Nöthen MM - Search Results

1

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects.

Erk S, Meyer-Lindenberg A, Linden DEJ, Lancaster T, Mohnke S, Grimm O, Degenhardt F, Holmans P, Pocklington A, Schmierer P, Haddad L, Mühleisen TW, Mattheisen M, Witt SH, Romanczuk-Seiferth N, Tost H, Schott BH, Cichon S, Nöthen MM, Rietschel M, Heinz A, Walter H. Erk S, et al. Among authors: nothen mm. Neuroimage. 2014 Jul 1;94:147-154. doi: 10.1016/j.neuroimage.2014.03.007. Epub 2014 Mar 16. Neuroimage. 2014. PMID: 24642287

2

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

3

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

4

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

5

[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.

6

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

7

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.

8

Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.

Dewald G, Nöthen MM, Cichon S. Dewald G, et al. Among authors: nothen mm. Biochem Biophys Res Commun. 1993 Jul 15;194(1):458-64. doi: 10.1006/bbrc.1993.1841. Biochem Biophys Res Commun. 1993. PMID: 8101442

9

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).

Cichon S, Nöthen MM, Erdmann J, Propping P. Cichon S, et al. Among authors: nothen mm. Hum Mol Genet. 1994 Jan;3(1):209. doi: 10.1093/hmg/3.1.209. Hum Mol Genet. 1994. PMID: 8162032 No abstract available.

10

Familial cosegregation of affective disorder and Hailey-Hailey disease.

Körner J, Rietschel M, Nöthen MM, Wilk CM, Bauer R, Propping P, Möller HJ. Körner J, et al. Among authors: nothen mm. Br J Psychiatry. 1993 Jul;163:109-10. doi: 10.1192/bjp.163.1.109. Br J Psychiatry. 1993. PMID: 8353676

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