Hochbegabtenberatung im Dienste des sächsischen Landesgymnasiums St. Afra

Etliche Beratungsstellen mit ganz unterschiedlichen Konzepten widmen sich dem Thema der Hochbegabtendiagnostik bzw. -förderung. Ziel dieses Artikels soll es sein, den Mehrwert und die Notwendigkeit von unmittelbarer pädagogisch-psychologischer Kooperation deutlich zu machen. Zum einen können Empfehlungen aus der Diagnostik direkt begleitet werden; zum anderen kann die Umsetzung im pädagogischen Alltag wiederum in die Einzelberatung rückwirkend im Sinne der Realisierbarkeit bestimmter Maßnahmen einfließen. (DIPF/Orig.

Visual search for featural singletons: No top-down modulation, only bottom-up priming.

The present study investigated the effect of top-down knowledge on search for a feature singleton (a "pop-out target"). In a singleton detection task, advance cueing of the dimension of upcoming singleton resulted in cueing costs and benefits (Experiment 1). When the search for the singleton stayed the same but only the response requirements were changed, advance cueing failed to have an effect (Experiments 2 and 3). In singleton search only bottom-up priming plays a role (Experiments 4 and 5). We conclude that expectancy-based, top-down knowledge cannot guide the search for a featural singleton. Bottom-up priming that does facilitate search for a featural singleton cannot be influenced by top-down control. The study demonstrates that effects often attributed to early top-down guidance may represent effects that occur later in processing or represent bottom-up priming effects. © 2006 Psychology Press Ltd

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Variability in SARS-CoV-2 susceptibility and COVID-19 disease severity between individuals is partly due to genetic factors. Here, we identify 4 genomic loci with suggestive associations for SARS-CoV-2 susceptibility and 19 for COVID-19 disease severity. Four of these 23 loci likely have an ethnicity-specific component. Genome-wide association study (GWAS) signals in 11 loci colocalize with expression quantitative trait loci (eQTLs) associated with the expression of 20 genes in 62 tissues/cell types (range: 1:43 tissues/gene), including lung, brain, heart, muscle, and skin as well as the digestive system and immune system. We perform genetic fine mapping to compute 99% credible SNP sets, which identify 10 GWAS loci that have eight or fewer SNPs in the credible set, including three loci with one single likely causal SNP. Our study suggests that the diverse symptoms and disease severity of COVID-19 observed between individuals is associated with variants across the genome, affecting gene expression levels in a wide variety of tissue types

Visual search for featural singletons: No top-down modulation, only bottom-up priming

The present study investigated the effect of top-down knowledge on search for a feature singleton (a ‘‘pop-out target’’). In a singleton detection task, advance cueing of the dimension of upcoming singleton resulted in cueing costs and benefits (Experiment 1). When the search for the singleton stayed the same but only the response requirements were changed, advance cueing failed to have an effect (Experiments 2 and 3). In singleton search only bottom-up priming plays a role (Experiments 4 and 5). We conclude that expectancy-based, top-down knowledge cannot guide the search for a featural singleton. Bottom-up priming that does facilitate search for a featural singleton cannot be influenced by top-down control. The study demonstrates that effects often attributed to early top-down guidance may represent effects that occur later in processing or represent bottom-up priming effects. Every day we spend a lot of time searching for important things such as a traffic sign at a busy crossroad, or one of our kids in a busy shopping centre. When searching for an object we have to keep in mind what we are looking for. A target template describing the target (its colour, its shape, its location, etc.) is kept in memory to guide our search process. For example when searching for one of our lost kids in a shopping centre, we try to remembe

Visual Search for Featural Singletons: No Top-Down Modulation, Only Bottom-Up Priming

The present study investigated the effect of top-down knowledge on search for a feature singleton (a `pop-out target'). In a singleton detection task, advance cueing of the dimension of upcoming singleton resulted in cueing costs and benefits (Experiment 1). When the search for the singleton stayed the same but only the response requirements were changed, advance cueing failed to have an effect (Experiment 2 and 3). In singleton search only bottom-up priming plays a role (Experiment 4 and 5). We conclude that expectancy-based, top-down knowledge cannot guide the search for a featural singleton. Bottom-up priming that does facilitate search for a featural singleton cannot be influenced by top-down control. The study demonstrates that effects often attributed to early top-down guidance may represent effects that occur later in processing or represent bottom-up priming effects

Sources of top-down control in visual search

Endogenous control of visual search can influence search guidance at the level of a supradimensional topographic saliency map [Wolfe, J. M. Guided Search 2.0: A revised model of visual search. Psychonomic Bulletin & Review, 1, 202–238, 1994], and modulate nonspatial mechanisms coding saliency in dimension-specific input modules [Müller, H. J., Reimann, B., & Krummenacher, J. Visual search for singleton feature targets across dimensions: Stimulus- and expectancy-driven effects in dimensional weighting. Journal of Experimental Psychology: Human Perception and Performance, 29, 1021–1035, 2003]. The current experiment used fMRI to dissociate these mechanisms in a singleton feature search task in which the likely target dimension (color or orientation) was semantically precued and target saliency in each dimension was varied parametrically. BOLD signal increases associated with increased demands for top–down guidance were observed within the fronto-parietal attention network and in the right anterior middle frontal gyrus. Decreasing requirements for top–down control led to BOLD signal increases in medial anterior prefrontal cortex, consistent with a gating mechanism in favor of stimulus-related processing [Burgess, P. W., Dumontheil, I., & Gilbert, S. J. The gateway hypothesis of rostral prefrontal cortex (area 10) function. Trends in Cognitive Sciences, 11, 290–298, 2007]. Another network of brain areas consisting of left lateral fronto-polar cortex, the left supramarginal gyrus, and the cerebellum, as well as a bilateral network consisting of the posterior orbital gyrus, the inferior frontal gyrus, and the pre-SMA were associated with top–down dimensional (re-) orienting. These data argue in favor of distinct endogenous control systems for visuospatial and dimension-based attentional processing. Finally, cue validity modulated saliency processing in the left temporo-parietal junction (TPJ), pointing to a crucial role of the left TPJ in integrating an endogenous dimension-based attention set with bottom–up saliency signals

Genome-wide association study of autopsy-confirmed Multiple System Atrophy identifies common variants near <i>ZIC1</i> and <i>ZIC4</i>

AbstractMultiple System Atrophy is a rare neurodegenerative disease with alpha-synuclein aggregation in glial cytoplasmic inclusions and either predominant olivopontocerebellar atrophy or striatonigral degeneration, leading to dysautonomia, parkinsonism, and cerebellar ataxia. One prior genome-wide association study in mainly clinically diagnosed patients with Multiple System Atrophy failed to identify genetic variants predisposing for the disease. Since the clinical diagnosis of Multiple System Atrophy yields a high rate of misdiagnosis when compared to the neuropathological gold standard, we studied common genetic variation in only autopsy-confirmed cases (N = 731) and controls (N = 2,898).The most strongly disease-associated markers were rs16859966 on chromosome 3 (P = 8.6 × 10−7, odds ratio (OR) = 1.58, [95% confidence interval (CI) = 1.32-1.89]), rs7013955 on chromosome 8 (P = 3.7 × 10−6, OR = 1.8 [1.40-2.31]), and rs116607983 on chromosome 4 (P = 4.0 × 10−6, OR = 2.93 [1.86-4.63]), all of which were supported by at least one additional genotyped and several imputed single nucleotide polymorphisms with P-values below 5 × 10−5. The genes closest to the chromosome 3 locus are ZIC1 and ZIC4 encoding the zinc finger proteins of cerebellum 1 and 4 (ZIC1 and ZIC4).Since mutations of ZIC1 and ZIC4 and paraneoplastic autoantibodies directed against ZIC4 are associated with severe cerebellar dysfunction, we conducted immunohistochemical analyses in brain tissue of the frontal cortex and the cerebellum from 24 Multiple System Atrophy patients. Strong immunohistochemical expression of ZIC4 was detected in a subset of neurons of the dentate nucleus in all healthy controls and in patients with striatonigral degeneration, whereas ZIC4 positive neurons were significantly reduced in patients with olivopontocerebellar atrophy.These findings point to a potential ZIC4-mediated vulnerability of neurons in Multiple System Atrophy.</jats:p

Common variants near ZIC1 and ZIC4 in autopsy-confirmed multiple system atrophy.

BACKGROUND: Multiple System Atrophy is a rare neurodegenerative disease with alpha-synuclein aggregation in glial cytoplasmic inclusions and either predominant olivopontocerebellar atrophy or striatonigral degeneration, leading to dysautonomia, parkinsonism, and cerebellar ataxia. One prior genome-wide association study in mainly clinically diagnosed patients with Multiple System Atrophy failed to identify genetic variants predisposing for the disease. OBJECTIVE: Since the clinical diagnosis of Multiple System Atrophy yields a high rate of misdiagnosis when compared to the neuropathological gold standard, we studied only autopsy-confirmed cases. METHODS: We studied common genetic variations in Multiple System Atrophy cases (N&nbsp;=&nbsp;731) and controls (N&nbsp;=&nbsp;2898). RESULTS: The most strongly disease-associated markers were rs16859966 on chromosome 3, rs7013955 on chromosome 8, and rs116607983 on chromosome 4 with P-values below 5 × 10-6 , all of which were supported by at least one additional genotyped and several imputed single nucleotide polymorphisms. The genes closest to the chromosome 3 locus are ZIC1 and ZIC4 encoding the zinc finger proteins of cerebellum 1 and 4 (ZIC1 and ZIC4). INTERPRETATION: Since mutations of ZIC1 and ZIC4 and paraneoplastic autoantibodies directed against ZIC4 are associated with severe cerebellar dysfunction, we conducted immunohistochemical analyses in brain tissue of the frontal cortex and the cerebellum from 24 Multiple System Atrophy patients. Strong immunohistochemical expression of ZIC4 was detected in a subset of neurons of the dentate nucleus in all healthy controls and in patients with striatonigral degeneration, whereas ZIC4-immunoreactive neurons were significantly reduced inpatients with olivopontocerebellar atrophy. These findings point to a potential ZIC4-mediated vulnerability of neurons in Multiple System Atrophy. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society