Nöthen MM - Search Results

1

Mutation in the beta amyloid precursor protein gene and schizophrenia.

Nöthen MM, Erdmann J, Propping P, Lanczik M, Rietschel M, Körner J, Maier W, Albus M, Ertl MA, Wildenauer DB. Nöthen MM, et al. Biol Psychiatry. 1993 Oct 1;34(7):502. doi: 10.1016/0006-3223(93)90244-8. Biol Psychiatry. 1993. PMID: 8268336 No abstract available.

2

Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder.

Nöthen MM, Erdmann J, Körner J, Lanczik M, Fritze J, Fimmers R, Grandy DK, O'Dowd B, Propping P. Nöthen MM, et al. Am J Psychiatry. 1992 Feb;149(2):199-201. doi: 10.1176/ajp.149.2.199. Am J Psychiatry. 1992. PMID: 1346486

3

Association and linkage studies in bipolar affective disorder.

Lanczik M, Nöthen M, Körner J, Rietschel M, Erdmann J, Stratmann M, Cichon S, Lichtermann D, Maier W, Propping P, et al. Lanczik M, et al. Clin Neuropharmacol. 1992;15 Suppl 1 Pt A:580A-581A. doi: 10.1097/00002826-199201001-00301. Clin Neuropharmacol. 1992. PMID: 1498960 No abstract available.

4

Tyrosine hydroxylase polymorphisms and manic-depressive illness.

Nöthen M, Körner J, Lanczik M, Fritze J, Propping P. Nöthen M, et al. Lancet. 1990 Sep 1;336(8714):575. doi: 10.1016/0140-6736(90)92138-8. Lancet. 1990. PMID: 1975076 No abstract available.

5

Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1.

Dawson E, Parfitt E, Roberts Q, Daniels J, Lim L, Sham P, Nöthen M, Propping P, Lanczik M, Maier W, et al. Dawson E, et al. Am J Med Genet. 1995 Apr 24;60(2):94-102. doi: 10.1002/ajmg.1320600203. Am J Med Genet. 1995. PMID: 7485258

6

Genetic variation of the 5-HT2A receptor and response to clozapine.

Nöthen MM, Rietschel M, Erdmann J, Oberländer H, Möller HJ, Nober D, Propping P. Nöthen MM, et al. Lancet. 1995 Sep 30;346(8979):908-9. doi: 10.1016/s0140-6736(95)92756-5. Lancet. 1995. PMID: 7564704 No abstract available.

7

Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls.

Nöthen MM, Eggermann K, Albus M, Borrmann M, Rietschel M, Körner J, Maier W, Minges J, Lichtermann D, Franzek E, et al. Nöthen MM, et al. Am J Hum Genet. 1995 Oct;57(4):975-8. Am J Hum Genet. 1995. PMID: 7573065 Free PMC article. No abstract available.

8

Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation.

Shimron-Abarbanell D, Nöthen MM, Erdmann J, Propping P. Shimron-Abarbanell D, et al. Among authors: nothen mm. Brain Res Mol Brain Res. 1995 Apr;29(2):387-90. doi: 10.1016/0169-328x(95)00003-b. Brain Res Mol Brain Res. 1995. PMID: 7609628

9

Schizophrenia: genetic tools for unraveling the nature of a complex disorder.

Propping P, Nöthen MM. Propping P, et al. Among authors: nothen mm. Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7607-8. doi: 10.1073/pnas.92.17.7607. Proc Natl Acad Sci U S A. 1995. PMID: 7644462 Free PMC article. Review. No abstract available.

10

An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia.

Dawson E, Powell JF, Nöthen MM, Crocq MA, Lanczik M, Körner J, Rietschel M, van Os J, Wright P, Gill M. Dawson E, et al. Among authors: nothen mm. Psychiatr Genet. 1994 Winter;4(4):215-8. doi: 10.1097/00041444-199400440-00005. Psychiatr Genet. 1994. PMID: 7712118

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