-
1
-
-
0027405968
-
Distorted distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase neurons in temporal lobe of schizophrenics implies anomalous cortical development
-
Akbarian, S., Bunney, W.E., Potkin, S.G., Wigal, S.B., Hagman, J.O., Sandman, C.A., and Jones, E.G. (1993a). Distorted distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase neurons in temporal lobe of schizophrenics implies anomalous cortical development. Arch. Gen. Psychiatry 50, 169-177.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 169-177
-
-
Akbarian, S.1
Bunney, W.E.2
Potkin, S.G.3
Wigal, S.B.4
Hagman, J.O.5
Sandman, C.A.6
Jones, E.G.7
-
2
-
-
0027394523
-
Altered distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase cells in frontal lobe of schizophrenics implies disturbances of cortical development
-
Akbarian, S., Vinuela, A., Kim, J.J., Potkin, S.G., Bunney, W.E., and Jones, E.G. (1993b). Altered distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase cells in frontal lobe of schizophrenics implies disturbances of cortical development. Arch. Gen. Psychiatry 50, 178-187.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 178-187
-
-
Akbarian, S.1
Vinuela, A.2
Kim, J.J.3
Potkin, S.G.4
Bunney, W.E.5
Jones, E.G.6
-
4
-
-
0030292383
-
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient
-
Angrist, M., Bolk, S., Halushka, M., Lapchak, P.A., and Chakravarti, A. (1996). Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient. Nature Genet. 14, 341-344.
-
(1996)
Nature Genet.
, vol.14
, pp. 341-344
-
-
Angrist, M.1
Bolk, S.2
Halushka, M.3
Lapchak, P.A.4
Chakravarti, A.5
-
5
-
-
0000913726
-
Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32
-
Antonarakis, S.E., Blouin, J.-L., Curran, M., Luebbert, H., Kazazian, H.H., Dombroski, B., Housman, D., Ton, C., Karayiorgou, M., Chakravarti, A., et al. (1996). Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32. Am. J. Hum. Genet. 59 (suppl.), A210.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, Issue.SUPPL.
-
-
Antonarakis, S.E.1
Blouin, J.-L.2
Curran, M.3
Luebbert, H.4
Kazazian, H.H.5
Dombroski, B.6
Housman, D.7
Ton, C.8
Karayiorgou, M.9
Chakravarti, A.10
-
6
-
-
0029100429
-
Association between clozapine response and allelic variation in 5-HT2A receptor gene
-
Arranz, M., Collier, D., Sodhi, M., Ball, D., Roberts, G., Price, J., Sham, P., and Kerwin, R. (1995). Association between clozapine response and allelic variation in 5-HT2A receptor gene. Lancet 346, 281-282.
-
(1995)
Lancet
, vol.346
, pp. 281-282
-
-
Arranz, M.1
Collier, D.2
Sodhi, M.3
Ball, D.4
Roberts, G.5
Price, J.6
Sham, P.7
Kerwin, R.8
-
7
-
-
0028198920
-
Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia?
-
Asherson, P., Walsh, C., Williams, J., Sargeant, M., Taylor, C., Clements, A., Gill, M., Owen, M., and McGuffin, P. (1994). Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia? Br. J. Psychiatry 164, 619-624.
-
(1994)
Br. J. Psychiatry
, vol.164
, pp. 619-624
-
-
Asherson, P.1
Walsh, C.2
Williams, J.3
Sargeant, M.4
Taylor, C.5
Clements, A.6
Gill, M.7
Owen, M.8
McGuffin, P.9
-
8
-
-
0028107678
-
Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred
-
Barr, C.L., Kennedy, J.L., Pakstis, A.J., Wetterberg, L., Sjogren, B., Bierut, L., Wadelius, C., Wahlstrom, J., Martinsson, T., Giuffra, L., et al. (1994). Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred. Am. J. Med. Genet. 54, 51-58.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 51-58
-
-
Barr, C.L.1
Kennedy, J.L.2
Pakstis, A.J.3
Wetterberg, L.4
Sjogren, B.5
Bierut, L.6
Wadelius, C.7
Wahlstrom, J.8
Martinsson, T.9
Giuffra, L.10
-
9
-
-
0026783363
-
Chromosomal aberrations and schizophrenia. Autosomes
-
Bassett, A.S. (1992). Chromosomal aberrations and schizophrenia. Autosomes. Br. J. Psychiatry 161, 323-334.
-
(1992)
Br. J. Psychiatry
, vol.161
, pp. 323-334
-
-
Bassett, A.S.1
-
10
-
-
0028215549
-
Evidence for anticipation in schizophrenia
-
Bassett, A.S., and Honer, W.G. (1994). Evidence for anticipation in schizophrenia. Am. J. Hum. Genet. 54, 864-870.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 864-870
-
-
Bassett, A.S.1
Honer, W.G.2
-
11
-
-
0023913272
-
Partial trisomy chromosome 5 cosegregating with schizophrenia
-
Bassett, A.S., McGillivray, B.C., Jones, B.D., and Pantzar, J.T. (1988). Partial trisomy chromosome 5 cosegregating with schizophrenia. Lancet 1, 799-801.
-
(1988)
Lancet
, vol.1
, pp. 799-801
-
-
Bassett, A.S.1
McGillivray, B.C.2
Jones, B.D.3
Pantzar, J.T.4
-
12
-
-
0343504177
-
Velocardiofacial syndrome and schizophrenia
-
Beatty, B., Squires, J., Weksberg, R., Chow, E., Hodgkinson, K., Bomba, M., Chen, M., and Bassett, A. (1996). Velocardiofacial syndrome and schizophrenia. Am. J. Hum Genet. 59 (suppl.), A87.
-
(1996)
Am. J. Hum Genet.
, vol.59
, Issue.SUPPL.
-
-
Beatty, B.1
Squires, J.2
Weksberg, R.3
Chow, E.4
Hodgkinson, K.5
Bomba, M.6
Chen, M.7
Bassett, A.8
-
13
-
-
85030304100
-
Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: Further support for a putative schizophrenia susceptibility locus at 5q21-23.1
-
in press
-
Bennett, R.L., Karayiorgou, M., Sobin, C.A., Norwood, T.H., and Kay, M. Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia susceptibility locus at 5q21-23.1. Am. J. Hum. Genet., in press.
-
Am. J. Hum. Genet.
-
-
Bennett, R.L.1
Karayiorgou, M.2
Sobin, C.A.3
Norwood, T.H.4
Kay, M.5
-
14
-
-
0028304859
-
Chromosome 18 DNA markers and manic-depressive illness: Evidence for a susceptibility gene
-
Berrettini, W.H., Ferraro, T.N., Goldin, L.R., Weeks, D.E., DeteraWadleigh, S., Nurnberger, J.I., Jr., and Gershon, E.S. (1994). Chromosome 18 DNA markers and manic-depressive illness: Evidence for a susceptibility gene. Proc. Natl. Acad. Sci. USA 91, 5918-5921.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 5918-5921
-
-
Berrettini, W.H.1
Ferraro, T.N.2
Goldin, L.R.3
Weeks, D.E.4
Deterawadleigh, S.5
Nurnberger J.I., Jr.6
Gershon, E.S.7
-
15
-
-
0025228017
-
Cognitive brain potentials and their applications
-
Blackwood, D.H.R., and Muir, W.J. (1990). Cognitive brain potentials and their applications. Br. J. Psychiatry 157 (suppl.), 96-99.
-
(1990)
Br. J. Psychiatry
, vol.157
, Issue.SUPPL.
, pp. 96-99
-
-
Blackwood, D.H.R.1
Muir, W.J.2
-
16
-
-
0026566108
-
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
-
Brook, J.D., McCurrach, M.E., Harley, H.G., Buckler, A.J., Church, D., Aburatani, H., Hunter, K., Stanton, V.P., Thirion, J.P., Hudson, T., et al. (1992). Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68, 799-808.
-
(1992)
Cell
, vol.68
, pp. 799-808
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
Buckler, A.J.4
Church, D.5
Aburatani, H.6
Hunter, K.7
Stanton, V.P.8
Thirion, J.P.9
Hudson, T.10
-
17
-
-
0026612908
-
Changes in dopamine D1, D2 and D3 receptor mRNA levels in rat brain following antipsychotic treatment
-
Buckland, P.R., O'Donovan, M., and McGuffin, P. (1992). Changes in dopamine D1, D2 and D3 receptor mRNA levels in rat brain following antipsychotic treatment. Psychopharmacology (Berl.) 106, 479-483.
-
(1992)
Psychopharmacology (Berl.)
, vol.106
, pp. 479-483
-
-
Buckland, P.R.1
O'Donovan, M.2
McGuffin, P.3
-
18
-
-
0028261615
-
Structural brain abnormalities as indicators of vulnerability to schizophrenia
-
Cannon, T.D., and Marco, E. (1994). Structural brain abnormalities as indicators of vulnerability to schizophrenia. Schizophr. Bull. 20, 89-102.
-
(1994)
Schizophr. Bull.
, vol.20
, pp. 89-102
-
-
Cannon, T.D.1
Marco, E.2
-
19
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
Cardon, L.R., Smith, S.D., Fulker, D.W., Kimberling, W.J., Pennington, B.F., and DeFries, J.C. (1994). Quantitative trait locus for reading disability on chromosome 6. Science 266, 276-279.
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
20
-
-
0028007447
-
Genetic anticipation. Expanding tandem repeats
-
Carpenter, N.J. (1994). Genetic anticipation. Expanding tandem repeats. Neurol. Clin. 12, 683-697.
-
(1994)
Neurol. Clin.
, vol.12
, pp. 683-697
-
-
Carpenter, N.J.1
-
21
-
-
10244219858
-
Accessing genetic information with high-density DNA arrays
-
Chee, M., and Fodor, S.P.A. (1996). Accessing genetic information with high-density DNA arrays. Science 274, 610-614.
-
(1996)
Science
, vol.274
, pp. 610-614
-
-
Chee, M.1
Fodor, S.P.A.2
-
22
-
-
0002694680
-
Schizotypy and schizophrenia
-
P. Bebbington and P. McGuffin, eds. (London: Heinemann)
-
Claridge, G. (1988). Schizotypy and schizophrenia. In Schizophrenia: The Major Issues, P. Bebbington and P. McGuffin, eds. (London: Heinemann), pp. 187-201.
-
(1988)
Schizophrenia: The Major Issues
, pp. 187-201
-
-
Claridge, G.1
-
23
-
-
0001470575
-
Tests of alternative models of the relationship of schizophrenic and affective psychoses
-
E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc.)
-
Cloninger, C.R. (1994). Tests of alternative models of the relationship of schizophrenic and affective psychoses. In Genetic Approaches to Mental Disorders, E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc.), pp. 149-162.
-
(1994)
Genetic Approaches to Mental Disorders
, pp. 149-162
-
-
Cloninger, C.R.1
-
24
-
-
0030927942
-
Catch me if you can: Are catechol-and indolamine genes pleiotropic QTLs for common mental disorders?
-
Collier, D.A., and Sham, P.C. (1997). Catch me if you can: are catechol-and indolamine genes pleiotropic QTLs for common mental disorders? Mol. Psychiatry 2, 181-183.
-
(1997)
Mol. Psychiatry
, vol.2
, pp. 181-183
-
-
Collier, D.A.1
Sham, P.C.2
-
25
-
-
0028147374
-
Genomic scan for genes predisposing to schizophrenia
-
Coon, H., Jensen, S., Holik, J., Hoff, M., Myles-Worsley, M., Reimherr, F., Wender, P., Waldo, M., Freedman, R., Leppert, M., and Byerley, W. (1994a). Genomic scan for genes predisposing to schizophrenia. Am. J. Med. Genet. 54, 59-71.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 59-71
-
-
Coon, H.1
Jensen, S.2
Holik, J.3
Hoff, M.4
Myles-Worsley, M.5
Reimherr, F.6
Wender, P.7
Waldo, M.8
Freedman, R.9
Leppert, M.10
Byerley, W.11
-
26
-
-
0028156726
-
Analysis of chromosome 22 markers in nine schizophrenia pedigrees
-
Coon, H., Holik, J., Hoff, M., Reimherr, F., Wender, P., Myles-Worsley, M., Waldo, M., Freedman, R., and Byerley, W. (1994b). Analysis of chromosome 22 markers in nine schizophrenia pedigrees. Am. J. Med. Genet. 54, 72-79.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 72-79
-
-
Coon, H.1
Holik, J.2
Hoff, M.3
Reimherr, F.4
Wender, P.5
Myles-Worsley, M.6
Waldo, M.7
Freedman, R.8
Byerley, W.9
-
27
-
-
0027076725
-
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene
-
Crocq, M.A., Mant, R., Asherson, P., Williams, J., Hode, Y., Mayerova, A., Collier, D., Lannfelt, L., Sokoloff, P., Schwartz, J.-C., et al. (1992). Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. J. Med. Genet. 29, 858-860.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 858-860
-
-
Crocq, M.A.1
Mant, R.2
Asherson, P.3
Williams, J.4
Hode, Y.5
Mayerova, A.6
Collier, D.7
Lannfelt, L.8
Sokoloff, P.9
Schwartz, J.-C.10
-
28
-
-
0028936444
-
Clinical and functional correlates of a dopamine D3 receptor polymorphism
-
Crocq, M.A., Duval, F., Mayerova, A., Sokoloff, P., Mokrani, M.C., and Macher, J.P. (1995). Clinical and functional correlates of a dopamine D3 receptor polymorphism. Hum. Psychopharmacol. 10, 19-24.
-
(1995)
Hum. Psychopharmacol.
, vol.10
, pp. 19-24
-
-
Crocq, M.A.1
Duval, F.2
Mayerova, A.3
Sokoloff, P.4
Mokrani, M.C.5
Macher, J.P.6
-
29
-
-
0002430055
-
The demise of the Kraepelinian binary system as a prelude to genetic advance
-
E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc.)
-
Crow, T.J. (1994). The demise of the Kraepelinian binary system as a prelude to genetic advance. In Genetic Approaches To Mental Disorders, E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc.), pp. 163-192.
-
(1994)
Genetic Approaches To Mental Disorders
, pp. 163-192
-
-
Crow, T.J.1
-
30
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies, J.L., Kawaguchi, Y., Bennett, S.T., Copeman, J.B., Cordell, H.J., Pritchard, LE., Reed, P.W., Gough, S.C.L., Jenkins, S.C., Palmer, S.M., et al. (1994). A genome-wide search for human type 1 diabetes susceptibility genes. Nature 371, 130-136.
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
Reed, P.W.7
Gough, S.C.L.8
Jenkins, S.C.9
Palmer, S.M.10
-
31
-
-
0028841035
-
An association study of a Neurotrophin-3 (NT-3) gene polymorphism with schizophrenia
-
Dawson, E., Powell, J.F., Sham, P.C., Nothen, M., Crocq, M.A., Propping, P., Korner, J., Rietschel, M., Vanos J., Wright, P., et al. (1995). An association study of a Neurotrophin-3 (NT-3) gene polymorphism with schizophrenia. Acta Psychiatr. Scand. 92, 425-428.
-
(1995)
Acta Psychiatr. Scand.
, vol.92
, pp. 425-428
-
-
Dawson, E.1
Powell, J.F.2
Sham, P.C.3
Nothen, M.4
Crocq, M.A.5
Propping, P.6
Korner, J.7
Rietschel, M.8
Vanos, J.9
Wright, P.10
-
32
-
-
0028064295
-
Schizophrenia and sex chromosome anomalies
-
Delisi, L.E., Friedrich, U., Wahlstrom, J., Boccio-Smith, A., Forsman, A., Eklund, K., and Crow, T.J. (1994). Schizophrenia and sex chromosome anomalies. Schizophr. Bull. 20, 495-505.
-
(1994)
Schizophr. Bull.
, vol.20
, pp. 495-505
-
-
Delisi, L.E.1
Friedrich, U.2
Wahlstrom, J.3
Boccio-Smith, A.4
Forsman, A.5
Eklund, K.6
Crow, T.J.7
-
33
-
-
0024385396
-
Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders
-
Detera-Wadleigh, S.D., Goldin, L.R., Sherrington, R., et al., (1989). Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders. Nature 340, 391-393.
-
(1989)
Nature
, vol.340
, pp. 391-393
-
-
Detera-Wadleigh, S.D.1
Goldin, L.R.2
Sherrington, R.3
-
34
-
-
0025886783
-
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
-
Dietz, H.C., Cutting, G.R., Pyeritz, R.E., Maslen, C.L., Sakai, L.Y., Corson, G.M., Puffenberger, E.G., Hamosh, A., Nanthakumar, E., Curristin, S., et al. (1991). Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 352, 337-339.
-
(1991)
Nature
, vol.352
, pp. 337-339
-
-
Dietz, H.C.1
Cutting, G.R.2
Pyeritz, R.E.3
Maslen, C.L.4
Sakai, L.Y.5
Corson, G.M.6
Puffenberger, E.G.7
Hamosh, A.8
Nanthakumar, E.9
Curristin, S.10
-
35
-
-
0029655911
-
Absence makes the search grow longer
-
Dobyns, W.B. (1996). Absence makes the search grow longer. Am. J. Hum. Genet. 58, 7-16.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 7-16
-
-
Dobyns, W.B.1
-
36
-
-
0027370619
-
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: Implications for genetic counselling and prenatal diagnosis
-
Driscoll, D.A., Salvin, J., Sellinger, B., Budarf, M.L., McDonald-McGinn, D.M., Zackai, E.H., and Emanuel, B.S. (1993). Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis. J. Med. Genet. 30, 813-817.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 813-817
-
-
Driscoll, D.A.1
Salvin, J.2
Sellinger, B.3
Budarf, M.L.4
McDonald-McGinn, D.M.5
Zackai, E.H.6
Emanuel, B.S.7
-
37
-
-
0026774331
-
Inter and intrafamilial heterogeneity: Effective sampling strategies and comparison analysis methods
-
Durner, M., Greenberg, D.A., and Hodge, S.E. (1992). Inter and intrafamilial heterogeneity: effective sampling strategies and comparison analysis methods. Am. J. Hum. Genet. 51, 859-870.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 859-870
-
-
Durner, M.1
Greenberg, D.A.2
Hodge, S.E.3
-
38
-
-
0029880896
-
Systematic screening for mutations in the human serotonin-2A (5HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia
-
Erdmann, J., Shimron-Abarbanell, D., and Rietschel, M. (1996). Systematic screening for mutations in the human serotonin-2A (5HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia. Hum. Genet. 97, 614-619.
-
(1996)
Hum. Genet.
, vol.97
, pp. 614-619
-
-
Erdmann, J.1
Shimron-Abarbanell, D.2
Rietschel, M.3
-
39
-
-
0023255401
-
Twin concordance for DSM-III schizophrenia: Scrutinising the validity of the definition
-
Farmer, A.E., McGuffin, P., and Gottesman, I.I. (1987). Twin concordance for DSM-III schizophrenia: scrutinising the validity of the definition. Arch. Gen. Psychiatry 44, 634-641.
-
(1987)
Arch. Gen. Psychiatry
, vol.44
, pp. 634-641
-
-
Farmer, A.E.1
McGuffin, P.2
Gottesman, I.I.3
-
40
-
-
0028798545
-
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
-
Flint, J., Wilkie, A.O.M., Buckle, V.J., Winter, R.M., Holland, A.J., and McDermid, H.E. (1995). The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nature Genet. 9, 132-139.
-
(1995)
Nature Genet.
, vol.9
, pp. 132-139
-
-
Flint, J.1
Wilkie, A.O.M.2
Buckle, V.J.3
Winter, R.M.4
Holland, A.J.5
McDermid, H.E.6
-
41
-
-
12644303225
-
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
-
Freedman, R., Coon, H., Myles-Worsley, M., Orr-Urtreger, A., Olincy, A., Davis, A., Polymeropoulos, M., Holik, J., Hopkins, J., Hoff, M., et al. (1997). Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proc. Natl. Acad. Sci. USA 94, 587-592.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 587-592
-
-
Freedman, R.1
Coon, H.2
Myles-Worsley, M.3
Orr-Urtreger, A.4
Olincy, A.5
Davis, A.6
Polymeropoulos, M.7
Holik, J.8
Hopkins, J.9
Hoff, M.10
-
42
-
-
0027165146
-
Evidence of chromosomal fragile sites in schizophrenic patients
-
Garofalo, G., Ragusa, R.M., Argiolas, A., Scavuzzo, C., Spina, E., and Barletta C. (1993). Evidence of chromosomal fragile sites in schizophrenic patients. Annales de Genetique 36, 132-135.
-
(1993)
Annales de Genetique
, vol.36
, pp. 132-135
-
-
Garofalo, G.1
Ragusa, R.M.2
Argiolas, A.3
Scavuzzo, C.4
Spina, E.5
Barletta, C.6
-
43
-
-
0028065409
-
Translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia
-
Gordon, C.T., Krasnewich, D., White, B., Lenane, M., and Rapoport, J.L. (1994). Translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia. J. Autism Dev. Disord. 24, 537-545.
-
(1994)
J. Autism Dev. Disord.
, vol.24
, pp. 537-545
-
-
Gordon, C.T.1
Krasnewich, D.2
White, B.3
Lenane, M.4
Rapoport, J.L.5
-
45
-
-
0024535782
-
Minor physical anomalies in schizophrenia
-
Green, M.F., Satz, P., Gaier, D.J., Ganzell, S., and Kharabi, F. (1989). Minor physical anomalies in schizophrenia. Schizophr. Bull. 15, 91-99.
-
(1989)
Schizophr. Bull.
, vol.15
, pp. 91-99
-
-
Green, M.F.1
Satz, P.2
Gaier, D.J.3
Ganzell, S.4
Kharabi, F.5
-
46
-
-
0020025405
-
Minor physical anomalies in alcoholic and schizophrenic adults and hyperactive and autistic children
-
Gualtieri, C.T., Adams, A., Shen, C.D., and Loiselle, D. (1982). Minor physical anomalies in alcoholic and schizophrenic adults and hyperactive and autistic children. Am. J. Psychiatry 139, 640-643.
-
(1982)
Am. J. Psychiatry
, vol.139
, pp. 640-643
-
-
Gualtieri, C.T.1
Adams, A.2
Shen, C.D.3
Loiselle, D.4
-
47
-
-
0021010884
-
The incidence of minor physical anomalies in adult male schizophrenics
-
Guy, J.D., Majorski, M.V., Wallace, C.J., and Guy, M.P. (1983). The incidence of minor physical anomalies in adult male schizophrenics. Schizophr. Bull. 9, 571-582.
-
(1983)
Schizophr. Bull.
, vol.9
, pp. 571-582
-
-
Guy, J.D.1
Majorski, M.V.2
Wallace, C.J.3
Guy, M.P.4
-
48
-
-
0013937338
-
Psychiatric disorders in foster home reared children of schizophrenic mothers
-
Heston, L.L. (1966). Psychiatric disorders in foster home reared children of schizophrenic mothers. Br. J. Psychiatry 112, 819-825.
-
(1966)
Br. J. Psychiatry
, vol.112
, pp. 819-825
-
-
Heston, L.L.1
-
49
-
-
0025355756
-
A balanced chromosomal translocation partially cosegregating with psychotic illness in a family
-
Holland, T., and Gosden, C. (1990). A balanced chromosomal translocation partially cosegregating with psychotic illness in a family. Psychol. Res. 32, 1-8.
-
(1990)
Psychol. Res.
, vol.32
, pp. 1-8
-
-
Holland, T.1
Gosden, C.2
-
50
-
-
0023894061
-
A single dominant gene can account for eye tracking dysfunctions and schizophrenia in offspring of discordant twins
-
Holzman, P.S., Kringlen, E., Matthysse, S., Flanagan, S.D., Lipton, R.B., Cramer, G., Levin, S., Lange, K., and Levy, D.L. (1988). A single dominant gene can account for eye tracking dysfunctions and schizophrenia in offspring of discordant twins. Arch. Gen. Psychiatry 45, 641-647.
-
(1988)
Arch. Gen. Psychiatry
, vol.45
, pp. 641-647
-
-
Holzman, P.S.1
Kringlen, E.2
Matthysse, S.3
Flanagan, S.D.4
Lipton, R.B.5
Cramer, G.6
Levin, S.7
Lange, K.8
Levy, D.L.9
-
51
-
-
0029988749
-
Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia
-
Inayama, Y., Yoneda, H., Sakai, T., Ishida, T., Nonomura, Y., Kono, Y., Takahata, R., Koh, J., Sakai, J., Takai, A., et al. (1996). Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia. Am. J. Med. Genet. 67, 103-105.
-
(1996)
Am. J. Med. Genet.
, vol.67
, pp. 103-105
-
-
Inayama, Y.1
Yoneda, H.2
Sakai, T.3
Ishida, T.4
Nonomura, Y.5
Kono, Y.6
Takahata, R.7
Koh, J.8
Sakai, J.9
Takai, A.10
-
52
-
-
4243822617
-
Interstitial deletions of chromosome 22q11 in very early onset schizophrenia
-
Jacobsen, L.K., Yan, W.L., Guan, X.Y., Krasnewich, D., Kumra, S., Long, R.T., Sidransky, E., Ginns, E.I, and Rapoport, J.L. (1996). Interstitial deletions of chromosome 22q11 in very early onset schizophrenia. Am. J. Hum. Genet. 59 (suppl.), A120.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, Issue.SUPPL.
-
-
Jacobsen, L.K.1
Yan, W.L.2
Guan, X.Y.3
Krasnewich, D.4
Kumra, S.5
Long, R.T.6
Sidransky, E.7
Ginns, E.I.8
Rapoport, J.L.9
-
53
-
-
0027262460
-
Lack of association between schizophrenia and alleles at the D3 receptor gene
-
Jonsson, E., Lannfelt, L., Sokoloff, P., Schwartz, J.C., and Sedvall, G. (1993). Lack of association between schizophrenia and alleles at the D3 receptor gene. Acta Psychiatr. Scand. 87, 345-349.
-
(1993)
Acta Psychiatr. Scand.
, vol.87
, pp. 345-349
-
-
Jonsson, E.1
Lannfelt, L.2
Sokoloff, P.3
Schwartz, J.C.4
Sedvall, G.5
-
54
-
-
0026529399
-
Sensory gating deficits in schizophrenia: New results
-
Judd, L.L., McAdams, L., Budnick, B., and Braff, D.L. (1992). Sensory gating deficits in schizophrenia: new results. Am. J. Psychiatry 149, 488-493.
-
(1992)
Am. J. Psychiatry
, vol.149
, pp. 488-493
-
-
Judd, L.L.1
McAdams, L.2
Budnick, B.3
Braff, D.L.4
-
56
-
-
0000606592
-
The genetic theory of schizophrenia: An analysis of 691 schizophrenic twin index families
-
Kallman, F.J. (1946). The genetic theory of schizophrenia: An analysis of 691 schizophrenic twin index families. Am. J. Psychiatry 103, 309-322.
-
(1946)
Am. J. Psychiatry
, vol.103
, pp. 309-322
-
-
Kallman, F.J.1
-
57
-
-
0028559999
-
The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia
-
Kalsi, G., Mankoo, B.S., Brynjolfsson, J., Curtis, D., Read, T., Murphy, P., Sharma, T., Petursson, H., and Gurling, H.M. (1994). The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia. Psychiatr. Genet. 4, 219-227.
-
(1994)
Psychiatr. Genet.
, vol.4
, pp. 219-227
-
-
Kalsi, G.1
Mankoo, B.S.2
Brynjolfsson, J.3
Curtis, D.4
Read, T.5
Murphy, P.6
Sharma, T.7
Petursson, H.8
Gurling, H.M.9
-
58
-
-
0028672996
-
Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model
-
Karayiorgou, M., Kasch, L., Lasseter, V.K., Hwang, J., Elango, R., Bernardini, D.J., Kimberland, M., Babb, R., Francomano, C.A., Wolyniec, P.S., et al. (1994). Report from the Maryland Epidemiology Schizophrenia Linkage Study: no evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model. Am. J. Med. Genet. 54, 345-353.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 345-353
-
-
Karayiorgou, M.1
Kasch, L.2
Lasseter, V.K.3
Hwang, J.4
Elango, R.5
Bernardini, D.J.6
Kimberland, M.7
Babb, R.8
Francomano, C.A.9
Wolyniec, P.S.10
-
59
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
Karayiorgou, M., Morris, M.A., Morrow, B., Shprintzen, R.J., Goldberg, R., Borrow, J., Gos, A., Nestadt, G., Wolyniec, P.S., Lasseter, V.K., et al. (1995). Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci. USA 92, 7612-7616.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
Shprintzen, R.J.4
Goldberg, R.5
Borrow, J.6
Gos, A.7
Nestadt, G.8
Wolyniec, P.S.9
Lasseter, V.K.10
-
60
-
-
12644271199
-
Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Karayiorgou, M., Gogos, J.A., Galke, B.L., Jeffery, J.A., Nestadt, G., Wolyniec, P.S., Antonarakis, S.E., Kazazian, H.H., Housman, D.E., Driscoll, D.A., and Pulver, A.E. (1996). Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus. In Cold Spring Harbor Symposia on Quantitative Biology, Vol. LXI (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press), pp. 835-843.
-
(1996)
Cold Spring Harbor Symposia on Quantitative Biology
, vol.61
, pp. 835-843
-
-
Karayiorgou, M.1
Gogos, J.A.2
Galke, B.L.3
Jeffery, J.A.4
Nestadt, G.5
Wolyniec, P.S.6
Antonarakis, S.E.7
Kazazian, H.H.8
Housman, D.E.9
Driscoll, D.A.10
Pulver, A.E.11
-
61
-
-
0343504179
-
Identification of sequence variants and analysis of the role of the COMT gene in schizophrenia susceptibility
-
in press
-
Karayiorgou, M., Gogos, J.A., Galke, B.L., Wolyniec, P.S., Nestadt, G., Antonarakis, S.E., Kazazian, H.H., Housman, D.E., and Pulver, A.E. (1997a). Identification of sequence variants and analysis of the role of the COMT gene in schizophrenia susceptibility. Biol. Psychiatry, in press.
-
(1997)
Biol. Psychiatry
-
-
Karayiorgou, M.1
Gogos, J.A.2
Galke, B.L.3
Wolyniec, P.S.4
Nestadt, G.5
Antonarakis, S.E.6
Kazazian, H.H.7
Housman, D.E.8
Pulver, A.E.9
-
62
-
-
0030895285
-
Genotype determining low COMT activity associated with increased susceptibility to obsessive-compulsive disorder
-
Karayiorgou, M., Altemus, M., Galke, B.L., Goldman, D., Murphy, D.L., Ott, J., and Gogos, J.A. (1997b). Genotype determining low COMT activity associated with increased susceptibility to obsessive-compulsive disorder. Proc. Natl. Acad. Sci. USA 94, 4572-4575.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 4572-4575
-
-
Karayiorgou, M.1
Altemus, M.2
Galke, B.L.3
Goldman, D.4
Murphy, D.L.5
Ott, J.6
Gogos, J.A.7
-
63
-
-
0024437794
-
Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish
-
Kelsoe, J.R., Ginns, E.I., Egeland, J.A., Gerhard, D.S., Goldstein, A.M., Bale, S.J., Pauls, D.L., Long, R.T., Kidd., K.K., and Conte, G. (1989). Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish. Nature 342, 238-243.
-
(1989)
Nature
, vol.342
, pp. 238-243
-
-
Kelsoe, J.R.1
Ginns, E.I.2
Egeland, J.A.3
Gerhard, D.S.4
Goldstein, A.M.5
Bale, S.J.6
Pauls, D.L.7
Long, R.T.8
Kidd, K.K.9
Conte, G.10
-
64
-
-
0027216273
-
The genetics of schizophrenia: A current, genetic-epidemiologic perspective
-
Kendler, K.S., and Diehl, S.R. (1993). The genetics of schizophrenia: a current, genetic-epidemiologic perspective. Schizophr. Bull. 19, 261-285.
-
(1993)
Schizophr. Bull.
, vol.19
, pp. 261-285
-
-
Kendler, K.S.1
Diehl, S.R.2
-
65
-
-
0027272195
-
The roscommon family study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives
-
Kendler, K.S., McGuire, M., Gruenberg, A.M., O'Hare, A., Spellman, M., and Walsh, D. (1993a). The Roscommon family study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives. Arch. Gen. Psychiatry 50, 527-540.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 527-540
-
-
Kendler, K.S.1
McGuire, M.2
Gruenberg, A.M.3
O'Hare, A.4
Spellman, M.5
Walsh, D.6
-
66
-
-
0027383067
-
The roscom mon family study. III. Schizophrenia-related personality disorders in relatives
-
Kendler, K.S., McGuire, M., Gruenberg, A.M., O'Hare, A., Spellman, M., and Walsh D. (1993b).The Roscom mon family study. III. Schizophrenia-related personality disorders in relatives. Arch. Gen. Psychiatry 50, 781-788.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 781-788
-
-
Kendler, K.S.1
McGuire, M.2
Gruenberg, A.M.3
O'Hare, A.4
Spellman, M.5
Walsh, D.6
-
67
-
-
0002906377
-
The biological and adoptive families of adopted individuals who become schizophrenic
-
L.C. Wynne, R.L. Cromwell, and S. Matthysse, eds. (New York: John Wiley and Sons)
-
Kety, S.S., Rosenthal, D., Wender, P.H., Schulsinger, F., and Jacobsen, B. (1978). The biological and adoptive families of adopted individuals who become schizophrenic. In The Nature of Schizophrenia, L.C. Wynne, R.L. Cromwell, and S. Matthysse, eds. (New York: John Wiley and Sons), pp. 25-37.
-
(1978)
The Nature of Schizophrenia
, pp. 25-37
-
-
Kety, S.S.1
Rosenthal, D.2
Wender, P.H.3
Schulsinger, F.4
Jacobsen, B.5
-
68
-
-
0028206470
-
Mental illness in the biological and adoptive relatives of schizophrenic adoptees: Replication of the Copenhagen study in the rest of Denmark
-
Kety, S.S., Wender, P., Jacobsen, B., Ingraham, L.J., Jansson, L., and Faber, B. (1994). Mental illness in the biological and adoptive relatives of schizophrenic adoptees: replication of the Copenhagen study in the rest of Denmark. Arch. Gen. Psychiatry 51, 442-455.
-
(1994)
Arch. Gen. Psychiatry
, vol.51
, pp. 442-455
-
-
Kety, S.S.1
Wender, P.2
Jacobsen, B.3
Ingraham, L.J.4
Jansson, L.5
Faber, B.6
-
69
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander, E.S., and Schork, N.J. (1994). Genetic dissection of complex traits. Science 265, 2037-2048.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
70
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander, E., and Kruglyak, L. (1995). Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nature Genet. 11, 241-247.
-
(1995)
Nature Genet.
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
71
-
-
0010587883
-
Minor physical anomalies in schizophrenia
-
Lane, A., Cassidy, B., Murphy, P., Sheppard, N., Horgan, R., Keenan, J., Waddington, J.L., Larkin, C., and O'Callaghan, E. (1993). Minor physical anomalies in schizophrenia. Ir. J. Med. Sci. 162 (suppl.), 27-28.
-
(1993)
Ir. J. Med. Sci.
, vol.162
, Issue.SUPPL.
, pp. 27-28
-
-
Lane, A.1
Cassidy, B.2
Murphy, P.3
Sheppard, N.4
Horgan, R.5
Keenan, J.6
Waddington, J.L.7
Larkin, C.8
O'Callaghan, E.9
-
72
-
-
0000101935
-
Amino-acid substitution in the dopamine D3 receptor as a useful polymorphism for investigating psychiatric disorders
-
Lannfelt, L., Sokoloff, P., Martres, M., et al. (1992). Amino-acid substitution in the dopamine D3 receptor as a useful polymorphism for investigating psychiatric disorders. Psychiatr. Genet. 2, 249-256.
-
(1992)
Psychiatr. Genet.
, vol.2
, pp. 249-256
-
-
Lannfelt, L.1
Sokoloff, P.2
Martres, M.3
-
73
-
-
0029651299
-
Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3
-
Lasseter, V.K., Pulver, A.E., Wolyniec, P.S., Nestadt, G., Meyers, D., Karayiorgou, M., Housman, D., Antonarakis, S., Kazazian, H., Kasch, L., et al. (1995). Follow-up report of potential linkage for schizophrenia on chromosome 22q: part 3. Am. J. Med. Genet. 60, 172-173.
-
(1995)
Am. J. Med. Genet.
, vol.60
, pp. 172-173
-
-
Lasseter, V.K.1
Pulver, A.E.2
Wolyniec, P.S.3
Nestadt, G.4
Meyers, D.5
Karayiorgou, M.6
Housman, D.7
Antonarakis, S.8
Kazazian, H.9
Kasch, L.10
-
74
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad, E., Wasco, W., Poorkaj, P., Romano, D.M., Oshima, J., Pettingell, H., Yu, C., Jondro, P.D., Schmidt, S.D., Wang, K., et al. (1995). Candidate gene for the chromosome 1 familial Alzheimer's disease locus. Science 269, 973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
Pettingell, H.6
Yu, C.7
Jondro, P.D.8
Schmidt, S.D.9
Wang, K.10
-
75
-
-
0029851636
-
Preferential transmission of the high activity allele of COMT in schizophrenia
-
Li, T., Sham, P.C., Vallada, H., Xie, T., Tang, X., Murray, R.M., Liu, X., and Collier, D.A. (1996). Preferential transmission of the high activity allele of COMT in schizophrenia. Psychiatr. Genet. 6, 131-133.
-
(1996)
Psychiatr. Genet.
, vol.6
, pp. 131-133
-
-
Li, T.1
Sham, P.C.2
Vallada, H.3
Xie, T.4
Tang, X.5
Murray, R.M.6
Liu, X.7
Collier, D.A.8
-
76
-
-
0029565202
-
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32
-
Lin, M.W., Curtis, D., Williams, N., Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, M., Gill, M., and Powell, J. (1995). Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatr. Genet. 5, 117-126.
-
(1995)
Psychiatr. Genet.
, vol.5
, pp. 117-126
-
-
Lin, M.W.1
Curtis, D.2
Williams, N.3
Arranz, M.4
Nanko, S.5
Collier, D.6
McGuffin, P.7
Murray, R.8
Owen, M.9
Gill, M.10
Powell, J.11
-
77
-
-
0029240699
-
Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method
-
Lindblad, K., Nylander, P., De Bruyn, A., Sourey, D., Zander, C., Endstrom, C., Holmgren, G., Hudson, T., Chotai, J., Mendlewicz, J., et al. (1995). Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method. Neurobiol. Dis. 2, 55-59.
-
(1995)
Neurobiol. Dis.
, vol.2
, pp. 55-59
-
-
Lindblad, K.1
Nylander, P.2
De Bruyn, A.3
Sourey, D.4
Zander, C.5
Endstrom, C.6
Holmgren, G.7
Hudson, T.8
Chotai, J.9
Mendlewicz, J.10
-
78
-
-
0026683152
-
Association of schizophrenia and partial trisomy of chromosome 5p. A case report
-
Malaspina, D., Warburton, D., Amador, X., Harris, M., and Kaufmann, C.A. (1992). Association of schizophrenia and partial trisomy of chromosome 5p. A case report. Schizophr. Res. 7, 191-196.
-
(1992)
Schizophr. Res.
, vol.7
, pp. 191-196
-
-
Malaspina, D.1
Warburton, D.2
Amador, X.3
Harris, M.4
Kaufmann, C.A.5
-
79
-
-
0027958429
-
Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia
-
Mant, R., Williams, J., Asherson, P., Parfitt, E., McGuffin, P., and Owen, M.J. (1994). Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia. Am. J. Med. Genet. 54, 21-26.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 21-26
-
-
Mant, R.1
Williams, J.2
Asherson, P.3
Parfitt, E.4
McGuffin, P.5
Owen, M.J.6
-
80
-
-
0029842548
-
Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33
-
Marquet, S., Abel, L., Hillaire, D., Dessin, H., Kalil, J., Feingold, J., Weissenbach, J., and Dessin, A.J. (1996). Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33. Nature Genet. 14, 181-184.
-
(1996)
Nature Genet.
, vol.14
, pp. 181-184
-
-
Marquet, S.1
Abel, L.2
Hillaire, D.3
Dessin, H.4
Kalil, J.5
Feingold, J.6
Weissenbach, J.7
Dessin, A.J.8
-
81
-
-
0027523934
-
A balanced 2:18 translocation and familial schizophrenia: Falling short of an association
-
Maziade, M., Debraekeleer, M., Genest, P., Cliche, D., Fournier, J.P., Garneau, Y., Shriqui, C., Roy, M.A., Nicole, L., and Raymond, V. (1993). A balanced 2:18 translocation and familial schizophrenia: falling short of an association. Arch. Gen. Psychiatry 50, 73-75.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 73-75
-
-
Maziade, M.1
Debraekeleer, M.2
Genest, P.3
Cliche, D.4
Fournier, J.P.5
Garneau, Y.6
Shriqui, C.7
Roy, M.A.8
Nicole, L.9
Raymond, V.10
-
82
-
-
0029165757
-
Perinatal risk factors and schizophrenia: Selective review and methodological concerns
-
McNeil, T.F. (1995). Perinatal risk factors and schizophrenia: selective review and methodological concerns. Epidemiol. Rev. 17, 107-112.
-
(1995)
Epidemiol. Rev.
, vol.17
, pp. 107-112
-
-
McNeil, T.F.1
-
83
-
-
0029242309
-
Mitral valve prolapse in a case of Marfan syndrome with congenital cardiac disease, chronic obstructive pulmonary disease and schizophrenia
-
Melissari, M., Giordano, G., Crafa, P., Martella, E.M., and Ricci, R. (1995). Mitral valve prolapse in a case of Marfan syndrome with congenital cardiac disease, chronic obstructive pulmonary disease and schizophrenia. Pathologica 87, 78-81.
-
(1995)
Pathologica
, vol.87
, pp. 78-81
-
-
Melissari, M.1
Giordano, G.2
Crafa, P.3
Martella, E.M.4
Ricci, R.5
-
84
-
-
0030896842
-
Association between psychiatric disorders and Marfan's syndrome in a large sardinian family with a high prevalence of cardiac abnormalities
-
Mercuro, G., Carpiniello, B., Ruscazio, M., Zoncu, S., Montisci, R., Rudas, N., and Cherchi, A. (1997). Association between psychiatric disorders and Marfan's syndrome in a large Sardinian family with a high prevalence of cardiac abnormalities.Clin. Cardiol. 20, 243-245.
-
(1997)
Clin. Cardiol.
, vol.20
, pp. 243-245
-
-
Mercuro, G.1
Carpiniello, B.2
Ruscazio, M.3
Zoncu, S.4
Montisci, R.5
Rudas, N.6
Cherchi, A.7
-
85
-
-
0028871785
-
An international two-stage genome-wide search for schizophrenia susceptibility genes
-
Moises, H.W., Yang, L., Kristbjarnarson, H., Wiese, C., Byerley, W., Macciardi, F., Arolt, V., Blackwood, D., Liu, X., Sjogren, B., et al. (1995a). An international two-stage genome-wide search for schizophrenia susceptibility genes. Nature Genet. 11, 321-325.
-
(1995)
Nature Genet.
, vol.11
, pp. 321-325
-
-
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
-
86
-
-
0028786445
-
Potential linkage disequilibrium between schizophrenia and locus D22s278 on the long arm of chromosome 22
-
Moises, H.W., Yang, L., Li, T., Havsteen, B., Fimmers, R., Baur, M.P., Liu, X., and Gottesman, I.I. (1995b). Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22. Am. J. Med. Genet. 60, 465-467.
-
(1995)
Am. J. Med. Genet.
, vol.60
, pp. 465-467
-
-
Moises, H.W.1
Yang, L.2
Li, T.3
Havsteen, B.4
Fimmers, R.5
Baur, M.P.6
Liu, X.7
Gottesman, I.I.8
-
87
-
-
0028784037
-
CAG repeat expansions and schizophrenia: Association with disease in females and with early age at onset
-
Morris, A.G., Gaitonde, E., McKenna, P.J., Mollon, J.D., and Hunt, D.M. (1995). CAG repeat expansions and schizophrenia: association with disease in females and with early age at onset. Hum. Mol. Genet. 4, 1957-1961.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1957-1961
-
-
Morris, A.G.1
Gaitonde, E.2
McKenna, P.J.3
Mollon, J.D.4
Hunt, D.M.5
-
88
-
-
0027992744
-
Neurodevelopmental schizophrenia: The rediscovery of dementia praecox
-
Murray, R.M. (1994). Neurodevelopmental schizophrenia: the rediscovery of dementia praecox. Br. J. Psychiatry 165 (suppl.), 6-12.
-
(1994)
Br. J. Psychiatry
, vol.165
, Issue.SUPPL.
, pp. 6-12
-
-
Murray, R.M.1
-
89
-
-
0023638471
-
Is schizophrenia a neurodevelopmental disorder?
-
Murray, R.M., and Lewis, S.W. (1987). Is schizophrenia a neurodevelopmental disorder? Br. Med. J. Clin. Res. Ed. 295, 681-682.
-
(1987)
Br. Med. J. Clin. Res. Ed.
, vol.295
, pp. 681-682
-
-
Murray, R.M.1
Lewis, S.W.2
-
90
-
-
0027420408
-
A study of the association between schizophrenia and the dopamine d3 receptor gene
-
Nanko, S., Sasaki, T., Fukuda, R., Hattori, M., Dai, X.Y., Kazamatsuri, H., Kuwata, S., Juji, T., and Gill, M. (1993a). A study of the association between schizophrenia and the dopamine D3 receptor gene. Hum. Genet. 92, 336-338.
-
(1993)
Hum. Genet.
, vol.92
, pp. 336-338
-
-
Nanko, S.1
Sasaki, T.2
Fukuda, R.3
Hattori, M.4
Dai, X.Y.5
Kazamatsuri, H.6
Kuwata, S.7
Juji, T.8
Gill, M.9
-
91
-
-
0027208102
-
Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia
-
Nanko, S., Kunugi, H., Sasaki, T., Fukuda, R., Kawate, T., and Kazamatsuri, H. (1993b). Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia. Biol. Psychiatry 33, 655-658.
-
(1993)
Biol. Psychiatry
, vol.33
, pp. 655-658
-
-
Nanko, S.1
Kunugi, H.2
Sasaki, T.3
Fukuda, R.4
Kawate, T.5
Kazamatsuri, H.6
-
92
-
-
0028286735
-
Neurotrophin-3 gene polymorphism associated with schizophrenia
-
Nanko, S., Hattori, M., Kuwata, S., Sasaki, T., Fukuda, R., Dai, X.Y., Yamaguchi, K., Shibata, Y., and Kazamatsuri, H. (1994). Neurotrophin-3 gene polymorphism associated with schizophrenia. Acta Psychiatr. Scand. 89, 390-392.
-
(1994)
Acta Psychiatr. Scand.
, vol.89
, pp. 390-392
-
-
Nanko, S.1
Hattori, M.2
Kuwata, S.3
Sasaki, T.4
Fukuda, R.5
Dai, X.Y.6
Yamaguchi, K.7
Shibata, Y.8
Kazamatsuri, H.9
-
93
-
-
0027142626
-
Association study of schizophrenia with dopamine D3 receptor gene polymorphisms: Probable effects of family history of schizophrenia?
-
Nimgaonkar, V.L., Zhang, X.R., Caldwell, J.G., Ganguli, R., and Chakravarti, A. (1993a). Association study of schizophrenia with dopamine D3 receptor gene polymorphisms: probable effects of family history of schizophrenia? Am. J. Med. Genet. 48, 214-217.
-
(1993)
Am. J. Med. Genet.
, vol.48
, pp. 214-217
-
-
Nimgaonkar, V.L.1
Zhang, X.R.2
Caldwell, J.G.3
Ganguli, R.4
Chakravarti, A.5
-
94
-
-
0027476382
-
A negative association of schizophrenia with an allele of the HLA DQB1 gene among African-Americans
-
Nimgaonkar, V.L., Ganguli, R., Rudert, W.A., Vavassori, C., Rabin, B.S., and Trucco, M. (1993b). A negative association of schizophrenia with an allele of the HLA DQB1 gene among African-Americans. Schizophr. Res. 8, 199-209.
-
(1993)
Schizophr. Res.
, vol.8
, pp. 199-209
-
-
Nimgaonkar, V.L.1
Ganguli, R.2
Rudert, W.A.3
Vavassori, C.4
Rabin, B.S.5
Trucco, M.6
-
95
-
-
0030044987
-
Further evidence for an association between schizophrenia and the HLA DQB1 gene locus
-
Nimgaonkar, V.L., Rudert, W.A., Zhang, X.R., Tsoi, W.F., Trucco, M., and Saha, N. (1995). Further evidence for an association between schizophrenia and the HLA DQB1 gene locus. Schizophr. Res. 18, 43-49.
-
(1995)
Schizophr. Res.
, vol.18
, pp. 43-49
-
-
Nimgaonkar, V.L.1
Rudert, W.A.2
Zhang, X.R.3
Tsoi, W.F.4
Trucco, M.5
Saha, N.6
-
96
-
-
0027650453
-
Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed
-
Nothen, M.M., Cichon, S., Propping, P., Fimmers, R., Schwab, S.G., and Wildenauer, D.B. (1993). Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed. J. Med. Genet. 30, 708-709.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 708-709
-
-
Nothen, M.M.1
Cichon, S.2
Propping, P.3
Fimmers, R.4
Schwab, S.G.5
Wildenauer, D.B.6
-
97
-
-
0030901160
-
Genetic alterations in leukemias and lymphomas: Impressive progress and continuing complexity
-
Nowell, P.C. (1997). Genetic alterations in leukemias and lymphomas: impressive progress and continuing complexity. Cancer Genet. Cytogenet. 94, 13-19.
-
(1997)
Cancer Genet. Cytogenet.
, vol.94
, pp. 13-19
-
-
Nowell, P.C.1
-
98
-
-
0029355769
-
Expanded CAG repeats in schizophrenia and bipolar disorder
-
O'Donovan, M.C., Guy, C., Craddock, N., Murphy, K.C., Cardno, A.G., Jones, L.A., Owen, M.J., and McGuffin, P. (1995). Expanded CAG repeats in schizophrenia and bipolar disorder. Nature Genet. 10, 380-381.
-
(1995)
Nature Genet.
, vol.10
, pp. 380-381
-
-
O'Donovan, M.C.1
Guy, C.2
Craddock, N.3
Murphy, K.C.4
Cardno, A.G.5
Jones, L.A.6
Owen, M.J.7
McGuffin, P.8
-
99
-
-
0029143989
-
Schizophrenia with karyotype mosaic 47,XXY/48,XXY+8
-
Ong, S.H., and Robertson, J.R. (1995). Schizophrenia with karyotype mosaic 47,XXY/48,XXY+8. Psychiatr. Genet. 5, 67-69.
-
(1995)
Psychiatr. Genet.
, vol.5
, pp. 67-69
-
-
Ong, S.H.1
Robertson, J.R.2
-
100
-
-
0025780277
-
Twin concordance for DSM-III-R schizophrenia
-
Onstad, S., Skre, I., Torgersen, S., and Kringlen, E. (1991). Twin concordance for DSM-III-R schizophrenia. Acta Psychiatr. Scand. 83, 395-401.
-
(1991)
Acta Psychiatr. Scand.
, vol.83
, pp. 395-401
-
-
Onstad, S.1
Skre, I.2
Torgersen, S.3
Kringlen, E.4
-
102
-
-
0027648368
-
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene
-
Owen, M.J., Williams, J., Mant, R., et al. (1993). Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. J. Med. Genet. 30, 708-709.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 708-709
-
-
Owen, M.J.1
Williams, J.2
Mant, R.3
-
103
-
-
0028470917
-
A contribution to the differential diagnosis of the "group of schizophrenias": Structural abnormality of chromosome 4
-
Palmour, R.M., Miller, S., Fielding, A., Vekemans, M., and Ervin, F.R. (1994). A contribution to the differential diagnosis of the "group of schizophrenias": structural abnormality of chromosome 4. J. Psychiatry Neurosci. 19, 270-277.
-
(1994)
J. Psychiatry Neurosci.
, vol.19
, pp. 270-277
-
-
Palmour, R.M.1
Miller, S.2
Fielding, A.3
Vekemans, M.4
Ervin, F.R.5
-
104
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos, D.F., Faedda, G.L., Veitm, S., Goldberg, R., Morrow, B., Kucherlapati, R., and Shprintzen, R.J. (1996). Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? Am. J. Psychiatry 153, 1541-1547.
-
(1996)
Am. J. Psychiatry
, vol.153
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veitm, S.3
Goldberg, R.4
Morrow, B.5
Kucherlapati, R.6
Shprintzen, R.J.7
-
105
-
-
0025853513
-
Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1)
-
Park, J.P., Moeschler, J.B., Berg, S.Z., and Wurster-Hill, D.H. (1991). Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1). J. Med. Genet. 28, 282-283.
-
(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
-
106
-
-
78651024089
-
The problem of anticipation in pedigrees of dystrophia myotonica
-
Penrose, L.S. (1948). The problem of anticipation in pedigrees of dystrophia myotonica. Ann. Eugenics 14, 125.
-
(1948)
Ann. Eugenics
, vol.14
, pp. 125
-
-
Penrose, L.S.1
-
107
-
-
0029198740
-
Genetic anticipation in schizophrenia: Pro and con
-
Petronis, A., Sherrington, R.P., Paterson, A.D., and Kennedy, J.L. (1995). Genetic anticipation in schizophrenia: pro and con. Clin. Neurosci. 3, 76-80.
-
(1995)
Clin. Neurosci.
, vol.3
, pp. 76-80
-
-
Petronis, A.1
Sherrington, R.P.2
Paterson, A.D.3
Kennedy, J.L.4
-
108
-
-
0000023267
-
Neuropsychological impairments are increased in siblings of schizophrenic patients
-
Pogue-Geile, M.F., Garrett, A.H., Brunke, J.J., and Hall, J.K. (1991). Neuropsychological impairments are increased in siblings of schizophrenic patients. Schizophr. Res. 4, 390.
-
(1991)
Schizophr. Res.
, vol.4
, pp. 390
-
-
Pogue-Geile, M.F.1
Garrett, A.H.2
Brunke, J.J.3
Hall, J.K.4
-
109
-
-
0028082293
-
Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12-q13.1: Part 1
-
Pulver, A.E., Karayiorgou, M., Wolyniec, P.S., Lasseter, V.K., Kasch, L., Nestadt, G., Antonarakis, S., Housman, D., Kazazian, H.H., Meyers, D., et al. (1994a). Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: part 1. Am. J. Med. Genet. 54, 36-43.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 36-43
-
-
Pulver, A.E.1
Karayiorgou, M.2
Wolyniec, P.S.3
Lasseter, V.K.4
Kasch, L.5
Nestadt, G.6
Antonarakis, S.7
Housman, D.8
Kazazian, H.H.9
Meyers, D.10
-
110
-
-
0027989917
-
Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives
-
Pulver, A.E., Nestadt, G., Goldberg, R., Shprintzen, R.J., Lamacz, M., Wolyniec, P.S., Morrow, B., Karayiorgou, M., Antonarakis, S.E., Housman, D., and Kucherlapati, R. (1994b). Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. J. Nerv. Ment. Dis. 182, 476-478.
-
(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
Kucherlapati, R.11
-
111
-
-
0029071768
-
Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes
-
Pulver, A.E., Lasseter, V.K., Kasch, L., Wolyniec, P., Nestadt, G., Blouin, J.-L., Kimberland, M., Babb, R., Vourlis, S., Chen, H., et al. (1995). Schizophrenia: a genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes. Am. J. Med. Genet. 60, 252-260.
-
(1995)
Am. J. Med. Genet.
, vol.60
, pp. 252-260
-
-
Pulver, A.E.1
Lasseter, V.K.2
Kasch, L.3
Wolyniec, P.4
Nestadt, G.5
Blouin, J.-L.6
Kimberland, M.7
Babb, R.8
Vourlis, S.9
Chen, H.10
-
112
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts, T.H. (1994). Chromosomal translocations in human cancer. Nature 372, 143-149.
-
(1994)
Nature
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
113
-
-
0029618655
-
A new case of trisomy 5 as sole cytogenetic anomaly in acute myeloid leukemia
-
Rios, R., Sole, F., Montes, C., Vicente, A., Perez, M.M., Valle, M., and Gascon, F. (1995). A new case of trisomy 5 as sole cytogenetic anomaly in acute myeloid leukemia. Cancer Genet. Cytogenet. 84, 120-122.
-
(1995)
Cancer Genet. Cytogenet.
, vol.84
, pp. 120-122
-
-
Rios, R.1
Sole, F.2
Montes, C.3
Vicente, A.4
Perez, M.M.5
Valle, M.6
Gascon, F.7
-
114
-
-
0001839206
-
Mapping genes for psychiatric disorders
-
E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc.)
-
Risch, N. (1994). Mapping genes for psychiatric disorders. In Genetic Approaches To Mental Disorders. E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc.), pp. 47-61.
-
(1994)
Genetic Approaches To Mental Disorders
, pp. 47-61
-
-
Risch, N.1
-
115
-
-
0021748268
-
Segregation analysis of schizophrenia and related disorders
-
Risch, N., and Baron, M. (1984). Segregation analysis of schizophrenia and related disorders. Am. J. Hum. Genet. 36, 1039-1059.
-
(1984)
Am. J. Hum. Genet.
, vol.36
, pp. 1039-1059
-
-
Risch, N.1
Baron, M.2
-
116
-
-
0029001682
-
Extreme discordant sib-pairs for mapping quantitative trait loci in humans
-
Risch, N., and Zhang, H. (1995). Extreme discordant sib-pairs for mapping quantitative trait loci in humans. Science 268, 1584-1589.
-
(1995)
Science
, vol.268
, pp. 1584-1589
-
-
Risch, N.1
Zhang, H.2
-
117
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N., and Merikangas, K. (1996). The future of genetic studies of complex human diseases. Science 273, 1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
118
-
-
0023284603
-
Marfan's syndrome and schizophrenia: A case report
-
Romano, J., and Linares, R.L. (1987). Marfan's syndrome and schizophrenia: a case report. Arch. Gen. Psychiatry 44, 190-192.
-
(1987)
Arch. Gen. Psychiatry
, vol.44
, pp. 190-192
-
-
Romano, J.1
Linares, R.L.2
-
119
-
-
0027953283
-
Failure to find evidence for linkage or association between dopamine D3 receptor gene and schizophrenia
-
Sabate, O., Campion, D., D'Amato, T., Martres, M.P., Sokoloff, P., Giros, B., Leboyer, M., Jay, M., Guedj, F., Thibaut, F., et al. (1994). Failure to find evidence for linkage or association between dopamine D3 receptor gene and schizophrenia. Am. J. Psychiatry 151, 107-111.
-
(1994)
Am. J. Psychiatry
, vol.151
, pp. 107-111
-
-
Sabate, O.1
Campion, D.2
D'Amato, T.3
Martres, M.P.4
Sokoloff, P.5
Giros, B.6
Leboyer, M.7
Jay, M.8
Guedj, F.9
Thibaut, F.10
-
120
-
-
16144368214
-
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease
-
Salomon, R., Attie, T., Pelet, A., Bidaud, C., Eng, C., Amiel, J., Sarnacki, S., Goulet, O., Ricour, C., Nihoul-Fekete, C., et al. (1996). Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease. Nature Genet. 14, 345-347.
-
(1996)
Nature Genet.
, vol.14
, pp. 345-347
-
-
Salomon, R.1
Attie, T.2
Pelet, A.3
Bidaud, C.4
Eng, C.5
Amiel, J.6
Sarnacki, S.7
Goulet, O.8
Ricour, C.9
Nihoul-Fekete, C.10
-
121
-
-
0030292368
-
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
-
Sanpei, K., Takano, H., Igarashi, S., Sato, T., Oyake, M., Sasaki, H., Wakisaka, A., Tashiro, K., Ishida, Y., Ikeuchi, T., et al. (1996). Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT. Nature Genet. 14, 277-284.
-
(1996)
Nature Genet.
, vol.14
, pp. 277-284
-
-
Sanpei, K.1
Takano, H.2
Igarashi, S.3
Sato, T.4
Oyake, M.5
Sasaki, H.6
Wakisaka, A.7
Tashiro, K.8
Ishida, Y.9
Ikeuchi, T.10
-
122
-
-
13344277348
-
Psychosis and genes with trinucleotide repeat polymorphism
-
Sasaki, T., Billett, E., Petronis, A., Ying, D., Parsons, T., Macciardi, F.M., Meltzer, H.Y., Lieberman, J., Joffe, R.T., Ross, C.A., et al. (1996). Psychosis and genes with trinucleotide repeat polymorphism. Hum. Genet. 97, 244-246.
-
(1996)
Hum. Genet.
, vol.97
, pp. 244-246
-
-
Sasaki, T.1
Billett, E.2
Petronis, A.3
Ying, D.4
Parsons, T.5
Macciardi, F.M.6
Meltzer, H.Y.7
Lieberman, J.8
Joffe, R.T.9
Ross, C.A.10
-
123
-
-
0029874880
-
A combined analysis of D22s278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12
-
Schizophrenia Collaborative Linkage Group for chromosome 22 (1996). A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Am. J. Med. Genet. 67, 40-45.
-
(1996)
Am. J. Med. Genet.
, vol.67
, pp. 40-45
-
-
-
124
-
-
0029845435
-
Additional support for schizophrenia linkage findings on chromosomes 6 and 8: A multicenter study
-
Schizophrenia Collaborative Linkage Group for chromosomes 3, 6, and 8. (1996). Additional support for schizophrenia linkage findings on chromosomes 6 and 8: a multicenter study. Am. J. Med. Genet. 67, 580-594.
-
(1996)
Am. J. Med. Genet.
, vol.67
, pp. 580-594
-
-
-
125
-
-
8244226000
-
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis
-
Schwab, S.G., Eckstein, G.N., Hallmayer, J., Lerer, B., Albus, M., Borrmann, M., Lichtermann, D., Ertl, M.A., Maier, W., and Wildenauer, D.B. (1997). Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis. Mol. Psychiatry 2, 156-160.
-
(1997)
Mol. Psychiatry
, vol.2
, pp. 156-160
-
-
Schwab, S.G.1
Eckstein, G.N.2
Hallmayer, J.3
Lerer, B.4
Albus, M.5
Borrmann, M.6
Lichtermann, D.7
Ertl, M.A.8
Maier, W.9
Wildenauer, D.B.10
-
126
-
-
0030433777
-
Cell biology of the β-amyloid precursor protein and the genetics of Alzheimer's disease
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Selkoe, D.J. (1996). Cell biology of the β-amyloid precursor protein and the genetics of Alzheimer's disease. In Cold Spring Harbor Symposia on Quantitative Biology, Vol. LXI (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press), pp. 587-596.
-
(1996)
Cold Spring Harbor Symposia on Quantitative Biology
, vol.61
, pp. 587-596
-
-
Selkoe, D.J.1
-
127
-
-
0028116099
-
Disease susceptibility genes and the sib-pair method: A review of recent methodology
-
Shah, S., and Green, J.R. (1994). Disease susceptibility genes and the sib-pair method: a review of recent methodology. Ann. Hum. Genet. 58, 381-395.
-
(1994)
Ann. Hum. Genet.
, vol.58
, pp. 381-395
-
-
Shah, S.1
Green, J.R.2
-
128
-
-
0030005962
-
Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia
-
Shaikh, S., Collier, D.A., Sham, P.C., Ball, D., Aitchison, K., Vallada, H., Smith, I., Gill, M., and Kerwin, R.W. (1996). Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia. Hum. Genet. 97, 714-719.
-
(1996)
Hum. Genet.
, vol.97
, pp. 714-719
-
-
Shaikh, S.1
Collier, D.A.2
Sham, P.C.3
Ball, D.4
Aitchison, K.5
Vallada, H.6
Smith, I.7
Gill, M.8
Kerwin, R.W.9
-
129
-
-
0023716504
-
Localization of a susceptibility locus for schizophrenia on chromosome 5
-
Sherrington, R., Brynjolfsson, J., Petursson, H., Potter, M., Dudleston, K., Barraclough, B., Wasmuth, J., Dobbs, M., and Gurling, H. (1988). Localization of a susceptibility locus for schizophrenia on chromosome 5. Nature 336, 164-167.
-
(1988)
Nature
, vol.336
, pp. 164-167
-
-
Sherrington, R.1
Brynjolfsson, J.2
Petursson, H.3
Potter, M.4
Dudleston, K.5
Barraclough, B.6
Wasmuth, J.7
Dobbs, M.8
Gurling, H.9
-
130
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early onset familial Alzheimer's disease
-
Sherrington, R., Rogaev, E., Liang, Y., Rogaeva, E., Levesque, G., Ikeda, M., Chi, H., Lin, C., Holman, K., Tsuda, T., et al. (1995). Cloning of a gene bearing missense mutations in early onset familial Alzheimer's disease. Nature 375, 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.2
Liang, Y.3
Rogaeva, E.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
-
131
-
-
0024992104
-
Schizophrenia and Marfan syndrome
-
Sirota, P., Frydman, M., and Sirota, L. (1990). Schizophrenia and Marfan syndrome. Br. J. Psychiatry 157, 433-436.
-
(1990)
Br. J. Psychiatry
, vol.157
, pp. 433-436
-
-
Sirota, P.1
Frydman, M.2
Sirota, L.3
-
132
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman, R.S., McGinnis, R.E., and Ewens, W.J. (1993). Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet. 52, 506-516.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
133
-
-
0030436489
-
Two homologous genes causing early-onset familial Alzheimer's disease
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
St. George-Hyslop, P.H., Levesque, G., Levesque, L., Rommens, J., Westaway, D., and Fraser, P.E. (1996). Two homologous genes causing early-onset familial Alzheimer's disease. In Cold Spring Harbor Symposia on Quantitative Biology, Vol. LXI (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press), pp 559-564.
-
(1996)
Cold Spring Harbor Symposia on Quantitative Biology
, vol.61
, pp. 559-564
-
-
St. George-Hyslop, P.H.1
Levesque, G.2
Levesque, L.3
Rommens, J.4
Westaway, D.5
Fraser, P.E.6
-
134
-
-
0028820161
-
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: Evidence for genetic heterogeneity
-
Straub, R.E., MacLean, C.J., O'Neill, F.A., Burke, J., Murphy, B., Duke, F., Shinkwin, R., Webb, B.T., Zhang, J., Walsh, D., and Kendler, K.S. (1995). A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. Nature Genet. 11, 287-293.
-
(1995)
Nature Genet.
, vol.11
, pp. 287-293
-
-
Straub, R.E.1
MacLean, C.J.2
O'Neill, F.A.3
Burke, J.4
Murphy, B.5
Duke, F.6
Shinkwin, R.7
Webb, B.T.8
Zhang, J.9
Walsh, D.10
Kendler, K.S.11
-
135
-
-
0030980118
-
Support for a possible schizophrenia vulnerability locus in region 5q21-q31 in Irish families
-
Straub, R.E., MacLean, C.J., O'Neill, F.A., Walsh, D., and Kendler, K.S. (1997). Support for a possible schizophrenia vulnerability locus in region 5q21-q31 in Irish families. Mol. Psychiatry 2, 148-155.
-
(1997)
Mol. Psychiatry
, vol.2
, pp. 148-155
-
-
Straub, R.E.1
MacLean, C.J.2
O'Neill, F.A.3
Walsh, D.4
Kendler, K.S.5
-
136
-
-
0002710362
-
Problems of replicating linkage claims in psychiatry
-
E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc)
-
Suarez, B.K., Hampe, C.L., and Van Eerdewegh, P. (1994). Problems of replicating linkage claims in psychiatry. In Genetic Approaches To Mental Disorders, E.S. Gershon and C.R. Cloninger, eds. (Washington, D.C.: American Psychiatric Press, Inc), pp. 23-46.
-
(1994)
Genetic Approaches To Mental Disorders
, pp. 23-46
-
-
Suarez, B.K.1
Hampe, C.L.2
Van Eerdewegh, P.3
-
137
-
-
0030021577
-
Schizophrenia after prenatal famine. Further evidence
-
Susser, E., Neugebauer, R., Hoek, H.W., Brown, A.S., Lin, S., Labovitz, D., and Gorman, J.M. (1996). Schizophrenia after prenatal famine. Further evidence. Arch. Gen. Psychiatry 53, 25-31.
-
(1996)
Arch. Gen. Psychiatry
, vol.53
, pp. 25-31
-
-
Susser, E.1
Neugebauer, R.2
Hoek, H.W.3
Brown, A.S.4
Lin, S.5
Labovitz, D.6
Gorman, J.M.7
-
138
-
-
0025345773
-
Developmental abnormalities of the corpus callosum in schizophrenia
-
Swayze, V.W., Andreasen, N.C., Ehrhardt, J.C., Yuh, W.T.C., Alliger, R.J., and Cohen, G.A. (1990). Developmental abnormalities of the corpus callosum in schizophrenia. Arch. Neurol. 47, 805-808.
-
(1990)
Arch. Neurol.
, vol.47
, pp. 805-808
-
-
Swayze, V.W.1
Andreasen, N.C.2
Ehrhardt, J.C.3
Yuh, W.T.C.4
Alliger, R.J.5
Cohen, G.A.6
-
139
-
-
0026494911
-
A haplotype-based "haplotype relative risk" approach to detecting allelic associations
-
Terwilliger, J., and Ott, J. (1992). A haplotype-based "haplotype relative risk" approach to detecting allelic associations. Hum. Hered. 42, 337-346.
-
(1992)
Hum. Hered.
, vol.42
, pp. 337-346
-
-
Terwilliger, J.1
Ott, J.2
-
140
-
-
0028858104
-
The case for heterogeneity in the etiology of schizophrenia
-
Tsuang, M.T., and Faraone, S.V. (1995). The case for heterogeneity in the etiology of schizophrenia. Schizophr. Res. 17, 161-175.
-
(1995)
Schizophr. Res.
, vol.17
, pp. 161-175
-
-
Tsuang, M.T.1
Faraone, S.V.2
-
141
-
-
0029561772
-
Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia
-
Vallada, H., Curtis, D., Sham, P.C., Murray, R.M., McGuffin, P., Nanko, S., Gill, M., Owen, M., and Collier, D.A. (1995). Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia. Psychiatr. Genet. 5, 127-130.
-
(1995)
Psychiatr. Genet.
, vol.5
, pp. 127-130
-
-
Vallada, H.1
Curtis, D.2
Sham, P.C.3
Murray, R.M.4
McGuffin, P.5
Nanko, S.6
Gill, M.7
Owen, M.8
Collier, D.A.9
-
142
-
-
0029045963
-
Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22
-
Wang, S., Sun, C.E., Walczak, C.A., Ziegle, J.S., Kipps, B.R., Goldin, L.R., and Diehl, S.R. (1995). Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22. Nature Genet. 10, 41-46.
-
(1995)
Nature Genet.
, vol.10
, pp. 41-46
-
-
Wang, S.1
Sun, C.E.2
Walczak, C.A.3
Ziegle, J.S.4
Kipps, B.R.5
Goldin, L.R.6
Diehl, S.R.7
-
143
-
-
0029102868
-
Association of polymorphic VNTR region in the first intron of the human TH gene with disturbances of the catecholamine pathway in schizophrenia
-
Wei, J., Ramchand, C.N., and Hemmings, G.P. (1995). Association of polymorphic VNTR region in the first intron of the human TH gene with disturbances of the catecholamine pathway in schizophrenia. Psychiatr. Genet. 5, 83-88.
-
(1995)
Psychiatr. Genet.
, vol.5
, pp. 83-88
-
-
Wei, J.1
Ramchand, C.N.2
Hemmings, G.P.3
-
144
-
-
0023215296
-
Implications of normal brain development for the pathogenesis of schizophrenia
-
Weinberger, D.R. (1987). Implications of normal brain development for the pathogenesis of schizophrenia. Arch. Gen. Psychiatry 44, 660-669.
-
(1987)
Arch. Gen. Psychiatry
, vol.44
, pp. 660-669
-
-
Weinberger, D.R.1
-
145
-
-
12644293808
-
Searching for susceptibility genes in schizophrenia by genetic linkage analysis
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Wildenauer, D.B., Hallmayer, J., Schwab, S.G., Albus, M., Eckstein, G.N., Zill, P., Honig, S., Strauss, M., Borrmann, M., Lichtermann, D., et al. (1996). Searching for susceptibility genes in schizophrenia by genetic linkage analysis. In Cold Spring Harbor Symposia on Quantitative Biology, Vol. LXI (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press), pp. 845-850.
-
(1996)
Cold Spring Harbor Symposia on Quantitative Biology
, vol.61
, pp. 845-850
-
-
Wildenauer, D.B.1
Hallmayer, J.2
Schwab, S.G.3
Albus, M.4
Eckstein, G.N.5
Zill, P.6
Honig, S.7
Strauss, M.8
Borrmann, M.9
Lichtermann, D.10
-
146
-
-
0029873266
-
Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) group
-
Williams, J., Spurlock, G., McGuffin, P., Mallet, J., Nothen, M.M, Gill, M., Aschauer, H., Nylander, P.O., Macciardi, F., and Owen, M.J. (1996). Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. Lancet 347, 1294-1296.
-
(1996)
Lancet
, vol.347
, pp. 1294-1296
-
-
Williams, J.1
Spurlock, G.2
McGuffin, P.3
Mallet, J.4
Nothen, M.M.5
Gill, M.6
Aschauer, H.7
Nylander, P.O.8
Macciardi, F.9
Owen, M.J.10
-
147
-
-
0343068160
-
A family-based association study of the dopamine D3 receptor gene and highly familial schizophrenia
-
in press
-
Williams, J., Mant, R., Holmans, P., McGuffin, P., Owen, M.J., Spurlock, G. et al. (1997). A family-based association study of the dopamine D3 receptor gene and highly familial schizophrenia. Am. J. Med. Genet., in press.
-
(1997)
Am. J. Med. Genet.
-
-
Williams, J.1
Mant, R.2
Holmans, P.3
McGuffin, P.4
Owen, M.J.5
Spurlock, G.6
-
148
-
-
0001883914
-
Prenatal influenza, immunogenes, and schizophrenia: A hypothesis and some recent findings
-
J.L. Waddington and P.F. Buckley, eds. (Austin,TX: R.G. Landes)
-
Wright, P., and Murray, R.M. (1996). Prenatal influenza, immunogenes, and schizophrenia: a hypothesis and some recent findings. In The Neurodevelopmental Basis of Schizophrenia, J.L. Waddington and P.F. Buckley, eds. (Austin,TX: R.G. Landes), pp. 43-59.
-
(1996)
The Neurodevelopmental Basis of Schizophrenia
, pp. 43-59
-
-
Wright, P.1
Murray, R.M.2
-
149
-
-
0029949697
-
Genetic association of the HLA DRB1 gene locus on chromosome 6p21.3 with schizophrenia
-
Wright, P., Donaldson, P.T., Underhill, J.A., Choudhuri, K., Doherty, D.G., and Murray, R.M. (1996). Genetic association of the HLA DRB1 gene locus on chromosome 6p21.3 with schizophrenia. Am. J. Psychiatry 153, 1530-1533.
-
(1996)
Am. J. Psychiatry
, vol.153
, pp. 1530-1533
-
-
Wright, P.1
Donaldson, P.T.2
Underhill, J.A.3
Choudhuri, K.4
Doherty, D.G.5
Murray, R.M.6
-
150
-
-
0027302882
-
No association between schizophrenia and homozygosity at the D3 dopamine receptor gene
-
Yang, L., Li, T., Wiese, C., Lannfelt, L., Sokoloff, P., Xu, C.T., Zeng, Z., Schwartz, J.C., Liu, X., and Moises, H.W. (1993). No association between schizophrenia and homozygosity at the D3 dopamine receptor gene. Am. J. Med. Genet. 48, 83-86.
-
(1993)
Am. J. Med. Genet.
, vol.48
, pp. 83-86
-
-
Yang, L.1
Li, T.2
Wiese, C.3
Lannfelt, L.4
Sokoloff, P.5
Xu, C.T.6
Zeng, Z.7
Schwartz, J.C.8
Liu, X.9
Moises, H.W.10
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