-
1
-
-
0000684708
-
Psychobiology of suicide, impulsivity, and related phenomena
-
H. Y. Meltzer, Ed., Raven Press, New York
-
Asberg, M., Schalling, D., and Traskman-Bendz, L. (1987). Psychobiology of suicide, impulsivity, and related phenomena. In "Psychopharmacology: The Third Generation of Progress" (H. Y. Meltzer, Ed.), pp. 665-668, Raven Press, New York.
-
(1987)
Psychopharmacology: The Third Generation of Progress
, pp. 665-668
-
-
Asberg, M.1
Schalling, D.2
Traskman-Bendz, L.3
-
2
-
-
0031414904
-
μ opioid receptor gene variants: Lack of association with alcohol dependence
-
Bergen, A. W., Kokoszka, J., Peterson, R., Long, J. C., Virkkunen, M., Linnoila, M., and Goldman, D. (1997). μ opioid receptor gene variants: Lack of association with alcohol dependence. Mol. Psychiatry 2: 490-494.
-
(1997)
Mol. Psychiatry
, vol.2
, pp. 490-494
-
-
Bergen, A.W.1
Kokoszka, J.2
Peterson, R.3
Long, J.C.4
Virkkunen, M.5
Linnoila, M.6
Goldman, D.7
-
3
-
-
0030792136
-
Human mu opioid receptor gene polymorphisms and vulnerability to substance abuse
-
Berrettini, W. H., Hoehe, M. R., Ferraro, T. N., DeMaria, P. A., and Gottheil, E. (1997). Human mu opioid receptor gene polymorphisms and vulnerability to substance abuse. Addict. Biol. 2: 303-308.
-
(1997)
Addict. Biol.
, vol.2
, pp. 303-308
-
-
Berrettini, W.H.1
Hoehe, M.R.2
Ferraro, T.N.3
DeMaria, P.A.4
Gottheil, E.5
-
4
-
-
0025918637
-
Localization of dopamine D3 receptor mRNA in the rat brain using in situ hybridization histochemistry: Comparison with dopamine D2 receptor mRNA
-
Bouthenet, M. L., Souil, E., Martres, M. P., Sokoloff, P., Giros, B., and Schwartz, J-C. (1991). Localization of dopamine D3 receptor mRNA in the rat brain using in situ hybridization histochemistry: Comparison with dopamine D2 receptor mRNA. Brain Res. 564: 203-219.
-
(1991)
Brain Res.
, vol.564
, pp. 203-219
-
-
Bouthenet, M.L.1
Souil, E.2
Martres, M.P.3
Sokoloff, P.4
Giros, B.5
Schwartz, J.-C.6
-
5
-
-
0027194404
-
Modulation of cocaine self administration in the rat through D-3 dopamine receptors
-
Caine, S. B., and Koob, G. F. (1993). Modulation of cocaine self administration in the rat through D-3 dopamine receptors. Science 260: 1814-1816.
-
(1993)
Science
, vol.260
, pp. 1814-1816
-
-
Caine, S.B.1
Koob, G.F.2
-
6
-
-
0003770396
-
-
Am. Psychiatric Press, Washington, DC
-
Coccaro, E. F., and Murphy, D. L. (Eds.) (1990). "Serotonin in Major Psychiatric Disorders," Am. Psychiatric Press, Washington, DC.
-
(1990)
Serotonin in Major Psychiatric Disorders
-
-
Coccaro, E.F.1
Murphy, D.L.2
-
7
-
-
0028987091
-
Association of attention-deficit disorder and the dopamine transporter gene
-
Cook, E. H., Jr., Stein, M. S., Krasowski, M. D., Cox, N. J., Olkon, D. M., Kieffer, J. E., and Leventhal, B. L. (1995). Association of attention-deficit disorder and the dopamine transporter gene. Am. J. Hum. Genet. 56: 993-996.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 993-996
-
-
Cook E.H., Jr.1
Stein, M.S.2
Krasowski, M.D.3
Cox, N.J.4
Olkon, D.M.5
Kieffer, J.E.6
Leventhal, B.L.7
-
8
-
-
0028305380
-
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
-
Corder, E. H., Saunders, A. M., Risch, N. J., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Jr., Rimmler, J. B., Locke, P. A., Conneally, P. M., Schmader, K. E., Small, G. W., Roses, A. D., Haines, J. L., and Pericak-Vance, M. A. (1994). Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease. Nature Genet. 7: 180-184.
-
(1994)
Nature Genet.
, vol.7
, pp. 180-184
-
-
Corder, E.H.1
Saunders, A.M.2
Risch, N.J.3
Strittmatter, W.J.4
Schmechel, D.E.5
Gaskell P.C., Jr.6
Rimmler, J.B.7
Locke, P.A.8
Conneally, P.M.9
Schmader, K.E.10
Small, G.W.11
Roses, A.D.12
Haines, J.L.13
Pericak-Vance, M.A.14
-
9
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., and Pericak-Vance, M. A. (1993). Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 261: 921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
Roses, A.D.7
Haines, J.L.8
Pericak-Vance, M.A.9
-
10
-
-
0027076725
-
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene
-
Crocq, M-A., Mant, R., Asherson, P., Williams, J., Hode, Y., Mayerova, D., Collier, D., Lannfelt, L., Sokoloff, P., Schwartz, J-C., Gill, M., Macher, J-P., McGuffin, P., and Owen, M. J. (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, D.6
Collier, D.7
Lannfelt, L.8
Sokoloff, P.9
Schwartz, J.-C.10
Gill, M.11
Macher, J.-P.12
McGuffin, P.13
Owen, M.J.14
-
11
-
-
0030793566
-
Population genetics of a functional variant of the dopamine β-hydroxylase gene (DBH)
-
Cubells, J. F., Kobayashi, K, Nagatsu, T., Kidd, K. K., Kidd, J. R., Calafell, F., Kranzler, H., Ichinose, H., and Gelernter, J. (1997). Population genetics of a functional variant of the dopamine β-hydroxylase gene (DBH). Am. J. Med. Genet. (Neuropsych. Genet.) 74: 374-379.
-
(1997)
Am. J. Med. Genet. (Neuropsych. Genet.)
, vol.74
, pp. 374-379
-
-
Cubells, J.F.1
Kobayashi, K.2
Nagatsu, T.3
Kidd, K.K.4
Kidd, J.R.5
Calafell, F.6
Kranzler, H.7
Ichinose, H.8
Gelernter, J.9
-
12
-
-
0028025498
-
Polymorphic admixture typing in human ethnic populations
-
Dean, M., Stephens, J. C., Winkler, C., Lomb, D. A., Ramsburg, M., Boaze, R., Stewart, C., Charbonneau, L., Goldman, D., Albaugh, B. J., Goedert, J. J., Beasley, R. P., Hwang, L-Y., Buchbinder, S., Weedon, M., Johnson, P. A., Eichelberger, M., and O'Brien, S. J. (1994). Polymorphic admixture typing in human ethnic populations. Am. J. Hum. Genet. 55: 788-808.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 788-808
-
-
Dean, M.1
Stephens, J.C.2
Winkler, C.3
Lomb, D.A.4
Ramsburg, M.5
Boaze, R.6
Stewart, C.7
Charbonneau, L.8
Goldman, D.9
Albaugh, B.J.10
Goedert, J.J.11
Beasley, R.P.12
Hwang, L.-Y.13
Buchbinder, S.14
Weedon, M.15
Johnson, P.A.16
Eichelberger, M.17
O'Brien, S.J.18
-
13
-
-
0029010561
-
Population genetic study of the human dopamine transporter gene (DAT1)
-
Doucette-Stamm, L. A., Blakely, D. J., Tian, J., Mockus, S., and Mao, J. (1995). Population genetic study of the human dopamine transporter gene (DAT1). Genet. Epidemiol. 12: 303-308.
-
(1995)
Genet. Epidemiol.
, vol.12
, pp. 303-308
-
-
Doucette-Stamm, L.A.1
Blakely, D.J.2
Tian, J.3
Mockus, S.4
Mao, J.5
-
14
-
-
0023235253
-
Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations
-
Falk, C. T., and Rubinstein, P. (1987). Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations. Ann. Hum. Genet. 51: 227-233.
-
(1987)
Ann. Hum. Genet.
, vol.51
, pp. 227-233
-
-
Falk, C.T.1
Rubinstein, P.2
-
15
-
-
0000054129
-
No association between D3 dopamine receptor (DRD3) alleles and cocaine dependence
-
Freimer, M., Kranzler, H., Satel, S., Lacobelle, J., Skipsey, K., Charney, D. S., and Gelernter, J. (1996). No association between D3 dopamine receptor (DRD3) alleles and cocaine dependence. Addict. Biol. 1: 281-287.
-
(1996)
Addict. Biol.
, vol.1
, pp. 281-287
-
-
Freimer, M.1
Kranzler, H.2
Satel, S.3
Lacobelle, J.4
Skipsey, K.5
Charney, D.S.6
Gelernter, J.7
-
16
-
-
0025925209
-
2 dopamine receptor gene (DRD2) and alcoholism
-
2 dopamine receptor gene (DRD2) and alcoholism. JAMA 266: 1801-1807.
-
(1991)
JAMA
, vol.266
, pp. 1801-1807
-
-
Gelernter, J.1
O'Malley, S.2
Risch, N.3
Kranzler, H.4
Krystal, J.5
Merikangas, K.6
Kennedy, J.7
Kidd, K.K.8
-
17
-
-
0028042409
-
Genetic association between dopamine transporter protein alleles and cocaine-induced paranoia
-
Gelernter, J., Kranzler, H. R., Satel, S. L., and Rao, P. A. (1994). Genetic association between dopamine transporter protein alleles and cocaine-induced paranoia. Neuropsychopharmacology 11: 195-200.
-
(1994)
Neuropsychopharmacology
, vol.11
, pp. 195-200
-
-
Gelernter, J.1
Kranzler, H.R.2
Satel, S.L.3
Rao, P.A.4
-
18
-
-
6244247470
-
Candidate genes and psychiatric genetics: Tomorrow never knows
-
Gelernter, J., and Crowe, R. R. (1997). Candidate genes and psychiatric genetics: Tomorrow never knows. Psychiatric Ann. 27: 262-267.
-
(1997)
Psychiatric Ann.
, vol.27
, pp. 262-267
-
-
Gelernter, J.1
Crowe, R.R.2
-
19
-
-
0030846211
-
Ciliary neurotrophic factor null allele frequency in schizophrenia, affective disorders, and Alzheimer's disease
-
Gelernter, J., Van Dyck, C., van Kammen, D. P., Malison, R., Price, L. H., Cubells, J., Berman, R., Charney, D. S., and Heninger, G. (1997a). Ciliary neurotrophic factor null allele frequency in schizophrenia, affective disorders, and Alzheimer's disease. Am. J. Med. Genet. (Neuropsych. Genet.) 74: 497-500.
-
(1997)
Am. J. Med. Genet. (Neuropsych. Genet.)
, vol.74
, pp. 497-500
-
-
Gelernter, J.1
Van Dyck, C.2
Van Kammen, D.P.3
Malison, R.4
Price, L.H.5
Cubells, J.6
Berman, R.7
Charney, D.S.8
Heninger, G.9
-
20
-
-
0031441095
-
Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African and European American and Japanese populations and in alcohol dependent subjects
-
Gelernter, J., Kranzler, H., and Cubells, J. F. (1997b). Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African and European American and Japanese populations and in alcohol dependent subjects. Hum. Genet. 101: 243-246.
-
(1997)
Hum. Genet.
, vol.101
, pp. 243-246
-
-
Gelernter, J.1
Kranzler, H.2
Cubells, J.F.3
-
21
-
-
0010402359
-
Population studies of polymorphisms of the serotonin transporter protein gene
-
in press
-
Gelernter, J., Cubells, J. F., Kidd, J. R., Pakstis, A. J., and Kidd, K. K. (1998a). Population studies of polymorphisms of the serotonin transporter protein gene. Am. J. Med. Genet. (Neuropsych. Genet.), in press.
-
(1998)
Am. J. Med. Genet. (Neuropsych. Genet.)
-
-
Gelernter, J.1
Cubells, J.F.2
Kidd, J.R.3
Pakstis, A.J.4
Kidd, K.K.5
-
22
-
-
0033084231
-
2 dopamine receptor (DRD2) "a" system alleles, or DRD2 haplotypes, and posttraumatic stress disorder (PTSD)
-
in press
-
2 dopamine receptor (DRD2) "A" system alleles, or DRD2 haplotypes, and posttraumatic stress disorder (PTSD). Biol. Psychiatry, in press.
-
(1998)
Biol. Psychiatry
-
-
Gelernter, J.1
Southwick, S.2
Goodson, S.3
Morgan, A.4
Nagy, L.5
Charney, D.S.6
-
23
-
-
0029925561
-
3 receptor gene: Organization, transcript variants, and polymorphism associated with schizophrenia
-
3 receptor gene: Organization, transcript variants, and polymorphism associated with schizophrenia. Am. J. Med. Genet. (Neuropsych. Genet.) 67: 63-70.
-
(1996)
Am. J. Med. Genet. (Neuropsych. Genet.)
, vol.67
, pp. 63-70
-
-
Griffon, N.1
Crocq, M.A.2
Pilon, C.3
Martres, M.P.4
Mayerova, A.5
Uyanik, G.6
Burgert, E.7
Duval, F.8
Macher, J.P.9
Javoy-Agid, F.10
Tamminga, C.A.11
Schwartz, J.C.12
Sokoloff, P.13
-
24
-
-
0010319430
-
A defense of beanbag genetics
-
Reprinted in "Selected Genetic Papers of J. B. S. Haldane" (K. R. Dronamraju, Ed.), Garland, New York and London, 1990
-
Haldane, J. B. S. (1964). A defense of beanbag genetics. Perspect. Biol. Med. 7: 343-359. [Reprinted in "Selected Genetic Papers of J. B. S. Haldane" (K. R. Dronamraju, Ed.), Garland, New York and London, 1990]
-
(1964)
Perspect. Biol. Med.
, vol.7
, pp. 343-359
-
-
Haldane, J.B.S.1
-
25
-
-
0026349433
-
The apolipoprotein E polymorphism: A comparison of allele frequencies and effects in nine populations
-
Hallman, D. M., Boerwinkle, E., Saha, N., Sandholzer, C., Menzel, H. J., Csazar, A., and Utermann, G. (1991). The apolipoprotein E polymorphism: A comparison of allele frequencies and effects in nine populations. Am. J. Hum. Genet. 49: 338-349.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 338-349
-
-
Hallman, D.M.1
Boerwinkle, E.2
Saha, N.3
Sandholzer, C.4
Menzel, H.J.5
Csazar, A.6
Utermann, G.7
-
26
-
-
0025257612
-
Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI
-
Hixson, J. E., and Vernier, D. T. (1990). Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI. J. Lipid Res. 31: 545-548.
-
(1990)
J. Lipid Res.
, vol.31
, pp. 545-548
-
-
Hixson, J.E.1
Vernier, D.T.2
-
27
-
-
0026076409
-
Ciliary neurotrophic factor enhances neuronal survival in embryonic rat hippocampal cultures
-
Ip, N. Y., Li, Y. P., van de Stadt, I., Panayotatos, N., Alderson, R. F., and Lindsay, R. M. (1991). Ciliary neurotrophic factor enhances neuronal survival in embryonic rat hippocampal cultures. J. Neurosci. 11: 3124-3134.
-
(1991)
J. Neurosci.
, vol.11
, pp. 3124-3134
-
-
Ip, N.Y.1
Li, Y.P.2
Van De Stadt, I.3
Panayotatos, N.4
Alderson, R.F.5
Lindsay, R.M.6
-
28
-
-
0027262460
-
Lack of association between schizophrenia and alleles in the dopamine D3 receptor gene
-
Jönsson, E., Lannfelt, L., Sokoloff, P., Schwartz, J-C., and Sedvall, G. (1993). Lack of association between schizophrenia and alleles in the dopamine D3 receptor gene. Acta Psychiatr. Scand. 87: 345-349.
-
(1993)
Acta Psychiatr. Scand.
, vol.87
, pp. 345-349
-
-
Jönsson, E.1
Lannfelt, L.2
Sokoloff, P.3
Schwartz, J.-C.4
Sedvall, G.5
-
29
-
-
0026307091
-
Studies of three Amerindian populations using nuclear DNA polymorphisms
-
Kidd, J. R., Black, F. L., Weiss, K. M., Balazs, I., and Kidd, K. K. (1991). Studies of three Amerindian populations using nuclear DNA polymorphisms. Hum. Biol. 63: 775-794.
-
(1991)
Hum. Biol.
, vol.63
, pp. 775-794
-
-
Kidd, J.R.1
Black, F.L.2
Weiss, K.M.3
Balazs, I.4
Kidd, K.K.5
-
30
-
-
0031659387
-
Association of alcohol or other drug dependence with alleles of the μ opioid receptor (OPRM1)
-
in press
-
Kranzler, H. A., Gelernter, J., O'Malley, S., Hernandez-Avila, C. A., and Kaufman, D. (1998). Association of alcohol or other drug dependence with alleles of the μ opioid receptor (OPRM1). Alcohol Clin. Exp. Res., in press.
-
(1998)
Alcohol Clin. Exp. Res.
-
-
Kranzler, H.A.1
Gelernter, J.2
O'Malley, S.3
Hernandez-Avila, C.A.4
Kaufman, D.5
-
31
-
-
0029157488
-
Minisatellites and human disease
-
Krontiris, T. G. (1995). Minisatellites and human disease. Science 269: 1682-1683.
-
(1995)
Science
, vol.269
, pp. 1682-1683
-
-
Krontiris, T.G.1
-
32
-
-
0026080111
-
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies
-
Lahiri, D. K., and Nurnberger, J. I. (1991). A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies. Nucleic Acids Res. 9: 5444.
-
(1991)
Nucleic Acids Res.
, vol.9
, pp. 5444
-
-
Lahiri, D.K.1
Nurnberger, J.I.2
-
33
-
-
0000101935
-
Amino acid substitution in the dopamine D3 receptor as a useful polymorphism for investigating psychiatric disorders
-
Lannfelt, L., Sokoloff, P., Martres, M. P., Pilon, C., Giros, B., Jonsson, E., Sedvall, G., and Schwartz, J-C. (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.P.3
Pilon, C.4
Giros, B.5
Jonsson, E.6
Sedvall, G.7
Schwartz, J.-C.8
-
34
-
-
0025942741
-
Chromosomal localization of the human D-3 dopamine receptor gene
-
Le Coniat, M., Sokoloff, P., Hillion, J., Martres, M-P., Giros, B., Pilon, C., Schwartz, J-C., and Berger, R. (1991). Chromosomal localization of the human D-3 dopamine receptor gene. Hum. Genet. 87: 618-620.
-
(1991)
Hum. Genet.
, vol.87
, pp. 618-620
-
-
Le Coniat, M.1
Sokoloff, P.2
Hillion, J.3
Martres, M.-P.4
Giros, B.5
Pilon, C.6
Schwartz, J.-C.7
Berger, R.8
-
35
-
-
0023412634
-
Assignment of human tryptophan hydroxylase locus to chromosome 11: Gene duplication and translocation in evolution of aromatic amino acid hydroxylases
-
Ledley, F. D., Grenett, H. E., Bartos, D. P., van Tuinen, P., Ledbetter, D. H., and Woo, S. L. (1987). Assignment of human tryptophan hydroxylase locus to chromosome 11: Gene duplication and translocation in evolution of aromatic amino acid hydroxylases. Somatic Cell Mol. Genet. 13: 575-580.
-
(1987)
Somatic Cell Mol. Genet.
, vol.13
, pp. 575-580
-
-
Ledley, F.D.1
Grenett, H.E.2
Bartos, D.P.3
Van Tuinen, P.4
Ledbetter, D.H.5
Woo, S.L.6
-
36
-
-
0027256846
-
Human ciliary neurotrophic factor: Localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat
-
Lev, A. A., Rosen, D. R., Kos, C., Clifford, E., Landes, G., Hauser, S. L., and Brown, R. H., Jr. (1993). Human ciliary neurotrophic factor: Localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat. Genomics 16: 539-541.
-
(1993)
Genomics
, vol.16
, pp. 539-541
-
-
Lev, A.A.1
Rosen, D.R.2
Kos, C.3
Clifford, E.4
Landes, G.5
Hauser, S.L.6
Brown R.H., Jr.7
-
37
-
-
0003765562
-
Genetic data analysis
-
Free program distributed by the authors over the Internet from the GDA home page
-
Lewis, P. O., and Zaykin, D. (1997). Genetic data analysis: Computer program for the analysis of allelic data. Version 1.0. Free program distributed by the authors over the Internet from the GDA home page at http://chee.unm.edu/gda/.
-
(1997)
Computer Program for the Analysis of Allelic Data. Version 1.0
-
-
Lewis, P.O.1
Zaykin, D.2
-
38
-
-
0030161652
-
CNTF and psychiatric disorders
-
Li, T., Vallada, H., Bell, R., Liu, X., Xie, T., and Collier, D. A. (1996). CNTF and psychiatric disorders [letter]. Nat. Genet. 13: 143-144.
-
(1996)
Nat. Genet.
, vol.13
, pp. 143-144
-
-
Li, T.1
Vallada, H.2
Bell, R.3
Liu, X.4
Xie, T.5
Collier, D.A.6
-
39
-
-
0028816355
-
Apolipoprotein E and Alzheimer's disease: Ethnic variation in genotypic risks
-
Maestre, G., Ottman, R., Stern, Y., Gurland, B., Chun, M., Tang, M-X., Shelanski, M., Tycko, B., and Mayeux, R. (1995). Apolipoprotein E and Alzheimer's disease: Ethnic variation in genotypic risks. Ann. Neurol. 37: 254-259.
-
(1995)
Ann. Neurol.
, vol.37
, pp. 254-259
-
-
Maestre, G.1
Ottman, R.2
Stern, Y.3
Gurland, B.4
Chun, M.5
Tang, M.-X.6
Shelanski, M.7
Tycko, B.8
Mayeux, R.9
-
40
-
-
0030770598
-
Possible association of a polymorphism of the tryptophan hydroxylase gene with suicidal behavior in depressed patients
-
Mann, J. J., Malone, K. M., Nielsen, D. A., Goldman, D., Erdos, J., and Gelernter, J. (1997). Possible association of a polymorphism of the tryptophan hydroxylase gene with suicidal behavior in depressed patients. Am. J. Psychiatry 154: 1451-1453.
-
(1997)
Am. J. Psychiatry
, vol.154
, pp. 1451-1453
-
-
Mann, J.J.1
Malone, K.M.2
Nielsen, D.A.3
Goldman, D.4
Erdos, J.5
Gelernter, J.6
-
41
-
-
0027958429
-
Relationship between homozygosity at the dopamine D3 receptor 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 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
-
42
-
-
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., et al. (1993). 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
-
43
-
-
0000655270
-
Genetic distance between populations
-
Nei, M. (1972). Genetic distance between populations. Am. Nat. 106: 283-292.
-
(1972)
Am. Nat.
, vol.106
, pp. 283-292
-
-
Nei, M.1
-
44
-
-
0032492114
-
Tryptophan hydroxylase genotype is associated with impulsive aggression measures: A preliminary study
-
New, A. S., Gelernter, J., Yovell, Y., Trestman, R. L., Nielsen, D. A., Silverman, J., Mitropoulou, V., and Siever, L. J. (1998). Tryptophan hydroxylase genotype is associated with impulsive aggression measures: A preliminary study. Am. J. Med. Genet. (Neuropsych. Genet.) 81: 13-17.
-
(1998)
Am. J. Med. Genet. (Neuropsych. Genet.)
, vol.81
, pp. 13-17
-
-
New, A.S.1
Gelernter, J.2
Yovell, Y.3
Trestman, R.L.4
Nielsen, D.A.5
Silverman, J.6
Mitropoulou, V.7
Siever, L.J.8
-
45
-
-
0026621825
-
Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism
-
Nielsen, D. A., Dean, M., and Goldman, D. (1992). Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism. Am. J. Hum. Genet. 51: 1366-1371.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1366-1371
-
-
Nielsen, D.A.1
Dean, M.2
Goldman, D.3
-
46
-
-
0028117344
-
Suicidality and 5-hydroxyindolacetic acid concentration associated with a tryptophan hydroxylase polymorphism
-
Nielsen, D. A., Goldman, D., Virkkunen, M., Tokola, R., Rawlings, R., and Linnoila, M. (1994). Suicidality and 5-hydroxyindolacetic acid concentration associated with a tryptophan hydroxylase polymorphism. Arch. Gen. Psychiatr. 51: 34-38.
-
(1994)
Arch. Gen. Psychiatr.
, vol.51
, pp. 34-38
-
-
Nielsen, D.A.1
Goldman, D.2
Virkkunen, M.3
Tokola, R.4
Rawlings, R.5
Linnoila, M.6
-
47
-
-
0031128233
-
Sequence, splice site and population frequency distribution analyses of the polymorphic human tryptophan hydroxylase intron 7
-
Nielsen, D. A., Jenkins, G. L., Stefanisko, K. M., Jefferson, K. K., and Goldman, D. (1997). Sequence, splice site and population frequency distribution analyses of the polymorphic human tryptophan hydroxylase intron 7. Mol. Brain Res. 45: 145-148.
-
(1997)
Mol. Brain Res.
, vol.45
, pp. 145-148
-
-
Nielsen, D.A.1
Jenkins, G.L.2
Stefanisko, K.M.3
Jefferson, K.K.4
Goldman, D.5
-
48
-
-
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. (1993). 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
-
49
-
-
17144437675
-
CNTF and psychiatric disorders
-
Nöthen, M. M., Cichon, S., Eggermann, K., Propping, P., Knapp, M., Maier, W., and Rietschel, M. (1996). CNTF and psychiatric disorders [letter]. Nat. Genet. 13: 142-143.
-
(1996)
Nat. Genet.
, vol.13
, pp. 142-143
-
-
Nöthen, M.M.1
Cichon, S.2
Eggermann, K.3
Propping, P.4
Knapp, M.5
Maier, W.6
Rietschel, M.7
-
50
-
-
0020434488
-
The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man
-
Olaisen, B., Teisberg, P., and Gedde-Dahl, T., Jr. (1982). The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man. Hum. Genet. 62: 233-236.
-
(1982)
Hum. Genet.
, vol.62
, pp. 233-236
-
-
Olaisen, B.1
Teisberg, P.2
Gedde-Dahl T., Jr.3
-
51
-
-
0344248890
-
-
Johns Hopkins Univ., Baltimore
-
Online Mendelian Inheritance in Man (OMIM). (1998). The Human Genome Data Base Project, Johns Hopkins Univ., Baltimore. [World Wide Web: http://gdbwww.gdb.org/omim/docs/omimtop.html]
-
(1998)
The Human Genome Data Base Project
-
-
-
52
-
-
0026498986
-
Naltrexone and coping skills therapy for alcohol dependence. A controlled study
-
O'Malley, S. S., Jaffe, A. J., Chang, G., Schottenfeld, R. S., Meyer, R. E., and Rounsaville, B. (1992). Naltrexone and coping skills therapy for alcohol dependence. A controlled study. Arch. Gen. Psychiatry 49: 881-887.
-
(1992)
Arch. Gen. Psychiatry
, vol.49
, pp. 881-887
-
-
O'Malley, S.S.1
Jaffe, A.J.2
Chang, G.3
Schottenfeld, R.S.4
Meyer, R.E.5
Rounsaville, B.6
-
54
-
-
0027460695
-
A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: No role in the genetic predisposition to bipolar affective disorder
-
Rietschel, M., Nöthen, M. M., Lannfelt, L., Sokoloff, P., Schwartz, J-C., Lanczik, M., and Fritze, J. (1993). A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: No role in the genetic predisposition to bipolar affective disorder. Psychiatry Res. 46: 253-259.
-
(1993)
Psychiatry Res.
, vol.46
, pp. 253-259
-
-
Rietschel, M.1
Nöthen, M.M.2
Lannfelt, L.3
Sokoloff, P.4
Schwartz, J.-C.5
Lanczik, M.6
Fritze, J.7
-
55
-
-
0031081813
-
Allelic association of a dopamine transporter gene polymorphism in alcohol dependence with withdrawal seizures or delirium
-
Sander, T., Harms, H., Podschus, J., Finckh, U., Nickel, B., Rolfs, A., Rommelspacher, H., and Schmidt, L. G. (1997). Allelic association of a dopamine transporter gene polymorphism in alcohol dependence with withdrawal seizures or delirium. Biol. Psychiatry 41: 299-304.
-
(1997)
Biol. Psychiatry
, vol.41
, pp. 299-304
-
-
Sander, T.1
Harms, H.2
Podschus, J.3
Finckh, U.4
Nickel, B.5
Rolfs, A.6
Rommelspacher, H.7
Schmidt, L.G.8
-
56
-
-
0028847829
-
High frequency of the apo ∈4 allele in Khoi San from South Africa
-
Sandholzer, C., Delport, R., Vermaak, H., and Utermann, G. (1995). High frequency of the apo ∈4 allele in Khoi San from South Africa. Hum. Genet. 95: 46-48.
-
(1995)
Hum. Genet.
, vol.95
, pp. 46-48
-
-
Sandholzer, C.1
Delport, R.2
Vermaak, H.3
Utermann, G.4
-
57
-
-
0027327267
-
Association of apolipoprotein E allele E4 with late-onset familial and sporadic Alzheimer's disease
-
Saunders, A. M., Strittmatter, W. J., Schmechel, D., St. George-Hyslop, P. H., Pericak-Vance, M. A., Joo, S. H., Rosi, B. L., Gusella, J. F., Crapper-MacLachlan, D. R., Alberts, M. J., Hulette, C., Crain, B., Goldgaber, D., and Roses, A. D. (1993). Association of apolipoprotein E allele E4 with late-onset familial and sporadic Alzheimer's disease. Neurology 43: 1467-1472.
-
(1993)
Neurology
, vol.43
, pp. 1467-1472
-
-
Saunders, A.M.1
Strittmatter, W.J.2
Schmechel, D.3
St. George-Hyslop, P.H.4
Pericak-Vance, M.A.5
Joo, S.H.6
Rosi, B.L.7
Gusella, J.F.8
Crapper-MacLachlan, D.R.9
Alberts, M.J.10
Hulette, C.11
Crain, B.12
Goldgaber, D.13
Roses, A.D.14
-
59
-
-
0028909113
-
Monte Carlo tests for associations between disease and alleles at highly polymorphic loci
-
Sham, P. C., and Curtis, D. (1995). Monte Carlo tests for associations between disease and alleles at highly polymorphic loci. Ann. Hum. Genet. 59: 97-105.
-
(1995)
Ann. Hum. Genet.
, vol.59
, pp. 97-105
-
-
Sham, P.C.1
Curtis, D.2
-
60
-
-
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: 506-16.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
62
-
-
0028021552
-
A null mutation in the human CNTF gene is not causally related to neurological diseases
-
Takahashi, R., Yokoji, H., Misawa, H., Hayashi, M., Hu, J., and Deguchi, T. (1994). A null mutation in the human CNTF gene is not causally related to neurological diseases. Nat. Genet. 7: 79-84.
-
(1994)
Nat. Genet.
, vol.7
, pp. 79-84
-
-
Takahashi, R.1
Yokoji, H.2
Misawa, H.3
Hayashi, M.4
Hu, J.5
Deguchi, T.6
-
63
-
-
19144373595
-
Relative risk of Alzheimer disease and age-at-onset distributions, based on APOE genotypes among elderly African Americans, Caucasians, and Hispanics in New York City
-
Tang, M. X., Maestre, G., Tsai, W. Y., Liu, X. H., Feng, L., Chung, W. Y., and Chun, M. (1996). Relative risk of Alzheimer disease and age-at-onset distributions, based on APOE genotypes among elderly African Americans, Caucasians, and Hispanics in New York City. Am. J. Hum. Genet. 58: 574-584.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 574-584
-
-
Tang, M.X.1
Maestre, G.2
Tsai, W.Y.3
Liu, X.H.4
Feng, L.5
Chung, W.Y.6
Chun, M.7
-
64
-
-
16144367111
-
CNTF and endogenous psychoses?
-
Thome, J., Kornhuber, J., Baumer, A., Rösler, M., Beckmann, H., and Riederer, P. (1996a). CNTF and endogenous psychoses? [letter]. Nat. Genet. 12: 123.
-
(1996)
Nat. Genet.
, vol.12
, pp. 123
-
-
Thome, J.1
Kornhuber, J.2
Baumer, A.3
Rösler, M.4
Beckmann, H.5
Riederer, P.6
-
65
-
-
0030026455
-
Association between a null mutation in the human ciliary neurotrophic factor (CNTF) gene and increased incidence of psychiatric diseases?
-
Thome, J., Kornhuber, J., Baumer, A., Rösler, M., Beckmann, H., and Riederer, P. (1996b). Association between a null mutation in the human ciliary neurotrophic factor (CNTF) gene and increased incidence of psychiatric diseases? Neurosci. Lett. 203: 109-110.
-
(1996)
Neurosci. Lett.
, vol.203
, pp. 109-110
-
-
Thome, J.1
Kornhuber, J.2
Baumer, A.3
Rösler, M.4
Beckmann, H.5
Riederer, P.6
-
66
-
-
84984767173
-
CNTF and psychiatric disorders
-
Thome, J., Rösler, M., Riederer, P., and Kornhuber, J. (1996c). In reply - CNTF and psychiatric disorders [letter]. Nat. Genet. 13: 144.
-
(1996)
Nat. Genet.
, vol.13
, pp. 144
-
-
Thome, J.1
Rösler, M.2
Riederer, P.3
Kornhuber, J.4
-
67
-
-
0028851862
-
Departure from Hardy-Weinberg equilibrium should be systematically tested in studies of association between genetic markers and disease
-
Tiret, L., and Cambien, F. (1995). Departure from Hardy-Weinberg equilibrium should be systematically tested in studies of association between genetic markers and disease [letter]. Circulation 92: 3364.
-
(1995)
Circulation
, vol.92
, pp. 3364
-
-
Tiret, L.1
Cambien, F.2
-
68
-
-
0029667388
-
Global patterns of linkage disequilibrium at the CD4 locus and modern human origins
-
Tishkoff, S. A., Dietzsch, E., Speed, W., Pakstis, A. J., Kidd, J. R., Cheung, K., Bonné-Tamir, B., Santachiara-Benerecetti, A. S., Moral, P., Krings, M., Pääbo, E., Watson, E., Risch, N., Jenkins, T., and Kidd, K. K. (1996). Global patterns of linkage disequilibrium at the CD4 locus and modern human origins. Science 271: 1380-1387.
-
(1996)
Science
, vol.271
, pp. 1380-1387
-
-
Tishkoff, S.A.1
Dietzsch, E.2
Speed, W.3
Pakstis, A.J.4
Kidd, J.R.5
Cheung, K.6
Bonné-Tamir, B.7
Santachiara-Benerecetti, A.S.8
Moral, P.9
Krings, M.10
Pääbo, E.11
Watson, E.12
Risch, N.13
Jenkins, T.14
Kidd, K.K.15
-
69
-
-
0028301820
-
Apolipoprotein E: Risk factor for Alzheimer's disease
-
Tsai, M. S., Tangalos, E. G., Petersen, R. C., Smiteh, G. E., Schaid, D. J., Kokmen, E., Ivnik, R. J., and Thibodeau, S. N. (1994). Apolipoprotein E: Risk factor for Alzheimer's disease. Am. J. Hum. Genet. 54: 643-649.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 643-649
-
-
Tsai, M.S.1
Tangalos, E.G.2
Petersen, R.C.3
Smiteh, G.E.4
Schaid, D.J.5
Kokmen, E.6
Ivnik, R.J.7
Thibodeau, S.N.8
-
70
-
-
0028031222
-
IDDM susceptibility associated with polymorphisms in the insulin gene region: A study of blacks, Caucasians, and Orientals
-
Undlien, D. E., Hamaguchi, K., Kimura, A., Tuomilehto-Wolf, E., Swai, A. B. M., McLarty, D. G, Tuomilehto, J., et al. (1994). IDDM susceptibility associated with polymorphisms in the insulin gene region: A study of blacks, Caucasians, and Orientals. Diabetologia 37: 745-749.
-
(1994)
Diabetologia
, vol.37
, pp. 745-749
-
-
Undlien, D.E.1
Hamaguchi, K.2
Kimura, A.3
Tuomilehto-Wolf, E.4
Swai, A.B.M.5
McLarty, D.G.6
Tuomilehto, J.7
-
71
-
-
0027078061
-
Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR
-
Vandenbergh, D. J., Persico, A. M., Hawkins, A. L., Griffin, C. A., Li, X., Jabs, E. W., and Uhl, G. R. (1992). Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR. Genomics 14: 1104-1106.
-
(1992)
Genomics
, vol.14
, pp. 1104-1106
-
-
Vandenbergh, D.J.1
Persico, A.M.2
Hawkins, A.L.3
Griffin, C.A.4
Li, X.5
Jabs, E.W.6
Uhl, G.R.7
-
72
-
-
0026591841
-
Naltrexone in the treatment of alcohol dependence
-
Volpicelli, J. R., Alterman, A. I., Hayashida, M., and O'Brien, C. P. (1992). Naltrexone in the treatment of alcohol dependence. Arch. Gen. Psychiatry 49: 876-880.
-
(1992)
Arch. Gen. Psychiatry
, vol.49
, pp. 876-880
-
-
Volpicelli, J.R.1
Alterman, A.I.2
Hayashida, M.3
O'Brien, C.P.4
-
73
-
-
0028089275
-
Human mu opiate receptor: cDNA and genomic clones, pharmacologic characterization and chromosomal assignment
-
Wang, J-B., Johnson, P. S., Persico, A. M., Hawkins, A. L., Griffin, C. A., and Uhl, G. R. (1994). Human mu opiate receptor: cDNA and genomic clones, pharmacologic characterization and chromosomal assignment. FEBS Lett. 338: 217-222.
-
(1994)
FEBS Lett.
, vol.338
, pp. 217-222
-
-
Wang, J.-B.1
Johnson, P.S.2
Persico, A.M.3
Hawkins, A.L.4
Griffin, C.A.5
Uhl, G.R.6
-
76
-
-
0019783892
-
Human E apoprotein heterogeneity: Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms
-
Weisgraber, K. H., Rall, S. C., Jr., and Mahley, R. W. (1981). Human E apoprotein heterogeneity: Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms. J. Biol. Chem. 256: 9077-9083.
-
(1981)
J. Biol. Chem.
, vol.256
, pp. 9077-9083
-
-
Weisgraber, K.H.1
Rall S.C., Jr.2
Mahley, R.W.3
-
77
-
-
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
|