Jennifer F. Linden

Affiliations: 
University College London, London, United Kingdom 
Area:
Auditory cortex
Google:
"Jennifer Linden"
Mean distance: 12.25 (cluster 17)
 
SNBCP
Cross-listing: CSD Tree

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Publications

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Gothner T, Gonçalves PJ, Sahani M, et al. (2020) Sustained Activation of PV+ Interneurons in Core Auditory Cortex Enables Robust Divisive Gain Control for Complex and Naturalistic Stimuli. Cerebral Cortex (New York, N.Y. : 1991)
Meyer AF, Poort J, O'Keefe J, et al. (2018) A Head-Mounted Camera System Integrates Detailed Behavioral Monitoring with Multichannel Electrophysiology in Freely Moving Mice. Neuron. 100: 46-60.e7
Anderson LA, Hesse LL, Pilati N, et al. (2018) Increased spontaneous firing rates in auditory midbrain following noise exposure are specifically abolished by a Kv3 channel modulator. Hearing Research
Hildebrandt KJ, Sahani M, Linden JF. (2017) The Impact of Anesthetic State on Spike-Sorting Success in the Cortex: A Comparison of Ketamine and Urethane Anesthesia. Frontiers in Neural Circuits. 11: 95
Burgess CP, Lak A, Steinmetz NA, et al. (2017) High-Yield Methods for Accurate Two-Alternative Visual Psychophysics in Head-Fixed Mice. Cell Reports. 20: 2513-2524
Meyer AF, Williamson RS, Linden JF, et al. (2016) Models of Neuronal Stimulus-Response Functions: Elaboration, Estimation, and Evaluation. Frontiers in Systems Neuroscience. 10: 109
Hesse LL, Bakay W, Ong HC, et al. (2016) Non-Monotonic Relation between Noise Exposure Severity and Neuronal Hyperactivity in the Auditory Midbrain. Frontiers in Neurology. 7: 133
Williamson RS, Ahrens MB, Linden JF, et al. (2016) Input-Specific Gain Modulation by Local Sensory Context Shapes Cortical and Thalamic Responses to Complex Sounds. Neuron
Anderson LA, Linden JF. (2016) Mind the Gap: Two Dissociable Mechanisms of Temporal Processing in the Auditory System. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 1977-95
Fuchs JC, Linden JF, Baldini A, et al. (2015) A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome. Human Molecular Genetics. 24: 1869-82
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