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Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.
Dempfle A, Wudy SA, Saar K, Hagemann S, Friedel S, Scherag A, Berthold LD, Alzen G, Gortner L, Blum WF, Hinney A, Nürnberg P, Schäfer H, Hebebrand J. Dempfle A, et al. Among authors: hebebrand j. Hum Mol Genet. 2006 Sep 15;15(18):2772-83. doi: 10.1093/hmg/ddl218. Epub 2006 Aug 11. Hum Mol Genet. 2006. PMID: 16905557
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
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.
Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature.
Wang HJ, Geller F, Dempfle A, Schäuble N, Friedel S, Lichtner P, Fontenla-Horro F, Wudy S, Hagemann S, Gortner L, Huse K, Remschmidt H, Bettecken T, Meitinger T, Schäfer H, Hebebrand J, Hinney A. Wang HJ, et al. Among authors: hebebrand j. J Clin Endocrinol Metab. 2004 Jan;89(1):157-62. doi: 10.1210/jc.2003-031395. J Clin Endocrinol Metab. 2004. PMID: 14715843
658 results