Thilo Kellermann

Thilo Kellermann

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

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Previous Organizations / Institutes

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Thilo Kellermann has a total of 233 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Reduced functional resting-state connectivity in chronic pain patients with small fiber neuropathy

    by Sebastian Scheliga, Han-Gue Jo, Maike F. Dohrn, Thilo Kellermann, Angelika Lampert, Roman Rolke, Greta Z. Peschke, Noortje W.M. van Den Braak, Annette Lischka, Robin Bekrater-Bodmann, et al.

  • Open Access

    Altered brain dynamics of facial emotion processing in schizophrenia: a combined EEG/fMRI study

    by Philippa Hüpen, Barbara Schulte Holthausen, Christina Regenbogen, Thilo Kellermann, Han-Gue Jo, Ute Habel

    Facial stimuli are relevant social cues for humans and essential signals for adequate social interaction. Impairments in face processing are well-documented in schizophrenia and linked to symptomatology, yet the underlying neural dynamics remain unclear. Here, we investigated the processing and underlying neural temporal dynamics of task-irrelevant emotional face stimuli using combined EEG/fMRI in 14 individuals with schizophrenia and 14 matched healthy controls. Specifically, fMRI-informed region-of-interests were subjected to EEG-Dynamic Causal Modeling (DCM) analyses. Among six fMRI-informed EEG-DCM models, alterations in effective connectivity emerged between the primary visual cortex (V1) and the left occipital fusiform gyrus (lOFG). Specifically, individuals with schizophrenia showed enhanced backward connectivity from the lOFG to V1 for stimuli preceded by fearful (but not happy or neutral) faces. Connectivity strength was strongly correlated with self-reported difficulties in comprehending, processing, or articulating emotions (as assessed by the Toronto Alexithymia Scale-20) in individuals with schizophrenia but not in healthy controls. Enhanced backward connectivity from the lOFG to V1 potentially indicates heightened attention towards fearful surroundings and a propensity to assign salience to these stimuli in individuals with schizophrenia. The link to TAS-20 scores indicates that this neural deficit has real-world implications for how individuals with schizophrenia perceive and relate to their emotions and the external world, potentially contributing to the social and cognitive difficulties observed in the disorder.


  • Open Access

    Reduced Gray Matter Volume and Cortical Thickness in Patients With Small-Fiber Neuropathy

    by Sebastian Scheliga, Maike F. Dohrn, Ute Habel, Angelika Lampert, Roman Rolke, Annette Lischka, Noortje van Den Braak, Marc Spehr, Han-Gue Jo, Thilo Kellermann


  • A neural mechanism underlying predictive visual motion processing in patients with schizophrenia

    by Sebastian Scheliga, Rosalie Schwank, Ruben Scholle, Ute Habel, Thilo Kellermann


  • Neural correlates of multisensory integration in the human brain: an ALE meta-analysis

    by Sebastian Scheliga, Thilo Kellermann, Angelika Lampert, Roman Rolke, Marc Spehr, Ute Habel

    Previous fMRI research identified superior temporal sulcus as central integration area for audiovisual stimuli. However, less is known about a general multisensory integration network across senses. Therefore, we conducted activation likelihood estimation meta-analysis with multiple sensory modalities to identify a common brain network. We included 49 studies covering all Aristotelian senses i.e., auditory, visual, tactile, gustatory, and olfactory stimuli. Analysis revealed significant activation in bilateral superior temporal gyrus, middle temporal gyrus, thalamus, right insula, and left inferior frontal gyrus. We assume these regions to be part of a general multisensory integration network comprising different functional roles. Here, thalamus operate as first subcortical relay projecting sensory information to higher cortical integration centers in superior temporal gyrus/sulcus while conflict-processing brain regions as insula and inferior frontal gyrus facilitate integration of incongruent information. We additionally performed meta-analytic connectivity modelling and found each brain region showed co-activations within the identified multisensory integration network. Therefore, by including multiple sensory modalities in our meta-analysis the results may provide evidence for a common brain network that supports different functional roles for multisensory integration.


  • Open Access

    Effects of exogenous testosterone application on network connectivity within emotion regulation systems

    by Mikhail Votinov, Lisa Wagels, Felix Hoffstaedter, Thilo Kellermann, Katharina S. Goerlich, Simon B. Eickhoff, Ute Habel

    Studies with steroid hormones underlined the vital role of testosterone on social-emotional processing. However, there is still a lack of studies investigating whether testosterone modulates network connectivity during resting-state. Here, we tested how the exogenous application of testosterone would affect functional connectivity between regions implicated in emotion regulation. In total, 96 male participants underwent resting-state fMRI scanning. Before the measurement, half of the subjects received 5 g TestimTM gel (containing 50 mg testosterone) and the other half a corresponding amount of placebo gel. Seeds for the connectivity analysis were meta-analytically defined. First, all regions associated with emotion regulation were chosen via Neurosynth (data driven). Among those, specific seeds were selected and categorized based on the neural model of emotion regulation by Etkin and colleagues (Etkin et al., 2015) (theory-guided). Resting-state connectivity analysis revealed decreased connectivity between the right DLPFC and the right amygdala as well as between the VMPFC and the left IPL for the testosterone group compared to the placebo group. A complementary dynamic causal modeling (DCM) analysis on findings from the resting-state connectivity analysis underlined a bidirectional coupling which was decreased close to zero by testosterone administration. Our results demonstrate that testosterone administration disrupts resting-state connectivity within fronto-subcortical and fronto-parietal circuits. The findings suggest that even without a specific task (e.g. challenge, reward processing) testosterone modulates brain networks important for social-emotional processing.


  • Open Access

    Task-dependent functional organizations of the visual ventral stream

    by Han-Gue Jo, Junji Ito, Barbara Schulte Holthausen, Conrad Baumann, Sonja Grün, Ute Habel, Thilo Kellermann

    The visual hierarchy of the ventral stream has been widely studied. However, it remains unclear how the hierarchical system organizes its functional coupling during top-down cognitive process. The present fMRI study investigated task-dependent functional connectivity along the ventral stream, while twenty-eight participants performed object recognition tasks that required different types of visual processing: i) searching or ii) memorizing visual objects embedded in natural scene images or iii) free viewing of the same images. Utilizing a seed-based approach that explicitly compared task-specific BOLD time-series, we identified task-dependent functional connectivity of the visual ventral stream, demonstrating different correlation structures. Searching for a target object manifested both correlated and anti-correlated structures, separating the visual areas V1 and V4 from the posterior part of the inferior temporal cortex (PIT). In contrast, the ventral stream structure remained correlated during memorizing objects, but increased the correlation between the right V4 and PIT. On the other hand, V1 and V4 showed task-dependent activation, whereas PIT was deactivated. These results highlight the context-dependent nature of the visual ventral stream and shed light on how the visual hierarchy is selectively organized to bias object recognition toward features of interest.


  • Cerebral and behavioural response to human voices is mediated by sex and sexual orientation

    by Elke Smith, Jessica Junger, Katharina Pauly, Thilo Kellermann, Birgit Dernt, Ute Habel


  • Gender incongruence and the brain – Behavioral and neural correlates of voice gender perception in transgender people

    by Elke Smith, Jessica Junger, Katharina Pauly, Thilo Kellermann, Joseph Neulen, Christiane Neuschaefer-Rube, Birgit Derntl, Ute Habel


  • Progressively analogous evidence of covert face recognition from functional magnetic resonance imaging and skin conductance responses studies involving a patient with dissociative amnesia

    by Natalya Chechko, Susanne Stickel, Thilo Kellermann, Andre Kirner, Ute Habel, Guillén Fernández, Frank Schneider, Nils Kohn

    This is a case study involving a female patient (NN) with complete loss of autobiographical memory and identity despite normal neurological assessment. To test the hypothesis that patients with dissociative amnesia (DA) possess the ability to covertly process facial identities they are unaware of, we conducted functional magnetic resonance imaging (fMRI) and assessed skin conductance responses (SCR) to (a) strangers, (b) celebrities, and (c) familiar faces not seen since the onset of DA. We also performed associative face‐name memory tasks to test the patient's ability to learn and recall newly learned face‐name pairs. Although NN did not recognize any of the faces of her friends and relatives, their images triggered a stronger involvement of the left fusiform gyrus, the bilateral hippocampus/amygdala region, the orbitofrontal cortex, the middle temporal regions, and the precuneus, along with higher SCR. During recollection of previously learned face‐name pairs, NN (compared to healthy controls) demonstrated a weaker involvement of the hippocampus. Our findings suggest that, in DA, specific arousal systems remain capable of being activated by familiar faces outside of conscious awareness. The decreased activation observed in the hippocampus demonstrates that the functioning of memory‐sensitive regions may be impaired by trauma.