| human | Q5 |
| P2381 | Academic Tree ID | 9052 |
| P268 | Bibliothèque nationale de France ID | 145630534 |
| P646 | Freebase ID | /m/0c5d7ng |
| P227 | GND ID | 115543929 |
| P269 | IdRef ID | 073313947 |
| P213 | ISNI | 0000000108940652 |
| P10553 | IxTheo authority ID | 07731929X |
| P9918 | Kallías ID | PE00642740 |
| P244 | Library of Congress authority ID | n95111154 |
| P2798 | Loop ID | 14096 |
| P8189 | National Library of Israel J9U ID | 987007424060905171 |
| P1006 | Nationale Thesaurus voor Auteursnamen ID | 261998366 |
| P1207 | NUKAT ID | n94200419 |
| P3762 | openMLOL author ID | 300249 |
| P3987 | SHARE Catalogue author ID | 772532 |
| P214 | VIAF ID | 45035234 |
| P10832 | WorldCat Entities ID | E39PBJcWqxfY3WggCxD4RmMByd |
| P27 | country of citizenship | Germany | Q183 |
| P735 | given name | Georg | Q1985538 |
| Georg | Q1985538 | ||
| P1412 | languages spoken, written or signed | English | Q1860 |
| P106 | occupation | psychiatrist | Q211346 |
| P21 | sex or gender | male | Q6581097 |
| P937 | work location | Magdeburg | Q1733 |
| Q38732885 | "Paradox of slow frequencies" - Are slow frequencies in upper cortical layers a neural predisposition of the level/state of consciousness (NPC)? |
| Q37889474 | A canadian perspective on ethics review and neuroimaging: tensions and solutions. |
| Q38045029 | A cultural neuroscience approach to the biosocial nature of the human brain |
| Q30374780 | A fallacious jar? The peculiar relation between descriptive premises and normative conclusions in neuroethics. |
| Q47592804 | A stochastic model of input effectiveness during irregular gamma rhythms |
| Q38782447 | Abnormal Time Experiences in Major Depression: An Empirical Qualitative Study |
| Q48312961 | Abnormal body perception and neural activity in the insula in depression: an fMRI study of the depressed "material me". |
| Q50950137 | Affective judgment and beneficial decision making: ventromedial prefrontal activity correlates with performance in the Iowa Gambling Task. |
| Q48841444 | Altered brain activity during emotional empathy in somatoform disorder |
| Q34048603 | Altered brain long-range functional interactions underlying the link between aberrant self-experience and self-other relationship in first-episode schizophrenia |
| Q47337175 | Altered negative BOLD responses in the default-mode network during emotion processing in depressed subjects |
| Q33960320 | Altered negative unconscious processing in major depressive disorder: an exploratory neuropsychological study |
| Q47865440 | Altered temporal variance and neural synchronization of spontaneous brain activity in anesthesia |
| Q48260024 | Anterior cingulate activity and the self in disorders of consciousness |
| Q41677729 | Anxious attachment style and hopelessness as predictors of burden in caregivers of patients with disorders of consciousness: a pilot study |
| Q34942618 | Are Auditory Hallucinations Related to the Brain's Resting State Activity? A 'Neurophenomenal Resting State Hypothesis'. |
| Q39793988 | Are emotions associated with activity during rest or interoception? An exploratory fMRI study in healthy subjects |
| Q30838949 | Associations of regional GABA and glutamate with intrinsic and extrinsic neural activity in humans—a review of multimodal imaging studies |
| Q48505720 | Attentional modulation of emotional stimulus processing in patients with major depression--alterations in prefrontal cortical regions |
| Q34471440 | Attentional modulation of emotional stimulus processing: an fMRI study using emotional expectancy |
| Q38855914 | Auditory Hallucinations and the Brain's Resting-State Networks: Findings and Methodological Observations |
| Q48735599 | Autoepistemic limitation and the brain's neural code: Comment on "Neuroontology, neurobiological naturalism, and consciousness: a challenge to scientific reduction and a solution" by Todd E. Feinberg |
| Q42538491 | Brain and self - a neurophilosophical account |
| Q39829406 | Brain imaging of the self--conceptual, anatomical and methodological issues |
| Q37057686 | Brain network informed subject community detection in early-onset schizophrenia |
| Q28305056 | Brain pathology in pedophilic offenders: evidence of volume reduction in the right amygdala and related diencephalic structures |
| Q42125358 | Catatonia in Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition |
| Q37098704 | Changes in brain activity of somatoform disorder patients during emotional empathy after multimodal psychodynamic psychotherapy |
| Q30462682 | Common brain activations for painful and non-painful aversive stimuli |
| Q51998679 | Cortical midline structures and the self. |
| Q46446674 | Culture modulates brain activity during empathy with anger |
| Q47668713 | Culture-sensitive neural substrates of human cognition: a transcultural neuroimaging approach |
| Q47655917 | Decoupled temporal variability and signal synchronization of spontaneous brain activity in loss of consciousness: An fMRI study in anesthesia |
| Q46423388 | Decreased neural activity in reward circuitry during personal reference in abstinent alcoholics--a fMRI study |
| Q48303799 | Decreased neuronal activity in reward circuitry of pathological gamblers during processing of personal relevant stimuli |
| Q48923197 | Deficit in decision making in catatonic schizophrenia: an exploratory study |
| Q34096181 | Delineating self-referential processing from episodic memory retrieval: common and dissociable networks |
| Q39265899 | Different neural manifestations of two slow frequency bands in resting functional magnetic resonance imaging: a systemic survey at regional, interregional, and network levels |
| Q48955073 | Differential alterations of resting-state functional connectivity in generalized anxiety disorder and panic disorder |
| Q50670285 | Differential modulation of valence and arousal in high-alexithymic and low-alexithymic individuals |
| Q50879691 | Differential parametric modulation of self-relatedness and emotions in different brain regions. |
| Q38666125 | Disrupted relationship between "resting state" connectivity and task-evoked activity during social perception in schizophrenia |
| Q48704184 | Dissociable networks for the expectancy and perception of emotional stimuli in the human brain |
| Q51017257 | Dissociation between anterior and posterior cortical regions during self-specificity and familiarity: a combined fMRI-meta-analytic study. |
| Q37992047 | Distinction between Externally vs. Internally Guided Decision-Making: Operational Differences, Meta-Analytical Comparisons and Their Theoretical Implications |
| Q50800522 | Distinguishing specific sexual and general emotional effects in fMRI-subcortical and cortical arousal during erotic picture viewing. |
| Q47753416 | Do brain lesions in stroke affect basic emotions and attachment? |
| Q38258488 | Do cortical midline variability and low frequency fluctuations mediate William James' "Stream of Consciousness"? "Neurophenomenal Balance Hypothesis" of "Inner Time Consciousness". |
| Q43197598 | Editorial: Reward- and aversion-related processing in the brain: translational evidence for separate and shared circuits |
| Q54993390 | Editorial: The Janus Face of Language: Where Are the Emotions in Words and Where Are the Words in Emotions? |
| Q52935607 | Effect of low-frequency transcranial magnetic stimulation on an affective go/no-go task in patients with major depression: role of stimulation site and depression severity. |
| Q48955519 | Emotional processing and executive functions in major depressive disorder: dorsal prefrontal activity correlates with performance in the intra-extra dimensional set shift |
| Q37064566 | Essentials of psychoanalytic process and change: how can we investigate the neural effects of psychodynamic psychotherapy in individualized neuro-imaging? |
| Q51986698 | Executive dysfunction, self, and ego pathology in schizophrenia: an exploratory study of neuropsychology and personality. |
| Q46032783 | Finite size effect induces stochastic gamma oscillation in inhibitory network with conduction delay. |
| Q42590077 | First-Person Neuroscience: a new methodological approach for linking mental and neuronal states |
| Q41890558 | From emotions to consciousness - a neuro-phenomenal and neuro-relational approach |
| Q53402596 | Functional connections between activated and deactivated brain regions mediate emotional interference during externally directed cognition. |
| Q46914797 | GABA concentrations in the human anterior cingulate cortex predict negative BOLD responses in fMRI. |
| Q26830571 | GABA in the insula - a predictor of the neural response to interoceptive awareness |
| Q30540638 | GABAA receptors predict aversion-related brain responses: an fMRI-PET investigation in healthy humans |
| Q38045099 | Gene, brains, and environment-genetic neuroimaging of depression |
| Q51084310 | Generation of the probabilistic template of default mode network derived from resting-state fMRI. |
| Q28485971 | Glutamate concentration in the medial prefrontal cortex predicts resting-state cortical-subcortical functional connectivity in humans |
| Q30363352 | Habits: bridging the gap between personhood and personal identity. |
| Q48366446 | High resolution fMRI of subcortical regions during visual erotic stimulation at 7 T. |
| Q47984988 | How are different neural networks related to consciousness? |
| Q37819255 | How can the brain's resting state activity generate hallucinations? A 'resting state hypothesis' of auditory verbal hallucinations |
| Q38929195 | How do abnormalities in the brain's spontaneous activity translate into symptoms in schizophrenia? From an overview of resting state activity findings to a proposed spatiotemporal psychopathology |
| Q31031248 | How do resting state changes in depression translate into psychopathological symptoms? From 'Spatiotemporal correspondence' to 'Spatiotemporal Psychopathology'. |
| Q47554805 | How do the brain's time and space mediate consciousness and its different dimensions? Temporo-spatial theory of consciousness (TTC). |
| Q50960392 | How do we modulate our emotions? Parametric fMRI reveals cortical midline structures as regions specifically involved in the processing of emotional valences. |
| Q36787757 | How does our brain constitute defense mechanisms? First-person neuroscience and psychoanalysis |
| Q47977703 | How does the 'rest-self overlap' mediate the qualitative and automatic features of self-reference? |
| Q46970449 | How is informed consent related to emotions and empathy? An exploratory neuroethical investigation |
| Q30367663 | How is our self altered in psychiatric disorders? A neurophenomenal approach to psychopathological symptoms. |
| Q34187105 | How is our self related to midline regions and the default-mode network? |
| Q47568223 | How much is enough-Can resting state fMRI provide a demarcation for neurosurgical resection in glioma? |
| Q36847668 | How to Link Brain and Experience? Spatiotemporal Psychopathology of the Lived Body |
| Q38181499 | How to investigate neuro-biochemical relationships on a regional level in humans? Methodological considerations for combining functional with biochemical imaging |
| Q37719941 | Humans, brains, and their environment: marriage between neuroscience and anthropology? |
| Q30472842 | Identifying a network of brain regions involved in aversion-related processing: a cross-species translational investigation |
| Q46987420 | Imbalance between left and right dorsolateral prefrontal cortex in major depression is linked to negative emotional judgment: an fMRI study in severe major depressive disorder |
| Q30418696 | Immanuel Kant's mind and the brain's resting state |
| Q48959417 | Impaired self-referential processing in mesial temporal lobe epilepsy: a functional MRI study |
| Q39388194 | Implicit and Explicit Routes to Recognize the Own Body: Evidence from Brain Damaged Patients |
| Q49072667 | Increased activation of the supragenual anterior cingulate cortex during visual emotional processing in male subjects with high degrees of alexithymia: an event-related fMRI study |
| Q47336234 | Increased self-focus in major depressive disorder is related to neural abnormalities in subcortical-cortical midline structures |
| Q41241367 | Integrative Processing of Touch and Affect in Social Perception: An fMRI Study |
| Q62489228 | Interindividual neural differences in moral decision-making are mediated by alpha power and delta/theta phase coherence |
| Q48646329 | Interoceptive awareness enhances neural activity during empathy |
| Q37001094 | Is Anorexia Nervosa a Disorder of the Self? A Psychological Approach |
| Q58583825 | Is Our Self Related to Personality? A Neuropsychodynamic Model |
| Q47356152 | Is There a Nonadditive Interaction Between Spontaneous and Evoked Activity? Phase-Dependence and Its Relation to the Temporal Structure of Scale-Free Brain Activity |
| Q48845548 | Is emotion regulation self-regulation? |
| Q37833254 | Is our self nothing but reward? |
| Q33521240 | Is our self nothing but reward? Neuronal overlap and distinction between reward and personal relevance and its relation to human personality |
| Q43148611 | Is schizophrenia a spatiotemporal disorder of the brain's resting state? |
| Q37643880 | Is subcortical-cortical midline activity in depression mediated by glutamate and GABA? A cross-species translational approach |
| Q38435777 | Is the Sense of Agency in Schizophrenia Influenced by Resting-State Variation in Self-Referential Regions of the Brain? |
| Q30380722 | Is the self a higher-order or fundamental function of the brain? The "basis model of self-specificity" and its encoding by the brain's spontaneous activity. |
| Q34171546 | Is there a valence-specific pattern in emotional conflict in major depressive disorder? An exploratory psychological study |
| Q48941642 | Left prefrontal repetitive transcranial magnetic stimulation impairs performance in affective go/no-go task |
| Q48605116 | Linear noise approximation for oscillations in a stochastic inhibitory network with delay |
| Q43205095 | Lorazepam modulates orbitofrontal signal changes during emotional processing in catatonia |
| Q28078489 | Methodological Problems on the Way to Integrative Human Neuroscience |
| Q51892123 | Multimodal psychodynamic psychotherapy induces normalization of reward related activity in somatoform disorder. |
| Q38418744 | NMDA hypofunction in the posterior cingulate as a model for schizophrenia: an exploratory ketamine administration study in fMRI. |
| Q35650264 | Neural activity during interoceptive awareness and its associations with alexithymia-An fMRI study in major depressive disorder and non-psychiatric controls |
| Q48058452 | Neural overlap between resting state and self-relevant activity in human subcallosal cingulate cortex--single unit recording in an intracranial study |
| Q35750376 | Neural substrates underlying intentional empathy |
| Q30593477 | Neuroimaging in pedophilia |
| Q31031649 | Neuroimaging markers of glutamatergic and GABAergic systems in drug addiction: Relationships to resting-state functional connectivity |
| Q58102931 | Neuronal variability of Resting State activity in Eating Disorders: increase and decoupling in Ventral Attention Network and relation with clinical symptoms |
| Q60634824 | Neuronal variability of Resting State activity in Eating Disorders: increase and decoupling in Ventral Attention Network and relation with clinical symptoms |
| Q51892998 | Neurophilosophical perspectives of neuroimaging in forensic psychiatry-giving way to a paradigm shift? |
| Q37093630 | Neuropsychiatry. An old discipline in a new gestalt bridging biological psychiatry, neuropsychology, and cognitive neurology |
| Q36381854 | Neuroscience of decision making and informed consent: an investigation in neuroethics |
| Q48326115 | Novelty seeking modulates medial prefrontal activity during the anticipation of emotional stimuli |
| Q33953456 | Options for the treatment of febrile catatonia |
| Q30947956 | Orbitofrontal cortical dysfunction in akinetic catatonia: a functional magnetic resonance imaging study during negative emotional stimulation |
| Q30457599 | Overview of potential procedural and participant-related confounds for neuroimaging of the resting state |
| Q47857071 | Patterns of microstructural white matter abnormalities and their impact on cognitive dysfunction in the various phases of type I bipolar disorder |
| Q34493952 | Personality functioning and the cortical midline structures--an exploratory FMRI study |
| Q33671243 | Posterior cingulate cross-hemispheric functional connectivity predicts the level of consciousness in traumatic brain injury |
| Q50879343 | Preceding attention and the dorsomedial prefrontal cortex: process specificity versus domain dependence. |
| Q39203411 | Psychoanalysis and the brain - why did freud abandon neuroscience? |
| Q30360626 | Psychopathology and pathophysiology of the self in depression - neuropsychiatric hypothesis. |
| Q51009371 | Reciprocal modulation and attenuation in the prefrontal cortex: an fMRI study on emotional-cognitive interaction. |
| Q49084889 | Reduced deactivation in reward circuitry and midline structures during emotion processing in borderline personality disorder |
| Q47333083 | Reduced negative BOLD responses in the default-mode network and increased self-focus in depression |
| Q33998242 | Reduced resting-state functional connectivity of the somatosensory cortex predicts psychopathological symptoms in women with bulimia nervosa |
| Q62082879 | Region-Based Approach versus Mechanism-Based Approach to the Brain |
| Q37708463 | Rest-stimulus interaction in the brain: a review |
| Q34701060 | Resting state activity and the "stream of consciousness" in schizophrenia--neurophenomenal hypotheses |
| Q42789642 | Resting state low-frequency fluctuations in prefrontal cortex reflect degrees of harm avoidance and novelty seeking: an exploratory NIRS study |
| Q48318613 | Resting-state EEG power predicts conflict-related brain activity in internally guided but not in externally guided decision-making |
| Q30747649 | Resting-state functional magnetic resonance imaging: review of neurosurgical applications |
| Q46546288 | S-ketamine and GABA-A-receptor interaction in humans: an exploratory study with I-123-iomazenil SPECT. |
| Q45838748 | SEEKING and depression in stroke patients: an exploratory study |
| Q48726299 | Segregated neural representation of distinct emotion dimensions in the prefrontal cortex-an fMRI study |
| Q48622365 | Segregated neural representation of psychological and somatic-vegetative symptoms in severe major depression |
| Q34492718 | Self-referential processing in our brain--a meta-analysis of imaging studies on the self |
| Q45036494 | Self-related processing in the sexual domain: a parametric event-related fMRI study reveals neural activity in ventral cortical midline structures |
| Q37050772 | Self-specific stimuli interact differently than non-self-specific stimuli with eyes-open versus eyes-closed spontaneous activity in auditory cortex |
| Q30371689 | Slow cortical potentials and "inner time consciousness" - A neuro-phenomenal hypothesis about the "width of present". |
| Q38527023 | Spatiotemporal Psychopathology II: How does a psychopathology of the brain's resting state look like? Spatiotemporal approach and the history of psychopathology |
| Q30967021 | Spatiotemporal psychopathology I: No rest for the brain's resting state activity in depression? Spatiotemporal psychopathology of depressive symptoms |
| Q47946473 | Temporal limits on rubber hand illusion reflect individuals' temporal resolution in multisensory perception |
| Q37824731 | The 'resting-state hypothesis' of major depressive disorder-a translational subcortical-cortical framework for a system disorder |
| Q41284948 | The Degree of Early Life Stress Predicts Decreased Medial Prefrontal Activations and the Shift from Internally to Externally Guided Decision Making: An Exploratory NIRS Study during Resting State and Self-Oriented Task |
| Q33692296 | The association of interoceptive awareness and alexithymia with neurotransmitter concentrations in insula and anterior cingulate |
| Q42738750 | The brain's intrinsic activity and inner time consciousness in schizophrenia |
| Q39212041 | The brain's spontaneous activity and its psychopathological symptoms - "Spatiotemporal binding and integration". |
| Q48450726 | The neuroanatomy of asomatognosia and somatoparaphrenia |
| Q46025910 | The relationship between aberrant neuronal activation in the pregenual anterior cingulate, altered glutamatergic metabolism, and anhedonia in major depression. |
| Q48093149 | The role of hippocampus dysfunction in deficient memory encoding and positive symptoms in schizophrenia |
| Q50702497 | The self and its resting state in consciousness: an investigation of the vegetative state. |
| Q47341473 | The temporal structure of resting-state brain activity in the medial prefrontal cortex predicts self-consciousness |
| Q30369986 | The trans-species concept of self and the subcortical-cortical midline system. |
| Q30369476 | The trans-species core SELF: the emergence of active cultural and neuro-ecological agents through self-related processing within subcortical-cortical midline networks. |
| Q38774384 | Too Fast or Too Slow? Time and Neuronal Variability in Bipolar Disorder-A Combined Theoretical and Empirical Investigation |
| Q40001453 | Translational neuroimaging of the mood and anxiety disorders |
| Q37624077 | Understanding the self: a cultural neuroscience approach |
| Q30588531 | Using fMRI to decode true thoughts independent of intention to conceal |
| Q51741127 | Vascular-metabolic and GABAergic Inhibitory Correlates of Neural Variability Modulation. A Combined fMRI and PET Study. |
| Q48691206 | Volume and neuron number of the mediodorsal thalamic nucleus in schizophrenia: a replication study |
| Q47269977 | What Can Different Motor Circuits Tell Us About Psychosis? An RDoC Perspective |
| Q58106915 | What Neuroscience and Neurophilosophy Can Tell Us About the Effects of Deep Brain Stimulation on the Self |
| Q48383782 | What are the subjective processes in our brain? Empirical and ethical implications of a relational concept of the brain |
| Q35213151 | What catatonia can tell us about "top-down modulation": a neuropsychiatric hypothesis |
| Q30381421 | What is neuroethics? Empirical and theoretical neuroethics. |
| Q38068704 | What the brain's intrinsic activity can tell us about consciousness? A tri-dimensional view |
| Q30400604 | Who Am I: The Conscious and the Unconscious Self |
| Q41982897 | Why and How is the Self-Related to the Brain Midline Regions? |
| Q34216839 | Why are cortical GABA neurons relevant to internal focus in depression? A cross-level model linking cellular, biochemical and neural network findings |
| Q30891056 | Why is the distinction between neural predispositions, prerequisites, and correlates of the level of consciousness clinically relevant?: Functional brain imaging in coma and vegetative state |
| Georg Northoff | wikipedia |
Search more.