6:	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.
	Abstract 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. BMC Genet. 2007 May 3;8(1):17

5:	M. C. Ochoa, C. Azcona, H. Biebermann, H. Brumm, C. Razquin, A.-K. Wermter, J. A. Martínez, J. Hebebrand, A. Hinney, M. J. Moreno-Aliaga, A. Marti and Grupo de Estudio Navarro de la Obesidad Infantil (GENOI)
	A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent population Clinical Endocrinology (2007) 66, 652–658

4:	Rettenbacher E, Tarnow P, Brumm H, Prayer D, Wermter AK, Hebebrand J, Biebermann H, Hinney A, Widhalm K.
	A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity. Exp Clin Endocrinol Diabetes. 2007 Jan;115(1):7-12.

3:	Hinney A, Bettecken T, Tarnow P, Brumm H, Reichwald K, Lichtner P, Scherag A, Nguyen TT, Schlumberger P, Rief W, Vollmert C, Illig T, Wichmann HE, Schafer H, Platzer M, Biebermann H, Meitinger T, Hebebrand J.
	Prevalence, Spectrum and Functional Characterization of Melanocortin-4 Receptor Gene Mutations in a Representative Population-based Sample and Obese Adults from Germany. J Clin Endocrinol Metab. 2006 May;91(5):1761-9.

2:	Brumm H, Pfeufer A, Biebermann H, Schnabel D, Deiss D, Gruters A.
	Congenital central hypothyroidism due to homozygous thyrotropin b 313DT mutation is caused by a founder effect. J Clin Endocrinol Metab. 2002 Oct;87(10):4811-6.

1:	Stoeva I, Peneva L, Grigorova R, Vassileva B, Brumm H, Gruters A.
	Neonatal TSH screening--an instrument of iodine supplementation monitoring in Bulgaria in comparison to Berlin--a preliminary report. Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:51-4.