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The Lancet. Neurology|June 22, 2007
Deciphering the role of heterozygous mutations in genes associated with parkinsonismChristine Klein, Katja Lohmann-Hedrich, Ekaterina Rogaeva, et al.Parkinsonism & Related Disorders|August 14, 2018
Field synopsis and systematic meta-analyses of genetic association studies in isolated dystoniaOlena Ohlei, Valerija Dobricic, Katja Lohmann, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2025
'What's in a Name?' Naming Genetically Determined Movement Disorders: Gap and ControversyConnie Marras, Alberto Albanese, Mark Hallett, et al.Parkinson'S Disease|March 26, 2011
PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1Aleksandar Rakovic, Anne Grünewald, Lisa Voges, et al.European Journal of Human Genetics : EJHG|July 20, 2007
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's diseaseSusan Winkler, Inke R König, Katja Lohmann-Hedrich, et al.Journal of Parkinson'S Disease|May 2, 2022
Pronounced Orthostatic Hypotension in GBA-Related Parkinson's DiseaseTatiana Usnich, Henrike Hanssen, Katja Lohmann, et al.Annals of Clinical and Translational Neurology|June 19, 2019
Discordance in monozygotic Parkinson's disease twins - continuum or dichotomy?Alexander Balck, Max Borsche, Meike Kasten, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 21, 2024
Genome Aggregation Database Version 4-Allele Frequency Changes and Impact on Variant Interpretation in DystoniaElisabetta Indelicato, Anna Eberl, Sylvia Boesch, et al.Plos One|March 17, 2011
Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblastsAleksandar Rakovic, Anne Grünewald, Jan Kottwitz, et al.Human Molecular Genetics|May 29, 2010
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patientsAleksandar Rakovic, Anne Grünewald, Philip Seibler, et al.Pageof 59