Roeper, Jochen

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Ramirez, A., Heimbach, A., Gründemann, J., Stiller, B., Hampshire, D., Cid, L. P., Goebel, I., Mubaidin, A. F., Wriekat, A.-L., Roeper, J., et al. (2006) · Nature Genetics

Parkinson's Disease Mechanisms and TreatmentsNeurological diseases and metabolism

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Unique properties of mesoprefrontal neurons within a dual mesocorticolimbic dopamine system

Lammel, S., Hetzel, A., Häckel, O., Jones, I., Liss, B., & Roeper, J. (2008) · Neuron

Neurotransmitter Receptor Influence on BehaviorNeuroscience and Neuropharmacology Research

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Projection-specific modulation of dopamine neuron synapses by aversive and rewarding stimuli

Lammel, S., Ion, D. I., Roeper, J., & Malenka, R. C. (2011) · Neuron

Neurotransmitter Receptor Influence on BehaviorNeuroscience and Neuropharmacology Research

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Inhibition of histone deacetylation rescues phenotype in a mouse model of Birk-Barel intellectual disability syndrome

Cooper, A., Butto, T., Hammer, N., Jagannath, S., Fend-Guella, D. L., Akhtar, J., Radyushkin, K., Lesage, F., Winter, J., Strand, S., et al. (2020) · Nature Communications

Genetic Syndromes and ImprintingGenetics and Neurodevelopmental Disorders

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