Sabine Purmann

Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease

Volker Arolt, Rebekka Lencer, Achim Nolte et al. · American Journal of Medical Genetics · 1996 · 193 citations

Life Sciences, Genetics, Psychiatry +16

Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted<i>DLK1/GTL2</i>gene cluster

Karin Buiting, Deniz Kanber, José I. Martı́n-Subero et al. · Human Mutation · 2008 · 71 citations

Life Sciences, Genetics, Molecular Genetics +17

Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia

Volker Arolt, Rebekka Lencer, Sabine Purmann et al. · American Journal of Medical Genetics · 1999 · 46 citations

Life Sciences, Genetics, Psychiatry +12

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

Jasmin Beygo, Alma Küchler, Gabriele Gillessen‐Kaesbach et al. · European Journal of Human Genetics · 2017 · 45 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Premutations in the <i>FMR1</i> gene as a modifying factor in <i>Parkin</i>‐associated Parkinson's disease?

Katja Hedrich, Peter P. Pramstaller, Katrin Stübke et al. · Movement Disorders · 2005 · 30 citations

Life Sciences, Genetics, Molecular Genetics +16