1994)
Schizophr Bull
, vol.20
, pp. 203-214
-
-
Riecher-Rossler, A.1
Hafner, H.2
Stumbaum, M.3
Maurer, K.4
Schmidt, R.5
-
75
-
-
0343729872
-
Main risk factors for schizophrenia: Increased familial loading and pre- and peri-natal complications antagonize the protective effect of oestrogen in women
-
Konnecke R, Hafner H, Maurer K, Loffler W, van der Heiden W. Main risk factors for schizophrenia: increased familial loading and pre- and peri-natal complications antagonize the protective effect of oestrogen in women. Schizophr Res 2000; 44: 81-93.
-
(2000)
Schizophr Res
, vol.44
, pp. 81-93
-
-
Konnecke, R.1
Hafner, H.2
Maurer, K.3
Loffler, W.4
Van Der Heiden, W.5
-
76
-
-
0035218794
-
Estradiol levels in psychotic disorders
-
Huber TJ, Rollnik J, Wilhelms J, von zur Muhlen A, Emrich HM, Schneider U. Estradiol levels in psychotic disorders. Psychoneuroendocrinology 2001; 26: 27-35.
-
(2001)
Psychoneuroendocrinology
, vol.26
, pp. 27-35
-
-
Huber, T.J.1
Rollnik, J.2
Wilhelms, J.3
Von Zur Muhlen, A.4
Emrich, H.M.5
Schneider, U.6
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