Petra Bruse

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease

Patrick Linsel‐Nitschke, Jörg Heeren, Zouhair Aherrahrou et al. · Atherosclerosis · 2009 · 159 citations

Chromosome 1P13.3, Allelic Variant, Genetic Determinant +11

The 4977bp deletion of mitochondrial DNA in human skeletal muscle, heart and different areas of the brain: A useful biomarker or more?

Petra Bruse, Salaheldien Ali Mohamed, Anja Schulz et al. · Experimental Gerontology · 2008 · 151 citations · Full text

Dna Sequencing, Dna, Mitochondrial Function +11

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

Jeanette Erdmann, Christina Willenborg, Janja Nahrstaedt et al. · European Heart Journal · 2010 · 143 citations · Full text

Lack of age-related increase of mitochondrial DNA amount in brain, skeletal muscle and human heart

Thomas Frahm, Salaheldien Ali Mohamed, Petra Bruse et al. · Mechanisms of Ageing and Development · 2005 · 102 citations

Mitochondrial Myopathy, Aging, Mitochondrial Function +9

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik et al. · Neurology Genetics · 2015 · 73 citations · Full text