Dagmar Nolte

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

Michael F. Waters, Natali A. Minassian, Giovanni Stévanin et al. · Nature Genetics · 2006 · 313 citations

Life Sciences, Genetics, Neuroscience +12

Specific sequence changes in multiple transcript system <i>DYT3</i> are associated with X-linked dystonia parkinsonism

Dagmar Nolte, Stephan Niemann, Ulrich Müller · Proceedings of the National Academy of Sciences · 2003 · 137 citations · Full text

Life Sciences, Molecular Genetics, Neurology +17

DNA analysis of Huntington’s disease

Franco Laccone, Ulrike Engel, Elke Holinski‐Feder et al. · Neurology · 1999 · 81 citations

Life Sciences, Genetics, Molecular Genetics +15

First case of X‐linked dystonia‐parkinsonism (“Lubag”) to demonstrate a response to bilateral pallidal stimulation

Virgilio Gerald H. Evidente, Mark Lyons, M T Wheeler et al. · Movement Disorders · 2007 · 80 citations

Medicine, Neurology, Neuroscience +13

Human O-GlcNAc transferase (OGT): genomic structure, analysis of splice variants, fine mapping in Xq13.1

Dagmar Nolte, Ulrich Müller · Mammalian Genome · 2002 · 79 citations

Life Sciences, Genetics, Molecular Genetics +14