Publications by authors named "Harald Brumm"

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Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness.
Jessica Mühlhaus, Carolin Pütter, Harald Brumm, Harald Grallert, Thomas Illig

Horm Res Paediatr· January 2013

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Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-through.
Harald Brumm, Jessica Mühlhaus, Florian Bolze, Susann Scherag, Anke Hinney

Obesity (Silver Spring)· May 2012

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A heterozygous mutation in the third transmembrane domain causes a dominant-negative effect on signalling capability of the MC4R.
Patrick Tarnow, Anne Rediger, Harald Brumm, Petra Ambrugger, Eva Rettenbacher

Obes Facts· January 2010

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A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesity.
Christian L Roth, Michael Ludwig, Joachim Woelfle, Zhen-Chuan Fan, Harald Brumm

Endocrine· August 2009

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Lifestyle intervention in obese children with variations in the melanocortin 4 receptor gene.
Thomas Reinehr, Johannes Hebebrand, Susann Friedel, André M Toschke, Harald Brumm

Obesity (Silver Spring)· February 2009

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Increased constraints on MC4R during primate and human evolution.
David A Hughes, Anke Hinney, Harald Brumm, Anne-Kathrin Wermter, Heike Biebermann

Hum Genet· January 2009

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Evolutionary aspects in evaluating mutations in the melanocortin 4 receptor.
Claudia Stäubert, Patrick Tarnow, Harald Brumm, Christian Pitra, Thomas Gudermann

Endocrinology· October 2007

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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.
Susann Friedel, Kathrin Reichwald, André Scherag, Harald Brumm, Anne-Kathrin Wermter

BMC Genet· May 2007

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Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany.
Anke Hinney, Thomas Bettecken, Patrick Tarnow, Harald Brumm, Kathrin Reichwald

J Clin Endocrinol Metab· May 2006

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Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect.
Harald Brumm, Arne Pfeufer, Heike Biebermann, Dirk Schnabel, Dorothee Deiss

J Clin Endocrinol Metab· October 2002

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