-
3
-
-
0021130337
-
Lifetime prevalence of specific psychiatric disorders in three sites
-
Robins LN, Helzer JE, Weissman MM, Orvaschel H, Gruenberg E, Burke JD Jr, Regier DA. Lifetime prevalence of specific psychiatric disorders in three sites. Arch Gen Psychiatry 1984;41:949-58.
-
(1984)
Arch Gen Psychiatry
, vol.41
, pp. 949-958
-
-
Robins, L.N.1
Helzer, J.E.2
Weissman, M.M.3
Orvaschel, H.4
Gruenberg, E.5
Burke J.D., Jr.6
Regier, D.A.7
-
4
-
-
0034535747
-
The genetic epidemiology of schizophrenia and of schizophrenia spectrum disorders
-
Lichtermann D, Karbe E, Maier W. The genetic epidemiology of schizophrenia and of schizophrenia spectrum disorders. Eur Arch Psychiatry Clin Neurosci 2000;250:304-10.
-
(2000)
Eur Arch Psychiatry Clin Neurosci
, vol.250
, pp. 304-310
-
-
Lichtermann, D.1
Karbe, E.2
Maier, W.3
-
5
-
-
0035121790
-
Genetics of schizophrenia and the new millennium: Progress and pitfalls
-
Baron M. Genetics of schizophrenia and the new millennium: progress and pitfalls. Am J Hum Genet 2001;68:299-312.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 299-312
-
-
Baron, M.1
-
6
-
-
0033580966
-
Chromosome Workshop: Chromosomes 11, 14, and 15
-
Craddock N, Lendon C. Chromosome Workshop: chromosomes 11, 14, and 15. Am J Med Genet 1999;88:244-54.
-
(1999)
Am J Med Genet
, vol.88
, pp. 244-254
-
-
Craddock, N.1
Lendon, C.2
-
7
-
-
0036024272
-
Genetic heterogeneity in schizophrenia. II. Conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q
-
Chiu YF, McGrath JA, Thornquist MH, Wolyniec PS, Nestadt G, Swartz KL, Lasseter VK, Liang KY, Pulver AE. Genetic heterogeneity in schizophrenia. II. Conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q. Mol Psychiatry 2002;7:658-64.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 658-664
-
-
Chiu, Y.F.1
McGrath, J.A.2
Thornquist, M.H.3
Wolyniec, P.S.4
Nestadt, G.5
Swartz, K.L.6
Lasseter, V.K.7
Liang, K.Y.8
Pulver, A.E.9
-
8
-
-
0017903859
-
Segregation of ABO, AK1 and ACONs in families with abnormalities of chromosome 9
-
Cook PJ, Robson EB, Buckton KE, Slaughter CA, Gray JE, Blank CE, James FE, Ridler MA, Insley J, Hulten M. Segregation of ABO, AK1 and ACONs in families with abnormalities of chromosome 9. Ann Hum Genet 1978;41:365-77.
-
(1978)
Ann Hum Genet
, vol.41
, pp. 365-377
-
-
Cook, P.J.1
Robson, E.B.2
Buckton, K.E.3
Slaughter, C.A.4
Gray, J.E.5
Blank, C.E.6
James, F.E.7
Ridler, M.A.8
Insley, J.9
Hulten, M.10
-
9
-
-
0035425831
-
Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes
-
Kamnasaran D, O'Brien PC, Schuffenhauer S, Quarrell O, Lupski JR, Grammatico P, Ferguson-Smith MA, Cox DW. Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes. Am J Med Genet 2001;102:173-82.
-
(2001)
Am J Med Genet
, vol.102
, pp. 173-182
-
-
Kamnasaran, D.1
O'Brien, P.C.2
Schuffenhauer, S.3
Quarrell, O.4
Lupski, J.R.5
Grammatico, P.6
Ferguson-Smith, M.A.7
Cox, D.W.8
-
10
-
-
0037623881
-
Mapping chromosome breakpoints using fibre-FISH in a family with a translocation t(9;14)(q34q13) chromosome and psychiatric illness
-
8th World Congress on Psychiatric Genetics. Abstract P327
-
Malloy MP, Cox DW, Kamnasaran D, Ferguson-Smith MA, Picard BS, Porteus DJ, Blackwood DR, Muir WJ. Mapping chromosome breakpoints using fibre-FISH in a family with a translocation t(9;14)(q34q13) chromosome and psychiatric illness. 8th World Congress on Psychiatric Genetics. Abstract P327 Am J Med Genet 2000;96:551-552..
-
(2000)
Am J Med Genet
, vol.96
, pp. 551-552
-
-
Malloy, M.P.1
Cox, D.W.2
Kamnasaran, D.3
Ferguson-Smith, M.A.4
Picard, B.S.5
Porteus, D.J.6
Blackwood, D.R.7
Muir, W.J.8
-
11
-
-
0032872915
-
Remembrance of things PAS: Regulation of development by bHLH-PAS proteins
-
Crews ST, Fan CM. Remembrance of things PAS: regulation of development by bHLH-PAS proteins. Curr Opin Genet Dev 1999;9:580-7.
-
(1999)
Curr Opin Genet Dev
, vol.9
, pp. 580-587
-
-
Crews, S.T.1
Fan, C.M.2
-
12
-
-
0032030839
-
Control of cell lineage-specific development and transcription by bHLH-PAS proteins
-
Crews ST. Control of cell lineage-specific development and transcription by bHLH-PAS proteins. Genes Dev 1998;12:607-20.
-
(1998)
Genes Dev
, vol.12
, pp. 607-620
-
-
Crews, S.T.1
-
13
-
-
0034705398
-
Impaired cued and contextual memory in NPAS2-deficient mice
-
Garcia JA, Zhang D, Estill SJ, Michnoff C, Rutter J, Reick M, Scott K, Diaz-Arrastia R, McKnight SL. Impaired cued and contextual memory in NPAS2-deficient mice. Science 2000;288:2226-30.
-
(2000)
Science
, vol.288
, pp. 2226-2230
-
-
Garcia, J.A.1
Zhang, D.2
Estill, S.J.3
Michnoff, C.4
Rutter, J.5
Reick, M.6
Scott, K.7
Diaz-Arrastia, R.8
McKnight, S.L.9
-
14
-
-
0035919618
-
NPAS2: An analog of clock operative in the mammalian forebrain
-
Reick M, Garcia JA, Dudley C, McKnight SL. NPAS2: an analog of clock operative in the mammalian forebrain. Science 2001;293:506-09.
-
(2001)
Science
, vol.293
, pp. 506-509
-
-
Reick, M.1
Garcia, J.A.2
Dudley, C.3
McKnight, S.L.4
-
15
-
-
0037067729
-
Differential regulation of gene expression by PITX2 isoforms
-
Cox CJ, Espinoza HM, McWilliams B, Chappell K, Morton L, Hjalt TA, Semina EV, Amendt BA. Differential regulation of gene expression by PITX2 isoforms. J Biol Chem 2002;277:25001-10.
-
(2002)
J Biol Chem
, vol.277
, pp. 25001-25010
-
-
Cox, C.J.1
Espinoza, H.M.2
McWilliams, B.3
Chappell, K.4
Morton, L.5
Hjalt, T.A.6
Semina, E.V.7
Amendt, B.A.8
-
16
-
-
0032835527
-
Characterization of Npas3, a novel basic helix-loop-helix PAS gene expressed in the developing mouse nervous system
-
Brunskill EW, Witte DP, Shreiner AB, Potter SS. Characterization of Npas3, a novel basic helix-loop-helix PAS gene expressed in the developing mouse nervous system. Mech Dev 1999;88:237-41.
-
(1999)
Mech Dev
, vol.88
, pp. 237-241
-
-
Brunskill, E.W.1
Witte, D.P.2
Shreiner, A.B.3
Potter, S.S.4
-
17
-
-
0033852958
-
Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome
-
Chrast R, Scott HS, Madani R, Huber L, Wolfer DP, Prinz M, Aguzzi A, Lipp HP, Antonarokis SE. Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome. Hum Mol Genet 2000;9:1853-64.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1853-1864
-
-
Chrast, R.1
Scott, H.S.2
Madani, R.3
Huber, L.4
Wolfer, D.P.5
Prinz, M.6
Aguzzi, A.7
Lipp, H.P.8
Antonarokis, S.E.9
-
19
-
-
0028871785
-
An international two-stage genome-wide search for schizophrenia susceptibility genes
-
Moises HW, Yang L, Kristbjarnarson H, Wiese C, Byerley W, Macciardi F, Arolt V, Blackwood D, Liu X, Sjogren B, Aschauer HN, Hwu GG, Jang K, Livelsley WJ, Kennedy JL, Zoega T, Ivarsson O, Bui MT, Yu MH, Havsteen B, Commenges D, Weissenbach J, Schwinger E, Gottesman II, Pakstis AJ, Wetterberg L, Kidd KK, Helgason T. An international two-stage genome-wide search for schizophrenia susceptibility genes. Nat Genet 1995;11:321-4.
-
(1995)
Nat Genet
, vol.11
, pp. 321-324
-
-
Moises, H.W.1
Yang, L.2
Kristbjarnarson, H.3
Wiese, C.4
Byerley, W.5
Macciardi, F.6
Arolt, V.7
Blackwood, D.8
Liu, X.9
Sjogren, B.10
Aschauer, H.N.11
Hwu, G.G.12
Jang, K.13
Livelsley, W.J.14
Kennedy, J.L.15
Zoega, T.16
Ivarsson, O.17
Bui, M.T.18
Yu, M.H.19
Havsteen, B.20
Commenges, D.21
Weissenbach, J.22
Schwinger, E.23
Gottesman, I.I.24
Pakstis, A.J.25
Wetterberg, L.26
Kidd, K.K.27
Helgason, T.28
more..
-
20
-
-
17344364477
-
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
-
Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, Balk KG, Neufeld K, Swartz KL, DeMarchi N, Papadimitriou GN, Dikeos DG, Stefanis CN, Chakravarti A, Childs B, Housmon DE, Kazazian HH, Antonarakis SE, Pulver AE. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet 1998;20:70-3
-
(1998)
Nat Genet
, vol.20
, pp. 70-73
-
-
Blouin, J.L.1
Dombroski, B.A.2
Nath, S.K.3
Lasseter, V.K.4
Wolyniec, P.S.5
Nestadt, G.6
Thornquist, M.7
Ullrich, G.8
McGrath, J.9
Kasch, L.10
Lamacz, M.11
Thomas, M.G.12
Gehrig, C.13
Radhakrishna, U.14
Snyder, S.E.15
Balk, K.G.16
Neufeld, K.17
Swartz, K.L.18
DeMarchi, N.19
Papadimitriou, G.N.20
Dikeos, D.G.21
Stefanis, C.N.22
Chakravarti, A.23
Childs, B.24
Housmon, D.E.25
Kazazian, H.H.26
Antonarakis, S.E.27
Pulver, A.E.28
more..
-
21
-
-
0034873749
-
Multipoint analysis using affected sib pairs: Incorporating linkage evidence from unlinked regions
-
Liang KY, Chiu YF, Beaty TH, Wjst M. Multipoint analysis using affected sib pairs: incorporating linkage evidence from unlinked regions. Genet Epidemiol 2001;21:105-22.
-
(2001)
Genet Epidemiol
, vol.21
, pp. 105-122
-
-
Liang, K.Y.1
Chiu, Y.F.2
Beaty, T.H.3
Wjst, M.4
-
22
-
-
0036181474
-
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency
-
Krude H, Schutz B, Biebermann H, von Moers A, Schnabel D, Neitzel H, Tonnies H, Weise D, Lafferty A, Schwarz S, DeFelice M, von Deimling A, van Landeghem F, DiLauro R, Gruters A. Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency. J Clin Invest 2002;109:475-80.
-
(2002)
J Clin Invest
, vol.109
, pp. 475-480
-
-
Krude, H.1
Schutz, B.2
Biebermann, H.3
Von Moers, A.4
Schnabel, D.5
Neitzel, H.6
Tonnies, H.7
Weise, D.8
Lafferty, A.9
Schwarz, S.10
DeFelice, M.11
Von Deimling, A.12
Van Landeghem, F.13
DiLauro, R.14
Gruters, A.15
-
23
-
-
18344393450
-
Mutations in TITF-1 are associated with benign hereditary chorea
-
Breedveld GJ, van Dongen JW, Danesino C, Guala A, Percy AK, Dure LS, Harper P, Lazarou LP, van der Linde H, Joosse M, Gruters A, MacDonald ME, de Vries BB, Arts WF, Oostro BA, Krude H, Heutink P. Mutations in TITF-1 are associated with benign hereditary chorea. Hum Mol Genet 2002;11:971-9.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 971-979
-
-
Breedveld, G.J.1
Van Dongen, J.W.2
Danesino, C.3
Guala, A.4
Percy, A.K.5
Dure, L.S.6
Harper, P.7
Lazarou, L.P.8
Van Der Linde, H.9
Joosse, M.10
Gruters, A.11
MacDonald, M.E.12
De Vries, B.B.13
Arts, W.F.14
Oostro, B.A.15
Krude, H.16
Heutink, P.17
-
24
-
-
0033795193
-
Abnormal myelination in a patient with deletion 14q11.2q13.1
-
Ramelli GP, Remonda L, Lovblad KO, Hirsiger H, Moser H Abnormal myelination in a patient with deletion 14q11.2q13.1. Pediatr Neurol 2000;23:170-2.
-
(2000)
Pediatr Neurol
, vol.23
, pp. 170-172
-
-
Ramelli, G.P.1
Remonda, L.2
Lovblad, K.O.3
Hirsiger, H.4
Moser, H.5
-
25
-
-
0036556243
-
Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia
-
Das P, Stockton DW, Bauer C, Shaffer LG, D'Souza RN, Wright T, Patel PI Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia. Hum Genet 2002;110:371-6.
-
(2002)
Hum Genet
, vol.110
, pp. 371-376
-
-
Das, P.1
Stockton, D.W.2
Bauer, C.3
Shaffer, L.G.4
D'Souza, R.N.5
Wright, T.6
Patel, P.I.7
-
26
-
-
0033358650
-
Identification of a lacus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease)
-
Geschwind DH, Loginov M, Stern JM. Identification of a lacus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Am J Hum Genet 1999;65:764-72.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 764-772
-
-
Geschwind, D.H.1
Loginov, M.2
Stern, J.M.3
-
27
-
-
0030799204
-
A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families
-
Riley BP, Tahir E, Rajagopalan S, Mogudi-Carter M, Faure S, Weissenboch J, Jenkins T, Williamson R. A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families. Psychiatr Genet 1997;7:57-74.
-
(1997)
Psychiatr Genet
, vol.7
, pp. 57-74
-
-
Riley, B.P.1
Tahir, E.2
Rajagopalan, S.3
Mogudi-Carter, M.4
Faure, S.5
Weissenboch, J.6
Jenkins, T.7
Williamson, R.8
-
28
-
-
0033588176
-
Mice with reduced NMDA receptor expression display behaviors related to schizophrenia
-
Mohn AR, Gainetdinov RR, Caron MG, Koller BH. Mice with reduced NMDA receptor expression display behaviors related to schizophrenia. Cell 1999;98:427-36.
-
(1999)
Cell
, vol.98
, pp. 427-436
-
-
Mohn, A.R.1
Gainetdinov, R.R.2
Caron, M.G.3
Koller, B.H.4
-
29
-
-
0025853513
-
Schizophrenia and mental retardation in an adult male with a de nova interstitial deletion 9(q32q34.1)
-
Park JP, Moeschler JB, Berg SZ, Wurster-Hill DH Schizophrenia and mental retardation in an adult male with a de nova interstitial deletion 9(q32q34.1). J Med Genet 1991;28:282-3.
-
(1991)
J Med Genet
, vol.28
, pp. 282-283
-
-
Park, J.P.1
Moeschler, J.B.2
Berg, S.Z.3
Wurster-Hill, D.H.4
|