H. Goldschmidt

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

B. Herpertz-Dahlmann, K. Konrad, J. Hebebrand, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents

K. Grzeschik, J. Hebebrand, A. Hinney, 2000, Acta Diabetologica.

Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation

K. Grzeschik, J. Hebebrand, A. Hinney, 2001, International Journal of Obesity.

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

J. Hebebrand, A. Hinney, A. Scherag, 2007, BMC Medical Genetics.

Genome scan for childhood and adolescent obesity in German families.

J. Hebebrand, A. Hinney, H. Remschmidt, 2003, Pediatrics.

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

J. Hebebrand, A. Hinney, H. Remschmidt, 2002, The Journal of clinical endocrinology and metabolism.

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.

Thomas Gudermann, Helmut Remschmidt, Johannes Hebebrand, 2003, The Journal of clinical endocrinology and metabolism.

Independent confirmation of a major locus for obesity on chromosome 10.

J. Hebebrand, A. Hinney, H. Remschmidt, 2000, The Journal of clinical endocrinology and metabolism.

Mutation analysis of the MCHR1 gene in human obesity.

K. Huse, O. Pedersen, K. Clément, 2005, European journal of endocrinology.

No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation.

J. Hebebrand, A. Hinney, H. Remschmidt, 2001, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

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

M. Platzer, W. Grassl, J. Hebebrand, 2005, The Journal of nutrition.

Nutrient-Gene Interactions Human Galanin ( GAL ) and Galanin 1 Receptor ( GALR 1 ) Variations Are Not Involved in Fat Intake and Early Onset Obesity 1 , 2

M. Platzer, W. Grassl, J. Hebebrand, 2005 .

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

J. Hebebrand, A. Hinney, H. Remschmidt, 2003, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

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

J. Hebebrand, A. Hinney, H. Remschmidt, 2002, Molecular genetics and metabolism.