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No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.
Müller TD, Reichwald K, Wermter AK, Brönner G, Nguyen TT, Friedel S, Koberwitz K, Engeli S, Lichtner P, Meitinger T, Schäfer H, Hebebrand J, Hinney A. Müller TD, et al. Among authors: friedel s. Mol Genet Metab. 2007 Apr;90(4):429-34. doi: 10.1016/j.ymgme.2007.01.002. Epub 2007 Feb 8. Mol Genet Metab. 2007. PMID: 17292652
Perspectives: molecular genetic research in human obesity.
Hebebrand J, Friedel S, Schäuble N, Geller F, Hinney A. Hebebrand J, et al. Among authors: friedel s. Obes Rev. 2003 Aug;4(3):139-46. doi: 10.1046/j.1467-789x.2003.00106.x. Obes Rev. 2003. PMID: 12916815 Review.
Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
Friedel S, Saar K, Sauer S, Dempfle A, Walitza S, Renner T, Romanos M, Freitag C, Seitz C, Palmason H, Scherag A, Windemuth-Kieselbach C, Schimmelmann BG, Wewetzer C, Meyer J, Warnke A, Lesch KP, Reinhardt R, Herpertz-Dahlmann B, Linder M, Hinney A, Remschmidt H, Schäfer H, Konrad K, Hübner N, Hebebrand J. Friedel S, et al. Mol Psychiatry. 2007 Oct;12(10):923-33. doi: 10.1038/sj.mp.4001986. Epub 2007 Apr 10. Mol Psychiatry. 2007. PMID: 17579611
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: friedel s. J Clin Endocrinol Metab. 2004 Jan;89(1):157-62. doi: 10.1210/jc.2003-031395. J Clin Endocrinol Metab. 2004. PMID: 14715843
Genetic risk factors in eating disorders.
Hinney A, Friedel S, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: friedel s. Am J Pharmacogenomics. 2004;4(4):209-23. doi: 10.2165/00129785-200404040-00001. Am J Pharmacogenomics. 2004. PMID: 15287815 Review.
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: friedel s. 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
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. 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
65 results