Prof. Dr. Mark W. Greenlee
Project members
Prof. Dr. Anton Beer, N. N.
Funding period
01.12.2018 – 31.12.2021
Renewal period
01.11.2024 - 31.10.2027
Dr. Mark W. Greenlee
Yih-Shiuan Lin (in cooperation with Prof. Dr. C.C. Chen, NTU Taipei)
01.07.2022 – 30.06.2025
Filling-in is the perceptual tendency of an observer to perceive a continuous visual pattern even when it is interrupted by a small "blank" area. Filling-in occurs at the blind spot, but also in scotomatous regions in patients with diseases of the visual pathways. Because filling-in occurs in an "empty" region, there is no physical stimulus to elicit a response in the visual cortex at this retinotopic location. Observers are usually asked to report on a trial when they experience filling-in. Neural responses to stimuli with and without filling-in can be compared to determine whether these responses differ on these two types of trials. Machine learning can be used to determine whether a classifier can distinguish between these two types of events. In univariate analysis, we found no difference between BOLD activation with and without filling-in. However, using a leave-one-out training procedure and a support vector machine, it was possible to classify percepts based on activation differences in early visual cortex (Lin, et al. 2020). We developed a paradigm to assess the presence or absence of filling-in. Observers are presented with periodic patterns of empty areas that serve as an artificial scotoma. By presenting a test stimulus in the empty region after filling-in has occurred, we can measure the neuronal response to the test stimulus and determine whether this response is affected by the presence of filling-in. The test stimulus will elicit a large enough neuronal response to allow reliable measurement of neuronal activity. We will vary the contrast of the test stimulus to determine the contrast transfer function in the presence of the eliciting stimulus. This will allow us to determine the contrast transfer function in response to the test stimulus. Variations in the physical properties of the eliciting stimulus and the test stimulus will be performed to separate response components attributable to these two types of stimuli, respectively.In a series of three studies, we will parametrically measure the response functions to the test stimulus using functional magnetic resonance imaging (fMRI), event-related potentials (ERP), and psychophysical experiments. The latter are performed to determine the range of action of the basic phenomena. The fMRI experiments will precisely identify the brain areas for filling-in. This precision is required because the area in the visual cortex considered to be the correlate for filling-in, V2, is small. The ERP trials will determine the temporal dynamics of the stimulus response with respect to the onset of filling-in. A model will be further tested to develop a new theory of filling-in.
(German) Filling-in ist die Wahrnehmungstendenz eines Beobachters, ein kontinuierliches visuelles Muster wahrzunehmen, selbst wenn dieses durch einen kleinen ?leeren“ Bereich unterbrochen ist. Filling-in tritt am blinden Fleck auf, aber auch in skotomat?sen Regionen bei Patienten mit Erkrankungen der Sehbahnen. Da das Filling-in in einer ?leeren“ Region auftritt, gibt es keinen physikalischen Reiz, der eine Reaktion im visuellen Kortex an dieser retinotopen Stelle ausl?st. Die Beobachter werden in der Regel aufgefordert, in einem Versuch zu berichten, wann sie das Filling-in erleben. Die neuronalen Reaktionen auf Stimuli mit und ohne Filling-in k?nnen verglichen werden, um festzustellen, ob sich diese Reaktionen bei diesen beiden Versuchsarten unterscheiden. Mit Hilfe von maschinellem Lernen kann ermittelt werden, ob ein Klassifikator zwischen diesen beiden Ereignistypen unterscheiden kann. Bei der univariaten Analyse fanden wir keinen Unterschied zwischen der BOLD-Aktivierung mit und ohne Filling-in. Mit einem Leave-One-Out-Trainingsverfahren und einer Support-Vector-Maschine war es jedoch m?glich, die Wahrnehmungen anhand der Aktivierungsunterschiede im frühen visuellen Kortex zu klassifizieren (Lin, et al. 2020). Wir entwickelten ein Paradigma , um das Vorhandensein oder Nichtvorhandensein von Filling-in zu beurteilen. Den Beobachtern werden periodische Muster mit leeren Bereichen pr?sentiert, die als künstliches Skotom dienen. Indem wir einen Testreiz in der leeren Region pr?sentieren, nachdem das Filling-in aufgetreten ist, k?nnen wir die neuronale Reaktion auf den Testreiz messen und feststellen, ob diese Reaktion durch das Vorhandensein des Filling-in beeinflusst wird. Der Testreiz wird eine ausreichend gro?e neuronale Reaktion hervorrufen, um so eine zuverl?ssige Messung der neuronalen Aktivit?t zu erm?glichen. Wir werden den Kontrast des Testreizes variieren, um die Kontrastübertragungsfunktion in Anwesenheit des ausl?senden Reizes zu bestimmen. bwin娱乐_bwin娱乐官网欢迎您@ erm?glicht uns, die Kontrastübertragungsfunktion als Antwort auf den Testreiz zu bestimmen. Variationen der physikalischen Eigenschaften des ausl?senden Reizes und des Testreizes werden durchgeführt, um Antwortkomponenten zu trennen, die jeweils diesen beiden Reizarten zuzuordnen sind.In einer Serie von drei Studien werden wir die Antwortfunktionen auf den Testreiz mit funktioneller Magnetresonanztomographie (fMRI), ereigniskorrelierten Potentialen (ERP) und psychophysischen Experimenten parametrisch messen. Letztere werden durchgeführt, um den Wirkungsbereich der Grundph?nomene zu ermitteln. Die fMRT-Experimente werden die Hirnareale für das Filling-in pr?zise identifizieren. bwin娱乐_bwin娱乐官网欢迎您@e Pr?zision ist erforderlich, da das Gebiet im visuellen Kortex, das als Korrelat für das Filling-in gilt, V2, klein ist. Die ERP-Versuche werden die zeitliche Dynamik der Reizantwort in Bezug auf den Beginn des Filling-in bestimmen. Ein Modell wird weiter getestet, um eine neue Theorie des Filling-in zu entwickeln.
Lin, Y.-S., Chen, C.-C., and Greenlee, M. W. (2020). Lateral modulation of orientation perception in center-surround sinusoidal stimuli: Divisive inhibition in perceptual filling-in.?Journal of Vision,?20(9), 5–5. doi.org/10.1167/jov.20.9.5
M.Sc. Edith Benkowitsch (in cooperation with Prof. Dr. med. Herbert J?gle, University Eye Hospital)
01.07.2021 – 30.06.2024
Retinal diseases such as macular degeneration usually lead to central vision loss, making the affected patients dependent on their peripheral residual vision. Often a kind of pseudo fovea (preferred retinal locus, PRL) develops in the peripheral visual field, which is then used in everyday life for the fixation of objects or faces, as well as for reading. These long-term adaptation processes are accompanied by certain neuroplastic changes in the visual cortex of the affected patients. Furthermore, appropriate training protocols, such as visual perceptual learning tasks, can help to further improve peripheral visual performance and even trigger neuronal plasticity. Our goal in this project is to investigate how these two neuroplastic processes of long-term adaptation and training act together and to uncover possible interrelations between the two. For this purpose, visual perceptual learning in the peripheral visual field will be applied, and it will be examined to what extent the learning success at the PRL of patients with central vision loss will be different from the learning success at a comparable peripheral site in the opposite visual hemifield (OppPRL) and from the learning success of normally sighted control persons, who are trained in the same visual task. The training measures will be accompanied by (functional) magnetic resonance imaging (fMRI) to reveal the neural correlates of learning in the visual cortex. Additionally, the biochemical changes caused by learning will be determined by magnetic resonance spectroscopy (MRS). To investigate possible changes in the cortical macro- and microstructure in grey and white matter of the visual cortex, structural and diffusion-weighted MRI will be performed. These measures will provide us with a more comprehensive picture of long and short term neuroplastic adaptation processes in patients with central vision loss and thus help to design even more efficient training protocols.
Netzhauterkrankungen wie Makuladegeneration führen meist zu zentralen Gesichtsfeldausf?llen, wodurch die betroffenen Patienten auf ihr peripheres Restsehverm?gen angewiesen sind. H?ufig entwickelt sich daraufhin im peripheren Gesichtsfeld eine Art Pseudo-Fovea (preferred retinal locus, PRL), die dann im Alltag zur Fixation von Objekten bzw. Gesichtern genutzt wird, sowie beim Lesen eingesetzt wird. bwin娱乐_bwin娱乐官网欢迎您@e langfristigen Anpassungsprozesse gehen mit gewissen neuroplastischen Ver?nderungen im visuellen Kortex der betroffenen Patienten einher. Des Weiteren k?nnen geeignete Trainingsprotokolle, wie z.B. visuelle perzeptuelle Lernaufgaben, helfen, die periphere Sehleistung weiter zu verbessern, und selbst neuronale Plastizit?t ansto?en. Unser Ziel im Rahmen dieses Projektes ist es, das Zusammenwirken dieser beiden neuroplastischen Prozesse der langfristigen Anpassung und des gezielten Trainings zu untersuchen und m?gliche Wechselwirkungen zwischen beiden aufzudecken. Hierzu soll visuelles perzeptuelles Lernen im peripheren Gesichtsfeld eingesetzt werden und überprüft werden, inwiefern sich der Lernerfolg am PRL von Patienten mit zentralem Gesichtsfeldausfall vom Lernerfolg an einer ?hnlich peripheren Stelle im gegenüberliegenden Gesichtsfeld (OppPRL) und vom Lernerfolg normalsichtiger Kontrollpersonen unterscheidet, die in derselben visuellen Aufgabe trainiert werden. Die Trainingsma?nahmen sollen von (funktionellen) Magnetresonanztomografie (fMRT)-Messungen begleitet werden, um die neuronalen Korrelate des Lernens im visuellen Kortex aufzudecken. Zus?tzlich sollen die biochemischen Ver?nderungen durch das Lernen mittels Magnetresonanzspektroskopie (MRS) ermittelt werden. Um m?gliche Ver?nderungen in der kortikalen Makro- und Mikrostruktur in grauer und wei?er Substanz des visuellen Kortex zu untersuchen, sollen strukturelle und diffusionsgewichtete MRT-Aufnahmen durchgeführt werden. Die genannten Ma?nahmen k?nnen uns ein umfassenderes Bild über lang- und kurzfristige neuroplastische Anpassungsvorg?nge bei Patienten mit zentralem Sehverlust liefern und so dabei helfen, noch effizientere Trainingsprotokolle zu entwerfen.
Contact
PD Dr. Tina Plank
tina.plank@ur.de
University of Regensburg
Institute for Experimental Psychology
93040 Regensburg, Germany
Tel: +49 941 943 3849
Fax: +49 941 943 3233
/humanwissenschaften/psychologie-greenlee/team/plank/index.html
Prof. Dr. Mark W. Greenlee
Project members
PD Dr. Anton Beer, M.Sc. Simon Wein
Funding period
01.12.2018 – 31.12.2021
Objectives
Our sensory systems allow us to experience our environment by the senses of touch, hearing, seeing, smell, and taste. Moreover, we have vestibular organs that inform us about self-motion and thus help us to keep our body in balance. In order to analyze the interactions between the visual and vestibular sensory systems for the sensation of self-motion, we will combine the method of caloric vestibular stimulation with visual stimulation. We want to use these stimulation types in order to investigate the neural interactions during simulated self-motion. Therefore, congruent and incongruent stimulus combinations will be applied in order to investigate their effect on the perception of self-motion, detecting its direction, and the relevant neural correlates of self-motion perception. We will assess the brain activity of healthy volunteers with the method of functional magnetic resonance imaging (fMRI). Moreover, we will apply the method of diffusion-weighted MRI combined with probabilistic fiber tracking in order to analyze the anatomical connecitivity between vestibular and visual cortical regions. By comparing structural and functional connectivity of the the human brain during rest (i.e., resting state) we want to show how parts of the visual-vestibular network are connected and how they interact with each other. Ultimately, we will also investigate the suppression of vestibular cortex during visual processing. If attention is directed towards visual motion stimuli, then activity in the vestibular cortex is suppressed. The method of repetitive transcranial magnetic stimulation (TMS) and functional MRI will be applied in order to determine the source of this inhibition in the vestibular cortex. The results of these studies will provide new insights into the multisensory integration of visual and vestibular information for the perception of self-motion.
Contact
PD Dr. rer. nat. Anton L. Beer?
anton.beer@ur.de
University of Regensburg
Institute for Experimental Psychology
93040 Regensburg, Germany
Tel: +49 941 943 3745?
Fax: +49 941 943 813745
Project leader
PD Dr. Gregor Volberg
Project members
Franziska Wei?, Anja Sch?ll
Funding period
01.11.2014 – 31.10.2017
Objectives
Synesthesia is a perceptual phenomenon where a stimulation in one sensory modality induces a concurrent sensation in a different modality or feature dimension that was not objectively stimulated. In this project we aim to identify the neuro-cognitive mechanisms of grapheme-color-synesthesia where written numbers or letters induce a concurrent sensation of color. Especially, we will investigate neural connectivity between grapheme and color processing brain areas and brain areas associated with visual-spatial selection. To this end, EEG experiments as well as combined EEG and fMRI studies will be conducted. The results of this project will improve our understanding of synesthesia and related topics in general psychology, like visual awareness or visual feature integration.
Contact
PD Dr. rer. nat. Gregor Volberg
gregor.volberg@ur.de
University of Regensburg
Institute for Experimental Psychology
93040 Regensburg, Germany
Tel: +49 941 943 3862
Fax: +49 941 943 3233
http://www.psychologie.uni-regensburg.de/Greenlee/team/volberg/volberg.html
Project leader
Prof. Dr. Mark W. Greenlee
Project members of the 2nd period
Dr. Katharina Rosengarth, Markus Goldhacker, Sabine Brandl-Rühle (in cooperation with Prof. Dr. med. Horst Helbig, Director, University Eye Hospital)
Project members of the 1st period
Dr. Tina Plank, Jozef Frolo, Sabine Brandl-Rühle (in cooperation with Prof. Dr. med. Horst Helbig, Director, University Eye Hospital)
Funding period
since 2008
Objectives
This 3-year project uses functional MRI to determine the extent to which macular degeneration induces neuroplastic alterations in the visual cortex of the affected patients. We will compare the results of a group of 20 patients with a juvenile form of macular degeneration (JMD) to those of patients with age-related macular degeneration (AMD). Our main focus will deal with the issue whether oculomotor training in AMD patients, assisting them to establish a new preferred retinal locus (PRL) for eccentric fixation, can promote cortical reorganization. The results will provide important feedback for therapeutic gains in patients with AMD. They will help guide new training protocols, thereby improving the patients' experienced quality of life.
For more information see: http://www.uni-regensburg.de/FOR1075/index.htm
Wein, Simon?(2022).
Lin, Yih-Shiuan?(2022).
Tallon, Miles?(2022).
Tahedl, Marlene?(2022).
Mohammadi Jooyandeh, Somayeh (2019).
Anna Maria Wirth (2019)
Goldhacker, Markus?(2017).
Frank, Sebastian (2017).
Lehner, Astrid (2016).
Dissertation at the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Dodoo-Schittko, Frank (2014).
Dissertation at the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Manuscript available at the Library of the University of Regensburg
under: 00/CZ 1320 D646. Further printed copies are also available at several German University libraries and at the German National Library (deutsche Nationalbibliothek).
Blurton, Steven (2014).
Dissertation at the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Manuscript available online.
Zunhammer, Matthias (2014).
Dissertation at the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg and the Institute of Psychiatry and Psychotherapy.
Manuscript available online.
Fischer, Volker (2011).
Dissertation at the Institute of Biophysics and Physical Biochemistry (supervisor Prof. Dr. E. W. Lang) in collaboration with the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Manuscript available online.
Alichniewicz, Karolina (2011).
Dissertation, University of Regensburg.
Manuscript available online.
Heckel, Andreas (2010).
Dissertation at the Institute of Psychiatry and Psychotherapy at the Medical Faculty (supervisor Prof. Dr. H. E. Klein) in collaboration with the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Manuscript available online.
Acs, Ferenc (2009).
Dissertation, University of Regensburg.
Manuscript available online.
Herpes, Martin (2009).
Dissertation at the Medical Faculty (supervisor Prof. Dr. U. Bogdahn) in collaboration with the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Manuscript available online.
Rosengarth, Katharina (2009).
Dissertation at the Philosophic Faculty IV (supervisor Prof. em. Dr. H. Brekle) in collaboration with the Institute of Experimental Psychology (supervisor Prof. Dr. M. W. Greenlee), University of Regensburg.
Manuscript available online.
Frank, Gabriele (2009).
Dissertation, University of Regensburg.
Manuscript available online.
Vallines García, Ignacio (2007).
Dissertation, University of Regensburg.
Manuscript available online.
Baumann, Oliver (2006).
Dissertation, University of Regensburg.
Manuscript available online.
Am Lehrstuhl besteht die M?glichkeit zur Betreuung von Abschlussarbeiten.
Eine Liste mit Themen bisher angefertigter Bachelor- und Masterarbeiten kann im Sekretariat angefordert werden.
Project leaders
Prof. Dr. Mark W. Greenlee, Dr. M. Gondan
Project members
Steven Blurton, Anja Wienbreyer
Funding period
01.04.2011 – 31.03.2013 (GR 988/20-2)
01.04.2009 – 31.03.2011 (GO 1855/1-1)
Objectives
We investigate basic mechanisms of integration of information provided by different sensory systems (e.g. auditory and visual). In basic speeded response tasks, participants receive either auditory information alone, visual information alone, or redundant information via both sensory modalities. Abundant evidence now exists that redundant information is pooled into a common channel (coactivation).? In our project we try to describe this process using a computational model (Diffusion Superposition Model, Schwarz, 1994, J Math Psychol): Based on the idea of simple additive superposition of channel activity, the model describes the reaction times observed in simple response tasks with redundant auditory and visual stimuli. In our project we investigate whether the model can equally explain reaction times observed in more complex tasks (Go/Nogo discrimination, choice reactions). Moreover, we manipulate task demands and spatial attention (e.g. Posner-task) to test whether the integration mechanism requires spatial attention. In an EEG study the computational model will be related to neurophysiological data.
Project leader
G. Kovacs
Project members of the 1st period
Christian Walther, Daniel Kaiser, Iulia Lavric
Funding period
2010-2012
Objectives
A given picture of a person might look different at different times. The previous encounters with other people or in other words, the temporal context of a given face modify its perception. In our present proposal we will study the effect of previous experiences on face perception using psychophysical, electrophysiological and neuroimaging methods. In most of our planned experiments we will use the powerful paradigm of face adaptation (Kovács et al, 2006), leading to specific, high level aftereffects. In the first set of experiments we will study the similarities and differences of two immediate repetition related phenomena, priming and aftereffects. In a second series of experiments we will study how the variation of the statistical properties of preceding stimuli affects face perception. For this we will use matrixes of multiple faces. In the last set of experiments we will study perceptual decisions, related to faces. In particular, we will compare the effects of bottom-up bias (such as caused by face adaptation) and top-down biases (caused by directed selective attention or by prior predictive information) on perceptual decisions. Altogether our experiments will shed light on the mechanisms of implicit and explicit face representations and on the related decisions that are important in social settings during our everyday life.
Project leader
Prof. Dr. Mark W. Greenlee
Project members
Dr. Katharina Rosengarth, Markus Goldhacker
Funding period
01.01.2008 - 30.06.2011
Objectives
"Perceptual Learning" is a BMBF network funded in the platform "Research collaborations on cognitive performance and relevant disorders in humans".
This collaborative research effort aims to explore the neural mechanisms underlying cortical plasticity in healthy subjects and in patients who learn or re-learn a perceptual task. Our approach is novel since it is strongly guided by methods from computational and cognitive neurosciences and directly applies them to problems arising in clinical neurology and neurorehabilitation. In the experimental part of the project, we plan to employ prototypical tasks that can be learned within a few hours or at most a few days with repeated practice. Before and after this extensive training, our participants will take part in functional and anatomical MR-scan sessions. We will ask the subjects to perform a task for the first time (e.g., speed discrimination of transparent motion). After a sufficient training period, the participants will be scanned again on the same task. We will then compare the MR-correlates of brain structure, brain activation, brain connectivity and neural information processing before and after this training (Project Greenlee).
Furthermore, we plan to examine patients with retrochiasmatic injury and homonymous visual field loss with respect to their global processing capacity in scene perception and in reading at the behavioural-neuropsychological and the functional-neurobiological level. To gain more insight into the neuronal processes underlying neuronal plasticity in adults, fMRI and neuropsychological studies will be conducted before and after an oculomotor training program in patients recovering from posterior infarctions and/or cerebral haemorrhaging (Project Zihl). The results of these basic and clinical investigations will be modelled with mean-field theory and computational models to get a better quantitative description of the neural processes underlying perceptual skill acquisition and reacquisition after brain damage (Projects Neumann, Lang, Deco). Powerful novel data-analysis techniques for functional MRI data will be developed and applied to enhance our ability to extract specific correlates of neuronal plasticity during neurorehabilitation.
A further aim of the research group is to gain a better understanding of how learning takes place in low-level sensory and sensorimotor circuits and compare these processes with those occurring in high-level cognitive learning. Some of the projects will focus on the low-level perceptual learning that occurs when healthy volunteers learn a new task. What changes take place in the brains of adults when they learn a new sensory or sensorimotor task? Moreover, we are interested in the brain changes that take place when patients recover from brain damage. At the macroanatomical level, the neural basis of “scaffolding” processes (Petersson, 1998), where additional brain circuits are temporally recruited to perform supplementary processing during the recovery period, will be investigated. At the microanatomical level, spike timing dependent plasticity (Masquelier and Thorpe, 2007) will be incorporated into models of higher-level motion processing required for velocity discrimination. It remains to be determined how exactly both these macro- and microanatomical changes take place. Finally, we hope to provide clinicians with new imaging approaches and diagnostic tools to map changes in grey and white matter that accompany neural learning processes.
Project leader
Prof. Dr. Mark W. Greenlee
Project members
Volker Fischer, Markus Raabe
Funding period
01.01.2007 - 30.06.2010
Objectives
"Visuo-spatial Cognition" is a BMBF network funded in the platform "Cognition research".
The goal is to model and analyze brain mechanisms underlying spatial cognition during visual search and visual exploration. A total of 4 German laboratories are collaborating on this project.
Karolina Alichniewicz, Florian Brunner, Helmut Nebl, Dr. Hans-Hermann Klünemann, Prof. Dr. Mark W. Greenlee
This study aims at exploring visuo-spatial information processing in healthy elderly and patients with amnestic mild cognitive impairment (aMCI). Participants undergo an extensive behavioral test battery with the main focus on working memory and attention. Subjects also participate in a pro-/anti-saccade task. With the help of two fMRI experiments we plan to investigate the neural correlates of cognitive processes relevant for working memory and saccadic control and to detect altered/compensatory brain activation patterns in aMCI patients.
In addition the project explores possible benefits of a short-term nordic walking program for aMCI patients and its impact on cognitive performance in behavioral tests as well as on neural brain activation.
Carolin M??nang, Gabriele Frank, Dr. Beate Winner, Prof. Dr. Jürgen Winkler, Prof. Dr. Mark W. Greenlee
Recent studies (e.g. Albers et al., 2006; Masaoka et al., 2007) point to the fact that already in early stages of Parkinson's disease (PD) the olfactory system shows distinct impairments additional to the well known pathological alterations in the basal ganglia. By presenting sniffing sticks as olfactory stimuli to 15 PD-patients and 15 age-matched healthy controls during the fMRI-session in a 3-Tesla-Scanner we will investigate the underlying neurofunctional correlates of this olfactory impairments. We hope to get new insights in the neuropathological processes of Parkinson's disease and to contribute to an effective and reliable diagnostic in early stages of this disease.
Gabriele Frank, Stefanie Feuerer, Dr. Hans-Hermann Klünemann, Prof. Dr. Mark W. Greenlee
This study deals with the neurofunctional correlates of an important aspect of semantic memory, the recognition of the faces of famous people in MCI-patients, age-matched controls and young healthy subjects by conducting an fMRI experiment (3-Tesla-Scanner). Because it is well known that Apolipoprotein E epsilon4 (APOE epsilon4) is an important genetic risk factor for the development of Alzheimer's disease, a main focus of our study lies on the impact of the APOE status on cortical activation as well as neuropsychological performance of the subject groups mentioned above.
Project coordinator
Prof. Dr. Mark W. Greenlee
Project members at University of Regensburg
Dr. Gyula Kovács, Markus Raabe
Funding period
2006 - 2009
Objectives
"Decisions in Motion" is a EU Commission project funded in the platform FP6 IST Cognitive Systems.
The goal is to model and implement fast sensory-based decision making in moving cognitive agents. A total of 8 European laboratories and 2 SMEs are collaborating on this project.
Project leaders
University Medical Center Regensburg, Department of Neurology, Prof. Dr. U. Bogdahn
University of Regensburg, Institute of Experimental Psychology, Prof. Dr. M. W. Greenlee
Project partners
Siemens AG
RAPID BioMedical GmbH
Funding period
2004 - 2007
Objectives
"BayernBrain3T" is a research and developmental project funded by Bayerische Forschungsstifung and dedicated to preclinical, neuropsychological and clinical research on a 3T high field MR scanner.
The goal of the project is to develop and optimise medical imaging techniques to evaluate diagnostic and therapeutic methods applied in the context of regeneration of CNS damage in particular and neuronal plasticity in general.
For more information see: http://www.forschungsstiftung.de/ (in German only)
Project leader
Prof. Dr. Mark W. Greenlee
Project members
Petra Behlmer-Elster, Markus Raabe, Markus Mühlhan, Jale ?zyurt
Funding period
2003 - 2005
Objectives
Attention deficit hyperacitvity disorder (ADHD) is a phenotypically heterogeneous neuropsychiatric disorder that usually manifests itself in early childhood. The pathogenetic factors that lead to ADHD are only partly understood and remain a matter of considerable dispute. Accumulating evidence from on-going research indicates, however, that ADHD reflects a dysfunction of cortical and subcortical systems, and that these neuronal substrates form the basis of executive functions. The goal of the present research proposal is to investigate well diagnosed subgroups of pediatric ADHD patients with functional magnetic resonance imaging (fMRI) and magnet resonance spectroscopy (MRS). Using fMRI we intend to explore the neural correlates of fundamental subprocesses that contribute to executive functioning (such as response inhibition and working memory). Behavorial data recorded during the fMRI experiments can be used to validate possible differences in brain activation. The use of MRS should focus on possible pathologically altered neurochemical processes in ADHD. Using both technologies, we plan to investigate de novo patients clinically diagnosed with ADHD and compare these findings with those collected after treatment with methlyphenidate (MPH; the neuroactive substance e.g. in Ritalin). Such a comparison should reveal the effect of stimulants on the fMRI-BOLD responses to challenging tasks and to altered brain metabolism as revealed by MRS. ADHD-specific patterns of brain activation recorded during tasks that require executive function and/or alterations in neurochemical markers might help to better understand the neural basis of ADHD and might serve as biological markers to objectively validate the diagnosis of the disorder.
Participating members
Prof. Dr. Mark W. Greenlee, Ignacio Vallines García (University of Regensburg), Riklef Weerda (University of Oldenburg)
For more information see: Progress reports 2002 and 2005