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Horst Obenhaus

Affiliations: 
Max Planck Institute for Medical Research, Heidelberg, Baden-Württemberg, Germany 
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"Horst Obenhaus"
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Edvard I. Moser post-doc
May-Britt Moser post-doc
Rolf Sprengel post-doc Kavli Institute for Systems Neuroscience and Centre for Neural Computation, NTNU

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Publications

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Gonzalo Cogno S, Obenhaus HA, Lautrup A, et al. (2023) Minute-scale oscillatory sequences in medial entorhinal cortex. Nature
Jacobsen RI, Nair RR, Obenhaus HA, et al. (2022) All-viral tracing of monosynaptic inputs to single birthdate-defined neurons in the intact brain. Cell Reports Methods. 2: 100221
Zong W, Obenhaus HA, Skytøen ER, et al. (2022) Large-scale two-photon calcium imaging in freely moving mice. Cell
Obenhaus HA, Zong W, Jacobsen RI, et al. (2022) Functional network topography of the medial entorhinal cortex. Proceedings of the National Academy of Sciences of the United States of America. 119
Bertocchi I, Eltokhi A, Rozov A, et al. (2021) Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca signaling promotes audiogenic seizures, attentional and cognitive deficits in mice. Communications Biology. 4: 187
Bertocchi I, Eltokhi A, Rozov A, et al. (2021) Voltage-independent GluN2A-type NMDA receptor Ca signaling promotes audiogenic seizures, attentional and cognitive deficits in mice. Communications Biology. 4: 59
Rowland DC, Obenhaus HA, Skytøen ER, et al. (2018) Functional properties of stellate cells in medial entorhinal cortex layer II. Elife. 7
Obenhaus HA, Rozov A, Bertocchi I, et al. (2016) Causal Interrogation of Neuronal Networks and Behavior through Virally Transduced Ivermectin Receptors. Frontiers in Molecular Neuroscience. 9: 75
Lissek T, Obenhaus HA, Ditzel DA, et al. (2016) General Anesthetic Conditions Induce Network Synchrony and Disrupt Sensory Processing in the Cortex. Frontiers in Cellular Neuroscience. 10: 64
Berkel S, Tang W, Treviño M, et al. (2012) Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology. Human Molecular Genetics. 21: 344-57
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