Publications - Salzburg Brain Dynamics Lab

Gehmacher, Q., Reisinger, P., Hartmann, T., Keintzel, T., Rösch, S., Schwarz, K., & Weisz, N.

Direct cochlear recordings in humans show a theta rhythmic modulation of the auditory nerve by selective attention bioRxiv, 2021.03.01.433316.

DOI: https://doi.org/10.1101/2021.03.01.433316

Rassi, E., Wutz, A., Peatfield, N., & Weisz, N.

Efficient prestimulus network integration of FFA biases face perception during binocular rivalry. BioRxiv, 2021.06.25.449883.

DOI: https://doi.org/10.1101/2021.06.25.449883

Suess, N., Hauswald, A., Reisinger, P., Roesch, S., Keitel, A., & Weisz, N.

Age-related decreases of cortical visuo-phonological transformation of unheard spectral fine-details. BioRxiv, 2021.04.13.439628.

DOI: https://doi.org/10.1101/2021.04.13.439628

Schmidt, F., Chen, Y.-P., Keitel, A., Roesch, S., Hannemann, R., Serman, M., Hauswald, A., & Weisz, N.

Neural speech tracking shifts from the syllabic to the modulation rate of speech as intelligibility decreases. BioRxiv, 2021.03.25.437033.

DOI: https://doi.org/10.1101/2021.03.25.437033

Popov, T., Gips, B., Weisz, N., & Jensen, O.

Brain areas associated with visual spatial attention display topographic organization during auditory spatial attention. bioRxiv, 2021.03.15.435371.

DOI: https://doi.org/10.1101/2021.03.15.435371

Suess, N., Hauswald, A., Zehentner, V., Depireux, J., Herzog, G., Rösch, S., & Weisz, N.

Influence of linguistic properties and hearing impairment on lip reading skills in the German language. PsyArXiv.

DOI: https://doi.org/10.31234/osf.io/rcfxv

Weise, A., Hartmann, T., Parmentier, F., Ruhnau, P., & Weisz, N.

Increases in parieto-occipital alpha-band power reflect involuntary spatial attention due to a task-distracting deviant sound. bioRxiv, 2020.06.29.161992

DOI: https://doi.org/10.1101/2020.06.29.161992

Partyka, M., Demarchi, G., Roesch, S., Suess, N., Sedley, W., Schlee, W. & Weisz, N.

Phantom auditory perception (tinnitus) is characterised by stronger anticipatory auditory predictions. bioRxiv, 869842.

DOI: https://doi.org/10.1101/869842

Partyka, M., Neff, P., Bacri, T., Michels, J., Weisz, N., & Schlee, W. (2021).

Gender differentiates effects of acoustic stimulation in patients with tinnitus. In Progress in Brain Research (Vol. 263, pp. 25–57). Elsevier.

DOI: https://doi.org/10.1016/bs.pbr.2021.04.010

Lundqvist, M., & Wutz, A. (2021).

New methods for oscillation analyses push new theories of discrete cognition. Psychophysiology.

DOI: https://doi.org/10.1111/psyp.13827

Schoisswohl, S., Schecklmann, M., Langguth, B., Schlee, W., & Neff, P. (2021).

Neurophysiological correlates of residual inhibition in tinnitus: Hints for trait-like EEG power spectra. Clinical Neurophysiology, 132(7), 1694-1707.

DOI: https://doi.org/10.1016/j.clinph.2021.03.038

Köhler, M. H. A., Demarchi, G., & Weisz, N. (2021).

Cochlear activity in silent cue-target intervals shows a theta-rhythmic pattern and is correlated to attentional alpha and theta modulations. BMC Biology, 19(1), 48.

DOI: https://doi.org/10.1186/s12915-021-00992-8

Zazio, A., Ruhnau, P., Weisz, N., & Wutz, A. (2021).

Pre‐stimulus alpha‐band power and phase fluctuations originate from different neural sources and exert distinct impact on stimulus‐evoked responses. European Journal of Neuroscience.

DOI: https://doi.org/10.1111/ejn.15138

Suess, N., Hartmann, T., & Weisz N. (2021).

Differential attention-dependent adjustment of frequency, power and phase in primary sensory and frontoparietal areas. Cortex, 137, 179–193.

DOI: https://doi.org/10.1016/j.cortex.2021.01.008

De Ridder, D., Schlee, W., Vanneste, S., Londero, A., Weisz, N., Kleinjung, T., Shekhawat, G. S., Elgoyhen, A. B., Song, J.-J., Andersson, G., Adhia, D., de Azevedo, A. A., Baguley, D. M., Biesinger, E., Binetti, A. C., Del Bo, L., Cederroth, C. R., Cima, R., Eggermont, J. J., … Langguth, B. (2021).

Tinnitus and tinnitus disorder: Theoretical and operational definitions (An international multidisciplinary proposal). In W. Schlee, B. Langguth, T. Kleinjung, S. Vanneste, & D. De Ridder (Eds.), Progress in Brain Research: Tinnitus - An Interdisciplinary Approach Towards Individualized Treatment: From Heterogeneity to Personalized Medicine (Vol. 260, pp. 1–25). Elsevier.

DOI: https://doi.org/10.1016/bs.pbr.2020.12.002

Melcher, D., Huber-Huber, C., & Wutz, A. (2021).

Enumerating the forest before the trees: The time courses of estimation-based and individuation-based numerical processing. Attention, Perception & Psychophysics, 83, 1215–1229.

DOI: https://doi.org/10.3758/s13414-020-02137-5

Hartmann, T., & Weisz, N. (2020).

An Introduction to the Objective Psychophysics Toolbox. Frontiers in Psychology, 11:585437.

DOI: https://doi.org/10.3389/fpsyg.2020.585437

Güntensperger, D., Kleinjung, T., Neff, P., Thüring, C., & Meyer, M. (2020).

Combining neurofeedback with source estimation: Evaluation of an sLORETA neurofeedback protocol for chronic tinnitus treatment. Restorative Neurology and Neuroscience, 38(4), 283–299.

DOI: https://doi.org/10.3233/RNN-200992

Wutz, A., Zazio, A., & Weisz, N. (2020).

Oscillatory bursts in parietal cortex reflect dynamic attention between multiple objects and ensembles. Journal of Neuroscience, 40(36), 6927–6937.

DOI: https://doi.org/10.1523/JNEUROSCI.0231-20.2020

Hauswald, A., Keitel, A., Chen, Y., Rösch, S., & Weisz, N. (2020).

Degradation levels of continuous speech affect neural speech tracking and alpha power differently. European Journal of Neuroscience, ejn.14912.

DOI: https://doi.org/10.1111/ejn.14912

Schmidt, F., Demarchi, G., Geyer, F., & Weisz, N. (2020).

A backward encoding approach to recover subcortical auditory activity. NeuroImage, 218, 116961.

DOI: https://doi.org/10.1016/j.neuroimage.2020.116961

Weisz, N., Kraft, N. G., & Demarchi, G. (2020).

Auditory cortical alpha/beta desynchronization prioritizes the representation of memory items during a retention period. eLife, 9, e55508.

DOI: https://doi.org/10.7554/eLife.55508

Sanchez, G., Hartmann, T., Fuscà, M., Demarchi, G., & Weisz, N. (2020).

Decoding across sensory modalities reveals common supramodal signatures of conscious perception. Proceedings of the National Academy of Sciences, 117(13), 7437-7446.

DOI: https://doi.org/10.1073/pnas.1912584117

Barchiesi, G., Demarchi, G., Wilhelm, F., Hauswald, A., Sanchez, G., & Weisz, N. (2020).

Head magnetomyography (hMMG): A novel approach to monitor face and whole head muscular activity. Psychophysiology, 57(3), e13507.

DOI: https://doi.org/10.1111/psyp.13507

Ferraro, S., Van Ackeren, M. J., Mai, R., Tassi, L., Cardinale, F., Nigri, A., Bruzzone, M. G., D’Incerti, L., Hartmann, T., Weisz, N., & Collignon, O. (2020).

Stereotactic electroencephalography in humans reveals multisensory signal in early visual and auditory cortices. Cortex, 126, 253-264.

DOI: http://dx.doi.org/10.1016/j.cortex.2019.12.032

Zeithamova, D., Mack, M. L., Braunlich, K., Davis, T., Seger, C. A., van Kesteren, M. T. R., & Wutz, A. (2019).

Brain mechanisms of concept learning. The Journal of Neuroscience, 39(42), 8259–8266.

DOI: https://doi.org/10.1523/JNEUROSCI.1166-19.2019

Hartmann, T., & Weisz, N. (2019).

Auditory cortical generators of the Frequency Following Response are modulated by intermodal attention. NeuroImage, 203, 116185.

DOI: https://doi.org/10.1016/j.neuroimage.2019.116185

Demarchi, G., Sanchez, G. & Weisz, N. (2019).

Automatic and feature-specific prediction-related neural activity in the human auditory system. Nature Communications, 10(1), 3440.

DOI: https://doi.org/10.1038/s41467-019-11440-1

Rassi, E., Fuscà, M., Weisz, N., Demarchi, G. (2019).

Detecting Pre-Stimulus Source-Level Effects on Object Perception with Magnetoencephalography. Journal of Visualized Experiments (149), e60120.

DOI: http://dx.doi.org/10.3791/60120

Rassi, E., Wutz, A., Müller-Voggel, N., & Weisz, N. (2019).

Prestimulus feedback connectivity biases the content of visual experiences. Proceedings of the National Academy of Sciences, 116(32), 16056-16061.

DOI: https://doi.org/10.1073/pnas.1817317116

Genitsaridi, E., Partyka, M., Gallus, S., Lopez-Escamez, J. A., Schecklmann, M., Mielczarek, M., Trpchevska, N., Santacruz, J. L., Schoisswohl, S., Riha, C., Lourenco, M., Biswas, R., Liyanage, N., Cederroth, C. R., Perez-Carpena, P., Devos, J., Fuller, T., Edvall, N. K., Hellberg, M. P., D'Antonio, A., Gerevini, S., Sereda, M., Rein, A., Kypraios, T., Hoare, D. J., Londero, A., Pryss, R., Schlee, W., & Hall, D. A. (2019).

Standardised profiling for tinnitus research: The European School for Interdisciplinary Tinnitus Research Screening Questionnaire (ESIT-SQ). Hearing Research, 377, 353-359.

DOI: https://doi.org/10.1016/j.heares.2019.02.017

De Pisapia, N., Barchiesi, G., Jovicich, J., & Cattaneo, L. (2019).

The role of medial prefrontal cortex in processing emotional self-referential information: a combined TMS/fMRI study. Brain Imaging and Behavior, 13(3), 603-614.

DOI: https://doi.org/10.1007/s11682-018-9867-3

Fuscà, M., Ruhnau, P., Neuling, T., & Weisz, N. (2018).

Local network-level integration mediates effects of transcranial Alternating Current Stimulation. Brain Connectivity, 8(4), 212-219.

DOI: https://doi.org/10.1089/brain.2017.0564

Hauswald, A., Tucciarelli, R. & Lingnau, A. (2018).

MEG adaptation reveals action representations in posterior occipitotemporal regions. Cortex, 103: 266-276.

DOI: https://doi.org/10.1016/j.cortex.2018.03.016

Hauswald, A., Lithari, C., Collignon, O., Leonardelli, E., & Weisz, N. (2018).

A visual cortical network for deriving phonological information from intelligible lip movements. Current Biology, 28(9), 1453–1459.

DOI: https://doi.org/10.1016/j.cub.2018.03.044

Hyvärinen, P., Choi, D., Demarchi, G., Aarnisalo, A., & Weisz, N. (2018).

tACS-mediated modulation of the auditory steady-state response as seen with MEG. Hearing Research, 364, 90-95.

DOI: https://doi.org/10.1016/j.heares.2018.03.023

Parmigiani, S., Zattera, B., Barchiesi, G., & Cattaneo, L. (2018).

Spatial and Temporal Characteristics of Set-Related Inhibitory and Excitatory Inputs from the Dorsal Premotor Cortex to the Ipsilateral Motor Cortex Assessed by Dual-Coil Transcranial Magnetic Stimulation. Brain Topography, 31(5), 795-810.

DOI: https://doi.org/10.1007/s10548-018-0635-x

Schlee, W., Hall, D.A., Canlon, B., Cima, R.F.F., de Kleine, E., Hauck, F., Huber, A., Gallus, S., Kleinjung, T., Kypraios, T., Langguth, B., Lopez-Escamez, J.A., Lugo, A., Meyer, M., Mielczarek, M., Norena, A., Pfiffner, F., Pryss, R.C., Reichert, M., Requena, T., Schecklmann, M., van Dijk, P., van de Heyning, P., Weisz, N., & Cederroth, C.R. (2018).

Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective. Frontiers in Aging Neuroscience, 9:447.

DOI: https://doi.org/10.3389/fnagi.2017.00447

Weise, A., Schröger, E., Horvath, J. (2018).

The detection of higher-order acoustic transitions is reflected in the N1 ERP. Psychophysiology, 55(7), e13063.

DOI: https://doi.org/10.1111/psyp.13063

Cashdollar, N., Ruhnau, P., Weisz, N., & Hasson, U. (2017).

The role of working memory in the probabilistic inference of future sensory events. Cerebral Cortex, 27 (5), 2955-2969.

DOI: https://doi.org/10.1093/cercor/bhw138

Kia, S. M., Vega-Pons, S., Weisz, N., & Passerini, A. (2017).

Interpretability of Multivariate Brain Maps in Linear Brain Decoding: Definition, and Heuristic Quantification in Multivariate Analysis of MEG Time-Locked Effects. Frontiers in Neuroscience, 10(619).

DOI: https://doi.org/10.3389/fnins.2016.00619

Neuling, T., Ruhnau, P., Weisz, N., Herrmann, C.S. &, Demarchi, G. (2017).

Faith and oscillations recovered: On analyzing EEG/MEG signals during tACS. NeuroImage, 147, 960–963.

DOI: https://doi.org/10.1016/j.neuroimage.2016.11.022

Weisz, N. & Lithari, C. (2017).

Amplitude modulation rate dependent topographic organization of the auditory steady-state response in human auditory cortex. Hearing Research, 354, 102-108.

DOI: https://doi.org/10.1016/j.heares.2017.09.003

Frey, J., Ruhnau, P., Leske, S., Siegel, M., Braun, C., & Weisz, N. (2016).

The tactile window to consciousness is characterized by frequency-specific integration and segregation of the primary somatosensory cortex. Scientific Reports, 6: 20805.

DOI: https://doi.org/10.1038/srep20805

Lithari, C., Moratti, S., & Weisz, N. (2016).

Limbic areas are functionally decoupled and visual cortex takes a more central role during fear conditioning in humans. Scientific Reports, 6: 29220.

DOI: https://doi.org/10.1038/srep29220

Lithari C., Sanchez-Garcia, C., Ruhnau, P., & Weisz, N. (2016).

Large-scale network-level processes during entrainment. Brain Research, 1635, 143–152.

DOI: https://doi.org/10.1016/j.brainres.2016.01.043

Magazzini, L., Ruhnau, P., & Weisz, N. (2016).

Alpha suppression and connectivity modulations in left temporal and parietal cortices index partial awareness of words. NeuroImage, 133, 279-287.

DOI: https://doi.org/10.1016/j.neuroimage.2016.03.025

Paoli, M., Weisz, N., Antolini, R., & Haase, A. (2016).

Spatially resolved time-frequency analysis of odour coding in the insect antennal lobe. European Journal of Neuroscience, 44 (6), 2387-2395.

DOI: https://doi.org/10.1111/ejn.13344

Peatfield, N.A., Choi, D., & Weisz, N. (2016).

Dynamical Network States as Predisposition of Perception. In Palva, S. (ed.). Multimodal Oscillation-based Connectivity Theory (pp. 19-27). Springer International Publishing.

DOI: https://doi.org/10.1007/978-3-319-32265-0_2

Ruhnau, P., Keitel, C., Lithari, C., Weisz, N., & Neuling, T. (2016).

Flicker-Driven Responses in Visual Cortex Change during Matched-Frequency Transcranial Alternating Current Stimulation. Frontiers in Human Neuroscience, 10:184.

DOI: https://doi.org/10.3389/fnhum.2016.00184

Ruhnau, P., Neuling, T., Fusca, M., Herrmann, C.S., Demarchi, G., & Weisz, N. (2016).

Eyes wide shut: Transcranial alternating current stimulation drives alpha rhythm in a state dependent manner. Scientific Reports, 6:27138.

DOI: https://doi.org/10.1038/srep27138

Turella, L., Tucciarelli, R., Oosterhof, N.N., Weisz, N., Rumiati, R., & Lingnau, A. (2016).

Beta Band Modulations underlie Action Representations for Movement Planning. Neuroimage, 136, 197–207.

DOI: https://doi.org/10.1016/j.neuroimage.2016.05.027

Weise, A., Hartmann, T., Schröger, E., Weisz, N., & Ruhnau, P. (2016).

Cross-modal distractors modulate oscillatory alpha power: the neural basis of impaired task performance. Psychophysiology, 53(11), 1651–1659.

DOI: https://doi.org/10.1111/psyp.12733

Wutz, A., Muschter, E., van Koningsbruggen, M.G., Weisz, N., & Melcher, D. (2016).

Temporal integration windows in neural processing and perception aligned to saccadic eye movements. Current Biology, 26, 1659–1668.

DOI: https://doi.org/10.1016/j.cub.2016.04.070

Hauswald, A., Übelacker, T., Leske, S., & Weisz, N. (2015).

What it means to be Zen: marked modulations of local and interareal synchronization during open monitoring meditation. NeuroImage, 108, 265-273.

DOI: https://doi.org/10.1016/j.neuroimage.2014.12.065

Frey, J., Ruhnau, P., & Weisz, N. (2015).

Not so different after all: the same oscillatory processes support different types of attention. Brain Research, 1626, 183-197.

DOI: https://doi.org/10.1016/j.brainres.2015.02.017

Leonardelli, E., Braun, C., Weisz, N., Lithari, C., Occelli, V., & Zampini, M. (2015).

Prestimulus oscillatory alpha power and connectivity patterns predispose perceptual integration of an audio and a tactile stimulus. Human Brain Mapping, 36(9), 3486-3498.

DOI: https://doi.org/10.1002/hbm.22857

Leske, S., Ruhnau, P., Frey, J., Lithari, C., Müller, N., Hartmann, T., & Weisz, N. (2015).

Prestimulus network integration of auditory cortex predisposes near-threshold perception independently of local excitability. Cerebral Cortex, 25 (12), 4898-4907.

DOI: https://doi.org/10.1093/cercor/bhv212

Lithari, C., Moratti, S. & Weisz, N. (2015).

Thalamocortical interactions underlying visual fear conditioning in humans. Human Brain Mapping, 36(11), 4592-4603.

DOI: https://doi.org/10.1002/hbm.22940

Müller, N., Leske, S., Hartmann, S., Szebeny, S., & Weisz, N. (2015).

Listen to yourself: The medial prefrontal cortex modulates auditory alpha power during speech preparation. Cerebral Cortex, 25(11), 4029-4037.

DOI: https://doi.org/10.1093/cercor/bhu117

Neuling, T., Ruhnau, P., Fusca, M., Demarchi, G., Herrmann, C., & Weisz, N. (2015).

Friends, not foes: magnetoencephalography as a tool to uncover brain dynamics during transcranial alternating current stimulation. Neuroimage, 118, 406-413.

DOI: https://doi.org/10.1016/j.neuroimage.2015.06.026

Tucciarelli, R, Turella, L., Oosterhof, N., Weisz, N., & Lingnau, A. (2015).

MEG multivariate analysis reveals early abstract action representations in the lateral occipitotemporal cortex. The Journal of Neuroscience, 35(49), 16034-16045.

DOI: https://doi.org/10.1523/JNEUROSCI.1422-15.2015

De Ridder, D., Vanneste, S., Weisz, N., Londero, A., Schlee, W., Elgoyhen, A.B. & Langguth, B. (2014).

An integrative model of auditory phantom perception: tinnitus as a unified percept of interacting separable subnetworks. Neuroscience and Biobehavioral Reviews, 44, 16-32.

DOI: https://doi.org/10.1016/j.neubiorev.2013.03.021

Frey, J., Mainy, N., Lachaux, J.P., Müller, N., Bertrand, O., & Weisz, N. (2014).

Selective modulation of auditory cortical alpha activity in an audiovisual spatial attention task. The Journal of Neuroscience, 34(19), 6634-6639.

DOI: https://doi.org/10.1523/JNEUROSCI.4813-13.2014

Hartmann, T., Lorenz, I., Müller, N., Langguth, B., & Weisz, N. (2014).

The effects of neurofeedback on oscillatory processes related to tinnitus. Brain Topography, 27, 149-157.

DOI: https://doi.org/10.1007/s10548-013-0295-9

Heimler, B., Weisz, N., & Collignon, O. (2014).

Revisiting the adaptive and maladaptive effects of crossmodal plasticity. Neuroscience, 283, 44–63.

DOI: https://doi.org/10.1016/j.neuroscience.2014.08.003

Keil, J., Müller, N., Hartmann, T., & Weisz, N. (2014).

Prestimulus beta power and phase synchrony influence the sound-induced flash illusion. Cerebral Cortex, 24, 1278–1288.

DOI: https://doi.org/10.1093/cercor/bhs409

Lange, J., Keil, J., Schnitzler, A., van Dijk, H., & Weisz, N. (2014).

The role of alpha oscillations for illusory perception. Behavioural Brain Research, 271, 294–301.

DOI: https://doi.org/10.1016/j.bbr.2014.06.015

Leske, S., Tse, A., Oosterhof, N.N., Hartmann, T., Müller, N., Keil, J. & Weisz, N. (2014).

The strength of alpha and beta oscillations parametrically scale with the strength of an illusory auditory percept. NeuroImage, 88, 69-78.

DOI: https://doi.org/10.1016/j.neuroimage.2013.11.014

Ruhnau, P., Hauswald, A., & Weisz, N. (2014).

Investigating ongoing brain oscillations and their influence on conscious perception – network states and the window to consciousness. Frontiers in Psychology, 5: 1230.

DOI: https://doi.org/10.3389/fpsyg.2014.01230

Schulz, H., Übelacker, T., Keil, J., Müller, N., & Weisz, N. (2014).

Now I am ready – now I am not: the influence of pre-TMS oscillations and corticomuscular coherence on motor evoked potentials. Cerebral Cortex, 24, 1708-1719.

DOI: https://doi.org/10.1093/cercor/bht024

Song, J.-J., De Ridder, D., Weisz, N., Schlee, W., Van de Heyning, P., & Vanneste, S. (2014).

Hyperacusis-associated pathological resting-state brain oscillations in the tinnitus brain: a hyperresponsiveness network with paradoxically inactive auditory cortex. Brain Structure and Function, 219(3), 1113-1128.

DOI: http://dx.doi.org/10.1007/s00429-013-0555-1

Weisz, N. & Obleser, J. (2014).

Synchronisation signatures in the listening brain: A perspective from non-invasive neuroelectrophysiology. Hearing Research, 307, 16-28.

DOI: https://doi.org/10.1016/j.heares.2013.07.009

Weisz, N., Lüchinger, C., Thut, G., & Müller, N. (2014).

Effects of individual alpha rTMS applied to the auditory cortex and its implications for the treatment of chronic tinnitus. Human Brain Mapping, 35, 14-29.

DOI: https://doi.org/10.1002/hbm.22152

Weisz, N., Müller, N., Jatzev, S., & Bertrand, O. (2014).

Oscillatory alpha modulations in right auditory regions reflect the validity of acoustic cues in an auditory spatial attention task. Cerebral Cortex, 24(10), 2579-2590.

DOI: https://doi.org/10.1093/cercor/bht113

Weisz, N., Wühle, A., Monittola, G. , Demarchi, G., Frey, J., Popov, T. , Braun, C. (2014).

Prestimulus oscillatory power and connectivity patterns predispose conscious somatosensory perception. PNAS USA, 111, E417-E425.

DOI: https://doi.org/10.1073/pnas.1317267111

Wutz, A., Weisz, N., Braun, C. & Melcher, D. (2014).

Temporal windows in visual processing: ‘Pre-stimulus brain state’ and ‘post-stimulus phase reset’ segregate visual transients on different temporal scales. The Journal of Neuroscience, 34, 1554-1565.

DOI: https://doi.org/10.1523/JNEUROSCI.3187-13.2014

Hauswald, A., Weisz, N., Bentin, S., & Kissler, J. (2013).

MEG premotor abnormalities in children with Asperger’s syndrome: Determinants of social behavior? Developmental Cognitive Neuroscience, 5, 95-105.

DOI: https://doi.org/10.1016/j.dcn.2013.02.002

Müller, N., Lorenz, I., Langguth, B., & Weisz, N. (2013).

rTMS induced tinnitus relief is related to an increase in auditory cortical alpha activity. PLoS One, 8(2): e55557.

DOI: https://doi.org/10.1371/journal.pone.0055557

Müller, N., Keil, J., Obleser, J., Schulz, H., Grunwald, T., Bernays, R.L., Huppertz, J., & Weisz, N. (2013).

You can’t stop the music: reduced auditory alpha power and coupling between auditory and memory regions facilitate the illusory perception of music during noise. Neuroimage, 79, 383-393.

DOI: https://doi.org/10.1016/j.neuroimage.2013.05.001

Popov, T., Miller, G., Rockstroh, B., & Weisz, N. (2013).

Modulation of alpha power and functional connectivity during facial affect recognition. The Journal of Neuroscience, 33, 6018-6026.

DOI: https://doi.org/10.1523/JNEUROSCI.2763-12.2013

Hartmann, T., Schlee, W., & Weisz, N. (2012).

It’s only in your head: Expectancy of aversive auditory stimulation modulates stimulus-induced auditory cortical alpha desynchronization. NeuroImage, 60, 170-178.

DOI: https://doi.org/10.1016/j.neuroimage.2011.12.034

Keil, J., Müller, N., Ihssen, N., & Weisz, N. (2012).

On the variability of the McGurk Effect: Audiovisual integration depends on prestimulus brain states. Cerebral Cortex, 22, 221-231.

DOI: https://doi.org/10.1093/cercor/bhr125

Langguth, B., Schecklmann, M., Lehner, A., Landgrebe, M., Poeppl, T.B., Kreuzer, P.M., Schlee, W., Weisz, N., Vanneste, S., & De Ridder, D. (2012).

Neuroimaging and neuromodulation: complementary approaches for identifying the neuronal correlates of tinnitus. Frontiers in Systems Neuroscience., 6:15.

DOI: https://dx.doi.org/10.3389%2Ffnsys.2012.00015

Müller, N. & Weisz, N. (2012).

Lateralized auditory cortical alpha band activity and interregional connectivity pattern reflect anticipation of target sounds. Cerebral Cortex, 22(7), 1604-1613.

DOI: https://doi.org/10.1093/cercor/bhr232

Obleser, J. & Weisz, N. (2012).

Suppressed Alpha Oscillations Predict Intelligibility of Speech and its Acoustic Details. Cerebral Cortex, 22(11), 2466-2477.

DOI: https://doi.org/10.1093/cercor/bhr325

Popov, T., Rockstroh, B., Weisz, N., Elbert, T., & Miller, G. (2012).

Adjusting brain dynamics in schizophrenia by means of perceptual and cognitive training. PLoS One, 7(7), e39051.

DOI: https://doi.org/10.1371/journal.pone.0039051

Popov, T., Steffen, A., Weisz, N., Miller, G., & Rockstroh, B. (2012).

Cross-frequency dynamics of neuromagnetic oscillatory activity: Two mechanisms of emotion regulation. Psychophysiology, 49, 1545-1557.

DOI: https://doi.org/10.1111/j.1469-8986.2012.01484.x

Schlee, W., Leirer, V., Kolassa, I., Weisz, N., & Elbert, T. (2012).

Age-related changes in neural functional connectivity and its behavioral relevance. BMC Neuroscience, 13: 16.

DOI: https://dx.doi.org/10.1186%2F1471-2202-13-16

Weisz, N., Steidle, L., & Lorenz, I. (2012).

Formerly known as inhibitory: effects of 1-Hz rTMS on auditory cortex are state-dependent. European Journal of Neuroscience, 36, 2077-2087.

DOI: https://doi.org/10.1111/j.1460-9568.2012.08097.x

Weisz, N., Lecaignard, F., Müller, N., & Bertrand, O. (2012).

The modulatory influence of a predictive cue on the auditory Steady-State Response. Human Brain Mapping, 33, 1417-1430.

DOI: https://doi.org/10.1002/hbm.21294

Hartmann, T., Lorenz, I., & Weisz, N. (2011).

Neurobiofeedback. In Møller, A., Langguth, B., De Ridder, D., & Kleinjung, T. (eds.). Textbook of Tinnitus (pp. 691-696). Humana-Springer.

DOI: https://doi.org/10.1007/978-1-60761-145-5_87

Hartmann, T., Schulz, H., & Weisz, N. (2011).

Probing of Brain States in Real-Time: Introducing the ConSole Environment. Frontiers in Psychology, 2: 36.

DOI: https://dx.doi.org/10.3389%2Ffpsyg.2011.00036

Jordanov, T., Popov, T., Weisz, N., Elbert, T., Paul-Jordanov, I., & Rockstroh, B. (2011).

Reduced mismatch negativity and increased variability of brain activity in schizophrenia. Clinical Neurophysiology, 122, 2365-2374.

DOI: https://dx.doi.org/10.1016/j.clinph.2011.05.002

Ortmann, M., Müller, N., Schlee, W., & Weisz, N. (2011).

Rapid increases of gamma power in the auditory cortex following noise trauma in humans. European Journal of Neuroscience, 33, 568-575.

DOI: https://doi.org/10.1111/j.1460-9568.2010.07542.x

Popov, T, Jordanov, T., Weisz, N., Elbert, T., Rockstroh, B., & Miller, G.. (2011).

Evoked and induced oscillatory activity contributes to abnormal auditory sensory gating in schizophrenia. NeuroImage, 56, 307-314.

DOI: https://doi.org/10.1016/j.neuroimage.2011.02.016

Schecklmann, M., Volberg, G., Frank, G., Hadersdorfer, J., Steffens, T., Weisz, N., Landgrebe, M., Hajak, G., Greenlee, M.W., Classen, J., & Langguth, B. (2011).

Paired associative stimulation of the auditory system: a proof-of-principle study. PLoS One, 6:e27008.

DOI: https://dx.doi.org/10.1371%2Fjournal.pone.0027088

Schlee, W., Lorenz, I., Hartmann, T., Müller, N., Schulz, H., & Weisz, N. (2011).

A global brain model of tinnitus. In Møller, A., Langguth, B., De Ridder, D., & Kleinjung, T. (eds.). Textbook of Tinnitus (pp. 161-169). Humana-Springer.

DOI: https://doi.org/10.1007/978-1-60761-145-5_20

Schlittmeier, S., Weisz, N., & Bertrand, O. (2011).

What Characterizes Changing-State Speech in Affecting Short-Term Memory? An EEG Study on the Irrelevant Sound Effect. Psychophysiology, 48, 1669-1680.

DOI: https://doi.org/10.1111/j.1469-8986.2011.01263.x

Weisz, N., Hartmann, T., Müller, N., Lorenz, I., & Obleser, J. (2011).

Alpha Rhythms in Audition: Cognitive and Clinical Perspectives. Frontiers in Psychology, 2: 73.

DOI: https://doi.org/10.3389/fpsyg.2011.00073

Keil, J., Weisz, N., Paul-Jordanov, I., & Wienbruch, C. (2010).

Localization of the magnetic equivalent of the ERN and induced oscillatory brain activity. NeuroImage, 51, 404-411.

DOI: https://doi.org/10.1016/j.neuroimage.2010.02.003

Lorenz, I., Müller, N., Schlee, W., Langguth, B., & Weisz, N. (2010).

Short-term effects of single repetitive TMS sessions on auditory evoked activity in patients with chronic tinnitus. Journal of Neurophysiology, 104, 1497-1505.

DOI: https://doi.org/10.1152/jn.00370.2010

Moazami-Gourdazi, M., Michels, L., Weisz, N., & Jeanmonod, D. (2010).

Temporo-insular enhancement of EEG low and high frequencies in patients with chronic tinnitus. QEEG study of chronic tinnitus patients. BMC Neuroscience, 11: 40.

DOI: https://dx.doi.org/10.1186/1471-2202-11-40

Weisz, N. & Langguth, B. (2010).

Kortikale Plastizität und Veränderungen bei Tinnitus – Therapeutische Optionen. HNO, 58, 983-989.

DOI: https://dx.doi.org/10.1007/s00106-010-2178-7

Foxton, J.M., Weisz, N., Bauchet-Lecaignard, F., Delpuech, C., & Bertrand, O. (2009).

The neural bases underlying pitch processing difficulties. NeuroImage, 45, 1305-1313.

DOI: https://doi.org/10.1016/j.neuroimage.2008.10.068

Hartmann, T., Weisz, N., Schlee, W., & Elbert, T. (2009).

Investigating the neural correlates of percepts using magnetencepholography and magnetic source imaging. n Pöppel, E., Balazs, G., & Kraft, E. (eds.). Neuronal Correlates of Thinking (pp. 51-64). Springer.

DOI: https://doi.org/10.1007/978-3-540-68044-4_4

Lorenz, I., Müller, N., Schlee, W., Hartmann, T., & Weisz, N. (2009).

Loss of alpha power is related to increased gamma synchronization – A marker of reduced inhibition in tinnitus? Neuroscience Letters, 453 (3), 225-228.

DOI: https://doi.org/10.1016/j.neulet.2009.02.028

Müller, N., Schlee, W., Hartmann, T., Lorenz, I., & Weisz, N. (2009).

Top-down modulation of the auditory steady-state response in a task-switch paradigm. Frontiers in Human Neuroscience, 3: 1.

DOI: https://dx.doi.org/10.3389%2Fneuro.09.001.2009

Schlee, W., Weisz, N., Hartmann, T., & Elbert, T. (2009).

Abnormal resting-state cortical coupling in chronic Tinnitus. BMC Neuroscience, 10: 11.

DOI: https://doi.org/10.1186/1471-2202-10-11

Schlee, W., Müller, N., Hartmann, T., Keil, J., Lorenz, I., & Weisz, N., (2009).

Mapping cortical hubs in tinnitus. BMC Biology, 7: 80.

DOI: https://doi.org/10.1186/1741-7007-7-80

Kahlbrock, N. & Weisz, N. (2008).

Transient reduction of tinnitus intensity is marked by concomitant reductions of delta band power. BMC Biology, 6: 4.

DOI: https://doi.org/10.1186/1741-7007-6-4

Schlee, W., Hartmann, T., Dohrmann, K., Lorenz, I., Müller, N., & Weisz, N. (2008).

Assessment and modification of the tinnitus-related cortical network. Seminars in Hearing, 29, 270-287.

DOI: https://dx.doi.org/10.1055/s-0028-1082033

Schlee, W., Weisz, N., Bertrand, O., Dohrmann, K., Hartmann, T., & Elbert, T. (2008).

Using auditory steady-state responses to outline the functional connectivity in the tinnitus brain. PLoS ONE, 3(11), e3720.

DOI: https://doi.org/10.1371/journal.pone.0003720

Dohrmann, K. , Weisz, N., Schlee, W., Hartmann, T., & Elbert, T. (2007).

Neurofeedback for treating tinnitus. Progress In Brain Research, 166, 473-554.

DOI: https://doi.org/10.1016/S0079-6123(07)66046-4

Dohrmann, K., Elbert, T., Schlee, W., & Weisz, N. (2007).

Tuning the tinnitus percept by modification of synchronous brain activity. Restorative Neurology and Neuroscience, 25, 1-8.

DOI: https://content.iospress.com/articles/restorative-neurology-and-neuroscience/rnn253418

Weisz, N., Kostadinov, B., Dohrmann, K., Hartmann, T., & Schlee, W. (2007).

Tracking short-term auditory cortical plasticity during classical conditioning using frequency-tagged stimuli. Cerebral Cortex, 17, 1867-1876.

DOI: https://doi.org/10.1093/cercor/bhl095

Weisz, N., Müller, S., Schlee, W., Dohrmann, K., Hartmann, & T., Elbert, T. (2007).

The neural code of auditory phantom perception. The Journal of Neuroscience, 27, 1479-1484.

DOI: https://doi.org/10.1523/JNEUROSCI.3711-06.2007

Weisz, N., Dohrmann, K., Schlee, W., Elbert, T. (2007).

The relevance of spontaneous activity for the coding of the tinnitus sensation. Progress In Brain Research, 166, 61-70.

DOI: https://doi.org/10.1016/S0079-6123(07)66006-3

Weisz, N. & Schlittmeier, S. (2006).

Detrimental effects of irrelevant speech on serial recall of visual items are reflected in reduced visual N1 and reduced theta activity. Cerebral Cortex, 16, 1097-1105.

DOI: https://doi.org/10.1093/cercor/bhj051

Weisz, N., Hartmann, T. Dohrmann, K., Schlee, W., & Noreña, A. (2006).

High-frequency tinnitus without hearing loss does not mean absence of deafferentation. Hearing Research, 222(1-2), 108-114.

DOI: https://doi.org/10.1016/j.heares.2006.09.003

Wienbruch, C., Paul, I., Weisz, N., Elbert, T., & Roberts, L. (2006).

Frequency organization of the 40-Hz auditory steady state response in normal hearing and in tinnitus. NeuroImage, 33, 180-194.

DOI: https://doi.org/10.1016/j.neuroimage.2006.06.023

Weisz, N., Dohrmann, K., & Elbert, T. (2005).

Der Klageton neuronaler Netze: Tinnitus aus neurowissenschaftlicher Perspektive. HNO-Nachrichten, 5, 32-35.

DOI: http://nbn-resolving.de/urn:nbn:de:bsz:352-opus-42624

Weisz, N., Moratti, S., Meinzer, M., Dohrmann, K., & Elbert, T. (2005).

Tinnitus perception and distress is related to abnormal spontaneous brain activity as measured by magnetencephalography. PLoS Medicine, 2, e153.

DOI: https://dx.doi.org/10.1371%2Fjournal.pmed.0020153

Weisz, N., Wienbruch, C., Dohrmann, K., & Elbert, T. (2005).

Neuromagnetic indicators of auditory cortical reorganization of tinnitus. Brain, 128, 2722-2731.

DOI: https://doi.org/10.1093/brain/awh588

Weisz, N., Wienbruch, C., Hoffmeister, S., & Elbert, T. (2004).

Tonotopic organization of the human auditory cortex probed with frequency-modulated tones. Hearing Research, 191, 49-58.

DOI: https://doi.org/10.1016/j.heares.2004.01.012

Weisz, N., Keil, A., Wienbruch, C., Hoffmeister, S., & Elbert, T. (2004).

One set of sounds, two tonotopic maps – exploring auditory cortex with amplitude-modulated tones. Clinical Neurophysiology, 115, 1248-1258.

DOI: https://doi.org/10.1016/j.clinph.2003.12.034

Weisz, N., Voss, S., Berg, P., & Elbert, T. (2004).

Abnormal auditory mismatch response in tinnitus sufferers with high-frequency hearing loss is associated with subjective distress level. BMC Neuroscience, 5, 8.

DOI: https://doi.org/10.1186/1471-2202-5-8

Duschek, S., Weisz, N., & Schandry, R. (2003).

Reduced cognitive performance and prolonged reaction time accompany moderate hypotension. Clinical Autonomic Research, 13, 427-432.

DOI: https://doi.org/10.1007/s10286-003-0124-4

Pantev, C., Weisz, N., Schulte, M., & Elbert, T. (2003).

Plasticity of the Human Auditory Cortex. In Pessoa, L. & De Weerd, P. (eds.). Filling-in: From perceptual completion to cortical reorganization (pp. 231-251). Oxford University Press.

DOI: https://dx.doi.org/10.1093/acprof:oso/9780195140132.003.0012

Weisz, N., Schandry, R., Jacobs, A.M., Mialet., J.-P., & Duschek, S. (2002).

Early contingent negative variation of the EEG and attentional flexibility are reduced in hypotension. International Journal of Psychophysiology, 45, 253-260.

DOI: https://doi.org/10.1016/S0167-8760(02)00032-6