Nöthen MM - Search Results

1

No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.

Georgi A, Jamra RA, Schumacher J, Becker T, Schmael C, Deschner M, Höfels S, Wulff M, Schwarz M, Klopp N, Illig T, Propping P, Cichon S, Nöthen MM, Rietschel M, Schulze TG. Georgi A, et al. Among authors: nothen mm. Psychiatr Genet. 2006 Oct;16(5):183-4. doi: 10.1097/01.ypg.0000242194.36150.2b. Psychiatr Genet. 2006. PMID: 16969270

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

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

5

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.

6

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

7

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.

8

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

9

Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls.

Körner J, Rietschel M, Hunt N, Castle D, Gill M, Nöthen MM, Craddock N, Daniels J, Owen M, Fimmers R, et al. Körner J, et al. Among authors: nothen mm. Psychiatr Genet. 1994 Fall;4(3):167-75. doi: 10.1097/00041444-199400430-00007. Psychiatr Genet. 1994. PMID: 7719703

10

Tyrosine hydroxylase gene and manic-depressive illness.

Rietschel M, Nöthen MM, Maier W, Albus M, Franzek E, Propping P. Rietschel M, et al. Among authors: nothen mm. Lancet. 1995 May 27;345(8961):1368. doi: 10.1016/s0140-6736(95)92566-x. Lancet. 1995. PMID: 7752774 No abstract available.

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