Nöthen MM - Search Results

1

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: nothen mm. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994

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

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

4

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.

5

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

6

Identification of genetic variation in the human serotonin 1D beta receptor gene.

Nöthen MM, Erdmann J, Shimron-Abarbanell D, Propping P. Nöthen MM, et al. Biochem Biophys Res Commun. 1994 Dec 15;205(2):1194-200. doi: 10.1006/bbrc.1994.2792. Biochem Biophys Res Commun. 1994. PMID: 7802650

7

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method.

Nöthen MM, Hebebrand J, Knapp M, Hebebrand K, Camps A, von Gontard A, Wettke-Schäfer R, Lisch S, Cichon S, Poustka F, et al. Nöthen MM, et al. Am J Med Genet. 1994 Sep 15;54(3):249-52. doi: 10.1002/ajmg.1320540311. Am J Med Genet. 1994. PMID: 7810582

8

[Genetic association in psychiatric diseases. Concepts and findings].

Propping P, Nöthen MM, Körner J, Rietschel M, Maier W. Propping P, et al. Among authors: nothen mm. Nervenarzt. 1994 Nov;65(11):725-40. Nervenarzt. 1994. PMID: 7816149 Review. German. No abstract available.

9

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.

Nöthen MM, Cichon S, Hemmer S, Hebebrand J, Remschmidt H, Lehmkuhl G, Poustka F, Schmidt M, Catalano M, Fimmers R, et al. Nöthen MM, et al. Hum Mol Genet. 1994 Dec;3(12):2207-12. doi: 10.1093/hmg/3.12.2207. Hum Mol Genet. 1994. PMID: 7881421

10

Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression.

Cichon S, Nöthen MM, Rietschel M, Körner J, Propping P. Cichon S, et al. Among authors: nothen mm. Biol Psychiatry. 1994 Dec 15;36(12):850-3. doi: 10.1016/0006-3223(94)90597-5. Biol Psychiatry. 1994. PMID: 7893850 Clinical Trial. No abstract available.

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