Karin Wiegers

Role of parkin mutations in 111 community‐based patients with early‐onset parkinsonism

Martin Kann, Helfried Jacobs, K. Mohrmann et al. · Annals of Neurology · 2002 · 140 citations

Life Sciences, Genetics, Neurology +14

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism

Christine Klein, Ana Djarmati, Katja Hedrich et al. · European Journal of Human Genetics · 2005 · 134 citations · Full text

Life Sciences, Genetics, Neurology +16

Myoclonus-dystonia: significance of large<i>SGCE</i>deletions

Anne Grünewald, Ana Djarmati, K. Lohmann-Hedrich et al. · Human Mutation · 2008 · 117 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

High mutation rate in dopa-responsive dystonia: Detection with comprehensive <i>GCHI</i> screening

J. Hagenah, Rachel Saunders‐Pullman, Katja Hedrich et al. · Neurology · 2005 · 97 citations

Life Sciences, Genetics, Molecular Genetics +15

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation

Sarah Doss, Katja Lohmann, Philip Seibler et al. · Journal of Neurology · 2013 · 46 citations

Life Sciences, Genetics, Molecular Genetics +14