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Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity.
Müller TD, Brönner G, Wandolski M, Carrie J, Nguyen TT, Greene BH, Scherag A, Grallert H, Vogel CI, Scherag S, Rief W, Wichmann HE, Illig T, Schäfer H, Hebebrand J, Hinney A. Müller TD, et al. Among authors: bronner g. BMC Med Genet. 2010 Jan 1;11:2. doi: 10.1186/1471-2350-11-2. BMC Med Genet. 2010. PMID: 20044928 Free PMC article.
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: bronner g. 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
Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups.
Vogel CI, Scherag A, Brönner G, Nguyen TT, Wang HJ, Grallert H, Bornhorst A, Rosskopf D, Völzke H, Reinehr T, Rief W, Illig T, Wichmann HE, Schäfer H, Hebebrand J, Hinney A. Vogel CI, et al. Among authors: bronner g. BMC Med Genet. 2009 Mar 2;10:19. doi: 10.1186/1471-2350-10-19. BMC Med Genet. 2009. PMID: 19254363 Free PMC article.
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.
Wermter AK, Scherag A, Meyre D, Reichwald K, Durand E, Nguyen TT, Koberwitz K, Lichtner P, Meitinger T, Schäfer H, Hinney A, Froguel P, Hebebrand J, Brönner G. Wermter AK, et al. Among authors: bronner g. Eur J Hum Genet. 2008 Sep;16(9):1126-34. doi: 10.1038/ejhg.2008.64. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398438
Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa.
Müller TD, Reichwald K, Brönner G, Kirschner J, Nguyen TT, Scherag A, Herzog W, Herpertz-Dahlmann B, Lichtner P, Meitinger T, Platzer M, Schäfer H, Hebebrand J, Hinney A. Müller TD, et al. Among authors: bronner g. Child Adolesc Psychiatry Ment Health. 2008 Nov 17;2(1):33. doi: 10.1186/1753-2000-2-33. Child Adolesc Psychiatry Ment Health. 2008. PMID: 19014633 Free PMC article.
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. Among authors: bronner g. 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
Genetic factors for overweight and CAD.
Brönner G, Erdmann J, Mayer B, Hinney A, Hebebrand J. Brönner G, et al. Herz. 2006 May;31(3):189-99. doi: 10.1007/s00059-006-2797-7. Herz. 2006. PMID: 16770554 Review.
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts.
Lyon HN, Emilsson V, Hinney A, Heid IM, Lasky-Su J, Zhu X, Thorleifsson G, Gunnarsdottir S, Walters GB, Thorsteinsdottir U, Kong A, Gulcher J, Nguyen TT, Scherag A, Pfeufer A, Meitinger T, Brönner G, Rief W, Soto-Quiros ME, Avila L, Klanderman B, Raby BA, Silverman EK, Weiss ST, Laird N, Ding X, Groop L, Tuomi T, Isomaa B, Bengtsson K, Butler JL, Cooper RS, Fox CS, O'Donnell CJ, Vollmert C, Celedón JC, Wichmann HE, Hebebrand J, Stefansson K, Lange C, Hirschhorn JN. Lyon HN, et al. Among authors: bronner g. PLoS Genet. 2007 Apr 27;3(4):e61. doi: 10.1371/journal.pgen.0030061. Epub 2007 Mar 7. PLoS Genet. 2007. PMID: 17465681 Free PMC article.
122 results