-
5
-
-
0004195717
-
-
London: Royal College of Psychiatrists
-
McGuffin P, Owen MJ, O'Donovan MC, Thapar A, Gottesman II. Seminars in psychiatric genetics. London: Royal College of Psychiatrists, 1994:87-109.
-
(1994)
Seminars in Psychiatric Genetics
, pp. 87-109
-
-
McGuffin, P.1
Owen, M.J.2
O'Donovan, M.C.3
Thapar, A.4
Gottesman, I.I.5
-
6
-
-
0000931729
-
Schizophrenia: Genetics
-
Sadock BJ, Sadock VA, eds. Philadelphia, PA; Lippincott, Williams and Wilkins
-
Kendler KS. Schizophrenia: genetics. In: Sadock BJ, Sadock VA, eds. Kapln and Sadock's comprehensive textbook of psychiatry, Vol 1. Philadelphia, PA; Lippincott, Williams and Wilkins, 2000:1147-59.
-
(2000)
Kapln and Sadock's Comprehensive Textbook of Psychiatry
, vol.1
, pp. 1147-1159
-
-
Kendler, K.S.1
-
7
-
-
0034060459
-
Twin studies of schizophrenia: From bow-and-arrow concordances to star wars Mx and functional genomics
-
Cardno AG, Gottesman II. Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics (review). Am J Med Genet 2000;97(1):12-7.
-
(2000)
Am J Med Genet
, vol.97
, Issue.1
, pp. 12-17
-
-
Cardno, A.G.1
Gottesman, I.I.2
-
9
-
-
0024670545
-
A single dominant gene still cannot account for the transmission of schizophrenia
-
McGue M, Gottesman II. A single dominant gene still cannot account for the transmission of schizophrenia. Arch Gen Psychiatry 1989;46:478-80.
-
(1989)
Arch Gen Psychiatry
, vol.46
, pp. 478-480
-
-
McGue, M.1
Gottesman, I.I.2
-
10
-
-
0025355888
-
Genetic linkage and complex diseases, with special reference to psychiatric disorders
-
discussion 17-45
-
Risch N. Genetic linkage and complex diseases, with special reference to psychiatric disorders. Genet Epidemiol 1990;7(1):3-16; discussion 17-45.
-
(1990)
Genet Epidemiol
, vol.7
, Issue.1
, pp. 3-16
-
-
Risch, N.1
-
11
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995;11:241-7.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
12
-
-
0002710362
-
Problems of replicating linkage claims in psychiatry
-
Gershon ES, Cloninger CR, eds. Washington, DC: American Psychiatric Press
-
Suarez BK, Hampe CL, Van Eerdewegh P. Problems of replicating linkage claims in psychiatry. In: Gershon ES, Cloninger CR, eds. Genetic approaches to mental disorders. Washington, DC: American Psychiatric Press, 1994:23-46.
-
(1994)
Genetic Approaches to Mental Disorders
, pp. 23-46
-
-
Suarez, B.K.1
Hampe, C.L.2
Van Eerdewegh, P.3
-
13
-
-
0036258079
-
Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia
-
Badner JA, Gershon ES. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 2002;7:405-11.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 405-411
-
-
Badner, J.A.1
Gershon, E.S.2
-
14
-
-
0038003196
-
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia
-
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Carver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lonnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR, Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoega T, Helgason T. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: schizophrenia. Am J Hum Genet 2003;73(1):34-48.
-
(2003)
Am J Hum Genet
, vol.73
, Issue.1
, pp. 34-48
-
-
Lewis, C.M.1
Levinson, D.F.2
Wise, L.H.3
Delisi, L.E.4
Straub, R.E.5
Hovatta, I.6
Williams, N.M.7
Schwab, S.G.8
Pulver, A.E.9
Faraone, S.V.10
Brzustowicz, L.M.11
Kaufmann, C.A.12
Carver, D.L.13
Gurling, H.M.14
Lindholm, E.15
Coon, H.16
Moises, H.W.17
Byerley, W.18
Shaw, S.H.19
Mesen, A.20
Sherrington, R.21
O'Neill, F.A.22
Walsh, D.23
Kendler, K.S.24
Ekelund, J.25
Paunio, T.26
Lonnqvist, J.27
Peltonen, L.28
O'Donovan, M.C.29
Owen, M.J.30
Wildenauer, D.B.31
Maier, W.32
Nestadt, G.33
Blouin, J.L.34
Antonarakis, S.E.35
Mowry, B.J.36
Silverman, J.M.37
Crowe, R.R.38
Cloninger, C.R.39
Tsuang, M.T.40
Malaspina, D.41
Harkavy-Friedman, J.M.42
Svrakic, D.M.43
Bassett, A.S.44
Holcomb, J.45
Kalsi, G.46
McQuillin, A.47
Brynjolfson, J.48
Sigmundsson, T.49
Petursson, H.50
Jazin, E.51
Zoega, T.52
Helgason, T.53
more..
-
15
-
-
0037336692
-
Dopamine D3 receptor gene Ser9Gly variant and schizophrenia: Association study and meta-analysis
-
Jonsson EG, Flyckt L, Burgert E, Crocq MA, Forslund K, Mattila-Evenden M, Rylander G, Asberg M, Nimgaonkar VL, Edman G, Bjerkenstedt L, Wiesel FA, Sedvall GC. Dopamine D3 receptor gene Ser9Gly variant and schizophrenia: association study and meta-analysis. Psychiatr Genet 2003;13:1-12.
-
(2003)
Psychiatr Genet
, vol.13
, pp. 1-12
-
-
Jonsson, E.G.1
Flyckt, L.2
Burgert, E.3
Crocq, M.A.4
Forslund, K.5
Mattila-Evenden, M.6
Rylander, G.7
Asberg, M.8
Nimgaonkar, V.L.9
Edman, G.10
Bjerkenstedt, L.11
Wiesel, F.A.12
Sedvall, G.C.13
-
16
-
-
0242552588
-
Meta-analysis identifies an association between the dopamine D2 receptor gene and schizophrenia
-
Glatt SJ, Faraone SV, Tsuang MT. Meta-analysis identifies an association between the dopamine D2 receptor gene and schizophrenia. Mol Psychiatry 2003;8:911-5.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 911-915
-
-
Glatt, S.J.1
Faraone, S.V.2
Tsuang, M.T.3
-
17
-
-
1642483062
-
Meta-analysis of association between the T102C polymorphism or the 5HT2a receptor gene and schizophrenia
-
Abdolmaleky HM, Faraone SV, Glatt SJ, Tsuang MT. Meta-analysis of association between the T102C polymorphism or the 5HT2a receptor gene and schizophrenia. Schizophr Res 2004;67:53-62.
-
(2004)
Schizophr Res
, vol.67
, pp. 53-62
-
-
Abdolmaleky, H.M.1
Faraone, S.V.2
Glatt, S.J.3
Tsuang, M.T.4
-
18
-
-
38149138747
-
Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population
-
Marti SB, Cichon S, Propping P, Nothen M. Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population. Am J Med Genet 2002;114:46-50.
-
(2002)
Am J Med Genet
, vol.114
, pp. 46-50
-
-
Marti, S.B.1
Cichon, S.2
Propping, P.3
Nothen, M.4
-
19
-
-
12444314603
-
Positive associations of polymorphisms in the metabotropic glutamate receptor type 3 gene (GRM3) with schizophrenia
-
Fujii Y, Shibata H, Kikuta R, Makino C, Tani A, Hirata N, Shibata A, Ninomiya H, Tashiro N, Fukumaki Y. Positive associations of polymorphisms in the metabotropic glutamate receptor type 3 gene (GRM3) with schizophrenia. Psychiatr Genet 2003;13:71-6.
-
(2003)
Psychiatr Genet
, vol.13
, pp. 71-76
-
-
Fujii, Y.1
Shibata, H.2
Kikuta, R.3
Makino, C.4
Tani, A.5
Hirata, N.6
Shibata, A.7
Ninomiya, H.8
Tashiro, N.9
Fukumaki, Y.10
-
20
-
-
4344624909
-
Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia
-
Egan MF, Straub RE, Goldberg TE, Yakub I, Callicott JH, Hariri AR, Mattay VS, Bertolino A, Hyde TM, Shannon-Weickert C, Akil M, Crook J, Vakkalanka RK, Balkissoon R, Gibbs RA, Kleinman JE, Weinberger DR. Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia. Proc Natl Acad Sci U S A 2004;101:12604-9.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 12604-12609
-
-
Egan, M.F.1
Straub, R.E.2
Goldberg, T.E.3
Yakub, I.4
Callicott, J.H.5
Hariri, A.R.6
Mattay, V.S.7
Bertolino, A.8
Hyde, T.M.9
Shannon-Weickert, C.10
Akil, M.11
Crook, J.12
Vakkalanka, R.K.13
Balkissoon, R.14
Gibbs, R.A.15
Kleinman, J.E.16
Weinberger, D.R.17
-
21
-
-
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, Harris-Kerr C, Wormley B, Sadek H, Kadambi B, Cesare AJ, Gibberman A, Wang X, O'Neill FA, Walsh D, Kendler KS. 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(2):337-48.
-
(2002)
Am J Hum Genet
, vol.71
, Issue.2
, 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
Harris-Kerr, C.7
Wormley, B.8
Sadek, H.9
Kadambi, B.10
Cesare, A.J.11
Gibberman, A.12
Wang, X.13
O'Neill, F.A.14
Walsh, D.15
Kendler, K.S.16
-
22
-
-
0037222276
-
Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families
-
Schwab SG, Knapp M, Mondaban S, Hallmayer J, Borrmann-Hassenbach M, Albus M, Lerer B, Rietschel M, Trixler M, Maier W, Wildenauer DB. Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. Am J Hum Genet 2003;72(1):185-90.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.1
, pp. 185-190
-
-
Schwab, S.G.1
Knapp, M.2
Mondaban, S.3
Hallmayer, J.4
Borrmann-Hassenbach, M.5
Albus, M.6
Lerer, B.7
Rietschel, M.8
Trixler, M.9
Maier, W.10
Wildenauer, D.B.11
-
23
-
-
11144356974
-
Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1)
-
Williams NM, Preece A, Morris DW, Spurlock G, Bray NJ, Stephens M, Norton N, Williams H, Clement M, Dwyer S, Curran C, Wilkinson J, Moskvina V, Waddington JL, Gill M, Corvin AP, Zammit S, Kirov G, Owen MJ, O'Donovan MC. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Arch Gen Psychiatr 2004;61:336-44.
-
(2004)
Arch Gen Psychiatr
, vol.61
, pp. 336-344
-
-
Williams, N.M.1
Preece, A.2
Morris, D.W.3
Spurlock, G.4
Bray, N.J.5
Stephens, M.6
Norton, N.7
Williams, H.8
Clement, M.9
Dwyer, S.10
Curran, C.11
Wilkinson, J.12
Moskvina, V.13
Waddington, J.L.14
Gill, M.15
Corvin, A.P.16
Zammit, S.17
Kirov, G.18
Owen, M.J.19
O'Donovan, M.C.20
more..
-
24
-
-
2342477899
-
Strong evidence for association between the dystrobrevin binding protein 1 (DTNBP1) gene and schizophrenia in 488 parent-offspring trios from Bulgaria
-
Kirov G, Ivanov D, Williams NM, Preece A, Nikolov I, Milev R, Koleva S, Dimitrova A, Toncheva D, O'Donovan MC, Owen MJ. Strong evidence for association between the dystrobrevin binding protein 1 (DTNBP1) gene and schizophrenia in 488 parent-offspring trios From Bulgaria. Biol Psychiatry 2004;55:971-5.
-
(2004)
Biol Psychiatry
, vol.55
, pp. 971-975
-
-
Kirov, G.1
Ivanov, D.2
Williams, N.M.3
Preece, A.4
Nikolov, I.5
Milev, R.6
Koleva, S.7
Dimitrova, A.8
Toncheva, D.9
O'Donovan, M.C.10
Owen, M.J.11
-
25
-
-
9144267763
-
The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease
-
Van Den Bogaert A, Schumacher J, Schulze TG, Otte AC, Ohlraun S, Kovalenko S, Becker T, Freudenberg J, Jonsson EG, Mattila-Evenden M, Sedvall GC, Czerski PM, Kapelski P, Hauser J, Maier W, Rietschel M, Propping P, Nothen MM, Cichon S. The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease. Am J Hum Genet 2003;73:1438-43.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1438-1443
-
-
Van Den Bogaert, A.1
Schumacher, J.2
Schulze, T.G.3
Otte, A.C.4
Ohlraun, S.5
Kovalenko, S.6
Becker, T.7
Freudenberg, J.8
Jonsson, E.G.9
Mattila-Evenden, M.10
Sedvall, G.C.11
Czerski, P.M.12
Kapelski, P.13
Hauser, J.14
Maier, W.15
Rietschel, M.16
Propping, P.17
Nothen, M.M.18
Cichon, S.19
-
26
-
-
8444250206
-
Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia
-
Numakawa T, Yagasaki Y, Ishimoto T, Okada T, Suzuki T, Iwata N, Ozaki N, Taguchi T, Tatsumi M, Kamijima K, Straub RE, Weinberger DR, Kunugi H, Hashimoto R. Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia. Hum Mol Genet 2004;13(21):2699-708.
-
(2004)
Hum Mol Genet
, vol.13
, Issue.21
, pp. 2699-2708
-
-
Numakawa, T.1
Yagasaki, Y.2
Ishimoto, T.3
Okada, T.4
Suzuki, T.5
Iwata, N.6
Ozaki, N.7
Taguchi, T.8
Tatsumi, M.9
Kamijima, K.10
Straub, R.E.11
Weinberger, D.R.12
Kunugi, H.13
Hashimoto, R.14
-
27
-
-
6344237686
-
Association of the DTNBP1 locus with schizophrenia in a U.S. population
-
Funke B, Finn CT, Plocik AM, Lake S, DeRosse P, Kane JM, Kucherlapoti R, Malhotra AK. Association of the DTNBP1 locus with schizophrenia in a U.S. population. Am J Hum Genet 2004;75(5):891-8.
-
(2004)
Am J Hum Genet
, vol.75
, Issue.5
, pp. 891-898
-
-
Funke, B.1
Finn, C.T.2
Plocik, A.M.3
Lake, S.4
Derosse, P.5
Kane, J.M.6
Kucherlapoti, R.7
Malhotra, A.K.8
-
28
-
-
0037395091
-
No evidence for association of the dysbindin gene (DTNBP1) with schizophrenia in an Irish population-based study
-
Morris DW, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP. No evidence for association of the dysbindin gene (DTNBP1) with schizophrenia in an Irish population-based study. Schizophr Res 2003;60:167-72.
-
(2003)
Schizophr Res
, vol.60
, pp. 167-172
-
-
Morris, D.W.1
McGhee, K.A.2
Schwaiger, S.3
Scully, P.4
Quinn, J.5
Meagher, D.6
Waddington, J.L.7
Gill, M.8
Corvin, A.P.9
-
29
-
-
0037623912
-
Cis-acting variation in the expression of a high proportion of genes in human brain
-
Bray NJ, Buckland PR, Owen MJ, O'Donovan MC. Cis-acting variation in the expression of a high proportion of genes in human brain. Hum Genet 2003;113:149-53.
-
(2003)
Hum Genet
, vol.113
, pp. 149-153
-
-
Bray, N.J.1
Buckland, P.R.2
Owen, M.J.3
O'Donovan, M.C.4
-
30
-
-
2942590969
-
Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain
-
Weickert CS, Straub RE, McClintock BW, Matsumoto M, Hashimoto R, Hyde TM, Herman MM, Weinberger DR, Kleinman JE. Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain. Arch Gen Psychiatry 2004;61:544-55.
-
(2004)
Arch Gen Psychiatry
, vol.61
, pp. 544-555
-
-
Weickert, C.S.1
Straub, R.E.2
McClintock, B.W.3
Matsumoto, M.4
Hashimoto, R.5
Hyde, T.M.6
Herman, M.M.7
Weinberger, D.R.8
Kleinman, J.E.9
-
31
-
-
2342512304
-
Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia
-
Talbot K, Eidem WL, Tinsley CL, Benson MA, Thompson EW, Smith RJ, Hahn CG, Siegel SJ, Trojanowski JQ, Gur RE, Blake DJ, Arnold SE. Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia. J Clin Invest 2004;113:1353-63.
-
(2004)
J Clin Invest
, vol.113
, pp. 1353-1363
-
-
Talbot, K.1
Eidem, W.L.2
Tinsley, C.L.3
Benson, M.A.4
Thompson, E.W.5
Smith, R.J.6
Hahn, C.G.7
Siegel, S.J.8
Trojanowski, J.Q.9
Gur, R.E.10
Blake, D.J.11
Arnold, S.E.12
-
32
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Gosh S, Brynjolfsson J, Gunnarsdottir S, Ivarsson O, Chou TT, Hjaltason O, Birgisdottir B, Jonsson H, Gudnadottir VG, Gudmundsdottir E, Bjornsson A, Ingvarsson B, Ingason A, Sigfusson S, Hardardottir H, Harvey RP, Lai D, Zhou M, Brunner D, Mutel V, Gonzalo A, Lemke G, Sainz J, Johannesson G, Andresson T, Gudbjartsson D, Manolescu A, Frigge ML, Gurney ME, Kong A, Gulcher JR, Petursson H, Stefonsson K. Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 2002;71:877-92.
-
(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
Gosh, S.6
Brynjolfsson, J.7
Gunnarsdottir, S.8
Ivarsson, O.9
Chou, T.T.10
Hjaltason, O.11
Birgisdottir, B.12
Jonsson, H.13
Gudnadottir, V.G.14
Gudmundsdottir, E.15
Bjornsson, A.16
Ingvarsson, B.17
Ingason, A.18
Sigfusson, S.19
Hardardottir, H.20
Harvey, R.P.21
Lai, D.22
Zhou, M.23
Brunner, D.24
Mutel, V.25
Gonzalo, A.26
Lemke, G.27
Sainz, J.28
Johannesson, G.29
Andresson, T.30
Gudbjartsson, D.31
Manolescu, A.32
Frigge, M.L.33
Gurney, M.E.34
Kong, A.35
Gulcher, J.R.36
Petursson, H.37
Stefonsson, K.38
more..
-
33
-
-
0037221589
-
Association of neuregulin 1 with schizophrenia confirmed in a Scottish population
-
Stefansson H, Sarginson J, Kong A, Yates P, Steinthorsdottir V, Gudfinnsson E, Gunnarsdottir S, Walker N, Petursson H, Crombie C, Ingason A, Gulcher JR, Stefansson K, St Clair D. Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. Am J Hum Genet 2003;72:83-7.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 83-87
-
-
Stefansson, H.1
Sarginson, J.2
Kong, A.3
Yates, P.4
Steinthorsdottir, V.5
Gudfinnsson, E.6
Gunnarsdottir, S.7
Walker, N.8
Petursson, H.9
Crombie, C.10
Ingason, A.11
Gulcher, J.R.12
Stefansson, K.13
St. Clair, D.14
-
34
-
-
9144220855
-
A systematic genomewide linkage study in 353 sib pairs with schizophrenia
-
Williams NM, Norton N, Williams H, Ekholm B, Hamshere ML, Lindblom Y, Chowdari KV, Cardno AG, Zammit S, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Jones G, Holmans P, Nimgaonkar V, Adolfson R, Osby U, Terenius L, Sedvall G, O'Donovan MC, Owen MJ. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. Am J Hum Genet 2003;73:1355-67.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1355-1367
-
-
Williams, N.M.1
Norton, N.2
Williams, H.3
Ekholm, B.4
Hamshere, M.L.5
Lindblom, Y.6
Chowdari, K.V.7
Cardno, A.G.8
Zammit, S.9
Jones, L.A.10
Murphy, K.C.11
Sanders, R.D.12
McCarthy, G.13
Gray, M.Y.14
Jones, G.15
Holmans, P.16
Nimgaonkar, V.17
Adolfson, R.18
Osby, U.19
Terenius, L.20
Sedvall, G.21
O'Donovan, M.C.22
Owen, M.J.23
more..
-
35
-
-
10744230431
-
Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus
-
Corvin AP, Morris DW, McGhee K, Schwaiger S, Scully P, Quinn J, Meagher D, Clair DS, Waddington JL, Gill M. Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus. Mol Psychiatry 2004;9:208-13.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 208-213
-
-
Corvin, A.P.1
Morris, D.W.2
McGhee, K.3
Schwaiger, S.4
Scully, P.5
Quinn, J.6
Meagher, D.7
Clair, D.S.8
Waddington, J.L.9
Gill, M.10
-
36
-
-
12444315127
-
Association study of neuregulin 1 gene with schizophrenia
-
Yang JZ, Si TM, Ruan Y, Ling YS, Han YH, Wang XL, Zhou M, Zhang HY, Kong QM, Liu C, Zhang DR, Yu YQ, Liu SZ, Ju GZ, Shu L, Ma DL, Zhang D. Association study of neuregulin 1 gene with schizophrenia. Mol Psychiatry 2003;8(7):706-9.
-
(2003)
Mol Psychiatry
, vol.8
, Issue.7
, pp. 706-709
-
-
Yang, J.Z.1
Si, T.M.2
Ruan, Y.3
Ling, Y.S.4
Han, Y.H.5
Wang, X.L.6
Zhou, M.7
Zhang, H.Y.8
Kong, Q.M.9
Liu, C.10
Zhang, D.R.11
Yu, Y.Q.12
Liu, S.Z.13
Ju, G.Z.14
Shu, L.15
Ma, D.L.16
Zhang, D.17
-
37
-
-
0842286652
-
Polymorphisms within 5′ end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population
-
Tang JX, Chen WY, He G, Zhou J, Gu NF, Feng GY, He L. Polymorphisms within 5′ end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population. Mol Psychiatry 2004;9:11-2.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 11-12
-
-
Tang, J.X.1
Chen, W.Y.2
He, G.3
Zhou, J.4
Gu, N.F.5
Feng, G.Y.6
He, L.7
-
38
-
-
9144257198
-
A case control and family based association study of the neuregulin 1 gene and schizophrenia
-
Zhao X, Shi Y, Tang J, Tang R, Yu L, Gu N, Feng G, Zhu S, Liu H, Xing Y, Zhao S, Sang H, Guan Y, St Clair D, He L. A case control and family based association study of the neuregulin 1 gene and schizophrenia. J Med Genet 2004;41:31-4.
-
(2004)
J Med Genet
, vol.41
, pp. 31-34
-
-
Zhao, X.1
Shi, Y.2
Tang, J.3
Tang, R.4
Yu, L.5
Gu, N.6
Feng, G.7
Zhu, S.8
Liu, H.9
Xing, Y.10
Zhao, S.11
Sang, H.12
Guan, Y.13
St. Clair, D.14
He, L.15
-
39
-
-
3042679816
-
Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but na association with the Icelandic/Scottish risk haplotype
-
Li T, Stefansson H, Gudfinnsson E, Cai G, Liu X, Murray RM, Steinthorsdottir V, Januel D, Gudnadottir VG, Petursson H, Ingason A, Gulcher JR, Stefansson K, Collier DA. Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but na association with the Icelandic/Scottish risk haplotype. Mol Psychiatr 2004;9:698-704.
-
(2004)
Mol Psychiatr
, vol.9
, pp. 698-704
-
-
Li, T.1
Stefansson, H.2
Gudfinnsson, E.3
Cai, G.4
Liu, X.5
Murray, R.M.6
Steinthorsdottir, V.7
Januel, D.8
Gudnadottir, V.G.9
Petursson, H.10
Ingason, A.11
Gulcher, J.R.12
Stefansson, K.13
Collier, D.A.14
-
40
-
-
3442888075
-
The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations
-
Hall D, Gogos JA, Karayiorgou M. The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations. Genes Brain Behav 2004;3:240-8.
-
(2004)
Genes Brain Behav
, vol.3
, pp. 240-248
-
-
Hall, D.1
Gogos, J.A.2
Karayiorgou, M.3
-
41
-
-
1542314863
-
No association with the neuregulin 1 haplotype to Japanese schizophrenia
-
Iwata N, Suzuki T, Ikeda M, Kitajima T, Yamanouchi Y, Inada T, Ozaki N. No association with the neuregulin 1 haplotype to Japanese schizophrenia. Mol Psychiatry 2004;9:126-7.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 126-127
-
-
Iwata, N.1
Suzuki, T.2
Ikeda, M.3
Kitajima, T.4
Yamanouchi, Y.5
Inada, T.6
Ozaki, N.7
-
42
-
-
4243147180
-
No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF)
-
Thiselton DL, Webb BT, Neale BM, Ribble RC, O'Neill FA, Walsh D, Riley BP, Kendler KS. No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF). Mol Psychiatry 2004;9:777-83.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 777-783
-
-
Thiselton, D.L.1
Webb, B.T.2
Neale, B.M.3
Ribble, R.C.4
O'Neill, F.A.5
Walsh, D.6
Riley, B.P.7
Kendler, K.S.8
-
43
-
-
3242759878
-
Case-control and family-based association studies between the neuregulin 1 (Arg38Gln) polymorphism and schizophrenia
-
Hong CJ, Huo SJ, Liao DL, Lee K, Wu JY, Tsai SJ. Case-control and family-based association studies between the neuregulin 1 (Arg38Gln) polymorphism and schizophrenia. Neurosci Lett 2004;366:158-61.
-
(2004)
Neurosci Lett
, vol.366
, pp. 158-161
-
-
Hong, C.J.1
Huo, S.J.2
Liao, D.L.3
Lee, K.4
Wu, J.Y.5
Tsai, S.J.6
-
44
-
-
1242314858
-
Neuregulin 1 and schizophrenia
-
Stefansson H, Steinthorsdottir V, Thorgeirsson TE, Gulcher JR, Stefonsson K. Neuregulin 1 and schizophrenia. Ann Med 2004;36:62-71.
-
(2004)
Ann Med
, vol.36
, pp. 62-71
-
-
Stefansson, H.1
Steinthorsdottir, V.2
Thorgeirsson, T.E.3
Gulcher, J.R.4
Stefonsson, K.5
-
45
-
-
1942469932
-
Expression analysis of neuregulin-1 in the dorsolateral prefrontal cortex in schizophrenia
-
Hashimoto R, Straub RE, Weickert CS, Hyde TM, Kleinman JE, Weinberger DR. Expression analysis of neuregulin-1 in the dorsolateral prefrontal cortex in schizophrenia. Mol Psychiatry 2004;9:299-307.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 299-307
-
-
Hashimoto, R.1
Straub, R.E.2
Weickert, C.S.3
Hyde, T.M.4
Kleinman, J.E.5
Weinberger, D.R.6
-
46
-
-
2542451853
-
Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia
-
Corfas G, Roy K, Buxbaum JD. Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia. Nat Neurosci 2004;7:575-80.
-
(2004)
Nat Neurosci
, vol.7
, pp. 575-580
-
-
Corfas, G.1
Roy, K.2
Buxbaum, J.D.3
-
47
-
-
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, Bougeueleret L, Barry C, Tanaka H, La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse S, Lissarrague S, Picard FP, Maurice K, Essioux L, Millasseau P, Grel P, Debailleul V, Simon AM, Caterina D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier S, Nasroune M, Peixoto H, Delaye A, Pinchot V, Bastucci M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni S, Aurich-Costa J, Cherif D, Gimalac A, van Duijn C, Gauvreau D, Ouelette G, Fortier I, Realson J, Sherbatich T, Riazanskaia N, Rogaev E, Raeymaekers P, Aerssens J, Konings F, Luyten W, Macciardi F, Sham PC, Straub RE, Weinberger DR, Cohen N, Cohen D. Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci U S A 2002;99:13675-80.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 13675-13680
-
-
Chumakov, I.1
Blumenfeld, M.2
Guerassimenko, O.3
Cavarec, L.4
Palicio, M.5
Abderrahim, H.6
Bougeueleret, L.7
Barry, C.8
Tanaka, H.9
La Rosa, P.10
Puech, A.11
Tahri, N.12
Cohen-Akenine, A.13
Delabrosse, S.14
Lissarrague, S.15
Picard, F.P.16
Maurice, K.17
Essioux, L.18
Millasseau, P.19
Grel, P.20
Debailleul, V.21
Simon, A.M.22
Caterina, D.23
Dufaure, I.24
Malekzadeh, K.25
Belova, M.26
Luan, J.J.27
Bouillot, M.28
Sambucy, J.L.29
Primas, G.30
Saumier, M.31
Boubkiri, N.32
Martin-Saumier, S.33
Nasroune, M.34
Peixoto, H.35
Delaye, A.36
Pinchot, V.37
Bastucci, M.38
Guillou, S.39
Chevillon, M.40
Sainz-Fuertes, R.41
Meguenni, S.42
Aurich-Costa, J.43
Cherif, D.44
Gimalac, A.45
Van Duijn, C.46
Gauvreau, D.47
Ouelette, G.48
Fortier, I.49
Realson, J.50
Sherbatich, T.51
Riazanskaia, N.52
Rogaev, E.53
Raeymaekers, P.54
Aerssens, J.55
Konings, F.56
Luyten, W.57
Macciardi, F.58
Sham, P.C.59
Straub, R.E.60
Weinberger, D.R.61
Cohen, N.62
Cohen, D.63
more..
-
48
-
-
10744232028
-
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
-
Schumacher J, Jamra RA, Freudenberg J, Becker T, Ohlraun S, Otte AC, Tullius M, Kovalenko S, Bogaert AV, Maier W, Rietschel M, Propping P, Nothen MM, Cichon S. Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder. Mol Psychiatry 2004;9:203-7.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 203-207
-
-
Schumacher, J.1
Jamra, R.A.2
Freudenberg, J.3
Becker, T.4
Ohlraun, S.5
Otte, A.C.6
Tullius, M.7
Kovalenko, S.8
Bogaert, A.V.9
Maier, W.10
Rietschel, M.11
Propping, P.12
Nothen, M.M.13
Cichon, S.14
-
49
-
-
2942521644
-
Association of G72/G30 with schizophrenia in the Chinese population
-
Wang X, He G, Gu N, Yang J, Tang J, Chen Q, Liu X, Shen Y, Qian X, Lin W, Duan Y, Feng G, He L. Association of G72/G30 with schizophrenia in the Chinese population. Biochem Biophys Res Commun 2004;319:1281-6.
-
(2004)
Biochem Biophys Res Commun
, vol.319
, pp. 1281-1286
-
-
Wang, X.1
He, G.2
Gu, N.3
Yang, J.4
Tang, J.5
Chen, Q.6
Liu, X.7
Shen, Y.8
Qian, X.9
Lin, W.10
Duan, Y.11
Feng, G.12
He, L.13
-
50
-
-
3242755008
-
Is the G72/G30 locus associated with schizophrenia? - Single nucleotide polymorphisms, haplotypes, and gene expression analysis
-
Korostishevsky M, Kaganovich M, Cholostoy A, Ashkenazi M, Ratner Y, Dahary D, Bernstein J, Bening-Abu-Shach U, Ben-Asher E, Lancet D, Ritsner M, Navon R. Is the G72/G30 locus associated with schizophrenia? - single nucleotide polymorphisms, haplotypes, and gene expression analysis. Biol Psychiatry 2004;56(3):169-76.
-
(2004)
Biol Psychiatry
, vol.56
, Issue.3
, pp. 169-176
-
-
Korostishevsky, M.1
Kaganovich, M.2
Cholostoy, A.3
Ashkenazi, M.4
Ratner, Y.5
Dahary, D.6
Bernstein, J.7
Bening-Abu-Shach, U.8
Ben-Asher, E.9
Lancet, D.10
Ritsner, M.11
Navon, R.12
-
51
-
-
2342541110
-
Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified
-
Addington AM, Gornick M, Sporn AL, Gogtay N, Greenstein D, Lenane M, Gochman P, Baker N, Balkissoon R, Vakkalanka RK, Weinberger DR, Straub RE, Rapoport JL. Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified. Biol Psychiatry 2004;55:976-80.
-
(2004)
Biol Psychiatry
, vol.55
, pp. 976-980
-
-
Addington, A.M.1
Gornick, M.2
Sporn, A.L.3
Gogtay, N.4
Greenstein, D.5
Lenane, M.6
Gochman, P.7
Baker, N.8
Balkissoon, R.9
Vakkalanka, R.K.10
Weinberger, D.R.11
Straub, R.E.12
Rapoport, J.L.13
-
52
-
-
71749085915
-
Association and linkage analyses of RGS4 polymorphisms in schizophrenia
-
Chowdari KV, Mimics K, Semwal P, Wood J, Lawrence E, Bhatia T, Deshpande SN, Thelma BK, Ferrell RE, Middleton FA, Devlin B, Levitt P, Lewis DA, Nimgaonkar VL. Association and linkage analyses of RGS4 polymorphisms in schizophrenia. Hum Mol Genet 2002;11:1373-80.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1373-1380
-
-
Chowdari, K.V.1
Mimics, K.2
Semwal, P.3
Wood, J.4
Lawrence, E.5
Bhatia, T.6
Deshpande, S.N.7
Thelma, B.K.8
Ferrell, R.E.9
Middleton, F.A.10
Devlin, B.11
Levitt, P.12
Lewis, D.A.13
Nimgaonkar, V.L.14
-
53
-
-
12144286093
-
Support for RGS4 as a susceptibility gene for schizophrenia
-
Williams NM, Preece A, Spurlock G, Norton N, Williams HJ, McCreadie RG, Buckland P, Sharkey V, Chowdari KV, Zammit S, Nimgaonkar V, Kirov G, Owen MJ, O'Donovan MC. Support for RGS4 as a susceptibility gene for schizophrenia. Biol Psychiatry 2004;55:192-5.
-
(2004)
Biol Psychiatry
, vol.55
, pp. 192-195
-
-
Williams, N.M.1
Preece, A.2
Spurlock, G.3
Norton, N.4
Williams, H.J.5
McCreadie, R.G.6
Buckland, P.7
Sharkey, V.8
Chowdari, K.V.9
Zammit, S.10
Nimgaonkar, V.11
Kirov, G.12
Owen, M.J.13
O'Donovan, M.C.14
-
54
-
-
3342875632
-
Regulator of G-protein signaling 4 (RGS4) gene is associated with schizophrenia in Irish high density families
-
Chen X, Dunham C, Kendler S, Wang X, O'Neill FA, Walsh D, Kendler KS. Regulator of G-protein signaling 4 (RGS4) gene is associated with schizophrenia in Irish high density families. Am J Med Genet 2004;129B:23-6.
-
(2004)
Am J Med Genet
, vol.129 B
, pp. 23-26
-
-
Chen, X.1
Dunham, C.2
Kendler, S.3
Wang, X.4
O'Neill, F.A.5
Walsh, D.6
Kendler, K.S.7
-
55
-
-
0942268965
-
Confirming RGS4 as a susceptibility gene for schizophrenia
-
Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP. Confirming RGS4 as a susceptibility gene for schizophrenia. Am J Med Genet 2004;125B:50-3.
-
(2004)
Am J Med Genet
, vol.125 B
, pp. 50-53
-
-
Morris, D.W.1
Rodgers, A.2
McGhee, K.A.3
Schwaiger, S.4
Scully, P.5
Quinn, J.6
Meagher, D.7
Waddington, J.L.8
Gill, M.9
Corvin, A.P.10
-
56
-
-
4444375953
-
Regulators of G-protein signaling 4: Modulation of 5-HT(1A)-mediated neurotransmitter release in vivo
-
Beyer CE, Ghavami A, Lin Q, Sung A, Rhodes KJ, Dawson LA, Schlechter LE, Young KH. Regulators of G-protein signaling 4: modulation of 5-HT(1A)-mediated neurotransmitter release in vivo. Brain Res 2004;1022:214-20.
-
(2004)
Brain Res
, vol.1022
, pp. 214-220
-
-
Beyer, C.E.1
Ghavami, A.2
Lin, Q.3
Sung, A.4
Rhodes, K.J.5
Dawson, L.A.6
Schlechter, L.E.7
Young, K.H.8
-
58
-
-
2342469971
-
Dopamine receptor-mediated regulation of RGS2 ana RGS4 mRNA differentially depends on ascending dopamine projections and time
-
Taymans JM, Kia HK, Claes R, Cruz C, Leysen J, Langlois X. Dopamine receptor-mediated regulation of RGS2 ana RGS4 mRNA differentially depends on ascending dopamine projections and time. Eur J Neurosci 2004;19:2249-60.
-
(2004)
Eur J Neurosci
, vol.19
, pp. 2249-2260
-
-
Taymans, J.M.1
Kia, H.K.2
Claes, R.3
Cruz, C.4
Leysen, J.5
Langlois, X.6
-
59
-
-
0037810425
-
Identification of novel ErbB3-interacting factors using the split-ubiquitin membrane yeast two-hybrid system
-
Thaminy S, Auerbach D, Arnoldo A, Stagljar I. Identification of novel ErbB3-interacting factors using the split-ubiquitin membrane yeast two-hybrid system. Genome Res 2003;13:1744-53.
-
(2003)
Genome Res
, vol.13
, pp. 1744-1753
-
-
Thaminy, S.1
Auerbach, D.2
Arnoldo, A.3
Stagljar, I.4
-
60
-
-
2342625339
-
Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22
-
Brzustowicz LM, Simone J, Mohseni P, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. Am J Hum Genet 2004;74(5):1057-63.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.5
, pp. 1057-1063
-
-
Brzustowicz, L.M.1
Simone, J.2
Mohseni, P.3
Hayter, J.E.4
Hodgkinson, K.A.5
Chow, E.W.6
Bassett, A.S.7
-
61
-
-
0042202624
-
Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit
-
Gerber DJ, Hall D, Miyakawa T, Demars S, Gogos JA, Karayiorgou M, Tonegawa S. Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit. Proc Natl Acad Sci U S A 2003;100:8993-8.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 8993-8998
-
-
Gerber, D.J.1
Hall, D.2
Miyakawa, T.3
Demars, S.4
Gogos, J.A.5
Karayiorgou, M.6
Tonegawa, S.7
-
62
-
-
4544225882
-
Polymorphisms in the Trace Amine Receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia
-
Duan J, Martinez M, Sanders AR, Hou C, Saitou N, Kitano T, Mowry BJ, Crowe RR, Silverman JM, Levinson DF, Gejman PV. Polymorphisms in the Trace Amine Receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia. Am J Hum Genet 2004;75:624-38.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 624-638
-
-
Duan, J.1
Martinez, M.2
Sanders, A.R.3
Hou, C.4
Saitou, N.5
Kitano, T.6
Mowry, B.J.7
Crowe, R.R.8
Silverman, J.M.9
Levinson, D.F.10
Gejman, P.V.11
-
63
-
-
0038513712
-
Chromosomal abnormalities and mental illness
-
MacIntyre DJ, Blackwood DH, Porteous DJ, Pickard BS, Muir WJ. Chromosomal abnormalities and mental illness. Mol Psychiatry 2003;8:275-87.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 275-287
-
-
MacIntyre, D.J.1
Blackwood, D.H.2
Porteous, D.J.3
Pickard, B.S.4
Muir, W.J.5
-
64
-
-
0027989917
-
Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives
-
Pulver AE, Nestadt G, Goldberg R, Shprintzen RJ, Lamacz M, Wolyniec PS, Morrow B, Karayiorgou M, Antonarakis SE, Housman D, Kucherlapoti RJ. Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. J Nerv Ment Dis 1994;182:476-8.
-
(1994)
J Nerv Ment Dis
, vol.182
, pp. 476-478
-
-
Pulver, A.E.1
Nestadt, G.2
Goldberg, R.3
Shprintzen, R.J.4
Lamacz, M.5
Wolyniec, P.S.6
Morrow, B.7
Karayiorgou, M.8
Antonarakis, S.E.9
Housman, D.10
Kucherlapoti, R.J.11
-
65
-
-
0032503887
-
22q11 deletion syndrome in adults with schizophrenia
-
Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. 22q11 deletion syndrome in adults with schizophrenia. Am J Med Genet 1998;81:328-37.
-
(1998)
Am J Med Genet
, vol.81
, pp. 328-337
-
-
Bassett, A.S.1
Hodgkinson, K.2
Chow, E.W.3
Correia, S.4
Scutt, L.E.5
Weksberg, R.6
-
66
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy KC, Jones LA, Owen MJ. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch Gen Psychiatry 1999;56:940-5.
-
(1999)
Arch Gen Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
67
-
-
10744220251
-
Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis: Molecular genetic study
-
Ivanov D, Kirov G, Norton N, Williams HJ, Williams NM, Nikolov I, Tzwetkova R, Stambolova SM, Murphy KC, Toncheva D, Thapor A, O'Donovan MC, Owen MJ. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis: molecular genetic study. Br J Psychiatry 2003;183:409-13.
-
(2003)
Br J Psychiatry
, vol.183
, pp. 409-413
-
-
Ivanov, D.1
Kirov, G.2
Norton, N.3
Williams, H.J.4
Williams, N.M.5
Nikolov, I.6
Tzwetkova, R.7
Stambolova, S.M.8
Murphy, K.C.9
Toncheva, D.10
Thapor, A.11
O'Donovan, M.C.12
Owen, M.J.13
-
68
-
-
6044246071
-
Variants in the catechol-O-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families
-
Chen X, Wang X, O'Neill AF, Walsh D, Kendler KS. Variants in the catechol-O-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families. Mol Psychiatry 2004;9:962-7.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 962-967
-
-
Chen, X.1
Wang, X.2
O'Neill, A.F.3
Walsh, D.4
Kendler, K.S.5
-
69
-
-
0035810850
-
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
-
Egan MF, Goldberg TE, Kolachana BS, Callicott JH, Mazzanti CM, Straub RE, Goldman D, Weinberger DR. Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proc Natl Acad Sci USA 2001;98:6917-22.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 6917-6922
-
-
Egan, M.F.1
Goldberg, T.E.2
Kolachana, B.S.3
Callicott, J.H.4
Mazzanti, C.M.5
Straub, R.E.6
Goldman, D.7
Weinberger, D.R.8
-
70
-
-
0036214991
-
A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition
-
Malhotra AK, Kestler LJ, Mazzanti C, Bates JA, Goldberg T, Goldman D. A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition. Am J Psychiatry 2002;159:652-4.
-
(2002)
Am J Psychiatry
, vol.159
, pp. 652-654
-
-
Malhotra, A.K.1
Kestler, L.J.2
Mazzanti, C.3
Bates, J.A.4
Goldberg, T.5
Goldman, D.6
-
71
-
-
0037365978
-
Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: Meta-analysis of case-control and family-based studies
-
Glatt SJ, Faraone SV, Tsuang MT. Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies. Am J Psychiatry 2003;160:469-76.
-
(2003)
Am J Psychiatry
, vol.160
, pp. 469-476
-
-
Glatt, S.J.1
Faraone, S.V.2
Tsuang, M.T.3
-
72
-
-
0033939936
-
Family-based linkage disequilibrium mapping using SNP marker haplotypes: Application to a potential locus for schizophrenia at chromosome 22q11
-
Li T, Ball D, Zhao J, Murray RM, Liu X, Sham PC, Collier DA. Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11. Mol Psychiatry 2000;5:452.
-
(2000)
Mol Psychiatry
, vol.5
, pp. 452
-
-
Li, T.1
Ball, D.2
Zhao, J.3
Murray, R.M.4
Liu, X.5
Sham, P.C.6
Collier, D.A.7
-
73
-
-
0036913209
-
A highly significant association between a COMT haplotype and schizophrenia
-
Shifman S, Bronstein M, Sternfeld M, Pisanté-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Beckmann JS, Yakir B, Risch N, Zak NB, Darvasi A. A highly significant association between a COMT haplotype and schizophrenia. Am J Hum Genet 2002;71:1296-302.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1296-1302
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
Pisanté-Shalom, A.4
Lev-Lehman, E.5
Weizman, A.6
Reznik, I.7
Spivak, B.8
Grisaru, N.9
Karp, L.10
Schiffer, R.11
Kotler, M.12
Strous, R.D.13
Swartz-Vanetik, M.14
Knobler, H.Y.15
Shinar, E.16
Beckmann, J.S.17
Yakir, B.18
Risch, N.19
Zak, N.B.20
Darvasi, A.21
more..
-
74
-
-
15044349389
-
Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia
-
Aug 31 [Epub ahead of print]
-
Sanders AR, Rusu I, Duan J, Molen JE, Hou C, Schwab SG, Wildenouer DB, Martinez M, Gejman PV. Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia. Mol Psychiatry 2004, Aug 31 [Epub ahead of print].
-
(2004)
Mol Psychiatry
-
-
Sanders, A.R.1
Rusu, I.2
Duan, J.3
Molen, J.E.4
Hou, C.5
Schwab, S.G.6
Wildenouer, D.B.7
Martinez, M.8
Gejman, P.V.9
-
75
-
-
20144368067
-
Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia
-
Oct 26 [Epub ahead of print]
-
Handoko HY, Nyholt DR, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ. Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. Mol Psychiatry 2004, Oct 26 [Epub ahead of print].
-
(2004)
Mol Psychiatry
-
-
Handoko, H.Y.1
Nyholt, D.R.2
Hayward, N.K.3
Nertney, D.A.4
Hannah, D.E.5
Windus, L.C.6
McCormack, C.M.7
Smith, H.J.8
Filippich, C.9
James, M.R.10
Mowry, B.J.11
-
76
-
-
0030004521
-
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders
-
Lachman HM, Papolos DF, Saito T, Yu YM, Szumlanski CL, Weinshilboum RM. Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics 1996;6(3):243-50.
-
(1996)
Pharmacogenetics
, vol.6
, Issue.3
, pp. 243-250
-
-
Lachman, H.M.1
Papolos, D.F.2
Saito, T.3
Yu, Y.M.4
Szumlanski, C.L.5
Weinshilboum, R.M.6
-
77
-
-
0032948179
-
The gene encoding proline dehydrogenase modulates sensorimotor gating in mice
-
Gogos JA, Santha M, Takacs Z, Beck KD, Luine V, Lucas LR, Nadler JV, Karayiorgou M. The gene encoding proline dehydrogenase modulates sensorimotor gating in mice. Nat Genet 1999;21:434-9.
-
(1999)
Nat Genet
, vol.21
, pp. 434-439
-
-
Gogos, J.A.1
Santha, M.2
Takacs, Z.3
Beck, K.D.4
Luine, V.5
Lucas, L.R.6
Nadler, J.V.7
Karayiorgou, M.8
-
78
-
-
18544366528
-
PRODH mutations and hyperprolinemia in a subset of schizophrenic patients
-
Jacquet H, Raux G, Thibaut F, Hecketsweiler B, Houy E, Demilly C, Haouzir S, Allio G, Fouldrin G, Drouin V, Bou J, Petit M, Campion D, Frebourg T. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Hum Mol Genet 2002;11:2243-9.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2243-2249
-
-
Jacquet, H.1
Raux, G.2
Thibaut, F.3
Hecketsweiler, B.4
Houy, E.5
Demilly, C.6
Haouzir, S.7
Allio, G.8
Fouldrin, G.9
Drouin, V.10
Bou, J.11
Petit, M.12
Campion, D.13
Frebourg, T.14
-
79
-
-
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, Lenane M, Robertson B, Wijsman EM, Rapoport JL, Gogos JA, Karayiorgou M. Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci USA 2002;99:3717-22.
-
(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
Lenane, M.7
Robertson, B.8
Wijsman, E.M.9
Rapoport, J.L.10
Gogos, J.A.11
Karayiorgou, M.12
-
80
-
-
3343019031
-
Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population
-
Li T, Ma X, Sham PC, Sun X, Hu X, Wang Q, Meng H, Deng W, Liu X, Murray RM, Collier DA. Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population. Am J Med Genet 2004;129B:13-5.
-
(2004)
Am J Med Genet
, vol.129 B
, pp. 13-15
-
-
Li, T.1
Ma, X.2
Sham, P.C.3
Sun, X.4
Hu, X.5
Wang, Q.6
Meng, H.7
Deng, W.8
Liu, X.9
Murray, R.M.10
Collier, D.A.11
-
81
-
-
12444266887
-
Association between PRODH and schizophrenia is not confirmed
-
Williams HJ, Williams N, Spurlock G, Norton N, Ivanov D, McCreadie RG, Preece A, Sharkey V, Jones S, Zammit S, Nikolov I, Kehaiov I, Thapar A, Murphy KC, Kirov G, Owen MJ, O'Donovan MC. Association between PRODH and schizophrenia is not confirmed. Mol Psychiatry 2003;8:644-5.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 644-645
-
-
Williams, H.J.1
Williams, N.2
Spurlock, G.3
Norton, N.4
Ivanov, D.5
McCreadie, R.G.6
Preece, A.7
Sharkey, V.8
Jones, S.9
Zammit, S.10
Nikolov, I.11
Kehaiov, I.12
Thapar, A.13
Murphy, K.C.14
Kirov, G.15
Owen, M.J.16
O'Donovan, M.C.17
-
82
-
-
9144237473
-
Failure to find association between PRODH deletion and schizophrenia
-
Ohtsuki T, Tanaka S, Ishiguro H, Noguchi E, Arinami T, Tanabe E, Yara K, Okubo T, Takahashi S, Matsuura M, Sakai T, Muto M, Kojima T, Matsushima E, Toru M, Inada T. Failure to find association between PRODH deletion and schizophrenia. Schizophr Res 2004;67:111-3.
-
(2004)
Schizophr Res
, vol.67
, pp. 111-113
-
-
Ohtsuki, T.1
Tanaka, S.2
Ishiguro, H.3
Noguchi, E.4
Arinami, T.5
Tanabe, E.6
Yara, K.7
Okubo, T.8
Takahashi, S.9
Matsuura, M.10
Sakai, T.11
Muto, M.12
Kojima, T.13
Matsushima, E.14
Toru, M.15
Inada, T.16
-
83
-
-
13844302130
-
Hyperprolinemia is a risk factor for schizoaffective disorder
-
Oct 19 [Epub ahead of print]
-
Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Menard JF, Dollfus S, D'Amato T, Petit M, Thibaut F, Frebourg T, Campion D. Hyperprolinemia is a risk factor for schizoaffective disorder. Mol Psychiatry 2004, Oct 19 [Epub ahead of print].
-
(2004)
Mol Psychiatry
-
-
Jacquet, H.1
Demily, C.2
Houy, E.3
Hecketsweiler, B.4
Bou, J.5
Raux, G.6
Lerond, J.7
Allio, G.8
Haouzir, S.9
Tillaux, A.10
Bellegou, C.11
Fouldrin, G.12
Delamillieure, P.13
Menard, J.F.14
Dollfus, S.15
D'Amato, T.16
Petit, M.17
Thibaut, F.18
Frebourg, T.19
Campion, D.20
more..
-
84
-
-
3042804077
-
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia
-
Mukai J, Liu H, Burt RA, Swor DE, Lai WS, Karayiorgou M, Gogos JA. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. Nat Genet 2004;36:725-31.
-
(2004)
Nat Genet
, vol.36
, pp. 725-731
-
-
Mukai, J.1
Liu, H.2
Burt, R.A.3
Swor, D.E.4
Lai, W.S.5
Karayiorgou, M.6
Gogos, J.A.7
-
85
-
-
9744268907
-
Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8
-
Chen WY, Shi YY, Zheng YL, Zhao XZ, Zhang GJ, Chen SQ, Yang PD, He L. Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Hum Mol Genet 2004;13(23):2991-5.
-
(2004)
Hum Mol Genet
, vol.13
, Issue.23
, pp. 2991-2995
-
-
Chen, W.Y.1
Shi, Y.Y.2
Zheng, Y.L.3
Zhao, X.Z.4
Zhang, G.J.5
Chen, S.Q.6
Yang, P.D.7
He, L.8
-
86
-
-
0034927864
-
Schizophrenia and affective disorders - Cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: Clinical and P300 findings in a family
-
Blackwood DH, Fordyce A, Walker MT, St Clair DM, Porteous DJ, Muir WJ. Schizophrenia and affective disorders - cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family. Am J Hum Genet 2001;69:428-33.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 428-433
-
-
Blackwood, D.H.1
Fordyce, A.2
Walker, M.T.3
St. Clair, D.M.4
Porteous, D.J.5
Muir, W.J.6
-
87
-
-
0034702026
-
Disruption of two novel genes by a translocation co-segregating with schizophrenia
-
Millar JK, Wilson-Annan JC, Anderson S, Christie S, Taylor MS, Semple CA, Devon RS, Clair DM, Muir WJ, Blackwood DH, Porteous DJ. Disruption of two novel genes by a translocation co-segregating with schizophrenia. Hum Mol Genet 2000;9:1415-23.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1415-1423
-
-
Millar, J.K.1
Wilson-Annan, J.C.2
Anderson, S.3
Christie, S.4
Taylor, M.S.5
Semple, C.A.6
Devon, R.S.7
Clair, D.M.8
Muir, W.J.9
Blackwood, D.H.10
Porteous, D.J.11
-
88
-
-
0035878561
-
Chromosome 1 loci in Finnish schizophrenia families
-
Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R, Suhonen J, Ellonen P, Chan G, Sinsheimer JS, Sobel E, Juvonen H, Arajarvi R, Partonen T, Suvisaari J, Lonnqvist J, Meyer J, Peltonen L. Chromosome 1 loci in Finnish schizophrenia families. Hum Mol Genet 2001;10:1611-7.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1611-1617
-
-
Ekelund, J.1
Hovatta, I.2
Parker, A.3
Paunio, T.4
Varilo, T.5
Martin, R.6
Suhonen, J.7
Ellonen, P.8
Chan, G.9
Sinsheimer, J.S.10
Sobel, E.11
Juvonen, H.12
Arajarvi, R.13
Partonen, T.14
Suvisaari, J.15
Lonnqvist, J.16
Meyer, J.17
Peltonen, L.18
-
89
-
-
8744231685
-
Replication of 1q42 linkage in Finnish schizophrenia pedigrees
-
Ekelund J, Hennah W, Hiekkalinna T, Parker A, Mever J, Lonnqvist J, Peltonen L. Replication of 1q42 linkage in Finnish schizophrenia pedigrees. Mol Psychiatry 2004;9(11):1037-41.
-
(2004)
Mol Psychiatry
, vol.9
, Issue.11
, pp. 1037-1041
-
-
Ekelund, J.1
Hennah, W.2
Hiekkalinna, T.3
Parker, A.4
Mever, J.5
Lonnqvist, J.6
Peltonen, L.7
-
90
-
-
0042622356
-
Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth
-
Miyoshi K, Honda A, Baba K, Taniguchi M, Oono K, Fujita T, Kuroda S, Katayama T, Tohyama M. Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth. Mol Psychiatry 2003;8:685-94.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 685-694
-
-
Miyoshi, K.1
Honda, A.2
Baba, K.3
Taniguchi, M.4
Oono, K.5
Fujita, T.6
Kuroda, S.7
Katayama, T.8
Tohyama, M.9
-
91
-
-
0037422609
-
Disrupted-in-schizophrenia-1 (DISC-1): Mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth
-
Ozeki Y, Tomoda T, Kleiderlein J, Kamiya A, Bard L, Fujii K, Okawa M, Yamada N, Hatten ME, Snyder SH, Ross CA, Sawa A. Disrupted-in-schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth. Proc Natl Acad Sci U S A 2003;100:289-94.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 289-294
-
-
Ozeki, Y.1
Tomoda, T.2
Kleiderlein, J.3
Kamiya, A.4
Bard, L.5
Fujii, K.6
Okawa, M.7
Yamada, N.8
Hatten, M.E.9
Snyder, S.H.10
Ross, C.A.11
Sawa, A.12
-
92
-
-
0034941967
-
Identification of polymorphisms within disrupted in Schizophrenia 1 and disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar disorder
-
Devon RS, Anderson S, Teague PW, Burgess P, Kipori TM, Semple CA, Millar JK, Muir WJ, Murray V, Pelosi AJ, Blackwood DH, Porteous DJ. Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar disorder. Psychiatr Genet 2002;11:71-8.
-
(2002)
Psychiatr Genet
, vol.11
, pp. 71-78
-
-
Devon, R.S.1
Anderson, S.2
Teague, P.W.3
Burgess, P.4
Kipori, T.M.5
Semple, C.A.6
Millar, J.K.7
Muir, W.J.8
Murray, V.9
Pelosi, A.J.10
Blackwood, D.H.11
Porteous, D.J.12
-
93
-
-
4444315059
-
Association study of polymorphisms in the 5′ upstream region of human DISC1 gene with schizophrenia
-
Kockelkorn TT, Arai M, Matsumoto H, Fukuda N, Yamada K, Minabe Y, Toyota T, Ujike H, Sora I, Mori N, Yoshikawa T, Itokawa M. Association study of polymorphisms in the 5′ upstream region of human DISC1 gene with schizophrenia. Neurosci Lett 2004;368(1):41-5.
-
(2004)
Neurosci Lett
, vol.368
, Issue.1
, pp. 41-45
-
-
Kockelkorn, T.T.1
Arai, M.2
Matsumoto, H.3
Fukuda, N.4
Yamada, K.5
Minabe, Y.6
Toyota, T.7
Ujike, H.8
Sora, I.9
Mori, N.10
Yoshikawa, T.11
Itokawa, M.12
-
94
-
-
0345530985
-
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects
-
Hennah W, Varilo T, Kestila M, Paunio T, Arajarvi R, Haukka J, Parker A, Martin R, Levitzky S, Partonen T, Meyer J, Lonnqvist J, Peltonen L, Ekelund J. Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects. Hum Mol Genet 2003;12:3151-9.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3151-3159
-
-
Hennah, W.1
Varilo, T.2
Kestila, M.3
Paunio, T.4
Arajarvi, R.5
Haukka, J.6
Parker, A.7
Martin, R.8
Levitzky, S.9
Partonen, T.10
Meyer, J.11
Lonnqvist, J.12
Peltonen, L.13
Ekelund, J.14
-
95
-
-
6344255274
-
Disrupted in schizophrenia 1 (DISC1): Association with schizophrenia, schizoaffective disorder, and bipolar disorder
-
Hodgkinson CA, Goldman D, Jaeger J, Persaud S, Kane JM, Lipsky RH, Malhotra AK. Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder. Am J Hum Genet 2004;75(5):862-72.
-
(2004)
Am J Hum Genet
, vol.75
, Issue.5
, pp. 862-872
-
-
Hodgkinson, C.A.1
Goldman, D.2
Jaeger, J.3
Persaud, S.4
Kane, J.M.5
Lipsky, R.H.6
Malhotra, A.K.7
-
96
-
-
0032803524
-
Genetics of bipolar disorder
-
Craddock N, Jones I. Genetics of bipolar disorder. J Med Genet 1999;36:585-94.
-
(1999)
J Med Genet
, vol.36
, pp. 585-594
-
-
Craddock, N.1
Jones, I.2
-
97
-
-
0012114353
-
Genetics of affective disorders
-
McGuffin P, Owen M, Gottesman II, eds. Oxford: Oxford University Press
-
Jones I, Kent L, Craddock N. Genetics of affective disorders, In: McGuffin P, Owen M, Gottesman II, eds. Psychiatric genetics and genomics. Oxford: Oxford University Press, 2002:211-245.
-
(2002)
Psychiatric Genetics and Genomics
, pp. 211-245
-
-
Jones, I.1
Kent, L.2
Craddock, N.3
-
98
-
-
0024428729
-
The genetics of depression and manic-depressive disorder
-
McGuffin P, Katz R. The genetics of depression and manic-depressive disorder. Br J Psychiatry 1989;155:294-304.
-
(1989)
Br J Psychiatry
, vol.155
, pp. 294-304
-
-
McGuffin, P.1
Katz, R.2
-
99
-
-
0037629099
-
The heritability of bipolar affective disorder and the genetic relationship to unipolar depression
-
McGuffin P, Rijsdijk F, Andrew M, Sham P, Katz R, Cardno A. The heritability of bipolar affective disorder and the genetic relationship to unipolar depression. Arch Gen Psychiatry 2003;60(5):497-502.
-
(2003)
Arch Gen Psychiatry
, vol.60
, Issue.5
, pp. 497-502
-
-
McGuffin, P.1
Rijsdijk, F.2
Andrew, M.3
Sham, P.4
Katz, R.5
Cardno, A.6
-
100
-
-
4744342062
-
High concordance of bipolar I disorder in a nationwide sample of twins
-
Kieseppa T, Partonen T, Haukka J, Kaprio J, Lonnqvist J. High concordance of bipolar I disorder in a nationwide sample of twins. Am J Psychiatry 2004;161(10):1814-21.
-
(2004)
Am J Psychiatry
, vol.161
, Issue.10
, pp. 1814-1821
-
-
Kieseppa, T.1
Partonen, T.2
Haukka, J.3
Kaprio, J.4
Lonnqvist, J.5
-
101
-
-
0029168042
-
Mathematical limits of multilocus models: The genetic transmission of bipolar disorder
-
Craddock N, Khodel V, Van Eerdewegh P, Reich T. Mathematical limits of multilocus models: the genetic transmission of bipolar disorder. Am J Hum Genet 1995;57:690-702.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 690-702
-
-
Craddock, N.1
Khodel, V.2
Van Eerdewegh, P.3
Reich, T.4
-
102
-
-
0038341184
-
Genome scan meta-analysis of schizophrenia and bipolar disorder, part iii: Bipolar disorder
-
Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI Jr, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lonnqvist J, Nothen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Borden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N. Genome scan meta-analysis of schizophrenia and bipolar disorder, part iii: bipolar disorder. Am J Hum Genet 2003;73(1):49-62.
-
(2003)
Am J Hum Genet
, vol.73
, Issue.1
, pp. 49-62
-
-
Segurado, R.1
Detera-Wadleigh, S.D.2
Levinson, D.F.3
Lewis, C.M.4
Gill, M.5
Nurnberger Jr., J.I.6
Craddock, N.7
DePaulo, J.R.8
Baron, M.9
Gershon, E.S.10
Ekholm, J.11
Cichon, S.12
Turecki, G.13
Claes, S.14
Kelsoe, J.R.15
Schofield, P.R.16
Badenhop, R.F.17
Morissette, J.18
Coon, H.19
Blackwood, D.20
McInnes, L.A.21
Foroud, T.22
Edenberg, H.J.23
Reich, T.24
Rice, J.P.25
Goate, A.26
McInnis, M.G.27
McMahon, F.J.28
Badner, J.A.29
Goldin, L.R.30
Bennett, P.31
Willour, V.L.32
Zandi, P.P.33
Liu, J.34
Gilliam, C.35
Juo, S.H.36
Berrettini, W.H.37
Yoshikawa, T.38
Peltonen, L.39
Lonnqvist, J.40
Nothen, M.M.41
Schumacher, J.42
Windemuth, C.43
Rietschel, M.44
Propping, P.45
Maier, W.46
Alda, M.47
Grof, P.48
Rouleau, G.A.49
Del-Favero, J.50
Van Broeckhoven, C.51
Mendlewicz, J.52
Adolfsson, R.53
Spence, M.A.54
Luebbert, H.55
Adams, L.J.56
Donald, J.A.57
Mitchell, P.B.58
Borden, N.59
Shink, E.60
Byerley, W.61
Muir, W.62
Visscher, P.M.63
Macgregor, S.64
Gurling, H.65
Kalsi, G.66
McQuillin, A.67
Escamilla, M.A.68
Reus, V.I.69
Leon, P.70
Freimer, N.B.71
Ewald, H.72
Kruse, T.A.73
Mors, O.74
Radhakrishna, U.75
Blouin, J.L.76
Antonarakis, S.E.77
Akarsu, N.78
more..
-
103
-
-
0036373344
-
A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3
-
Ewald H, Flint T, Kruse TA, Mors O. A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3. Mol Psychiatry 2002;7(7):734-44.
-
(2002)
Mol Psychiatry
, vol.7
, Issue.7
, pp. 734-744
-
-
Ewald, H.1
Flint, T.2
Kruse, T.A.3
Mors, O.4
-
104
-
-
12344262032
-
A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12
-
Oct 19 [Epub ahead of print]
-
Shink E, Morissette J, Sherrington R, Barden N. A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12. Mol Psychiatry 2004, Oct 19 [Epub ahead of print].
-
(2004)
Mol Psychiatry
-
-
Shink, E.1
Morissette, J.2
Sherrington, R.3
Barden, N.4
-
105
-
-
0028205803
-
Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis)
-
Craddock N, Owen M, Burge S, Kurian B, Thomas P, McGuffin P. Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis). Br J Psychiatry 1994;164:355-8.
-
(1994)
Br J Psychiatry
, vol.164
, pp. 355-358
-
-
Craddock, N.1
Owen, M.2
Burge, S.3
Kurian, B.4
Thomas, P.5
McGuffin, P.6
-
106
-
-
85047697286
-
Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease
-
Jones I, Jacobsen N, Green EK, Elvidge GP, Owen MJ, Craddock N. Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease. Mol Psychiatry 2002;7:424-7.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 424-427
-
-
Jones, I.1
Jacobsen, N.2
Green, E.K.3
Elvidge, G.P.4
Owen, M.J.5
Craddock, N.6
-
107
-
-
11844305917
-
Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-24 region in two pedigrees with bipolar disorder and Darier's disease
-
Green E, Elvidge G, Jacobsen N, Glaser B, Jones I, O'Donovan MC, Kirov G, Owen MJ, Craddock N. Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-24 region in two pedigrees with bipolar disorder and Darier's disease. Am J Psychiatry 2005;162(1):35-42.
-
(2005)
Am J Psychiatry
, vol.162
, Issue.1
, pp. 35-42
-
-
Green, E.1
Elvidge, G.2
Jacobsen, N.3
Glaser, B.4
Jones, I.5
O'Donovan, M.C.6
Kirov, G.7
Owen, M.J.8
Craddock, N.9
-
109
-
-
12944257360
-
Association between bipolar disorder and monoamine oxidase A gene polymorphisms: Results of a multicenter study
-
Preisig M, Bellivier F, Fenton BT, Baud P, Berney A, Courtet P, Hardy P, Golaz J, Leboyer M, Mallet J, Matthey ML, Mouthon D Neidhart E, Nosten-Bertrand M, Stadelmann-Dubuis E, Guimon J, Ferrero F, Buresi C, Malafosse A. Association between bipolar disorder and monoamine oxidase A gene polymorphisms: results of a multicenter study. Am J Psychiatry 2000;157:948-55.
-
(2000)
Am J Psychiatry
, vol.157
, pp. 948-955
-
-
Preisig, M.1
Bellivier, F.2
Fenton, B.T.3
Baud, P.4
Berney, A.5
Courtet, P.6
Hardy, P.7
Golaz, J.8
Leboyer, M.9
Mallet, J.10
Matthey, M.L.11
Mouthon, D.12
Neidhart, E.13
Nosten-Bertrand, M.14
Stadelmann-Dubuis, E.15
Guimon, J.16
Ferrero, F.17
Buresi, C.18
Malafosse, A.19
-
110
-
-
0034982256
-
Candidate gene studies of bipolar disorder
-
Jones I, Craddock N. Candidate gene studies of bipolar disorder. Ann Med 2001;33:248-56.
-
(2001)
Ann Med
, vol.33
, pp. 248-256
-
-
Jones, I.1
Craddock, N.2
-
111
-
-
0041346384
-
A systematic review for association studies investigating genes coding for serotonin receptors and the serotonin transporter: I. Affective disorders
-
Anguelova M, Benkelfat C, Turecki G. A systematic review for association studies investigating genes coding for serotonin receptors and the serotonin transporter: I. Affective disorders. Mol Psychiatry 2003;8:574-91.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 574-591
-
-
Anguelova, M.1
Benkelfat, C.2
Turecki, G.3
-
112
-
-
15044348745
-
Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders
-
Dec 2 [Epub ahead of print]
-
Lasky-Su JA, Faraone SV, Glatt SJ, Tsuang MT. Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders. Am J Med Genet 2004, Dec 2 [Epub ahead of print].
-
(2004)
Am J Med Genet
-
-
Lasky-Su, J.A.1
Faraone, S.V.2
Glatt, S.J.3
Tsuang, M.T.4
-
113
-
-
3042806953
-
COMT: A common susceptibility gene in bipolar disorder and schizophrenia
-
Shifman S, Bronstein M, Sternfeld M, Pisante A, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Yakir B, Zak NB, Darvasi A. COMT: a common susceptibility gene in bipolar disorder and schizophrenia. Am J Med Genet 2004;128B(1):61-4.
-
(2004)
Am J Med Genet
, vol.128 B
, Issue.1
, pp. 61-64
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
Pisante, A.4
Weizman, A.5
Reznik, I.6
Spivak, B.7
Grisaru, N.8
Karp, L.9
Schiffer, R.10
Kotler, M.11
Strous, R.D.12
Swartz-Vanetik, M.13
Knobler, H.Y.14
Shinar, E.15
Yakir, B.16
Zak, N.B.17
Darvasi, A.18
-
114
-
-
0037730178
-
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series
-
Hattori E, Liu C, Badner JA, Bonner TI, Christian SL, Maheshwari M, Detera-Wadleigh SD, Gibbs RA, Gershon ES. Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. Am J Hum Genet 2003;72:1131-40.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1131-1140
-
-
Hattori, E.1
Liu, C.2
Badner, J.A.3
Bonner, T.I.4
Christian, S.L.5
Maheshwari, M.6
Detera-Wadleigh, S.D.7
Gibbs, R.A.8
Gershon, E.S.9
-
115
-
-
0842308210
-
Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33
-
Chen YS, Akula N, Detera-Wadleigh SD, Schulze TG, Thomas J, Potash JB, DePaulo JR, McInnis MG, Cox NJ, McMahon FJ. Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33. Mol Psychiatry 2004;9:87-92.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 87-92
-
-
Chen, Y.S.1
Akula, N.2
Detera-Wadleigh, S.D.3
Schulze, T.G.4
Thomas, J.5
Potash, J.B.6
DePaulo, J.R.7
McInnis, M.G.8
Cox, N.J.9
McMahon, F.J.10
-
116
-
-
20144385695
-
Evidence for linkage disequilibrium at both G72/G30 and D-amino acid oxidase with genetic risk for bipolar disorder
-
Green EK, Dimitrova A, Grozeva D, McGregor S, Nikolov I, Dwyer S, Preece A, Norton N, Williams H, Williams NM, Jones L, Jones I, O'Donovan MC, Owen MJ, Kirov G, Craddock N. Evidence for linkage disequilibrium at both G72/G30 and D-amino acid oxidase with genetic risk for bipolar disorder (abstract). Am J Med Genet 2004;130B(1):26.
-
(2004)
Am J Med Genet
, vol.130 B
, Issue.1
, pp. 26
-
-
Green, E.K.1
Dimitrova, A.2
Grozeva, D.3
McGregor, S.4
Nikolov, I.5
Dwyer, S.6
Preece, A.7
Norton, N.8
Williams, H.9
Williams, N.M.10
Jones, L.11
Jones, I.12
O'Donovan, M.C.13
Owen, M.J.14
Kirov, G.15
Craddock, N.16
-
117
-
-
2942633780
-
Brain-derived neurotrophic factor as a potential risk locus for bipolar disorder: Evidence, limitations, and implications
-
Green E, Craddock N. Brain-derived neurotrophic factor as a potential risk locus for bipolar disorder: evidence, limitations, and implications. Curr Psychiatry Rep 2003;5(6):469-76.
-
(2003)
Curr Psychiatry Rep
, vol.5
, Issue.6
, pp. 469-476
-
-
Green, E.1
Craddock, N.2
-
118
-
-
0001903586
-
The neurochemistry of mood disorders: Preclinical studies
-
Charney DS, Nestler EJ, Bunney BS, eds. New York: Oxford University Press
-
Duman RS. The neurochemistry of mood disorders: preclinical studies. In: Charney DS, Nestler EJ, Bunney BS, eds. The neurobiology of mental illness. New York: Oxford University Press, 1999:333-47.
-
(1999)
The Neurobiology of Mental Illness
, pp. 333-347
-
-
Duman, R.S.1
-
119
-
-
0030050741
-
Cellular processing of the neurotrophin precursors of NT3 and BDNF by the mammalian proprotein convertases
-
Seidah NG, Benjannet S, Pareek S, Chretien M, Murphy RA. Cellular processing of the neurotrophin precursors of NT3 and BDNF by the mammalian proprotein convertases. FEBS Lett 1996;379:247-50.
-
(1996)
FEBS Lett
, vol.379
, pp. 247-250
-
-
Seidah, N.G.1
Benjannet, S.2
Pareek, S.3
Chretien, M.4
Murphy, R.A.5
-
120
-
-
0037462449
-
The BDNF Val66Met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function
-
Egan MF, Kojima M, Callicott JH, Goldberg TE, Kolachana BS, Zaistev E, Bertolino A, Gol B, Goldman D, Dean M, Lu B, Weinberger DR. The BDNF Val66Met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function. Cell 2003;112:257-69.
-
(2003)
Cell
, vol.112
, pp. 257-269
-
-
Egan, M.F.1
Kojima, M.2
Callicott, J.H.3
Goldberg, T.E.4
Kolachana, B.S.5
Zaistev, E.6
Bertolino, A.7
Gol, B.8
Goldman, D.9
Dean, M.10
Lu, B.11
Weinberger, D.R.12
-
121
-
-
0036347948
-
Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neurotrophic factor
-
Sklar P, Gabriel SB, McInnis MG, Bennett P, Lim YM, Tsan G, Schaffner S, Kirov G, Jones I, Owen M, Craddock N, DePaulo JR, Lander ES. Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neurotrophic factor. Mol Psychiatry 2002;7:579-93.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 579-593
-
-
Sklar, P.1
Gabriel, S.B.2
McInnis, M.G.3
Bennett, P.4
Lim, Y.M.5
Tsan, G.6
Schaffner, S.7
Kirov, G.8
Jones, I.9
Owen, M.10
Craddock, N.11
DePaulo, J.R.12
Lander, E.S.13
-
122
-
-
0036724341
-
The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: Evidence from a family-based association study
-
Neves-Pereira M, Mundo E, Muglia P, King N, Macciardi F, Kennedy JL. The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: evidence from a family-based association study. Am J Hum Genet 2002;71:651-5.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 651-655
-
-
Neves-Pereira, M.1
Mundo, E.2
Muglia, P.3
King, N.4
Macciardi, F.5
Kennedy, J.L.6
-
123
-
-
4444322215
-
Linkage disequilibrium of the brain-derived neurotrophic factor Val66Met polymorphism in children with a prepubertal and early adolescent bipolar disorder phenotype
-
Geller B, Badner JA, Tillman R, Christian SL, Bolhofner K, Cook EH Jr. Linkage disequilibrium of the brain-derived neurotrophic factor Val66Met polymorphism in children with a prepubertal and early adolescent bipolar disorder phenotype. Am J Psychiatry 2004;161(9):1698-700.
-
(2004)
Am J Psychiatry
, vol.161
, Issue.9
, pp. 1698-1700
-
-
Geller, B.1
Badner, J.A.2
Tillman, R.3
Christian, S.L.4
Bolhofner, K.5
Cook Jr., E.H.6
-
124
-
-
3343026159
-
Non-replication of the brain-derived neurotrophic factor (BDNF) association in bipolar affective disorder: A Belgian patient-control study
-
Oswald P, Del-Favero J, Massat I, Souery D, Claes S, Van Broeckhoven C, Mendlewicz J. Non-replication of the brain-derived neurotrophic factor (BDNF) association in bipolar affective disorder: a Belgian patient-control study. Am J Med Genet 2004;129B(1):34-5.
-
(2004)
Am J Med Genet
, vol.129 B
, Issue.1
, pp. 34-35
-
-
Oswald, P.1
Del-Favero, J.2
Massat, I.3
Souery, D.4
Claes, S.5
Van Broeckhoven, C.6
Mendlewicz, J.7
-
125
-
-
15044352385
-
Association analysis of brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism in schizophrenia and bipolar affective disorder
-
Skibinska M, Hauser J, Czerski PM, Leszczynska-Rodziewicz A, Kosmowska M, Kapelski P, Slopien A, Zakrzewska M, Rybakowski JK. Association analysis of brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism in schizophrenia and bipolar affective disorder. World J Biol Psychiatry 2004;5(4):215-20.
-
(2004)
World J Biol Psychiatry
, vol.5
, Issue.4
, pp. 215-220
-
-
Skibinska, M.1
Hauser, J.2
Czerski, P.M.3
Leszczynska-Rodziewicz, A.4
Kosmowska, M.5
Kapelski, P.6
Slopien, A.7
Zakrzewska, M.8
Rybakowski, J.K.9
-
126
-
-
0347380124
-
Association study of a brain-derived neurotrophic-factor genetic polymorphism and mood disorders, age of onset and suicidal behavior
-
Hong CJ, Huo SJ, Yen FC, Tung CL, Pan GM, Tsai SJ. Association study of a brain-derived neurotrophic-factor genetic polymorphism and mood disorders, age of onset and suicidal behavior. Neuropsychobiology 2003;48(4):180-9.
-
(2003)
Neuropsychobiology
, vol.48
, Issue.4
, pp. 180-189
-
-
Hong, C.J.1
Huo, S.J.2
Yen, F.C.3
Tung, C.L.4
Pan, G.M.5
Tsai, S.J.6
-
127
-
-
0037472372
-
Association study of brain-derived neurotrophic factor (BDNF) gene with bipolar disorder
-
Nakata K, Ujike H, Sakai A, Uchida N, Nomura A, Imamura T, Katsu T, Tanaka Y, Hamamura T, Kuroda S. Association study of brain-derived neurotrophic factor (BDNF) gene with bipolar disorder. Neurosci Lett 2003;337:17-20.
-
(2003)
Neurosci Lett
, vol.337
, pp. 17-20
-
-
Nakata, K.1
Ujike, H.2
Sakai, A.3
Uchida, N.4
Nomura, A.5
Imamura, T.6
Katsu, T.7
Tanaka, Y.8
Hamamura, T.9
Kuroda, S.10
-
128
-
-
10744223787
-
Evidence that a single nucleotide polymorphism in the promoter of the G protein receptor kinase 3 gene is associated with bipolar disorder
-
Barrett TB, Hauger RL, Kennedy JL, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Alexander M, Shaw SH, Kelsoe JR. Evidence that a single nucleotide polymorphism in the promoter of the G protein receptor kinase 3 gene is associated with bipolar disorder. Mol Psychiatry 2003;8(5):546-57.
-
(2003)
Mol Psychiatry
, vol.8
, Issue.5
, pp. 546-557
-
-
Barrett, T.B.1
Hauger, R.L.2
Kennedy, J.L.3
Sadovnick, A.D.4
Remick, R.A.5
Keck, P.E.6
McElroy, S.L.7
Alexander, M.8
Shaw, S.H.9
Kelsoe, J.R.10
-
129
-
-
0141730405
-
Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder
-
Kakiuchi C, Iwamoto K, Ishiwata M, Bundo M, Kasahara T, Kusumi I, Tsujita T, Okazaki Y, Nanko S, Kunugi H, Sasaki T, Kata T. Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder. Nat Genet 2003;35(2):171-5.
-
(2003)
Nat Genet
, vol.35
, Issue.2
, pp. 171-175
-
-
Kakiuchi, C.1
Iwamoto, K.2
Ishiwata, M.3
Bundo, M.4
Kasahara, T.5
Kusumi, I.6
Tsujita, T.7
Okazaki, Y.8
Nanko, S.9
Kunugi, H.10
Sasaki, T.11
Kata, T.12
-
130
-
-
3543015566
-
Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin
-
Cichon S, Buervenich S, Kirov G, Akula N, Dimitrova A, Green E, Schumacher J, Klopp N, Becker T, Ohlraun S, Schulze TG, Tullius M, Gross MM, Jones L, Krastev S, Nikolov I, Hamshere M, Jones I, Czerski PM, Leszczynska-Rodziewicz A, Kapelski P, Bogaert AV, Illig T, Hauser J, Maier W, Berrettini W, Byerley W, Coryell W, Gershon ES, Kelsoe JR, McInnis MG, Murphy DL, Nurnberger JI, Reich T, Scheftner W, O'Donovan MC, Propping P, Owen MJ, Rietschel M, Nothen MM, McMahon FJ, Craddock N. Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nat Genet 2004;36(8):783-4.
-
(2004)
Nat Genet
, vol.36
, Issue.8
, pp. 783-784
-
-
Cichon, S.1
Buervenich, S.2
Kirov, G.3
Akula, N.4
Dimitrova, A.5
Green, E.6
Schumacher, J.7
Klopp, N.8
Becker, T.9
Ohlraun, S.10
Schulze, T.G.11
Tullius, M.12
Gross, M.M.13
Jones, L.14
Krastev, S.15
Nikolov, I.16
Hamshere, M.17
Jones, I.18
Czerski, P.M.19
Leszczynska-Rodziewicz, A.20
Kapelski, P.21
Bogaert, A.V.22
Illig, T.23
Hauser, J.24
Maier, W.25
Berrettini, W.26
Byerley, W.27
Coryell, W.28
Gershon, E.S.29
Kelsoe, J.R.30
McInnis, M.G.31
Murphy, D.L.32
Nurnberger, J.I.33
Reich, T.34
Scheftner, W.35
O'Donovan, M.C.36
Propping, P.37
Owen, M.J.38
Rietschel, M.39
Nothen, M.M.40
McMahon, F.J.41
Craddock, N.42
more..
-
131
-
-
20144375416
-
Identification and characterisation of a gene predisposing to both bipolar and unipolar affective disorders
-
Barden N, Harvey M, Shink E, Tremblay M, Gagné B, Raymond C, Labbé M, St-Onge L, Stadler H, Sillaber I, Paez-Pareda M, Muller-Mysok B, Binder E, Holsboer F. Identification and characterisation of a gene predisposing to both bipolar and unipolar affective disorders (abstract). Am J Med Gen 2004;130B(1):122.
-
(2004)
Am J Med Gen
, vol.130 B
, Issue.1
, pp. 122
-
-
Barden, N.1
Harvey, M.2
Shink, E.3
Tremblay, M.4
Gagné, B.5
Raymond, C.6
Labbé, M.7
St-Onge, L.8
Stadler, H.9
Sillaber, I.10
Paez-Pareda, M.11
Muller-Mysok, B.12
Binder, E.13
Holsboer, F.14
-
132
-
-
7344247646
-
Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder
-
Kirov G, Murphy KC, Arranz MJ, Jones I, McCandles F, Kunugi H, Murray RM, McGuffin P, Collier DA, Owen MJ, Craddock N. Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Mol Psychiatry 1998;3:342-5.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 342-345
-
-
Kirov, G.1
Murphy, K.C.2
Arranz, M.J.3
Jones, I.4
McCandles, F.5
Kunugi, H.6
Murray, R.M.7
McGuffin, P.8
Collier, D.A.9
Owen, M.J.10
Craddock, N.11
-
133
-
-
17944371887
-
Mapping susceptibility genes for bipolar disorder: A pharmacogenetic approach based on excellent response to lithium
-
Turecki G, Grof P, Grof E, D'Souza V, Lebuis L, Marineau C, Cavazzoni P, Duffy A, Betard C, Zvolsky P, Robertson C, Brewer C, Hudson TJ, Rouleau GA, Alda M. Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium. Mol Psychiatry 2001;6(5):570-8.
-
(2001)
Mol Psychiatry
, vol.6
, Issue.5
, pp. 570-578
-
-
Turecki, G.1
Grof, P.2
Grof, E.3
D'Souza, V.4
Lebuis, L.5
Marineau, C.6
Cavazzoni, P.7
Duffy, A.8
Betard, C.9
Zvolsky, P.10
Robertson, C.11
Brewer, C.12
Hudson, T.J.13
Rouleau, G.A.14
Alda, M.15
-
134
-
-
0034975406
-
Familiality of the puerperal trigger in bipolar disorder: Results of a family study
-
Jones I, Craddock N. Familiality of the puerperal trigger in bipolar disorder: results of a family study. Am J Psychiatry 2001;158:913-7.
-
(2001)
Am J Psychiatry
, vol.158
, pp. 913-917
-
-
Jones, I.1
Craddock, N.2
-
135
-
-
0034727432
-
Variation at the serotonin transporter gene influences susceptibility to bipolar affective puerperal psychosis
-
Coyle N, Jones I, Robertson E, Lendon C, Craddock N. Variation at the serotonin transporter gene influences susceptibility to bipolar affective puerperal psychosis. Lancet 2000;356:1490-1.
-
(2000)
Lancet
, vol.356
, pp. 1490-1491
-
-
Coyle, N.1
Jones, I.2
Robertson, E.3
Lendon, C.4
Craddock, N.5
-
136
-
-
1842533141
-
Three potential susceptibility loci shown by a genome-wide scan for regions influencing the age at onset of mania
-
Faraone SV, Glatt SJ, Su J, Tsuang MT. Three potential susceptibility loci shown by a genome-wide scan for regions influencing the age at onset of mania. Am J Psychiatry 2004;161(4):025-30.
-
(2004)
Am J Psychiatry
, vol.161
, Issue.4
, pp. 25-30
-
-
Faraone, S.V.1
Glatt, S.J.2
Su, J.3
Tsuang, M.T.4
-
137
-
-
0036133633
-
Sibling pairs with affective disorders: Resemblance of demographic and clinical features
-
O'Mahony E, Corvin A, O'Connell R, Comerford C, Larsen B, Jones R, McCandless F, Kirov G, Cardno AG, Craddock N, Gill M. Sibling pairs with affective disorders: resemblance of demographic and clinical features. Psychol Med 2002;32(1):55-61.
-
(2002)
Psychol Med
, vol.32
, Issue.1
, pp. 55-61
-
-
O'Mahony, E.1
Corvin, A.2
O'Connell, R.3
Comerford, C.4
Larsen, B.5
Jones, R.6
McCandless, F.7
Kirov, G.8
Cardno, A.G.9
Craddock, N.10
Gill, M.11
-
138
-
-
12944327712
-
The Bipolar Affective Disorder Dimension Scale (BADDS) - A dimensional scale for rating lifetime psychopathology in bipolar spectrum disorders
-
Craddock N, Jones I, Kirov G, Jones L. The Bipolar Affective Disorder Dimension Scale (BADDS) - a dimensional scale for rating lifetime psychopathology in bipolar spectrum disorders. BMC Psychiatry 2004;4:19.
-
(2004)
BMC Psychiatry
, vol.4
, pp. 19
-
-
Craddock, N.1
Jones, I.2
Kirov, G.3
Jones, L.4
-
139
-
-
0038135178
-
Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder
-
Potash JB, Zandi PP, Willour VL, Lan TH, Huo Y, Avramopoulos D, Shugart YY, MacKinnon DF, Simpson SG, McMahon FJ, DePaulo JR Jr, McInnis MG. Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. Am J Psychiatry 2003;160(4):680-6.
-
(2003)
Am J Psychiatry
, vol.160
, Issue.4
, pp. 680-686
-
-
Potash, J.B.1
Zandi, P.P.2
Willour, V.L.3
Lan, T.H.4
Huo, Y.5
Avramopoulos, D.6
Shugart, Y.Y.7
MacKinnon, D.F.8
Simpson, S.G.9
McMahon, F.J.10
DePaulo Jr., J.R.11
McInnis, M.G.12
-
143
-
-
0025285865
-
The continuum or psychosis and its genetic origins. The sixty-fifth Maudsley lecture
-
Crow TJ. The continuum or psychosis and its genetic origins. The sixty-fifth Maudsley lecture. Br J Psychiatry 1990;156:788-97.
-
(1990)
Br J Psychiatry
, vol.156
, pp. 788-797
-
-
Crow, T.J.1
-
144
-
-
0019975573
-
Family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands
-
Gershon ES, Hamovit J, Guroff JJ, Dibble E, Leckman JF, Sceery W, Targum SD, Nurnberger JI Jr, Goldin LR, Bunney WE Jr. family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands. Arch Gen Psychiatry 1982;39:1157-67.
-
(1982)
Arch Gen Psychiatry
, vol.39
, pp. 1157-1167
-
-
Gershon, E.S.1
Hamovit, J.2
Guroff, J.J.3
Dibble, E.4
Leckman, J.F.5
Sceery, W.6
Targum, S.D.7
Nurnberger Jr., J.I.8
Goldin, L.R.9
Bunney Jr., W.E.10
-
145
-
-
0022401190
-
Prevalence of DSM III schizophrenia among the first-degree relatives of schizophrenic probands
-
Frangos E, Athanassenas G, Tsitourides S, Katsanou N, Alexandrakou P. Prevalence of DSM III schizophrenia among the first-degree relatives of schizophrenic probands. Acta Psychiatr Scand 1985;72:382-6.
-
(1985)
Acta Psychiatr Scand
, vol.72
, pp. 382-386
-
-
Frangos, E.1
Athanassenas, G.2
Tsitourides, S.3
Katsanou, N.4
Alexandrakou, P.5
-
146
-
-
0020068075
-
Schizoaffective illness, schizophrenia and affective disorders: Morbidity risk and genetic transmission
-
Baron M, Gruen R, Asnis L, Kane J. Schizoaffective illness, schizophrenia and affective disorders: morbidity risk and genetic transmission. Acta Psychiatr Scand 1982;65:253-62.
-
(1982)
Acta Psychiatr Scand
, vol.65
, pp. 253-262
-
-
Baron, M.1
Gruen, R.2
Asnis, L.3
Kane, J.4
-
147
-
-
0025241022
-
Schizophrenic individuals with bipolar first-degree relatives: Analysis of two pedigrees
-
Pope HG Jr, Yurgelun-Todd D. Schizophrenic individuals with bipolar first-degree relatives: analysis of two pedigrees. J Clin Psychiatry 1990;51:97-101.
-
(1990)
J Clin Psychiatry
, vol.51
, pp. 97-101
-
-
Pope Jr., H.G.1
Yurgelun-Todd, D.2
-
148
-
-
0019143717
-
Morbidity risks of schizophrenia and affective disorders among first degree relatives of patients with schizophrenia, mania, depression and surgical conditions
-
Tsuang MT, Winokur G, Crowe RR. Morbidity risks of schizophrenia and affective disorders among first degree relatives of patients with schizophrenia, mania, depression and surgical conditions. Br J Psychiatry 1980;137:497-504.
-
(1980)
Br J Psychiatry
, vol.137
, pp. 497-504
-
-
Tsuang, M.T.1
Winokur, G.2
Crowe, R.R.3
-
149
-
-
0034615867
-
Increased morbid risk for schizophrenia in families of in-patients with bipolar illness
-
Valles V, Van Os J, Guillamat R, Gutiérrez B, Campillo M, Gento P, Fañanás L. Increased morbid risk for schizophrenia in families of in-patients with bipolar illness. Schizophr Res 2000;42:83-90.
-
(2000)
Schizophr Res
, vol.42
, pp. 83-90
-
-
Valles, V.1
Van Os, J.2
Guillamat, R.3
Gutiérrez, B.4
Campillo, M.5
Gento, P.6
Fañanás, L.7
-
150
-
-
0031798932
-
The structure of psychosis: Latent class analysis of probands from the Roscommon Family Study
-
Kendler KS, Karkowski LM, Walsh D. The structure of psychosis: latent class analysis of probands from the Roscommon Family Study. Arch Gen Psychiatry 1998;55:492-9.
-
(1998)
Arch Gen Psychiatry
, vol.55
, pp. 492-499
-
-
Kendler, K.S.1
Karkowski, L.M.2
Walsh, D.3
-
151
-
-
0023185858
-
The familial transmission of bipolar illness
-
Rice J, Reich T, Andreasen NC, Endicott J, Van Eerdewegh M, Fishman R, Hirschfeld RM, Klerman GL. The familial transmission of bipolar illness. Arch Gen Psychiatry 1987;44:441-7.
-
(1987)
Arch Gen Psychiatry
, vol.44
, pp. 441-447
-
-
Rice, J.1
Reich, T.2
Andreasen, N.C.3
Endicott, J.4
Van Eerdewegh, M.5
Fishman, R.6
Hirschfeld, R.M.7
Klerman, G.L.8
-
152
-
-
0036212511
-
A twin study of genetic relationships between psychotic symptoms
-
Cardno AG, Rijsdijk FV, Sham PC, Murray RM, McGuffin P. A twin study of genetic relationships between psychotic symptoms. Am J Psychiatry 2002;159:539-45.
-
(2002)
Am J Psychiatry
, vol.159
, pp. 539-545
-
-
Cardno, A.G.1
Rijsdijk, F.V.2
Sham, P.C.3
Murray, R.M.4
McGuffin, P.5
-
154
-
-
0242385651
-
Evidence for shared susceptibility in bipolar disorder and schizophrenia
-
Berrettini W. Evidence for shared susceptibility in bipolar disorder and schizophrenia. Am J Med Genet 2003;123C:59-64.
-
(2003)
Am J Med Genet
, vol.123 C
, pp. 59-64
-
-
Berrettini, W.1
-
155
-
-
20144379092
-
Evidence for linkage (LOD = 3.54) at IQ42 close to DISC1 in a genome scan of functional psychosis pedigrees including at least one member with schizoaffective disorder of bipolar type
-
Hamshere ML, Williams NM, Segurado R, Lambert D, Jones LA, Holmans P, Kirov G, Corvin A, Jones I, O'Donovan MC, Gill M, Owen MJ, Craddock N. Evidence for linkage (LOD = 3.54) at IQ42 close to DISC1 in a genome scan of functional psychosis pedigrees including at least one member with schizoaffective disorder of bipolar type (abstract). Am J Med Genet 2004;130B(1):127.
-
(2004)
Am J Med Genet
, vol.130 B
, Issue.1
, pp. 127
-
-
Hamshere, M.L.1
Williams, N.M.2
Segurado, R.3
Lambert, D.4
Jones, L.A.5
Holmans, P.6
Kirov, G.7
Corvin, A.8
Jones, I.9
O'Donovan, M.C.10
Gill, M.11
Owen, M.J.12
Craddock, N.13
-
156
-
-
11244302487
-
A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42
-
Macgregor S, Visscher PM, Knott SA, Thomson P, Porteous DJ, Millar JK, Devon RS, Blackwood D, Muir WJ. A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42. Mol Psychiatry 2004;9(12):1083-90.
-
(2004)
Mol Psychiatry
, vol.9
, Issue.12
, pp. 1083-1090
-
-
Macgregor, S.1
Visscher, P.M.2
Knott, S.A.3
Thomson, P.4
Porteous, D.J.5
Millar, J.K.6
Devon, R.S.7
Blackwood, D.8
Muir, W.J.9
-
157
-
-
20144370504
-
The schizophrenia susceptibility gene, Neuregulin 1 (NRG1), operates across traditional diagnostic boundaries to increase risk for bipolar disorder
-
in press
-
Green EK, Raybould R, Macgregor S, Gordon-Smith K, Heron J, Hyde S, Grozeva D, Hamshere M, Williams N, Owen MJ, O'Donovan MC, Jones L, Jones I, Kirov G, Craddock N. The schizophrenia susceptibility gene, Neuregulin 1 (NRG1), operates across traditional diagnostic boundaries to increase risk for bipolar disorder. Arch Gen Psychiatry (in press).
-
Arch Gen Psychiatry
-
-
Green, E.K.1
Raybould, R.2
Macgregor, S.3
Gordon-Smith, K.4
Heron, J.5
Hyde, S.6
Grozeva, D.7
Hamshere, M.8
Williams, N.9
Owen, M.J.10
O'Donovan, M.C.11
Jones, L.12
Jones, I.13
Kirov, G.14
Craddock, N.15
-
158
-
-
11244312972
-
Neuregulin 1: Genetic support for schizophrenia subtypes
-
Bakker SC, Hoogendoorn MLC, Selten J-P, Verduijn W, Pearson PL, Sinke RJ, Kahn RS. Neuregulin 1: genetic support for schizophrenia subtypes. Mol Psychiatry 2004;9:1061-3.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 1061-1063
-
-
Bakker, S.C.1
Hoogendoorn, M.L.C.2
Selten, J.-P.3
Verduijn, W.4
Pearson, P.L.5
Sinke, R.J.6
Kahn, R.S.7
-
159
-
-
18644386195
-
The beginning of the end for the Kraepelinian dichotomy
-
in press
-
Craddock N, Owen MJ. The beginning of the end for the Kraepelinian dichotomy. Br J Psychiatry (in press).
-
Br J Psychiatry
-
-
Craddock, N.1
Owen, M.J.2
-
160
-
-
0037308528
-
Genes for schizophrenia? Recent findings and their pathophysiological implications
-
Harrison PJ, Owen MJ. Genes for schizophrenia? Recent findings and their pathophysiological implications. Lancet 2003;361(9355):417-9.
-
(2003)
Lancet
, vol.361
, Issue.9355
, pp. 417-419
-
-
Harrison, P.J.1
Owen, M.J.2
-
161
-
-
9144254700
-
Heritability of adult body height: A comparative study of twin cohorts in eight countries
-
Silvontoinen K, Sammalisto S, Perola M, Boomsma DI, Cornes BK, Davis C, Dunkel L, De Lange M, Harris JR, Hjelmborg JV, Luciano M, Martin NG, Mortensen J, Nistico L, Pedersen NL, Skytthe A, Spector TD, Stazi MA, Willemsen G, Kaprio J. Heritability of adult body height: a comparative study of twin cohorts in eight countries. Twin Res 2003;6(5):399-408.
-
(2003)
Twin Res
, vol.6
, Issue.5
, pp. 399-408
-
-
Silvontoinen, K.1
Sammalisto, S.2
Perola, M.3
Boomsma, D.I.4
Cornes, B.K.5
Davis, C.6
Dunkel, L.7
De Lange, M.8
Harris, J.R.9
Hjelmborg, J.V.10
Luciano, M.11
Martin, N.G.12
Mortensen, J.13
Nistico, L.14
Pedersen, N.L.15
Skytthe, A.16
Spector, T.D.17
Stazi, M.A.18
Willemsen, G.19
Kaprio, J.20
more..
-
162
-
-
0029128706
-
Concordance rates of insulin dependent diabetes mellitus: A population based study of young Danish twins
-
Kyvik KO, Green A, Beck-Nielsen H. Concordance rates of insulin dependent diabetes mellitus: a population based study of young Danish twins. BMJ 1995;311(7010):913-7.
-
(1995)
BMJ
, vol.311
, Issue.7010
, pp. 913-917
-
-
Kyvik, K.O.1
Green, A.2
Beck-Nielsen, H.3
-
163
-
-
0345505676
-
Genetic liability of type 1 diabetes and the onset age among 22,650 young Finnish twin pairs: A nationwide follow-up study
-
Hyttinen V, Kaprio J, Kinnunen L, Koskenvuo M, Tuomilehto J. Genetic liability of type 1 diabetes and the onset age among 22,650 young Finnish twin pairs: a nationwide follow-up study. Diabetes 2003;52(4):1052-5.
-
(2003)
Diabetes
, vol.52
, Issue.4
, pp. 1052-1055
-
-
Hyttinen, V.1
Kaprio, J.2
Kinnunen, L.3
Koskenvuo, M.4
Tuomilehto, J.5
-
164
-
-
1942467078
-
The heritability of breast cancer: A Bayesian correlated frailty model applied to Swedish twins data
-
Locatelli I, Lichtenstein P, Yashin AI. The heritability of breast cancer: a Bayesian correlated frailty model applied to Swedish twins data. Twin Res 2004;7(2):182-91.
-
(2004)
Twin Res
, vol.7
, Issue.2
, pp. 182-191
-
-
Locatelli, I.1
Lichtenstein, P.2
Yashin, A.I.3
-
165
-
-
0036378360
-
Heritability of death from coronary heart disease: A 36-year follow-up of 20 966 Swedish twins
-
Zdravkovic S, Wienke A, Pedersen NL. Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins. J Intern Med 2002;252(3):247-54.
-
(2002)
J Intern Med
, vol.252
, Issue.3
, pp. 247-254
-
-
Zdravkovic, S.1
Wienke, A.2
Pedersen, N.L.3
-
166
-
-
0032953097
-
Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance - A population-based twin study
-
Poulsen P, Kyvik KO, Vaag A, Beck-Nielsen H. Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance - a population-based twin study. Diabetologia 1999;42(2):139-45.
-
(1999)
Diabetologia
, vol.42
, Issue.2
, pp. 139-145
-
-
Poulsen, P.1
Kyvik, K.O.2
Vaag, A.3
Beck-Nielsen, H.4
-
167
-
-
0035125598
-
An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree
-
Radhakrishna U, Senol S, Herken H, Gucuyener K, Gehrig C, Blouin JL, Akarsu NA, Antonarakis SE. An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree. Eur J Hum Genet 2001;9(1):39-44.
-
(2001)
Eur J Hum Genet
, vol.9
, Issue.1
, pp. 39-44
-
-
Radhakrishna, U.1
Senol, S.2
Herken, H.3
Gucuyener, K.4
Gehrig, C.5
Blouin, J.L.6
Akarsu, N.A.7
Antonarakis, S.E.8
-
168
-
-
0031960735
-
A susceptibility locus for bipolar affective disorder on chromosome 4q35
-
Adams LJ, Mitchell PB, Fielder SL, Rosso A, Donald JA, Schofield PR. A susceptibility locus for bipolar affective disorder on chromosome 4q35. Am J Hum Genet 1998;62(5):1084-91.
-
(1998)
Am J Hum Genet
, vol.62
, Issue.5
, pp. 1084-1091
-
-
Adams, L.J.1
Mitchell, P.B.2
Fielder, S.L.3
Rosso, A.4
Donald, J.A.5
Schofield, P.R.6
-
169
-
-
13344281025
-
A locus for bipolar affective disorder on chromosome 4p
-
Blackwood DH, He L, Morris SW, McLean A, Whitton C, Thomson M, Walker MT, Woodburn K, Sharp CM, Wright AF, Shibasaki Y, St Clair DM, Porteous DJ, Muir WJ. A locus for bipolar affective disorder on chromosome 4p. Nat Genet 1996;12(4):427-30.
-
(1996)
Nat Genet
, vol.12
, Issue.4
, pp. 427-430
-
-
Blackwood, D.H.1
He, L.2
Morris, S.W.3
McLean, A.4
Whitton, C.5
Thomson, M.6
Walker, M.T.7
Woodburn, K.8
Sharp, C.M.9
Wright, A.F.10
Shibasaki, Y.11
St. Clair, D.M.12
Porteous, D.J.13
Muir, W.J.14
-
170
-
-
20144363659
-
The Wellcome Trust Ireland/UK bipolar disorder sibling pair study: Stage II analysis
-
Lambert DBJ, Hamshere ML, Segurado R, Bennett P, Jones I, McCandless F, Jones L, Raybould R, Heron J, Green E, Nokolov I, Corvin A, O'Mahony E, Owen M, Middle F, Kirov G, Holmans P, Craddock N, Gill M. The Wellcome Trust Ireland/UK bipolar disorder sibling pair study: stage II analysis (abstract). Am J Med Genet 2004;130B:51.
-
(2004)
Am J Med Genet
, vol.130 B
, pp. 51
-
-
Lambert, D.B.J.1
Hamshere, M.L.2
Segurado, R.3
Bennett, P.4
Jones, I.5
McCandless, F.6
Jones, L.7
Raybould, R.8
Heron, J.9
Green, E.10
Nokolov, I.11
Corvin, A.12
O'Mahony, E.13
Owen, M.14
Middle, F.15
Kirov, G.16
Holmans, P.17
Craddock, N.18
Gill, M.19
-
171
-
-
3242728424
-
Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families
-
Fallin MD, Lasseter VK, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Liang KY, Pulver AE. Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families. Am J Hum Genet 2004;75(2):204-19.
-
(2004)
Am J Hum Genet
, vol.75
, Issue.2
, pp. 204-219
-
-
Fallin, M.D.1
Lasseter, V.K.2
Wolyniec, P.S.3
McGrath, J.A.4
Nestadt, G.5
Valle, D.6
Liang, K.Y.7
Pulver, A.E.8
-
172
-
-
2342635193
-
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: A comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22
-
Middleton FA, Pato MT, Gentile KL, Morley CP, Zhao X, Eisener AF, Brawn A, Petryshen TL, Kirby AN, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Azevedo MH, Kennedy JL, Daly MJ, Sklar P, Pato CN. Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. Am J Hum Genet 2004;74(5):886-97.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.5
, pp. 886-897
-
-
Middleton, F.A.1
Pato, M.T.2
Gentile, K.L.3
Morley, C.P.4
Zhao, X.5
Eisener, A.F.6
Brawn, A.7
Petryshen, T.L.8
Kirby, A.N.9
Medeiros, H.10
Carvalho, C.11
Macedo, A.12
Dourado, A.13
Coelho, I.14
Valente, J.15
Soares, M.J.16
Ferreira, C.P.17
Lei, M.18
Azevedo, M.H.19
Kennedy, J.L.20
Daly, M.J.21
Sklar, P.22
Pato, C.N.23
more..
-
173
-
-
0038389850
-
Genomewide linkage analyses of bipolar disorder: A new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative
-
Dick DM, Foroud T, Flury L, Bowman ES, Miller MJ, Rau NL, Moe PR, Samavedy N, El-Mallakh R, Manji H, Glitz DA, Meyer ET, Smiley C, Hahn R, Widmark C, McKinney R, Sutton L, Ballas C, Grice D, Berrettini W, Byerley W, Coryell W, DePaulo R, MacKinnon DF, Gershon ES, Kelsoe JR, McMahon FJ, McInnis M, Murphy DL, Reich T, Scheftner W, Nurnberger JI Jr. Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. Am J Hum Genet 2003;73(1):107-14 (erratum in: Am J Hum Genet 2003;73(4):979).
-
(2003)
Am J Hum Genet
, vol.73
, Issue.1
, pp. 107-114
-
-
Dick, D.M.1
Foroud, T.2
Flury, L.3
Bowman, E.S.4
Miller, M.J.5
Rau, N.L.6
Moe, P.R.7
Samavedy, N.8
El-Mallakh, R.9
Manji, H.10
Glitz, D.A.11
Meyer, E.T.12
Smiley, C.13
Hahn, R.14
Widmark, C.15
McKinney, R.16
Sutton, L.17
Ballas, C.18
Grice, D.19
Berrettini, W.20
Byerley, W.21
Coryell, W.22
DePaulo, R.23
MacKinnon, D.F.24
Gershon, E.S.25
Kelsoe, J.R.26
McMahon, F.J.27
McInnis, M.28
Murphy, D.L.29
Reich, T.30
Scheftner, W.31
Nurnberger Jr., J.I.32
more..
-
174
-
-
0038389850
-
Erratum
-
Dick DM, Foroud T, Flury L, Bowman ES, Miller MJ, Rau NL, Moe PR, Samavedy N, El-Mallakh R, Manji H, Glitz DA, Meyer ET, Smiley C, Hahn R, Widmark C, McKinney R, Sutton L, Ballas C, Grice D, Berrettini W, Byerley W, Coryell W, DePaulo R, MacKinnon DF, Gershon ES, Kelsoe JR, McMahon FJ, McInnis M, Murphy DL, Reich T, Scheftner W, Nurnberger JI Jr. Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. Am J Hum Genet 2003;73(1):107-14 (erratum in: Am J Hum Genet 2003;73(4):979).
-
(2003)
Am J Hum Genet
, vol.73
, Issue.4
, pp. 979
-
-
-
175
-
-
0037042063
-
Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees
-
Dick DM, Foroud T, Edenberg HJ, Miller M, Bowman E, Rau NL, DePaulo JR, McInnis M, Gershon E, McMahon F, Rice JP, Bierut LJ, Reich T, Nurnberger J Jr. Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees. Am J Med Genet 2002;114(4):407-12.
-
(2002)
Am J Med Genet
, vol.114
, Issue.4
, pp. 407-412
-
-
Dick, D.M.1
Foroud, T.2
Edenberg, H.J.3
Miller, M.4
Bowman, E.5
Rau, N.L.6
DePaulo, J.R.7
McInnis, M.8
Gershon, E.9
McMahon, F.10
Rice, J.P.11
Bierut, L.J.12
Reich, T.13
Nurnberger Jr., J.14
-
176
-
-
0042821693
-
Enome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21
-
Willour VL, Zandi PP, Huo Y, Diggs TL, Chellis JL, MacKinnon DF, Simpson SG, McMahon FJ, Potash JB, Gershon ES, Reich T, Foroud T, Nurnberger JI Jr, DePaulo JR Jr, McInnis MG. enome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: chromosomes 4, 7, 9, 18, 19, 20, and 21. Am J Med Genet 2003;121B(1):21-7.
-
(2003)
Am J Med Genet
, vol.121 B
, Issue.1
, pp. 21-27
-
-
Willour, V.L.1
Zandi, P.P.2
Huo, Y.3
Diggs, T.L.4
Chellis, J.L.5
MacKinnon, D.F.6
Simpson, S.G.7
McMahon, F.J.8
Potash, J.B.9
Gershon, E.S.10
Reich, T.11
Foroud, T.12
Nurnberger Jr., J.I.13
DePaulo Jr., J.R.14
McInnis, M.G.15
-
177
-
-
10744226840
-
Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: Chromosomes 2, 11, 13, 14, and X
-
Zandi PP, Willour VL, Huo Y, Chellis J, Potash JB, MacKinnon DF, Simpson SG, McMahon FJ, Gershon E, Reich T, Foroud T, Nurnberger J Jr, DePaulo JR Jr, McInnis MG, National Institute of Mental Health Genetics Initiative Bipolar Group. Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X. Am J Med Genet 2003;119B(1):69-76.
-
(2003)
Am J Med Genet
, vol.119 B
, Issue.1
, pp. 69-76
-
-
Zandi, P.P.1
Willour, V.L.2
Huo, Y.3
Chellis, J.4
Potash, J.B.5
MacKinnon, D.F.6
Simpson, S.G.7
McMahon, F.J.8
Gershon, E.9
Reich, T.10
Foroud, T.11
Nurnberger Jr., J.12
DePaulo Jr., J.R.13
McInnis, M.G.14
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