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Results: 1-25 | 26-43
Results: 1-25/43
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26
Authors: Cichon, S Schmidt-Wolf, G Schumacher, J Muller, DJ Hurter, M Schulze, TG Albus, M Borrmann-Hassenbach, M Franzek, E Lanczik, M Fritze, J Kreiner, R Weigelt, B Minges, J Lichtermann, D Lerer, B Kanyas, K Strauch, K Windemuth, C Baur, MP Wienker, TF Maier, W Rietschel, M Propping, P Nothen, MM
Citation: S. Cichon et al., A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26, MOL PSYCHI, 6(3), 2001, pp. 342-349
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach
Authors: Wang, T Franke, P Neidt, H Cichon, S Knapp, M Lichtermann, D Maier, W Propping, P Nothen, MM
Citation: T. Wang et al., Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach, MOL PSYCHI, 6(1), 2001, pp. 109-111
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease
Authors: Betz, RC Schoser, BGH Kasper, D Ricker, K Ramirez, A Stein, V Torbergsen, T Lee, YA Nothen, MM Wienker, TF Malin, JP Propping, P Reis, A Mortier, W Jentsch, TJ Vorgerd, M Kubisch, C
Citation: Rc. Betz et al., Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease, NAT GENET, 28(3), 2001, pp. 218-219
Association between the 5 ' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder
Authors: Niesler, B Flohr, T Nothen, MM Fischer, C Rietschel, M Franzek, E Albus, M Propping, P Rappold, GA
Citation: B. Niesler et al., Association between the 5 ' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder, PHARMACOGEN, 11(6), 2001, pp. 471-475
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients
Authors: Niesler, B Weiss, B Fischer, C Nothen, MM Propping, P Bondy, B Rietschel, M Maier, W Albus, M Franzek, E Rappold, GA
Citation: B. Niesler et al., Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients, PHARMACOGEN, 11(1), 2001, pp. 21-27
Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?
Authors: Schulze, TG Muller, DJ Krauss, H Marwinski, K Maroldt, AO Fernandez, ANY Fimmers, R Held, T Maier, W Nothen, MM Rietschel, M
Citation: Tg. Schulze et al., Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?, EUR PSYCHIA, 16(1), 2001, pp. 71-74
Mutational analysis of TSC1 and TSC2 genes in gangliogliomas
Authors: Becker, AJ Lobach, M Klein, H Normann, S Nothen, MM von Deimling, A Mizuguchi, M Elger, CE Schramm, J Wiestler, OD Blumcke, I
Citation: Aj. Becker et al., Mutational analysis of TSC1 and TSC2 genes in gangliogliomas, NEUROP AP N, 27(2), 2001, pp. 105-114
Different familial transmission patterns in bipolar I disorder with onset before and after age 25
Authors: Grigoroiu-Serbanescu, M Martinez, M Nothen, MM Grinberg, M Sima, D Propping, P Marinescu, E Hrestic, M
Citation: M. Grigoroiu-serbanescu et al., Different familial transmission patterns in bipolar I disorder with onset before and after age 25, AM J MED G, 105(8), 2001, pp. 765-773
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and Tardive dyskinesia in schizophrenia
Authors: Schulze, TG Schumacher, J Muller, DJ Krauss, H Alfter, D Maroldt, A Ahle, G Maroldt, AO Fernandez, ANY Weber, T Held, T Propping, P Maier, W Nothen, MM Rietschel, M
Citation: Tg. Schulze et al., Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and Tardive dyskinesia in schizophrenia, AM J MED G, 105(6), 2001, pp. 498-501
No association between a promoter dopamine D-4 receptor gene variant and schizophrenia
Authors: Jonsson, EG Ivo, R Forslund, K Mattila-Evenden, M Rylander, G Cichon, S Propping, P Nothen, MM Asberg, M Sedvall, GC
Citation: Eg. Jonsson et al., No association between a promoter dopamine D-4 receptor gene variant and schizophrenia, AM J MED G, 105(6), 2001, pp. 525-528
Brief research communication - Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios
Authors: Schulze, TG Muller, DJ Krauss, H Gross, M Bauer, I Fangerau-Lefevre, H Illes, F Ohlraun, S Fimmers, R Cichon, S Held, T Propping, P Nothen, MM Maier, W Rietschell, M
Citation: Tg. Schulze et al., Brief research communication - Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios, AM J MED G, 105(4), 2001, pp. 351-353
Nonreplication of association between mu-opioid-receptor gene (OPRM1) A(118)G polymorphism and substance dependence
Authors: Franke, P Wang, T Nothen, MM Knapp, M Neidt, H Albrecht, S Jahnes, E Propping, P Maier, W
Citation: P. Franke et al., Nonreplication of association between mu-opioid-receptor gene (OPRM1) A(118)G polymorphism and substance dependence, AM J MED G, 105(1), 2001, pp. 114-119
Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder
Authors: Barr, CL Xu, C Kroft, J Feng, Y Wigg, K Zai, G Tannock, R Schachar, R Malone, M Roberts, W Nothen, MM Grunhage, F Vandenbergh, DJ Uhl, G Sunohara, G King, N Kennedy, JL
Citation: Cl. Barr et al., Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder, BIOL PSYCHI, 49(4), 2001, pp. 333-339
Variant 1859G -> A (Arg620Gln) of the "hairless" gene: Absence of association with papular atrichia or androgenetic alopecia
Authors: Hillmer, AM Kruse, R Betz, RC Schumacher, J Heyn, U Propping, P Nothen, MM Cichon, S
Citation: Am. Hillmer et al., Variant 1859G -> A (Arg620Gln) of the "hairless" gene: Absence of association with papular atrichia or androgenetic alopecia, AM J HU GEN, 69(1), 2001, pp. 235-237
Familial occurrence of tardive dyskinesia
Authors: Muller, DJ Schulze, TG Knapp, M Held, T Krauss, H Weber, T Ahle, G Maroldt, A Alfter, D Maier, W Nothen, MM Rietschel, M
Citation: Dj. Muller et al., Familial occurrence of tardive dyskinesia, ACT PSYC SC, 104(5), 2001, pp. 375-379
Novel 5 '-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder
Authors: Deckert, J Meyer, J Catalano, M Bosi, M Sand, P DiBella, D Ortega, G Stober, G Franke, P Nothen, MM Fritze, J Maier, W Beckmann, H Propping, P Bellodi, L Lesch, KP
Citation: J. Deckert et al., Novel 5 '-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder, IN J NEUROP, 3(4), 2000, pp. 321-325
Systematic screening for DNA sequence Variation in the coding region of the human dopamine transporter gene (DAT1)
Authors: Grunhage, F Schulze, TG Muller, DJ Lanczik, M Franzek, E Albus, M Borrmann-Hassenbach, M Knapp, M Cichon, S Maier, W Rietschel, M Propping, P Nothen, MM
Citation: F. Grunhage et al., Systematic screening for DNA sequence Variation in the coding region of the human dopamine transporter gene (DAT1), MOL PSYCHI, 5(3), 2000, pp. 275-282
Analysis of parental-origin effects in linkage data - Reply
Authors: Strauch, K Fimmers, R Wienker, TF Baur, MP Cichon, S Propping, P Nothen, MM
Citation: K. Strauch et al., Analysis of parental-origin effects in linkage data - Reply, MOL PSYCHI, 5(2), 2000, pp. 126-127
DRD4 exon IIIVNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach
Authors: Franke, P Nothen, MM Wang, T Knapp, M Lichtermann, D Neidt, H Sander, T Propping, P Maier, W
Citation: P. Franke et al., DRD4 exon IIIVNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach, MOL PSYCHI, 5(1), 2000, pp. 101-104
Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach
Authors: Franke, P Wang, T Nothen, MM Knapp, M Neith, H Lichtermann, D Zur Capellen, KM Sander, T Propping, P Maier, W
Citation: P. Franke et al., Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach, ADDICT BIOL, 5(3), 2000, pp. 289-295
Pharmacological properties of naturally occurring variants of the human norepinephrine transporter
Authors: Runkel, F Bruss, M Nothen, MM Stober, G Propping, P Bonisch, H
Citation: F. Runkel et al., Pharmacological properties of naturally occurring variants of the human norepinephrine transporter, PHARMACOGEN, 10(5), 2000, pp. 397-405
Dopamine D-3 receptor variant and tardive dyskinesia
Authors: Rietschel, M Krauss, H Muller, DJ Schulze, TG Knapp, M Marwinski, K Maroldt, AO Paus, S Grunhage, F Propping, P Maier, W Held, T Nothen, MM
Citation: M. Rietschel et al., Dopamine D-3 receptor variant and tardive dyskinesia, EUR ARCH PS, 250(1), 2000, pp. 31-35
Pharmacogenetics of schizophrenia
Authors: Cichon, S Nothen, MM Rietschel, M Propping, P
Citation: S. Cichon et al., Pharmacogenetics of schizophrenia, AM J MED G, 97(1), 2000, pp. 98-106
Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder
Authors: Schulze, TG Muller, DJ Krauss, H Scherk, H Ohlraun, S Syagailo, YV Windemuth, C Neidt, H Grassle, M Papassotiropoulos, A Heun, R Nothen, MM Maier, W Lesch, KP Rietschel, M
Citation: Tg. Schulze et al., Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder, AM J MED G, 96(6), 2000, pp. 801-803
Association study of the tryptophan hydroxylase gene and bipolar affectivedisorder using family-based internal controls
Authors: Rietschel, M Schorr, A Albus, M Franzek, E Kreiner, R Held, T Knapp, M Muller, DJ Schulze, TG Propping, P Maier, W Nothen, MM
Citation: M. Rietschel et al., Association study of the tryptophan hydroxylase gene and bipolar affectivedisorder using family-based internal controls, AM J MED G, 96(3), 2000, pp. 310-311
Risultati: 1-25 | 26-43