Nöthen MM - Search Results

1

5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity.

Hinney A, Ziegler A, Nöthen MM, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: nothen mm. Lancet. 1997 Nov 1;350(9087):1324-5. doi: 10.1016/S0140-6736(05)62485-3. Lancet. 1997. PMID: 9357428 No abstract available.

2

Tourette's syndrome and homozygosity for the dopamine D3 receptor gene. German Tourette's Syndrome Collaborative Research Group.

Hebebrand J, Nöthen MM, Lehmkuhl G, Poustka F, Schmidt M, Propping P, Remschmidt H. Hebebrand J, et al. Among authors: nothen mm. Lancet. 1993 Jun 5;341(8858):1483-4. doi: 10.1016/0140-6736(93)90931-6. Lancet. 1993. PMID: 8099184 No abstract available.

3

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome.

Hebebrand J, Nöthen MM, Ziegler A, Klug B, Neidt H, Eggermann K, Lehmkuhl G, Poustka F, Schmidt MH, Propping P, Remschmidt H. Hebebrand J, et al. Among authors: nothen mm. Am J Hum Genet. 1997 Jul;61(1):238-9. doi: 10.1016/S0002-9297(07)64298-0. Am J Hum Genet. 1997. PMID: 9246007 Free PMC article. No abstract available.

4

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

5

Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.

Stöber G, Hebebrand J, Cichon S, Brüss M, Bönisch H, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Propping P, Nöthen MM. Stöber G, et al. Among authors: nothen mm. Am J Med Genet. 1999 Apr 16;88(2):158-63. doi: 10.1002/(sici)1096-8628(19990416)88:2<158::aid-ajmg12>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10206236

6

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

7

Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?

Le Hellard S, Theisen FM, Haberhausen M, Raeder MB, Fernø J, Gebhardt S, Hinney A, Remschmidt H, Krieg JC, Mehler-Wex C, Nöthen MM, Hebebrand J, Steen VM. Le Hellard S, et al. Among authors: nothen mm. Mol Psychiatry. 2009 Mar;14(3):308-17. doi: 10.1038/sj.mp.4002133. Epub 2008 Jan 15. Mol Psychiatry. 2009. PMID: 18195716

8

TCF7L2 polymorphism rs7903146 and predisposition for type 2 diabetes mellitus in obese children.

Roth CL, Hinney A, Reinehr T, Schreiner F, Nguyen TT, Müller T, Scholl C, Woelfle J, Karpushova A, Schäfer H, Nöthen MM, Hebebrand J. Roth CL, et al. Among authors: nothen mm. Horm Metab Res. 2008 Oct;40(10):713-7. doi: 10.1055/s-2008-1078720. Epub 2008 Jun 10. Horm Metab Res. 2008. PMID: 18546086

9

Genetic variation of the 5-HT2A receptor and response to clozapine.

Nöthen MM, Rietschel M, Erdmann J, Oberländer H, Möller HJ, Nober D, Propping P. Nöthen MM, et al. Lancet. 1995 Sep 30;346(8979):908-9. doi: 10.1016/s0140-6736(95)92756-5. Lancet. 1995. PMID: 7564704 No abstract available.

10

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.

Scherag A, Dina C, Hinney A, Vatin V, Scherag S, Vogel CI, Müller TD, Grallert H, Wichmann HE, Balkau B, Heude B, Jarvelin MR, Hartikainen AL, Levy-Marchal C, Weill J, Delplanque J, Körner A, Kiess W, Kovacs P, Rayner NW, Prokopenko I, McCarthy MI, Schäfer H, Jarick I, Boeing H, Fisher E, Reinehr T, Heinrich J, Rzehak P, Berdel D, Borte M, Biebermann H, Krude H, Rosskopf D, Rimmbach C, Rief W, Fromme T, Klingenspor M, Schürmann A, Schulz N, Nöthen MM, Mühleisen TW, Erbel R, Jöckel KH, Moebus S, Boes T, Illig T, Froguel P, Hebebrand J, Meyre D. Scherag A, et al. Among authors: nothen mm. PLoS Genet. 2010 Apr 22;6(4):e1000916. doi: 10.1371/journal.pgen.1000916. PLoS Genet. 2010. PMID: 20421936 Free PMC article.

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