Siegfried W - Search Results

1

Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.

Friedel S, Horro FF, Wermter AK, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt HP, Siegfried W, Remschmidt H, Hinney A, Hebebrand J. Friedel S, et al. Among authors: siegfried w. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9. doi: 10.1002/ajmg.b.30090. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15457498

2

Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students.

Hinney A, Hoch A, Geller F, Schäfer H, Siegfried W, Goldschmidt H, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: siegfried w. J Clin Endocrinol Metab. 2002 Jun;87(6):2716. doi: 10.1210/jcem.87.6.8672. J Clin Endocrinol Metab. 2002. PMID: 12050239

3

Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents.

Hölter K, Wermter AK, Scherag A, Siegfried W, Goldschmidt H, Hebebrand J, Hinney A. Hölter K, et al. Among authors: siegfried w. BMC Med Genet. 2007 Apr 19;8:21. doi: 10.1186/1471-2350-8-21. BMC Med Genet. 2007. PMID: 17445271 Free PMC article.

4

No evidence for involvement of polymorphisms of the dopamine D4 receptor gene in anorexia nervosa, underweight, and obesity.

Hinney A, Schneider J, Ziegler A, Lehmkuhl G, Poustka F, Schmidt MH, Mayer H, Siegfried W, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: siegfried w. Am J Med Genet. 1999 Dec 15;88(6):594-7. Am J Med Genet. 1999. PMID: 10581473

5

No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans.

Schäuble N, Geller F, Siegfried W, Goldschmidt H, Remschmidt H, Hinney A, Hebebrand J. Schäuble N, et al. Among authors: siegfried w. Exp Clin Endocrinol Diabetes. 2003 Apr;111(2):73-6. doi: 10.1055/s-2003-39232. Exp Clin Endocrinol Diabetes. 2003. PMID: 12746756

6

Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene.

Sina M, Hinney A, Ziegler A, Neupert T, Mayer H, Siegfried W, Blum WF, Remschmidt H, Hebebrand J. Sina M, et al. Among authors: siegfried w. Am J Hum Genet. 1999 Dec;65(6):1501-7. doi: 10.1086/302660. Am J Hum Genet. 1999. PMID: 10577903 Free PMC article.

7

No evidence for involvement of the calpain-10 gene 'high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity.

Hinney A, Antwerpen B, Geller F, Schäfer H, Siegfried W, Goldschmidt H, Remschmidt H, Ziegler A, Hebebrand J. Hinney A, et al. Among authors: siegfried w. Mol Genet Metab. 2002 Jun;76(2):152-6. doi: 10.1016/s1096-7192(02)00035-5. Mol Genet Metab. 2002. PMID: 12083814

8

Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.

Hinney A, Hohmann S, Geller F, Vogel C, Hess C, Wermter AK, Brokamp B, Goldschmidt H, Siegfried W, Remschmidt H, Schäfer H, Gudermann T, Hebebrand J. Hinney A, et al. Among authors: siegfried w. J Clin Endocrinol Metab. 2003 Sep;88(9):4258-67. doi: 10.1210/jc.2003-030233. J Clin Endocrinol Metab. 2003. PMID: 12970296 Free article. Clinical Trial.

9

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity.

Schäuble N, Reichwald K, Grassl W, Bechstein H, Müller HC, Scherag A, Geller F, Utting M, Siegfried W, Goldschmidt H, Blundell J, Lawton C, Alam R, Whybrow S, Stubbs J, Platzer M, Hebebrand J, Hinney A. Schäuble N, et al. Among authors: siegfried w. J Nutr. 2005 Jun;135(6):1387-92. doi: 10.1093/jn/135.6.1387. J Nutr. 2005. PMID: 15930442 Free article.

10

Mutation analysis of the MCHR1 gene in human obesity.

Wermter AK, Reichwald K, Büch T, Geller F, Platzer C, Huse K, Hess C, Remschmidt H, Gudermann T, Preibisch G, Siegfried W, Goldschmidt HP, Li WD, Price RA, Biebermann H, Krude H, Vollmert C, Wichmann HE, Illig T, Sørensen TI, Astrup A, Larsen LH, Pedersen O, Eberlé D, Clément K, Blundell J, Wabitsch M, Schäfer H, Platzer M, Hinney A, Hebebrand J. Wermter AK, et al. Among authors: siegfried w. Eur J Endocrinol. 2005 Jun;152(6):851-62. doi: 10.1530/eje.1.01917. Eur J Endocrinol. 2005. PMID: 15941924

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