Schulze T - Search Results

1

Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study.

Souery D, Van Gestel S, Massat I, Blairy S, Adolfsson R, Blackwood D, Del-Favero J, Dikeos D, Jakovljevic M, Kaneva R, Lattuada E, Lerer B, Lilli R, Milanova V, Muir W, Nöthen M, Oruc L, Papadimitriou G, Propping P, Schulze T, Serretti A, Shapira B, Smeraldi E, Stefanis C, Thomson M, Van Broeckhoven C, Mendlewicz J. Souery D, et al. Among authors: schulze t. Biol Psychiatry. 2001 Mar 1;49(5):405-9. doi: 10.1016/s0006-3223(00)01043-x. Biol Psychiatry. 2001. PMID: 11274651

2

Dopamine D3 receptor variant and tardive dyskinesia.

Rietschel M, Krauss H, Müller DJ, Schulze TG, Knapp M, Marwinski K, Maroldt AO, Paus S, Grünhage F, Propping P, Maier W, Held T, Nöthen MM. Rietschel M, et al. Among authors: schulze tg. Eur Arch Psychiatry Clin Neurosci. 2000;250(1):31-5. doi: 10.1007/pl00007536. Eur Arch Psychiatry Clin Neurosci. 2000. PMID: 10738862

3

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1).

Grünhage F, Schulze TG, Müller DJ, Lanczik M, Franzek E, Albus M, Borrmann-Hassenbach M, Knapp M, Cichon S, Maier W, Rietschel M, Propping P, Nöthen MM. Grünhage F, et al. Among authors: schulze tg. Mol Psychiatry. 2000 May;5(3):275-82. doi: 10.1038/sj.mp.4000711. Mol Psychiatry. 2000. PMID: 10889530

4

Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia.

Vogt IR, Shimron-Abarbanell D, Neidt H, Erdmann J, Cichon S, Schulze TG, Müller DJ, Maier W, Albus M, Borrmann-Hassenbach M, Knapp M, Rietschel M, Propping P, Nöthen MM. Vogt IR, et al. Among authors: schulze tg. Am J Med Genet. 2000 Apr 3;96(2):217-21. Am J Med Genet. 2000. PMID: 10893499

5

Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls.

Rietschel M, Schorr A, Albus M, Franzek E, Kreiner R, Held T, Knapp M, Müller DJ, Schulze TG, Propping P, Maier W, Nöthen MM. Rietschel M, et al. Among authors: schulze tg. Am J Med Genet. 2000 Jun 12;96(3):310-1. doi: 10.1002/1096-8628(20000612)96:3<310::aid-ajmg15>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10898906

6

Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder.

Schulze TG, Müller DJ, Krauss H, Scherk H, Ohlraun S, Syagailo YV, Windemuth C, Neidt H, Grässle M, Papassotiropoulos A, Heun R, Nöthen MM, Maier W, Lesch KP, Rietschel M. Schulze TG, et al. Am J Med Genet. 2000 Dec 4;96(6):801-3. Am J Med Genet. 2000. PMID: 11121185

7

Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?

Schulze TG, Müller DJ, Krauss H, Marwinski K, Maroldt AO, Novo Y Fernández A, Fimmers R, Held T, Maier W, Nöthen MM, Rietschel M. Schulze TG, et al. Eur Psychiatry. 2001 Feb;16(1):71-4. doi: 10.1016/s0924-9338(00)00539-3. Eur Psychiatry. 2001. PMID: 11246296

8

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26.

Cichon S, Schmidt-Wolf G, Schumacher J, Müller DJ, Hürter 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, Nöthen MM. Cichon S, et al. Among authors: schulze tg. Mol Psychiatry. 2001 May;6(3):342-9. doi: 10.1038/sj.mp.4000864. Mol Psychiatry. 2001. PMID: 11326307

9

Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios.

Schulze TG, Müller DJ, Krauss H, Gross M, Bauer I, Fangerau-Lefèvre H, Illes F, Ohlraun S, Fimmers R, Cichon S, Held T, Propping P, Nöthen MM, Maier W, Rietschel M. Schulze TG, et al. Am J Med Genet. 2001 May 8;105(4):351-3. doi: 10.1002/ajmg.1348. Am J Med Genet. 2001. PMID: 11378849

10

Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.

Schulze TG, Schumacher J, Müller DJ, Krauss H, Alfter D, Maroldt A, Ahle G, Maroldt AO, Novo y Fernández A, Weber T, Held T, Propping P, Maier W, Nöthen MM, Rietschel M. Schulze TG, et al. Am J Med Genet. 2001 Aug 8;105(6):498-501. doi: 10.1002/ajmg.1472. Am J Med Genet. 2001. PMID: 11496364

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