373 results on '"Daniel, Brandeis"'
Search Results
352. Brain mapping reveals covert orienting deficits of ADD-children in a continuous performance test
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T. H. van Leeuwen, H.-Ch. Steinhausen, and Daniel Brandeis
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Covert ,General Neuroscience ,Neurology (clinical) ,Psychology ,Brain mapping ,Cognitive psychology ,Test (assessment) - Published
- 1997
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353. Effects of input modality on brain activation during phonological processing: A fMRI study
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Th. Loenneker, P. Joeri, Daniel Brandeis, Ernst Martin, Thierry A.G.M. Huisman, D. Ekatodramis, Deborah Vitacco, and H. Rumpel
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Brain activation ,Modality (human–computer interaction) ,Neurology ,Cognitive Neuroscience ,Psychology ,Cognitive psychology - Published
- 1996
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354. Functional mapping of dyslexia in children using language-evoked potentials
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Daniel Brandeis, D. Vitacco, and H. C. Steinhausen
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Functional mapping ,medicine.medical_specialty ,General Neuroscience ,Dyslexia ,medicine ,Neurology (clinical) ,Audiology ,medicine.disease ,Psychology - Published
- 1995
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355. Neurophysiological signs of rapidly emerging visual expertise for symbol strings.
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Silvia Brem, Anette Lang-Dullenkopf, Urs Maurer, Pascal Halder, Kerstin Bucher, and Daniel Brandeis
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- 2005
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356. Altered responses to tone and phoneme mismatch in kindergartners at familial dyslexia risk.
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Urs Maurer, Kerstin Bucher, Silvia Brem, and Daniel Brandeis
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- 2003
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357. Cognitive flexibility in adolescence: Neural and behavioral mechanisms of reward prediction error processing in adaptive decision making during development
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Silvia Brem, Daniel Brandeis, Tobias U. Hauser, Susanne Walitza, Reto Iannaccone, University of Zurich, and Hauser, Tobias U
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Male ,2805 Cognitive Neuroscience ,Adolescent ,Cognitive Neuroscience ,Decision Making ,Ventromedial prefrontal cortex ,Context (language use) ,610 Medicine & health ,Adolescence ,Development ,Cognitive flexibility ,Functional magnetic resonance imaging (fMRI) ,Reward prediction errors ,050105 experimental psychology ,Article ,Developmental psychology ,03 medical and health sciences ,0302 clinical medicine ,Cognition ,Reward ,medicine ,Reinforcement learning ,Humans ,Learning ,0501 psychology and cognitive sciences ,10064 Neuroscience Center Zurich ,Child ,Computational model ,Brain Mapping ,medicine.diagnostic_test ,05 social sciences ,Perspective (graphical) ,Brain ,10058 Department of Child and Adolescent Psychiatry ,Magnetic Resonance Imaging ,medicine.anatomical_structure ,Neurology ,10076 Center for Integrative Human Physiology ,2808 Neurology ,570 Life sciences ,biology ,Female ,Adaptive learning ,Functional magnetic resonance imaging ,Psychology ,030217 neurology & neurosurgery ,Cognitive psychology - Abstract
Adolescence is associated with quickly changing environmental demands which require excellent adaptive skills and high cognitive flexibility. Feedback-guided adaptive learning and cognitive flexibility are driven by reward prediction error (RPE) signals, which indicate the accuracy of expectations and can be estimated using computational models. Despite the importance of cognitive flexibility during adolescence, only little is known about how RPE processing in cognitive flexibility deviates between adolescence and adulthood. In this study, we investigated the developmental aspects of cognitive flexibility by means of computational models and functional magnetic resonance imaging (fMRI). We compared the neural and behavioral correlates of cognitive flexibility in healthy adolescents (12–16 years) to adults performing a probabilistic reversal learning task. Using a modified risk-sensitive reinforcement learning model, we found that adolescents learned faster from negative RPEs than adults. The fMRI analysis revealed that within the RPE network, the adolescents had a significantly altered RPE-response in the anterior insula. This effect seemed to be mainly driven by increased responses to negative prediction errors. In summary, our findings indicate that decision making in adolescence goes beyond merely increased reward-seeking behavior and provides a developmental perspective to the behavioral and neural mechanisms underlying cognitive flexibility in the context of reinforcement learning., NeuroImage, 104, ISSN:1053-8119, ISSN:1095-9572
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358. Neurophysiological Correlates of Attentional Fluctuation in Attention-Deficit/Hyperactivity Disorder
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Gráinne McLoughlin, Daniel Brandeis, Jonna Kuntsi, Philip Asherson, Tobias Banaschewski, Celeste H. M. Cheung, University of Zurich, and Kuntsi, Jonna
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Male ,Neurology ,Electroencephalography ,Audiology ,Developmental psychology ,0302 clinical medicine ,Attention ,EEG ,10064 Neuroscience Center Zurich ,Genetic risk ,Evoked Potentials ,medicine.diagnostic_test ,Radiological and Ultrasound Technology ,P3 ,10058 Department of Child and Adolescent Psychiatry ,2702 Anatomy ,Contingent negative variation ,2728 Neurology (clinical) ,Radiology Nuclear Medicine and imaging ,10076 Center for Integrative Human Physiology ,Female ,Anatomy ,Psychology ,ERP ,medicine.medical_specialty ,Adolescent ,Reaction time variability ,CNV ,Clinical Neurology ,Contingent Negative Variation ,610 Medicine & health ,Context (language use) ,behavioral disciplines and activities ,Young Adult ,03 medical and health sciences ,mental disorders ,Reaction Time ,Journal Article ,medicine ,Humans ,ADHD ,2741 Radiology, Nuclear Medicine and Imaging ,Attention deficit hyperactivity disorder ,Radiology, Nuclear Medicine and imaging ,Effects of sleep deprivation on cognitive performance ,3614 Radiological and Ultrasound Technology ,Original Paper ,Neurophysiology ,medicine.disease ,Event-Related Potentials, P300 ,030227 psychiatry ,Attention Deficit Disorder with Hyperactivity ,Case-Control Studies ,2808 Neurology ,Neurology (clinical) ,030217 neurology & neurosurgery - Abstract
Cognitive performance in attention-deficit/hyperactivity disorder (ADHD) is characterised, in part, by frequent fluctuations in response speed, resulting in high reaction time variability (RTV). RTV captures a large proportion of the genetic risk in ADHD but, importantly, is malleable, improving significantly in a fast-paced, rewarded task condition. Using the temporal precision offered by event-related potentials (ERPs), we aimed to examine the neurophysiological measures of attention allocation (P3 amplitudes) and preparation (contingent negative variation, CNV), and their associations with the fluctuating RT performance and its improvement in ADHD. 93 participants with ADHD and 174 controls completed the baseline and fast-incentive conditions of a four-choice reaction time task, while EEG was simultaneously recorded. Compared to controls, individuals with ADHD showed both increased RTV and reduced P3 amplitudes during performance on the RT task. In the participants with ADHD, attenuated P3 amplitudes were significantly associated with high RTV, and the increase in P3 amplitudes from a slow baseline to a fast-paced, rewarded condition was significantly associated with the RTV decrease. Yet, the individuals with ADHD did not show the same increase in CNV from baseline to fast-incentive condition as observed in controls. ADHD is associated both with a neurophysiological impairment of attention allocation (P3 amplitudes) and an inability to adjust the preparatory state (CNV) in a changed context. Our findings suggest that both neurophysiological and cognitive performance measures of attention are malleable in ADHD, which are potential targets for non-pharmacological interventions. Electronic supplementary material The online version of this article (doi:10.1007/s10548-017-0554-2) contains supplementary material, which is available to authorized users.
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359. Segments of event-related potential map series reveal landscape changes with visual attention and subjective contours
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Daniel Brandeis and Dietrich Lehmann
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Adult ,Male ,Visual perception ,genetic structures ,Brain activity and meditation ,Computer science ,media_common.quotation_subject ,Map series ,Retina ,Event-related potential ,Perception ,Humans ,Attention ,media_common ,Communication ,Brain Mapping ,business.industry ,General Neuroscience ,Cognition ,Form Perception ,EEG microstates ,Female ,sense organs ,Neurology (clinical) ,business ,Cartography ,Photic Stimulation ,Vigilance (psychology) - Abstract
Changes of the event-related potential (ERP) map landscape with time and condition were used to identify qualitative changes in the ERP generating process which are indicative of a change in the functional microstate. Twelve subjects attended or ignored unilaterally presented visual stimuli with and without subjective contours. ERP map series from 16 electrodes were adaptively segmented to identify periods of stable map landscape, using topographic descriptions (map maxima and minima). Attention as well as the subjective contours changed the map topography and increased the map amplitude. From 170 to 380 msec, they had similar effects on the antero-posterior map topography. Topographic differences between the effects of attention and subjective contours were also present, but affected mainly the left-right topography. The results are in line with the notion of attentional involvement in subjective contour perception and show that global modulation of exogenous brain activity cannot account for topographic changes with attention or with subjective contours. They further establish space-oriented data reduction as a powerful tool to identify components and to distinguish among hypotheses about the underlying generator processes.
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- 1989
360. Sleep deprivation: effect on sleep stages and EEG power density in man
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Daniel Brandeis, Alexander A. Borbély, Dietrich Lehmann, Inge Strauch, and Fritz Baumann
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Adult ,Male ,Sleep Stages ,medicine.medical_specialty ,medicine.diagnostic_test ,General Neuroscience ,Electroencephalography ,Audiology ,Sleep time ,Sleep in non-human animals ,Developmental psychology ,Sleep deprivation ,Duration (music) ,medicine ,Reaction Time ,Humans ,Sleep Deprivation ,Spectral analysis ,Female ,Neurology (clinical) ,medicine.symptom ,Psychology ,Power density - Abstract
Sleep was analysed in 8 young adults subjects during two baseline nights and two recovery nights following 40.5 h sleep deprivation. Sleep stages were scored from the polygraph records according to conventional criteria. In addition, the EEG records of the entire nights were subjected to spectral analysis to compute the frequency distribution of the power density in the 0.25-25 Hz range for 0.5 Hz or 1.0 Hz bins. In the first recovery night, the power density in the delta band was significantly higher than baseline for total sleep time as well as for sleep stages 2, 3 and 4, 4 and REM. These changes were not restricted to the delta band, but extended to higher frequency bands. Minor, but significant, effects of sleep deprivation were seen in the power density distribution of the second recovery night. In the baseline nights, a progressive reduction of power density in the delta/theta range was present for successive non-REM-REM sleep cycles for total sleep time and stages 2, 3 and 4, and 4. The results show that effects of sleep deprivation as well as trends within the sleep periods are readily apparent from spectral analysis, but are inadequately reflected by conventional sleep scoring. When the power density values were integrated over the entire frequency range (0.75-25 Hz) for each non-REM-REM sleep cycle, an exponential decline from cycle 1 to cycle 3 was suggested. The present findings support the hypothesis that the EEG power density in the low frequency range is an indicator of a progressively declining process during sleep whose initial value is determined by the duration of prior waking.
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- 1981
361. Event-related potentials of the brain and cognitive processes: approaches and applications
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Dietrich Lehmann and Daniel Brandeis
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Cognitive Neuroscience ,Experimental and Cognitive Psychology ,Electroencephalography ,Brain mapping ,Dichotic Listening Tests ,Behavioral Neuroscience ,Cognition ,Event-related potential ,medicine ,Psychophysics ,Reaction Time ,Humans ,Attention ,Evoked Potentials ,Language ,Communication ,Brain Mapping ,medicine.diagnostic_test ,business.industry ,Subliminal stimuli ,Information processing ,Form Perception ,Covert ,Visual Perception ,Psychology ,business ,N2pc ,Cognitive psychology - Abstract
Event-related potentials (ERPs) are recordings of the electric field which the brain produces in fixed time-relation to an event. ERPs open a time and space window onto covert steps of brain information processing which need not be accompanied by overt behavior or private experiences. ERPs are the only noninvasive method which resolves the dynamic pattern of events in the human brain down to the millisecond range. Early ERP components are valuable tools in clinical testing of the afferent sensory systems in the absence of anamnestic or clinical pathology. Later components (e.g. the 'P300') index intermediate, covert steps of information processing and have clarified the time course and the contingencies of processes in attention, decisions and language. ERP waveshapes show electric potential differences between two recording points. Conventional analysis often ignores the fact that there is no unique voltage amplitude or signal latency for a single point, and interprets ambiguous results. Although important insights have emerged with such strategies, full utilization of ERP data requires unambiguous ERP assessment and converging evidence from neuropsychological and cognitive experimentation. Sequences of field distribution maps offer an unbiased display of ERP data. Spatial analysis yields unambiguous values for further comprehensive assessment, and should precede analysis over time. Examples of spatial analysis have shown that different ERP field configurations follow the presentation of noun and verb meaning of homophone words; that the ERP effects to subjective contours resemble those to attention in time course and topography; that the 'cognitive' P300 component reflects the specific stimulus location; and that subliminal information influences the configuration of late ERP fields.
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- 1986
362. Electrophysiological evidence for abnormal preparatory states and inhibitory processing in adult ADHD
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Tobias Banaschewski, Aribert Rothenberger, Daniel Brandeis, B. Albrecht, Jonna Kuntsi, Gráinne McLoughlin, Philip Asherson, University of Zurich, and McLoughlin, G
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Adult ,Male ,2805 Cognitive Neuroscience ,medicine.medical_specialty ,Neurology ,Adolescent ,Cognitive Neuroscience ,610 Medicine & health ,Audiology ,behavioral disciplines and activities ,lcsh:RC346-429 ,050105 experimental psychology ,Developmental psychology ,03 medical and health sciences ,Behavioral Neuroscience ,0302 clinical medicine ,Neurodevelopmental disorder ,2802 Behavioral Neuroscience ,mental disorders ,medicine ,Humans ,Attention deficit hyperactivity disorder ,Attention ,0501 psychology and cognitive sciences ,Evoked Potentials ,lcsh:Neurology. Diseases of the nervous system ,Biological Psychiatry ,Cued speech ,10093 Institute of Psychology ,Research ,05 social sciences ,Brain ,Cognition ,General Medicine ,10058 Department of Child and Adolescent Psychiatry ,Executive functions ,medicine.disease ,Contingent negative variation ,Inhibition, Psychological ,Electrophysiology ,Attention Deficit Disorder with Hyperactivity ,10036 Medical Clinic ,10076 Center for Integrative Human Physiology ,570 Life sciences ,biology ,150 Psychology ,Psychology ,2803 Biological Psychiatry ,Psychomotor Performance ,030217 neurology & neurosurgery - Abstract
Background Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder that starts in childhood and frequently persists in adults. Several theories postulate deficits in ADHD that have effects across many executive functions or in more narrowly defined aspects, such as response inhibition. Electrophysiological studies on children, however, indicate that ADHD is not associated with a core deficit of response inhibition, as abnormal inhibitory processing is typically preceded or accompanied by other processing deficits. It is not yet known if this pattern of abnormal processing is evident in adult ADHD. Methods The objective of this paper was to investigate event-related potential indices of preparatory states and subsequent response inhibition processing in adults with ADHD. Two cued continuous performance tasks were presented to 21 adults meeting current criteria for adult ADHD and combined type ADHD in childhood, and 20 controls. Results The ADHD group exhibited significantly weaker orienting attention to cues, cognitive preparation processes and inhibitory processing. In addition, we observed a strong correlation between the resources allocated to orienting to cues and the strength of the subsequent response strength control processes, suggesting that orienting deficits partly predict and determine response control deficits in ADHD. Conclusions These findings closely resemble those previously found in children with ADHD, which indicate that there is not a core response inhibition deficit in ADHD. These findings therefore suggest the possibility of developmental stability into adulthood of the underlying abnormal processes in ADHD.
363. Cognitive-electrophysiological indices of attentional and inhibitory processing in adults with ADHD: familial effects
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Gráinne McLoughlin, Philip Asherson, B. Albrecht, Tobias Banaschewski, Jonna Kuntsi, Aribert Rothenberger, Daniel Brandeis, University of Zurich, and McLoughlin, G
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2805 Cognitive Neuroscience ,Adult ,Male ,medicine.medical_specialty ,Neurology ,Adolescent ,Cognitive Neuroscience ,610 Medicine & health ,Audiology ,behavioral disciplines and activities ,lcsh:RC346-429 ,Developmental psychology ,Young Adult ,03 medical and health sciences ,Behavioral Neuroscience ,Cognition ,0302 clinical medicine ,Neurodevelopmental disorder ,Continuous performance task ,2802 Behavioral Neuroscience ,mental disorders ,Reaction Time ,medicine ,Humans ,Attention deficit hyperactivity disorder ,Attention ,Young adult ,Association (psychology) ,Evoked Potentials ,lcsh:Neurology. Diseases of the nervous system ,Biological Psychiatry ,Retrospective Studies ,Cued speech ,medicine.diagnostic_test ,Research ,Age Factors ,General Medicine ,10058 Department of Child and Adolescent Psychiatry ,Middle Aged ,medicine.disease ,Electrophysiological Phenomena ,030227 psychiatry ,Inhibition, Psychological ,Attention Deficit Disorder with Hyperactivity ,Psychology ,2803 Biological Psychiatry ,Psychomotor Performance ,030217 neurology & neurosurgery - Abstract
Background Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder that starts in childhood and frequently persists in adults. In a comparison of adults with ADHD and a matched control sample, we previously showed that abnormal inhibitory processing is typically preceded or accompanied by other processing deficits in adult ADHD. We now compare these data further to additional data from first-degree relatives (fathers) of children with ADHD to identify whether this pattern of abnormal processing shares familial influences with ADHD in adults. Methods Using a family design, we compared 20 fathers of children with the combined subtype of ADHD with 21 adults with ADHD combined subtype and 20 controls in event-related potential indices of preparatory states and subsequent response inhibition processing as elicited by a cued continuous performance task. Results Fathers of children with ADHD exhibited significantly weaker orienting attention to cues and inhibitory processing than the controls but not the ADHD sample. Conclusions These findings provide evidence for the familial association of attentional orienting and response inhibition processes with ADHD in adults and indicate a familial and neurobiological link between ADHD in children and adults.
364. Late EP negativity and perception of Kanizsa triangle
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D. Lehmann, Daniel Brandeis, and R.U. Mueller
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medicine.medical_specialty ,Neuropsychology and Physiological Psychology ,General Neuroscience ,Perception ,media_common.quotation_subject ,medicine ,Negativity effect ,Audiology ,Psychology ,media_common - Published
- 1985
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365. Lateral evoked potential distribution for effects of attention and figure perception, related to stimulated hemisphere
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D. Lehmann, Daniel Brandeis, R.U. Mueller, and G.C. Jin
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Neuropsychology and Physiological Psychology ,Distribution (number theory) ,General Neuroscience ,Perception ,media_common.quotation_subject ,Evoked potential ,Psychology ,Neuroscience ,media_common - Published
- 1985
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366. Spatial analysis of the scalp potential: Determination of baseline and definition of components
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Daniel Brandeis
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medicine.medical_specialty ,Neuropsychology and Physiological Psychology ,medicine.anatomical_structure ,business.industry ,General Neuroscience ,Scalp ,medicine ,Audiology ,business ,Baseline (configuration management) - Published
- 1985
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367. Adaptive segmentation of event-related potential map series into components defined by map configuration
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A. Horst, Wolfgang Skrandies, I. Pal, Daniel Brandeis, G.C. Jin, and Dietrich Lehmann
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Quasi-open map ,Event-related potential ,Computer science ,business.industry ,General Neuroscience ,Pattern recognition ,Segmentation ,Neurology (clinical) ,Artificial intelligence ,business ,Map series - Published
- 1985
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368. While on the subject of closure…
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Daniel Brandeis and Enoch Callaway
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Orthodontics ,Behavioral Neuroscience ,Neuropsychology and Physiological Psychology ,Physiology ,Closure (topology) ,Subject (philosophy) ,Psychology - Published
- 1988
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369. Impaired tuning of a fast occipito-temporal response for print in dyslexic children learning to read.
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Urs Maurer, Silvia Brem, Kerstin Bucher, Felicitas Kranz, Rosmarie Benz, Hans-Christoph Steinhausen, and Daniel Brandeis
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CHILDREN with dyslexia ,LANGUAGE disorders ,CHILD development ,READING disability - Abstract
Developmental dyslexia is defined as a disorder of learning to read. It is thus critical to examine the neural processes that impair learning to read during the early phase of reading acquisition, before compensatory mechanisms are adapted by older readers with dyslexia. Using electroencephalography-based event-related imaging, we investigated how tuning of visual activity for print advances in the same children before and after initial reading training in school. The focus was on a fast, coarse form of visual tuning for print, measured as an increase of the occipito-temporal N1 response at 150–270 ms in the event-related potential (ERP) to words compared to symbol strings. The results demonstrate that the initial development of reading skills and visual tuning for print progressed more slowly in those children who became dyslexic than in their control peers. Print-specific tuning in 2nd grade strongly distinguished dyslexic children from controls. It was maximal in the inferior occipito-temporal cortex, left-lateralized in controls, and reduced in dyslexic children. The results suggest that delayed initial visual tuning for print critically contributes to the development of dyslexia. [ABSTRACT FROM AUTHOR]
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- 2007
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370. Imbalanced social-communicative and restricted repetitive behavior subtypes of autism spectrum disorder exhibit different neural circuitry
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Meng-Chuan Lai, Elena Maria Busuoli, Antonio M. Persico, Bonnie Auyeung, Eva Loth, Sarah Durston, Andreas Meyer-Lindenberg, Sven Bölte, Carolin Moessnang, Stavros Trakoshis, Marianne Oldehinkel, Prantik Kundu, Steve C.R. Williams, Jan K. Buitelaar, Sarah Baumeister, Tony Charman, Michael V. Lombardo, Isotta Landi, Richard A. I. Bethlehem, Rosemary Holt, Veronica Mandelli, Christine Ecker, Natasha Bertelsen, Julian Tillmann, Declan G. Murphy, Christian F. Beckmann, Jakob Seidlitz, Eleonora Satta, Mark H. Johnson, Will Spooren, Simon Baron-Cohen, Guillaume Dumas, Luke Mason, Emily J.H. Jones, Thomas Bourgeron, Istituto Italiano di Tecnologia (IIT), University of Trento [Trento], University of Cambridge [UK] (CAM), Children’s Hospital of Philadelphia (CHOP ), University of Pennsylvania, University of Cyprus [Nicosia] (UCY), University of Edinburgh, King‘s College London, Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Universität Heidelberg [Heidelberg] = Heidelberg University, Radboud University Medical Center [Nijmegen], Karolinska Institutet [Stockholm], Stockholm Health Care Services (SLSO), Curtin University [Perth], Planning and Transport Research Centre (PATREC), University Medical Center [Utrecht], Goethe-Universität Frankfurt am Main, University of London [London], Monash University [Melbourne], University of Messina, Università Campus Bio-Medico di Roma / University Campus Bio-Medico of Rome ( UCBM), University of Vienna [Vienna], Roche Pharma Research and Early Development [Basel] (pRED), F. Hoffmann-La Roche [Basel], Centre for Addiction and Mental Health [Toronto] (CAMH), The Hospital for sick children [Toronto] (SickKids), University of Toronto, National Taiwan University [Taiwan] (NTU), This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme under grant agreement No 755816 (ERC Starting Grant to MVL). This work was also supported by EU-AIMS and EU AIMS-2-TRIALS, which both received support from the Innovative Medicines Initiative Joint Undertaking under Grant Agreement No. 115300 and the Innovative Medicines Initiative 2 Joint Undertaking under Grant Agreement No. 777394, the resources of which are composed of financial contributions from the European Union’s Seventh Framework Programme (Grant No. FP7/2007–2013), from the European Federation of Pharmaceutical Industries and Associations companies’ in-kind contributions, and from Autism Speaks, Autistica and the Simons Foundation for Autism Research Initiative. The views expressed are those of the author(s) and not necessarily those of the IMI 2JU. This work was also supported by the Netherlands Organization for Scientific Research through Vidi grants (Grant No. 864.12.003 [to CFB]), from the FP7 (Grant Nos. 602805) (AGGRESSOTYPE) (to JKB), 603016 (MATRICS), and 278948 (TACTICS), and from the European Community’s Horizon 2020 Programme (H2020/2014–2020) (Grant Nos. 643051 [MiND] and 642996 (BRAINVIEW). This work received funding from the Wellcome Trust UK Strategic Award (Award No. 098369/Z/12/Z) and from the National Institute for Health Research Maudsley Biomedical Research Centre (to DGMM). M-CL was supported by the Academic Scholars Award from the Department of Psychiatry, University of Toronto, the Slaight Family Child and Youth Mental Health Innovation Fund from the CAMH Foundation, the Ontario Brain Institute via the Province of Ontario Neurodevelopmental Disorders (POND) Network (IDS-I l-02), the Canadian Institutes of Health Research Sex and Gender Science Chair (GSB 171373), and the Innovation Fund of the Alternative Funding Plan for the Academic Health Sciences Centres of Ontario (CAM-20-004). R.A.I.B acknowledges research support by the Autism Research Trust and a British Academy Fellowship (PF2\180017). MHJ, TC, and EJHJ acknowledge support from a UK MRC Programme Grant., the EU-AIMS LEAP group : Jumana Ahmad, Sara Ambrosino, Bonnie Auyeung, Tobias Banaschewski, Simon Baron-Cohen, Sarah Baumeister, Christian F. Beckmann, Sven Bölte, Thomas Bourgeron, Carsten Bours, Michael Brammer, Daniel Brandeis, Claudia Brogna, Yvette de Bruijn, Jan K. Buitelaar, Bhismadev Chakrabarti, Tony Charman, Chris Chatham, Ineke Cornelissen, Daisy Crawley, Flavio Dell’Acqua, Guillaume Dumas, Sarah Durston, Christine Ecker, Jessica Faulkner, Vincent Frouin, Pilar Garcés, David Goyard, Lindsay Ham, Hannah Hayward, Joerg Hipp, Rosemary J. Holt, Mark H. Johnson, Emily J. H. Jones, Prantik Kundu, Meng-Chuan Lai, Xavier Liogier D’ardhuy, Michael V. Lombardo, Eva Loth, David J. Lythgoe, René Mandl, Andre Marquand, Luke Mason, Maarten Mennes, Andreas Meyer-Lindenberg, Carolin Moessnang, Nico Mueller, Declan G. M. Murphy, Bethany Oakley, Laurence O’Dwyer, Marianne Oldehinkel, Bob Oranje, Gahan Pandina, Antonio M. Persico, Barbara Ruggeri, Amber N. V. Ruigrok, Jessica Sabet, Roberto Sacco, Antonia San José Cáceres, Emily Simonoff, Will Spooren, Julian Tillmann, Roberto Toro, Heike Tost, Jack Waldman, Steve C. R. Williams, Caroline Wooldridge & Marcel P. Zwiers, European Project: 0755816(2008), European Project: 115300,EC:FP7:SP1-JTI,IMI-JU-03-2010,EU-AIMS(2012), European Project: 602805,EC:FP7:HEALTH,FP7-HEALTH-2013-INNOVATION-1,AGGRESSOTYPE(2013), European Project: 603016,EC:FP7:HEALTH,FP7-HEALTH-2013-INNOVATION-1,MATRICS(2014), European Project: 278948,EC:FP7:HEALTH,FP7-HEALTH-2011-two-stage,TACTICS(2012), European Project: 643051,H2020,H2020-MSCA-ITN-2014,MiND(2015), European Project: 642996,H2020,H2020-MSCA-ITN-2014,BRAINVIEW(2015), University of Pennsylvania [Philadelphia], University of Cyprus (UCY), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), Universität Heidelberg [Heidelberg], Bethlehem, Richard A I [0000-0002-0714-0685], Seidlitz, Jakob [0000-0002-8164-7476], Bourgeron, Thomas [0000-0001-8164-9220], Charman, Tony [0000-0003-1993-6549], Persico, Antonio M [0000-0001-8910-4479], Lombardo, Michael V [0000-0001-6780-8619], Apollo - University of Cambridge Repository, and Bethlehem, Richard AI [0000-0002-0714-0685]
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Male ,0301 basic medicine ,Autism Spectrum Disorder ,Stress-related disorders Donders Center for Medical Neuroscience [Radboudumc 13] ,Medicine (miscellaneous) ,MESH: Magnetic Resonance Imaging ,0302 clinical medicine ,130 000 Cognitive Neurology & Memory ,MESH: Child ,Neural Pathways ,Biology (General) ,Child ,MESH: Autism Spectrum Disorder ,MESH: Child Behavior Disorders ,Communication ,220 Statistical Imaging Neuroscience ,Hyperconnectivity ,Autism spectrum disorders ,Magnetic Resonance Imaging ,Autism spectrum disorder ,Female ,MESH: Communication ,General Agricultural and Biological Sciences ,MESH: Stereotyped Behavior ,QH301-705.5 ,autism spectrum disorders ,Child Behavior Disorders ,Biology ,Article ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,All institutes and research themes of the Radboud University Medical Center ,Neuroimaging ,mental disorders ,medicine ,Biological neural network ,Humans ,Association (psychology) ,MESH: Neurodevelopmental Disorders ,Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7] ,MESH: Humans ,Resting state fMRI ,Genetic heterogeneity ,MESH: Neural Pathways ,[SCCO.NEUR]Cognitive science/Neuroscience ,medicine.disease ,MESH: Male ,030104 developmental biology ,Neurodevelopmental Disorders ,Autism ,Stereotyped Behavior ,Neuroscience ,MESH: Female ,030217 neurology & neurosurgery - Abstract
Social-communication (SC) and restricted repetitive behaviors (RRB) are autism diagnostic symptom domains. SC and RRB severity can markedly differ within and between individuals and may be underpinned by different neural circuitry and genetic mechanisms. Modeling SC-RRB balance could help identify how neural circuitry and genetic mechanisms map onto such phenotypic heterogeneity. Here, we developed a phenotypic stratification model that makes highly accurate (97–99%) out-of-sample SC = RRB, SC > RRB, and RRB > SC subtype predictions. Applying this model to resting state fMRI data from the EU-AIMS LEAP dataset (n = 509), we find that while the phenotypic subtypes share many commonalities in terms of intrinsic functional connectivity, they also show replicable differences within some networks compared to a typically-developing group (TD). Specifically, the somatomotor network is hypoconnected with perisylvian circuitry in SC > RRB and visual association circuitry in SC = RRB. The SC = RRB subtype show hyperconnectivity between medial motor and anterior salience circuitry. Genes that are highly expressed within these networks show a differential enrichment pattern with known autism-associated genes, indicating that such circuits are affected by differing autism-associated genomic mechanisms. These results suggest that SC-RRB imbalance subtypes share many commonalities, but also express subtle differences in functional neural circuitry and the genomic underpinnings behind such circuitry., Natasha Bertelsen et al. develop a computational model to categorize patients with autism spectrum disorder (ASD) into distinct subgroups, based on social-communicative or restricted repetitive behaviors. By integrating publicly available neuroimaging and genetic data, they report neural and molecular signatures in two of these subgroups, altogether highlighting subtle differences in neural circuitry and genomic networks that could underlie phenotypic differences among ASD patients.
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- 2021
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371. Testing Geometrical Discrimination within an Enzyme Active Site: Constrained Hydrogen Bonding in the Ketosteroid Isomerase Oxyanion Hole
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Herschlag, Daniel [Brandeis]
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- 2008
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372. Investigating the factors underlying adaptive functioning in autism in the EU-AIMS Longitudinal European Autism Project
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Tillmann, Julian, San José Cáceres, Antonia, Chatham, Chris H., Crawley, Daisy, Holt, Rosemary, Oakley, Bethany, Banaschewski, Tobias, Baron-Cohen, Simon, Bölte, Sven, Buitelaar, Jan K., Durston, Sarah, Ham, Lindsay, Loth, Eva, Simonoff, Emily, Spooren, Will, Murphy, Declan G., Charman, Tony, Ahmad, Jumana, Ambrosino, Sara, Auyeung, Bonnie, Baumeister, Sarah, Beckmann, Christian, Bourgeron, Thomas, Bours, Carsten, Brammer, Michael, Brandeis, Daniel, Brogna, Claudia, de Bruijn, Yvette, Chakrabarti, Bhismadev, Cornelissen, Ineke, Dell’ Acqua, Flavio, Dumas, Guillaume, Ecker, Christine, Faulkner, Jessica, Frouin, Vincent, Garcés, Pilar, Goyard, David, Hayward, Hannah, Hipp, Joerg, Johnson, Mark H., Jones, Emily J. H., Kundu, Prantik, Lai, Meng-Chuan, D'Ardhuy, Xavier Liogier, Lombardo, Michael, Lythgoe, David J., Mandl, René, Mason, Luke, Meyer-Lindenberg, Andreas, Moessnang, Carolin, Mueller, Nico, O'Dwyer, Laurence, Oldehinkel, Marianne, Oranje, Bob, Pandina, Gahan, Persico, Antonio M., Ruggeri, Barbara, Ruigrok, Amber, Sabet, Jessica, Sacco, Roberto, Toro, Roberto, Tost, Heike, Waldman, Jack, Williams, Steve C. R., Wooldridge, Caroline, Zwiers, Marcel P., Institute of Psychiatry, Psychology & Neuroscience, King's College London, King‘s College London, University of Vienna [Vienna], F. Hoffmann-La Roche [Basel], University of Cambridge [UK] (CAM), Department of Child and Adolescent Psychiatry and Psychotherapy [Mannheim], Universität Heidelberg [Heidelberg] = Heidelberg University, Central Institute of Mental Health [Mannheim], University Hospital Mannheim | Universitätsmedizin Mannheim, Karolinska Institutet [Stockholm], Donders Institute for Brain, Cognition and Behaviour, Radboud University [Nijmegen], Stockholm County Council, University Medical Center [Utrecht], Karakter Child and Adolescent Psychiatry University Centre [Nijmegen], South London and Maudsley NHS Foundation Trust, This work was supported by EU‐AIMS (European Autism Interventions), which receives support from the Innovative Medicines Initiative Joint Undertaking under grant agreement no. 115300, the resources of which are composed of financial contributions from the European Union's Seventh Framework Programme (grant FP7/2007‐2013), from the European Federation of Pharmaceutical Industries and Associations companies' in‐kind contributions, and from Autism Speaks, The EU‐AIMS LEAP group : Jumana Ahmad, Sara Ambrosino, Bonnie Auyeung, Sarah Baumeister, Christian Beckmann, Thomas Bourgeron, Carsten Bours, Michael Brammer, Daniel Brandeis, Claudia Brogna, Yvette de Bruijn, Bhismadev Chakrabarti, Ineke Cornelissen, Flavio Dell’ Acqua, Guillaume Dumas, Christine Ecker, Jessica Faulkner, Vincent Frouin, Pilar Garcés, David Goyard, Hannah Hayward, Joerg Hipp, Mark H. Johnson, Emily J.H. Jones, Prantik Kundu, Meng‐Chuan Lai, Xavier Liogier D'ardhuy, Michael Lombardo, David J. Lythgoe, René Mandl, Luke Mason, Andreas Meyer‐Lindenberg, Carolin Moessnang, Nico Mueller, Laurence O'Dwyer, Marianne Oldehinkel, Bob Oranje, Gahan Pandina, Antonio M. Persico, Barbara Ruggeri, Amber Ruigrok, Jessica Sabet, Roberto Sacco, Roberto Toro, Heike Tost, Jack Waldman, Steve C.R. Williams, Caroline Wooldridge, and Marcel P. Zwiers., We thank all participants and their families for their efforts to participate in the study., European Project: 115300,EC:FP7:SP1-JTI,IMI-JU-03-2010,EU-AIMS(2012), Universität Heidelberg [Heidelberg], Medical Faculty [Mannheim], Radboud university [Nijmegen], Tillmann, Julian [0000-0001-9574-9855], Bölte, Sven [0000-0002-4579-4970], Charman, Tony [0000-0003-1993-6549], and Apollo - University of Cambridge Repository
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Male ,Intelligence ,Psychological intervention ,Severity of Illness Index ,Cohort Studies ,0302 clinical medicine ,Borderline intellectual functioning ,Activities of Daily Living ,Psychology ,Longitudinal Studies ,Child ,Genetics (clinical) ,Research Articles ,Adaptive behavior ,General Neuroscience ,05 social sciences ,Age Factors ,Cognition ,Europe ,symptom severity ,Phenotype ,Autism spectrum disorder ,Cohort ,Anxiety ,Female ,medicine.symptom ,adaptive functioning ,autism spectrum disorder ,intellectual functioning ,psychiatric symptoms ,Neuroscience (all) ,Neurology (clinical) ,050104 developmental & child psychology ,Clinical psychology ,Research Article ,Adult ,Adolescent ,03 medical and health sciences ,Young Adult ,Sex Factors ,mental disorders ,medicine ,Humans ,0501 psychology and cognitive sciences ,Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7] ,medicine.disease ,[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,Autism ,030217 neurology & neurosurgery - Abstract
Contains fulltext : 204820.pdf (Publisher’s version ) (Closed access) Individuals with autism spectrum disorder (ASD) exhibit significant impairments in adaptive functioning that impact on their ability to meet the demands of everyday life. A recurrent finding is that there is a pronounced discrepancy between level of cognitive ability and adaptive functioning, and this is particularly prominent among higher-ability individuals. However, the key clinical and demographic associations of these discrepancies remain unclear. This study included a sample of 417 children, adolescents, and adults with ASD as part of the EU-AIMS LEAP cohort. We examined how age, sex, IQ, levels of ASD symptom and autistic trait severity and psychiatric symptomatology are associated with adaptive functioning as measured by the Vineland Adaptive Behavior Scales-Second Edition and IQ-adaptive functioning discrepancies. Older age, lower IQ and higher social-communication symptoms were associated with lower adaptive functioning. Results also demonstrate that older age, higher IQ and higher social-communication symptoms are associated with greater IQ-adaptive functioning discrepancy scores. By contrast, sensory ASD symptoms, repetitive and restricted behaviors, as well as symptoms of attention deficit/hyperactivity disorder (ADHD), anxiety and depression, were not associated with adaptive functioning or IQ-adaptive functioning discrepancy scores. These findings suggest that it is the core social communication problems that define ASD that contribute to adaptive function impairments that people with ASD experience. They show for the first time that sensory symptoms, repetitive behavior and associated psychiatric symptoms do not independently contribute to adaptive function impairments. Individuals with ASD require supportive interventions across the lifespan that take account of social-communicative ASD symptom severity. Autism Res 2019, 12: 645-657. (c) 2019 The Authors. Autism Research published by International Society for Autism Research published by Wiley Periodicals, Inc. LAY SUMMARY: This study investigated key clinical and demographic associations of adaptive functioning impairments in individuals with autism. We found that older age, lower IQ and more severe social-communicative symptoms, but not sensory or repetitive symptoms or co-occurring psychiatric symptoms, are associated with lower adaptive functioning and greater ability-adaptive function discrepancies. This suggests that interventions targeting adaptive skills acquisition should be flexible in their timing and intensity across developmental periods, levels of cognitive ability and take account of social-communicative ASD symptom severity.
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- 2019
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373. Cognitive and neurophysiological markers of ADHD persistence and remission.
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Cheung CH, Rijsdijk F, McLoughlin G, Brandeis D, Banaschewski T, Asherson P, and Kuntsi J
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- Actigraphy, Adolescent, Child, Electroencephalography, Female, Follow-Up Studies, Humans, Male, Remission, Spontaneous, Siblings, Arousal physiology, Attention Deficit Disorder with Hyperactivity physiopathology, Disease Progression, Evoked Potentials physiology, Executive Function physiology, Intelligence physiology
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Background: Attention-deficit hyperactivity disorder (ADHD) persists in around two-thirds of individuals in adolescence and early adulthood., Aims: To examine the cognitive and neurophysiological processes underlying the persistence or remission of ADHD., Method: Follow-up data were obtained from 110 young people with childhood ADHD and 169 controls on cognitive, electroencephalogram frequency, event-related potential (ERP) and actigraph movement measures after 6 years., Results: ADHD persisters differed from remitters on preparation-vigilance measures (contingent negative variation, delta activity, reaction time variability and omission errors), IQ and actigraph count, but not on executive control measures of inhibition or working memory (nogo-P3 amplitudes, commission errors and digit span backwards)., Conclusions: Preparation-vigilance measures were markers of remission, improving concurrently with ADHD symptoms, whereas executive control measures were not sensitive to ADHD persistence/remission. For IQ, the present and previous results combined suggest a role in moderating ADHD outcome. These findings fit with previously identified aetiological separation of the cognitive impairments in ADHD. The strongest candidates for the development of non-pharmacological interventions involving cognitive training and neurofeedback are the preparation-vigilance processes that were markers of ADHD remission., (© The Royal College of Psychiatrists 2016.)
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- 2016
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