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Harald Brumm

Research Profile

Chemicals & Drugs

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Physiology

Genes & Molecular Sequences

Single Nucleotide Polymorphism

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Germany

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Publications

TOP 3
F Bolze; Harald Brumm; C Kless; R Kühn; S Mocek; N Rink; J Rozman; A-E Schwarz; W Wurst; Heike Biebermann; Martin Klingenspor
Characterization of the melanocortin-4-receptor nonsense mutation W16X in vitro and in vivo.
Harald Brumm; Annette Grüters; Johannes Hebebrand; Anke Hinney; Martin Klingenspor; Heiko Krude; Jessica Mühlhaus; Susann Scherag; Susanna Wiegand; Florian Bolze; Heike Biebermann
Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-through.
Jessica Mühlhaus; Wilfried Pott; Carolin Pütter; Thomas Reinehr; Susann Scherag; Hai-Jun Wang; Susanna Wiegand; Özgür Albayrak; Anne-Madeleine Bau; Heike Biebermann; Harald Brumm; Harald Grallert; Annette Grüters; Johannes Hebebrand; Anke Hinney; Thomas Illig; Heiko Krude; André Scherag
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness.

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All Publications

2013: F Bolze; Harald Brumm; C Kless; R Kühn; S Mocek; N Rink; J Rozman; A-E Schwarz; W Wurst; Heike Biebermann; Martin Klingenspor
Characterization of the melanocortin-4-receptor nonsense mutation W16X in vitro and in vivo.
The pharmacogenomics journal 2013;13(1):80-93.
2012: Harald Brumm; Annette Grüters; Johannes Hebebrand; Anke Hinney; Martin Klingenspor; Heiko Krude; Jessica Mühlhaus; Susann Scherag; Susanna Wiegand; Florian Bolze; Heike Biebermann
Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-through.
Obesity (Silver Spring, Md.) 2012;20(5):1074-81.
2012: Jessica Mühlhaus; Wilfried Pott; Carolin Pütter; Thomas Reinehr; Susann Scherag; Hai-Jun Wang; Susanna Wiegand; Özgür Albayrak; Anne-Madeleine Bau; Heike Biebermann; Harald Brumm; Harald Grallert; Annette Grüters; Johannes Hebebrand; Anke Hinney; Thomas Illig; Heiko Krude; André Scherag
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness.
Hormone research in pædiatrics 2012;77(6):358-68.
2007: Claudia Stäubert; Patrick Tarnow; Harald Brumm; Christian Pitra; Thomas Gudermann; Annette Grüters; Torsten Schöneberg; Heike Biebermann; Holger Römpler
Evolutionary aspects in evaluating mutations in the melanocortin 4 receptor.
Endocrinology 2007;148(10):4642-8.
2007: María C Ochoa; Cristina Azcona; Heike Biebermann; Harald Brumm; C Razquin; Anne-Kathrin Wermter; J Alfredo Martínez; Johannes Hebebrand; Anke Hinney; María J Moreno-Aliaga; Amelia Marti; Ana Patiño; María Chueca; M Oyarzabal; R Pelach
A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent population.
Clinical endocrinology 2007;66(5):652-8.
2007: Susann Friedel; Kathrin Reichwald; André Scherag; Harald Brumm; Anne-Kathrin Wermter; Hans-Rudolf Fries; Kerstin Koberwitz; Martin Wabitsch; Thomas Meitinger; Matthias Platzer; Heike Biebermann; Anke Hinney; Johannes Hebebrand
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 genetics 2007;8():17.
2007: E Rettenbacher; Patrick Tarnow; Harald Brumm; D Prayer; Anne-Kathrin Wermter; Johannes Hebebrand; Heike Biebermann; Anke Hinney; K Widhalm
A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2007;115(1):7-12.
2006: Anke Hinney; Thomas Bettecken; Patrick Tarnow; Harald Brumm; Kathrin Reichwald; Peter Lichtner; André Scherag; Thuy Trang Nguyen; Pia Schlumberger; Winfried Rief; Caren Vollmert; Thomas Illig; H-Erich Wichmann; Helmut Schäfer; Matthias Platzer; Heike Biebermann; Thomas Meitinger; Johannes Hebebrand
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany.
The Journal of clinical endocrinology and metabolism 2006;91(5):1761-9.
2002: Harald Brumm; Arne Pfeufer; Heike Biebermann; Dirk Schnabel; Dorothee Deiss; Annette Grüters
Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect.
The Journal of clinical endocrinology and metabolism 2002;87(10):4811-6.
1997: I Stoeva; L Peneva; R Grigorova; B Vassileva; Harald Brumm; Annette Grüters
Neonatal TSH screening--an instrument of iodine supplementation monitoring in Bulgaria in comparison to Berlin--a preliminary report.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 1997;105 Suppl 4():51-4.