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 · 310 citations

Channelopathies, Molecular Neuroscience, Developmental Biology +10

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 · 133 citations · Full text

Genetics, Disease Gene, Clinical Neuroscience +17

DNA analysis of Huntington’s disease

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

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

Neurological Disorder, Clinical Neurology, Cerebral Palsy +19

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

Allelic Variant, Somatic Variant, Medicine +8