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Wolfgang Siegfried

Research Profile

Disorders

Physiology

Genes & Molecular Sequences

Concepts & Ideas

Phenomena

Polymorphism, Single-Stranded Conformational

Geographic Areas

Germany

Chemicals & Drugs

Procedures

Case Control Studies

Living Beings

Nuclear Family

Co-author Network

Publications

TOP 3
Anne-Kathrin Wermter; André Scherag; Katja Holter; Kathrin Reichwald; Peter Lichtner; Wolfgang Siegfried; John Blundell; Clare Lawton; Stephen Whybrow; James Stubbs; Jonathan R Arch; Thomas Meitinger; Matthias Platzer; Anke Hinney; Johannes Hebebrand
Procolipase gene: no association with early-onset obesity or fat intake.
Anika Hennings; Anja Hilbert; Jobst Thomas; Wolfgang Siegfried; Winfried Rief
[Reduction of stigma against obese people: effects of an educational film].
Katja Hölter; Anne-Kathrin Wermter; André Scherag; Wolfgang Siegfried; Hanspeter Goldschmidt; Johannes Hebebrand; Anke Hinney
Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents.

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All Publications

2009: Anne-Kathrin Wermter; André Scherag; Katja Holter; Kathrin Reichwald; Peter Lichtner; Wolfgang Siegfried; John Blundell; Clare Lawton; Stephen Whybrow; James Stubbs; Jonathan R Arch; Thomas Meitinger; Matthias Platzer; Anke Hinney; Johannes Hebebrand
Procolipase gene: no association with early-onset obesity or fat intake.
Obesity facts 2009;2(1):40-4.
2007: Anika Hennings; Anja Hilbert; Jobst Thomas; Wolfgang Siegfried; Winfried Rief
[Reduction of stigma against obese people: effects of an educational film].
Psychotherapie, Psychosomatik, medizinische Psychologie 2007;57(9-10):359-63.
2007: Katja Hölter; Anne-Kathrin Wermter; André Scherag; Wolfgang Siegfried; Hanspeter Goldschmidt; Johannes Hebebrand; Anke Hinney
Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents.
BMC medical genetics 2007;8():21.
2005: Nadine Schäuble; Kathrin Reichwald; Wolfgang Grassl; Helen Bechstein; Hans-Christian Müller; André Scherag; Frank Geller; Michael Utting; Wolfgang Siegfried; Hanspeter Goldschmidt; John Blundell; Clare L Lawton; Rahul Alam; Stephen Whybrow; James Stubbs; Matthias Platzer; Johannes Hebebrand; Anke Hinney
Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity.
The Journal of nutrition 2005;135(6):1387-92.
2005: Susann Friedel; F Fontenla Horro; Anne-Kathrin Wermter; Frank Geller; Astrid Dempfle; Kathrin Reichwald; Judith Smidt; Günter Brönner; Kerstin Konrad; Beate Herpertz-Dahlmann; Andreas Warnke; U Hemminger; Martin Linder; H Kiefl; Hanspeter Goldschmidt; Wolfgang Siegfried; Helmut Remschmidt; Anke Hinney; Johannes Hebebrand
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.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;132B(1):96-9.
2003: Anke Hinney; Sarah Hohmann; Frank Geller; Constanze Vogel; Claudia Hess; Anne-Kathrin Wermter; Britta Brokamp; Hanspeter Goldschmidt; Wolfgang Siegfried; Helmut Remschmidt; Helmut Schäfer; Thomas Gudermann; Johannes Hebebrand
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.
The Journal of clinical endocrinology and metabolism 2003;88(9):4258-67.
2003: Nadine Schäuble; Frank Geller; Wolfgang Siegfried; Hanspeter Goldschmidt; Helmut Remschmidt; Anke Hinney; Johannes Hebebrand
No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2003;111(2):73-6.
2003: Kathrin Saar; Frank Geller; Franz Rüschendorf; André Reis; Susann Friedel; Nadine Schäuble; Peter Nürnberg; Wolfgang Siegfried; Hans-Peter Goldschmidt; Helmut Schäfer; Andreas Ziegler; Helmut Remschmidt; Anke Hinney; Johannes Hebebrand
Genome scan for childhood and adolescent obesity in German families.
Pediatrics 2003;111(2):321-7.
2002: Anke Hinney; Benjamin Antwerpen; Frank Geller; Helmut Schäfer; Wolfgang Siegfried; Hanspeter Goldschmidt; Helmut Remschmidt; Andreas Ziegler; Johannes Hebebrand
No evidence for involvement of the calpain-10 gene 'high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity.
Molecular genetics and metabolism 2002;76(2):152-6.
2002: Anke Hinney; Anne Hoch; Frank Geller; Helmut Schäfer; Wolfgang Siegfried; Hanspeter Goldschmidt; Helmut Remschmidt; Johannes Hebebrand
Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students.
The Journal of clinical endocrinology and metabolism 2002;87(6):2716.
2001: Frank Oeffner; Tina Korn; H Roth; Andreas Ziegler; Anke Hinney; Hanspeter Goldschmidt; Wolfgang Siegfried; Johannes Hebebrand; Karl-Heinz Grzeschik
Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2001;25(6):767-9.
2001: Anke Hinney; Frank Geller; T Neupert; C Sommerlad; G Gerber; Tilman Görg; Wolfgang Siegfried; Hanspeter Goldschmidt; Helmut Remschmidt; Andreas Ziegler; Johannes Hebebrand
No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2001;109(8):402-5.
2000: B Britz; Wolfgang Siegfried; Andreas Ziegler; C Lamertz; Beate Herpertz-Dahlmann; Helmut Remschmidt; H U Wittchen; Johannes Hebebrand
Rates of psychiatric disorders in a clinical study group of adolescents with extreme obesity and in obese adolescents ascertained via a population based study.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2000;24(12):1707-14.
2000: Anke Hinney; Andreas Ziegler; Frank Oeffner; C Wedewardt; M Vogel; H Wulftange; Frank Geller; K Stübing; Wolfgang Siegfried; Hanspeter Goldschmidt; Helmut Remschmidt; Johannes Hebebrand
Independent confirmation of a major locus for obesity on chromosome 10.
The Journal of clinical endocrinology and metabolism 2000;85(8):2962-5.
2000: Frank Oeffner; Dorothea Bornholdt; Andreas Ziegler; Anke Hinney; Tilman Görg; G Gerber; Hanspeter Goldschmidt; Wolfgang Siegfried; A Wright; Johannes Hebebrand; Karl-Heinz Grzeschik
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents.
Acta diabetologica 2000;37(2):93-101.
1999: Anke Hinney; J Schneider; Andreas Ziegler; Gerd Lehmkuhl; Fritz Poustka; Martin H Schmidt; H Mayer; Wolfgang Siegfried; Helmut Remschmidt; Johannes Hebebrand
No evidence for involvement of polymorphisms of the dopamine D4 receptor gene in anorexia nervosa, underweight, and obesity.
American journal of medical genetics 1999;88(6):594-7.
1999: M Sina; Anke Hinney; Andreas Ziegler; T Neupert; H Mayer; Wolfgang Siegfried; Werner F Blum; Helmut Remschmidt; Johannes Hebebrand
Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene.
American journal of human genetics 1999;65(6):1501-7.
1999: Anke Hinney; H Herrmann; T Löhr; K Rosenkranz; Andreas Ziegler; Gerd Lehmkuhl; Fritz Poustka; Martin H Schmidt; H Mayer; Wolfgang Siegfried; Helmut Remschmidt; Johannes Hebebrand
No evidence for an involvement of alleles of polymorphisms in the serotonin1Dbeta and 7 receptor genes in obesity, underweight or anorexia nervosa.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 1999;23(7):760-3.
1999: Anke Hinney; A Schmidt; K Nottebom; O Heibült; I Becker; Andreas Ziegler; G Gerber; M Sina; Tilman Görg; H Mayer; Wolfgang Siegfried; Manfred Fichter; Helmut Remschmidt; Johannes Hebebrand
Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans.
The Journal of clinical endocrinology and metabolism 1999;84(4):1483-6.
1998: K Rosenkranz; Anke Hinney; Andreas Ziegler; H Hermann; Manfred Fichter; H Mayer; Wolfgang Siegfried; John Young; Helmut Remschmidt; Johannes Hebebrand
Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: identification of several genetic variants.
The Journal of clinical endocrinology and metabolism 1998;83(12):4524-7.
1998: H Roth; Tina Korn; K Rosenkranz; Anke Hinney; Andreas Ziegler; Juergen Kunz; Wolfgang Siegfried; H Mayer; Johannes Hebebrand; Karl-Heinz Grzeschik
Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents.
Human genetics 1998;103(5):540-6.
1998: Anke Hinney; A Bornscheuer; M Depenbusch; B Mierke; A Tölle; K Middeke; Andreas Ziegler; H Roth; G Gerber; Karin Zamzow; Anne Ballauff; A Hamann; H Mayer; Wolfgang Siegfried; Gerd Lehmkuhl; Fritz Poustka; Martin H Schmidt; H Hermann; Beate Herpertz-Dahlmann; Manfred Fichter; Helmut Remschmidt; Johannes Hebebrand
No evidence for involvement of the leptin gene in anorexia nervosa, bulimia nervosa, underweight or early onset extreme obesity: identification of two novel mutations in the coding sequence and a novel polymorphism in the leptin gene linked upstream region.
Molecular psychiatry 1998;3(6):539-43.
1998: Anke Hinney; I Becker; O Heibült; K Nottebom; A Schmidt; Andreas Ziegler; H Mayer; Wolfgang Siegfried; Werner F Blum; Helmut Remschmidt; Johannes Hebebrand
Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes.
The Journal of clinical endocrinology and metabolism 1998;83(10):3737-41.
1998: K Rosenkranz; Anke Hinney; Andreas Ziegler; S von Prittwitz; Nikolaus Barth; H Roth; H Mayer; Wolfgang Siegfried; Gerd Lehmkuhl; Fritz Poustka; M Schmidt; Helmut Schäfer; Helmut Remschmidt; Johannes Hebebrand
Screening for mutations in the neuropeptide Y Y5 receptor gene in cohorts belonging to different weight extremes.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 1998;22(2):157-63.
1997: Anke Hinney; A Bornscheuer; M Depenbusch; B Mierke; A Tölle; H Mayer; Wolfgang Siegfried; Helmut Remschmidt; Johannes Hebebrand
Absence of leptin deficiency mutation in extremely obese German children and adolescents.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 1997;21(12):1190.
1997: H Roth; Anke Hinney; Andreas Ziegler; Nikolaus Barth; G Gerber; K Stein; Torsten Brömel; H Mayer; Wolfgang Siegfried; Helmut Schäfer; Helmut Remschmidt; Karl-Heinz Grzeschik; Johannes Hebebrand
Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 1997;105(6):341-4.