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Page 1
Estimated prevalence of potentially damaging variants in the leptin gene.
Nunziata A, Borck G, Funcke JB, Kohlsdorf K, Brandt S, Hinney A, Moepps B, Gierschik P, Debatin KM, Fischer-Posovszky P, Wabitsch M. Nunziata A, et al. Among authors: hinney a. Mol Cell Pediatr. 2017 Nov 3;4(1):10. doi: 10.1186/s40348-017-0074-x. Mol Cell Pediatr. 2017. PMID: 29101506 Free PMC article.
Mutation analysis of the MCHR1 gene in human obesity.
Wermter AK, Reichwald K, Büch T, Geller F, Platzer C, Huse K, Hess C, Remschmidt H, Gudermann T, Preibisch G, Siegfried W, Goldschmidt HP, Li WD, Price RA, Biebermann H, Krude H, Vollmert C, Wichmann HE, Illig T, Sørensen TI, Astrup A, Larsen LH, Pedersen O, Eberlé D, Clément K, Blundell J, Wabitsch M, Schäfer H, Platzer M, Hinney A, Hebebrand J. Wermter AK, et al. Among authors: hinney a. Eur J Endocrinol. 2005 Jun;152(6):851-62. doi: 10.1530/eje.1.01917. Eur J Endocrinol. 2005. PMID: 15941924
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.
Friedel S, Reichwald K, Scherag A, Brumm H, Wermter AK, Fries HR, Koberwitz K, Wabitsch M, Meitinger T, Platzer M, Biebermann H, Hinney A, Hebebrand J. Friedel S, et al. Among authors: hinney a. BMC Genet. 2007 May 3;8:17. doi: 10.1186/1471-2156-8-17. BMC Genet. 2007. PMID: 17477860 Free PMC article.
Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants.
Volckmar AL, Bolze F, Jarick I, Knoll N, Scherag A, Reinehr T, Illig T, Grallert H, Wichmann HE, Wiegand S, Biebermann H, Krude H, Fischer-Posovszky P, Rief W, Wabitsch M, Klingenspor M, Hebebrand J, Hinney A. Volckmar AL, et al. Among authors: hinney a. BMC Med Genomics. 2012 Dec 27;5:65. doi: 10.1186/1755-8794-5-65. BMC Med Genomics. 2012. PMID: 23270367 Free PMC article.
Mitochondrial DNA variants in obesity.
Knoll N, Jarick I, Volckmar AL, Klingenspor M, Illig T, Grallert H, Gieger C, Wichmann HE, Peters A, Wiegand S, Biebermann H, Fischer-Posovszky P, Wabitsch M, Völzke H, Nauck M, Teumer A, Rosskopf D, Rimmbach C, Schreiber S, Jacobs G, Lieb W, Franke A, Hebebrand J, Hinney A. Knoll N, et al. Among authors: hinney a. PLoS One. 2014 May 2;9(5):e94882. doi: 10.1371/journal.pone.0094882. eCollection 2014. PLoS One. 2014. PMID: 24788344 Free PMC article.
Unexpected identification of obesity-associated mutations in LEP and MC4R genes in patients with anorexia nervosa.
Rajcsanyi LS, Zheng Y, Herpertz-Dahlmann B, Seitz J, de Zwaan M, Herzog W, Ehrlich S, Zipfel S, Giel K, Egberts K, Burghardt R, Föcker M, Antel J, Fischer-Posovszky P, Hebebrand J, Hinney A. Rajcsanyi LS, et al. Among authors: hinney a. Sci Rep. 2024 Mar 25;14(1):7067. doi: 10.1038/s41598-024-57517-w. Sci Rep. 2024. PMID: 38528040 Free PMC article.
No evidence for involvement of the leptin gene in anorexia nervosa, bulimia nervosa, underweight or early onset extreme obesity: identification of two novel mutations in the coding sequence and a novel polymorphism in the leptin gene linked upstream region.
Hinney A, Bornscheuer A, Depenbusch M, Mierke B, Tölle A, Middeke K, Ziegler A, Roth H, Gerber G, Zamzow K, Ballauff A, Hamann A, Mayer H, Siegfried W, Lehmkuhl G, Poustka F, Schmidt MH, Hermann H, Herpertz-Dahlmann BM, Fichter M, Remschmidt H, Hebebrand J. Hinney A, et al. Mol Psychiatry. 1998 Nov;3(6):539-43. doi: 10.1038/sj.mp.4000394. Mol Psychiatry. 1998. PMID: 9857981
301 results