<i>DJ-1 (PARK7)</i> mutations are less frequent than <i>Parkin (PARK2)</i> mutations in early-onset Parkinson disease

Katja Hedrich, Ana Djarmati, Niklas Schäfer, +14

Neurology

GeneticsEopd PatientsDisease Gene IdentificationEarly-onset Parkinson DiseaseSynaptic Signaling +16

Ube2w and Ataxin-3 Coordinately Regulate the Ubiquitin Ligase CHIP

K. Matthew Scaglione, Eszter Zavodszky, Sokol V. Todi, +9

Molecular Cell

Molecular RegulationNatural SciencesGene RegulationMolecular BiologyGene Regulatory Network +4

Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study

Ana Djarmati, Susanne A. Schneider, Katja Lohmann, +16

The Lancet Neurology

PhoniatricsGeneticsPediatric DysphoniaGenetic Screening StudyProminent Spasmodic Dysphonia

The Machado–Joseph disease-associated mutant form of ataxin-3 regulates parkin ubiquitination and stability

Thomas M. Durcan, Maria Kontogiannea, Thorhildur Thorarinsdottir, +6

Human Molecular Genetics

Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease

Katja Hedrich, Johann Hagenah, Ana Djarmati, +14

Archives of Neurology

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

Christine Klein, Ana Djarmati, Katja Hedrich, +14

European Journal of Human Genetics

Early-onset ParkinsonismDj-1 MutationsMendelian DisorderNeurological DisorderParkinson Disease +6

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Manu Sharma, John P. A. Ioannidis, Jan Aasly, +150

Neurology

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

Anne Grünewald, Ana Djarmati, K. Lohmann-Hedrich, +21

Human Mutation

Recessively Inherited Parkinsonism

Norbert Brüggemann, Johann Hagenah, Kathrin Reetz, +13

Archives of Neurology

<i>ATP13A2</i> variants in early‐onset Parkinson's disease patients and controls

Ana Djarmati, Johann Hagenah, Kathrin Reetz, +16

Movement Disorders