Hebebrand J - Search Results

1

Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.

Albayrak Ö, Pütter C, Volckmar AL, Cichon S, Hoffmann P, Nöthen MM, Jöckel KH, Schreiber S, Wichmann HE, Faraone SV, Neale BM, Herpertz-Dahlmann B, Lehmkuhl G, Sinzig J, Renner TJ, Romanos M, Warnke A, Lesch KP, Reif A, Schimmelmann BG, Scherag A, Hebebrand J, Hinney A; Psychiatric GWAS Consortium: ADHD Subgroup. Albayrak Ö, et al. Among authors: hebebrand j. Am J Med Genet B Neuropsychiatr Genet. 2013 Jun;162B(4):295-305. doi: 10.1002/ajmg.b.32144. Epub 2013 Mar 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23533005

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: hebebrand j. J Clin Endocrinol Metab. 2002 Jun;87(6):2716. doi: 10.1210/jcem.87.6.8672. J Clin Endocrinol Metab. 2002. PMID: 12050239

3

Glucose transporter 4 gene: association studies pertaining to alleles of two polymorphisms in extremely obese children and adolescents and in normal and underweight controls.

Friedel S, Antwerpen B, Hoch A, Vogel C, Grassl W, Geller F, Hebebrand J, Hinney A. Friedel S, et al. Among authors: hebebrand j. Ann N Y Acad Sci. 2002 Jun;967:554-7. Ann N Y Acad Sci. 2002. PMID: 12079888

4

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: hebebrand j. Mol Genet Metab. 2002 Jun;76(2):152-6. doi: 10.1016/s1096-7192(02)00035-5. Mol Genet Metab. 2002. PMID: 12083814

5

Secular trends in body mass index measurements in preschool children from the City of Aachen, Germany.

Herpertz-Dahlmann B, Geller F, Böhle C, Khalil C, Trost-Brinkhues G, Ziegler A, Hebebrand J. Herpertz-Dahlmann B, et al. Among authors: hebebrand j. Eur J Pediatr. 2003 Feb;162(2):104-9. doi: 10.1007/s00431-002-1056-z. Epub 2003 Jan 9. Eur J Pediatr. 2003. PMID: 12548387

6

Genome scan for childhood and adolescent obesity in German families.

Saar K, Geller F, Rüschendorf F, Reis A, Friedel S, Schäuble N, Nürnberg P, Siegfried W, Goldschmidt HP, Schäfer H, Ziegler A, Remschmidt H, Hinney A, Hebebrand J. Saar K, et al. Among authors: hebebrand j. Pediatrics. 2003 Feb;111(2):321-7. doi: 10.1542/peds.111.2.321. Pediatrics. 2003. PMID: 12563058

7

Confidence intervals for genotype relative risks and allele frequencies from the case parent trio design for candidate-gene studies.

Scherag A, Dempfle A, Hinney A, Hebebrand J, Schäfer H. Scherag A, et al. Among authors: hebebrand j. Hum Hered. 2002;54(4):210-7. doi: 10.1159/000070666. Hum Hered. 2002. PMID: 12771553

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: hebebrand j. 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

Elevated physical activity and low leptin levels co-occur in patients with anorexia nervosa.

Holtkamp K, Herpertz-Dahlmann B, Mika C, Heer M, Heussen N, Fichter M, Herpertz S, Senf W, Blum WF, Schweiger U, Warnke A, Ballauff A, Remschmidt H, Hebebrand J. Holtkamp K, et al. Among authors: hebebrand j. J Clin Endocrinol Metab. 2003 Nov;88(11):5169-74. doi: 10.1210/jc.2003-030569. J Clin Endocrinol Metab. 2003. PMID: 14602745

10

Data adaptive interim modification of sample sizes for candidate-gene association studies.

Scherag A, Müller HH, Dempfle A, Hebebrand J, Schäfer H. Scherag A, et al. Among authors: hebebrand j. Hum Hered. 2003;56(1-3):56-62. doi: 10.1159/000073733. Hum Hered. 2003. PMID: 14614239

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