Karsten M. Strauss

Organization of the human serotonin transporter gene

Klaus‐Peter Lesch, U. Balling, Karsten M. Strauss et al. · Journal of Neural Transmission · 1994 · 626 citations

Molecular Physiology, Neurotransmitter, Molecular Biology +4

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

Karsten M. Strauss, L. Miguel Martins, Hélène Plun‐Favreau et al. · Human Molecular Genetics · 2005 · 563 citations · Full text

Mitophagy, Mitochondrial Dysfunction, Genetics +16

Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)

Robert Hering, Karsten M. Strauss, Xiao Tao et al. · Human Mutation · 2004 · 124 citations

The proteasomal subunit S6 ATPase is a novel synphilin‐1 interacting protein—implications for Parkinson's disease

Frank P. Marx, Anne S. Soehn, Daniela Berg et al. · The FASEB Journal · 2007 · 54 citations

Mitophagy, Proteasome, Molecular Biology +19

Mutation analysis of the neurofilament M gene in Parkinson's disease

Rejko Krüger, Christian Fischer, Thorsten Schulte et al. · Neuroscience Letters · 2003 · 35 citations

Mendelian Disorder, Neurofilament M Gene, Genetic Disorder +7