Nöthen MM - Search Results

1

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Nöthen MM, Cichon S, Mühleisen TW. Priebe L, et al. Among authors: nothen mm. Mol Psychiatry. 2012 Apr;17(4):421-32. doi: 10.1038/mp.2011.8. Epub 2011 Mar 1. Mol Psychiatry. 2012. PMID: 21358712

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

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.

7

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

8

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.

9

Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding region.

Deckert J, Nöthen MM, Bryant SP, Ren H, Wolf HK, Stiles GL, Spurr NK, Propping P. Deckert J, et al. Among authors: nothen mm. Biochem Biophys Res Commun. 1995 Sep 14;214(2):614-21. doi: 10.1006/bbrc.1995.2330. Biochem Biophys Res Commun. 1995. PMID: 7677773

10

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

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