Nöthen MM - Search Results

1

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene.

Luo XJ, Li M, Huang L, Steinberg S, Mattheisen M, Liang G, Donohoe G, Shi Y, Chen C, Yue W, Alkelai A, Lerer B, Li Z, Yi Q, Rietschel M, Cichon S, Collier DA, Tosato S, Suvisaari J, Rujescu D, Golimbet V, Silagadze T, Durmishi N, Milovancevic MP, Stefansson H, Schulze TG, Nöthen MM, Chen C, Lyne R, Morris DW, Gill M, Corvin A, Zhang D, Dong Q, Moyzis RK, Stefansson K, Sigurdsson E, Hu F; MooDS SCZ Consortium; Su B, Gan L. Luo XJ, et al. Among authors: nothen mm. Mol Psychiatry. 2014 Jul;19(7):774-83. doi: 10.1038/mp.2013.103. Epub 2013 Aug 20. Mol Psychiatry. 2014. PMID: 23958956

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

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

6

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.

7

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

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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