-
3
-
-
0031914649
-
Association between the tryptophan hydroxylase gene and manic-depressive illness
-
(1998)
Arch Gen Psychiatry
, vol.55
, pp. 33-37
-
-
Bellivier, F.1
Leboyer, M.2
Courtet, P.3
Buresi, C.4
Beaufils, B.5
Samolyk, D.6
Allilaire, J.F.7
Feingold, J.8
Mallet, J.9
Malafosse, A.10
-
4
-
-
0034088511
-
Tryptophan hydroxylase polymorphisms in suicide victims
-
(2000)
Psychiatr Genet
, vol.10
, pp. 13-17
-
-
Bennett, P.J.1
McMahon, W.M.2
Watabe, J.3
Achilles, J.4
Bacon, M.5
Coon, H.6
Grey, T.7
Keller, T.8
Tate, D.9
Tcaciuc, I.10
Workman, J.11
Gray, D.12
-
6
-
-
2142702029
-
Genome-wide search for schizophrenia susceptibility loci: The NIMH Genetics Initiative and Millennium Consortium
-
(1998)
Am J Med Genet
, vol.81
, pp. 275-281
-
-
Cloninger, C.R.1
Kaufmann, C.A.2
Faraone, S.V.3
Malaspina, D.4
Svrakic, D.M.5
Harkavy-Friedman, J.6
Suarez, B.K.7
Matise, T.C.8
Shore, D.9
Lee, H.10
Hampe, C.L.11
Wynne, D.12
Drain, C.13
Markel, P.D.14
Zambuto, C.T.15
Schmitt, K.16
Tsuang, M.T.17
-
7
-
-
0032871864
-
Association of unipolar major depressive disorder with genes of the serotonergic and dopaminergic pathways
-
(1999)
Mol Psychiatry
, vol.4
, pp. 389-392
-
-
Frisch, A.1
Postilnick, D.2
Rockah, R.3
Michaelovsky, E.4
Postilnick, S.5
Birman, E.6
Laor, N.7
Rauchverger, B.8
Kreinin, A.9
Poyurovsky, M.10
Schneidman, M.11
Modai, I.12
Weizman, R.13
-
8
-
-
0032496310
-
No association of the tryptophan hydroxylase gene with bipolar affective disorder, unipolar affective disorder, or suicidal behavior in major affective disorder
-
(1998)
Am J Med Genet
, vol.81
, pp. 245-247
-
-
Furlong, R.A.1
Ho, L.2
Rubinsztein, J.S.3
Walsh, C.4
Paykel, E.S.5
Rubinsztein, D.C.6
-
10
-
-
0031684199
-
Systematic search for variations in the tyrosine hydroxylase gene and their associations with schizophrenia, affective disorders, and alcoholism
-
(1998)
Am J Med Genet
, vol.81
, pp. 388-396
-
-
Ishiguro, H.1
Arinami, T.2
Saito, T.3
Akazawa, S.4
Enomoto, M.5
Mitushio, H.6
Fujishiro, H.7
Tada, K.8
Akimoto, Y.9
Mifune, H.10
Shiozuka, S.11
Hamaguchi, H.12
Toru, M.13
Shibuya, H.14
-
13
-
-
0027251133
-
The dopamine hypothesis of schizophrenia: Limbic interactions with serotonin and norepinephrine
-
(1993)
Psychopharmacology
, vol.112
-
-
Joyce, J.N.1
-
19
-
-
0030035985
-
Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1023-1028
-
-
Ludecke, B.1
Knappskog, P.M.2
Clayton, P.T.3
Surtees, R.A.4
Clelland, J.D.5
Heales, S.J.6
Brand, M.P.7
Bartholome, K.8
Flatmark, T.9
-
21
-
-
0029084535
-
A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patients
-
(1995)
Comptes Rendus De L Academie Des Sciences-Serie Iii, Sciences De La Vie
, vol.318
, pp. 803-809
-
-
Meloni, R.1
Laurent, C.2
Campion, D.3
Ben Hadjali, B.4
Thibaut, F.5
Dollfus, S.6
Petit, M.7
Samolyk, D.8
Martinez, M.9
Poirier, M.F.10
Mallet, J.11
-
22
-
-
0032492114
-
Tryptophan hydroxylase genotype is associated with impulsive-aggression measures: A preliminary study
-
(1998)
Am J Med 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
-
25
-
-
0031872284
-
A tryptophan hydroxylase gene marker for suicidality and alcoholism
-
(1998)
Arch Gen Psychiatry
, vol.55
, pp. 593-602
-
-
Nielsen, D.A.1
Virkkunen, M.2
Lappalainen, J.3
Eggert, M.4
Brown, G.L.5
Long, J.C.6
Goldman, D.7
Linnoila, M.8
-
28
-
-
0033965134
-
Identification and analysis of new sequence variants in the human tryptophan hydroxylase (TpH) gene
-
(2000)
Mol Psychiatry
, vol.5
, pp. 49-55
-
-
Paoloni-Giacobino, A.1
Mouthon, D.2
Lambercy, C.3
Vessaz, M.4
Coutant-Zimmerli, S.5
Rudolph, W.6
Malafosse, A.7
Buresi, C.8
-
31
-
-
0002156245
-
Phenylalanine hydroxylase gene mutation associated with schizophrenia and African-American ethnic status
-
(1999)
Schizophr Res
, vol.36
, pp. 95
-
-
Richardson, M.A.1
Guttler, F.2
Guldberg, P.3
Reilly, M.4
Suckow, R.5
Read, L.6
Chao, H.7
Clelland, J.8
-
32
-
-
0033986264
-
PAHdb: A locus-specific knowledge base
-
(2000)
Hum Mutat
, vol.15
, pp. 99-104
-
-
Scriver, C.R.1
Waters, P.J.2
Sarkissian, C.3
Ryan, S.4
Prevost, L.5
Cote, D.6
Novak, J.7
Teebi, S.8
Nowacki, P.M.9
-
34
-
-
0031901965
-
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-dopa-responsive dystonia in the Dutch population
-
(1998)
Hum Genet
, vol.102
, pp. 644-646
-
-
Van den Heuvel, L.P.1
Luiten, B.2
Smeitink, J.A.3
De Rijk-van Andel, J.F.4
Hyland, K.5
Steenbergen-Spanjers, G.C.6
Janssen, R.J.7
Wevers, R.A.8
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