Nöthen MM - Search Results

1

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

2

No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndrome.

Hebebrand J, Nöthen MM, Klug B, Wettke-Schäfer R, Camps A, Lisch S, Hemmer S, von Gontard A, Poustka F, Lehmkuhl G, et al. Hebebrand J, et al. Among authors: nothen mm. Biol Psychiatry. 1995 Feb 1;37(3):209-11. doi: 10.1016/0006-3223(94)00214-n. Biol Psychiatry. 1995. PMID: 7727632 No abstract available.

3

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

4

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.

5

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.

6

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

7

Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.

Nöthen MM, Schulte-Körne G, Grimm T, Cichon S, Vogt IR, Müller-Myhsok B, Propping P, Remschmidt H. Nöthen MM, et al. Eur Child Adolesc Psychiatry. 1999;8 Suppl 3:56-9. doi: 10.1007/pl00010696. Eur Child Adolesc Psychiatry. 1999. PMID: 10638372

8

Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder.

Schumacher J, Jamra RA, Freudenberg J, Becker T, Ohlraun S, Otte AC, Tullius M, Kovalenko S, Bogaert AV, Maier W, Rietschel M, Propping P, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: nothen mm. Mol Psychiatry. 2004 Feb;9(2):203-7. doi: 10.1038/sj.mp.4001421. Mol Psychiatry. 2004. PMID: 14966479

9

Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene.

Gadzicki D, Müller-Vahl KR, Heller D, Ossege S, Nöthen MM, Hebebrand J, Stuhrmann M. Gadzicki D, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):97-103. doi: 10.1002/ajmg.b.20159. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15108190

10

Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.

Abou Jamra R, Becker T, Georgi A, Feulner T, Schumacher J, Stromaier J, Schirmbeck F, Schulze TG, Propping P, Rietschel M, Nöthen MM, Cichon S. Abou Jamra R, et al. Among authors: nothen mm. Mol Psychiatry. 2008 Mar;13(3):277-84. doi: 10.1038/sj.mp.4002111. Epub 2007 Oct 16. Mol Psychiatry. 2008. PMID: 17938632

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