Christian Prehn

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

J.-M. Lee, E.M. Ramos, J.-H. Lee et al. · Neurology · 2012 · 391 citations · Full text

Life Sciences, Genetics, Neurology +15

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Davina J. Hensman Moss, Antonio F. Pardiñas, Douglas R. Langbehn et al. · The Lancet Neurology · 2017 · 332 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Role of a neuronal small non-messenger RNA: behavioural alterations in BC1 RNA-deleted mice

Lars Lewejohann, Boris V. Skryabin, Norbert Sachser et al. · Behavioural Brain Research · 2004 · 146 citations

Life Sciences, Neurobiology, Neuroscience +9

Cortical and Subcortical Grey and White Matter Atrophy in Myotonic Dystrophies Type 1 and 2 Is Associated with Cognitive Impairment, Depression and Daytime Sleepiness

Christiane Schneider‐Gold, Barbara Bellenberg, Christian Prehn et al. · PLoS ONE · 2015 · 88 citations · Full text

Medicine, Neurology, Neuroscience +17

Evaluation of CNS involvement in myotonic dystrophy type 1 and type 2 by transcranial sonography

Christos Krogias, Barbara Bellenberg, Christian Prehn et al. · Journal of Neurology · 2014 · 25 citations

Medicine, Neurology, Neuroscience +10