[PDF] Top 20 Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

... the neural basis of emotion processing in 22q11DS ...mixed emotional facial expressions be- tween eight individuals with 22q11DS and nine ...differentiate neural responses as a function of the type ... See full document

... 60. Schneider M, Debbané M, Bassett AS, Chow EWC, Fung WLA, van den Bree MBM, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, Vorstman J, Duijff SN, Klaassen PWJ, ... See full document

... a deletion at chromosome ...atypical neural structures and brain functioning and have identified less insular and frontal cortical activation and relatively more activation in bilateral occipital cortex ... See full document

... of socio-emotional intervention pro- grams aimed at improving efficiency in visual explor- ation and correcting face scanning from the very first fixations in individuals with developmental delay [53, ... See full document

... intelligence quotient (IQ) derived from standardized tests of intelligence, and as such, an analysis of the relationship between EI and IQ in children with 22q11.2DS is included in this study. To date, studies into the ... See full document

... Boredom is a mental state that is poorly understood and defined differently. Eastwood et al. (2012) defined it as “the aversive state that occurs when we (a) are not able to successfully engage attention with internal ... See full document

... of neural adaptation beyond HG activity (see ...numerous correlates of neural adaptation ...of neural adaptation is a systematic reduction in HG activity to commonly presented stimuli, we were ... See full document

... subtle emotional expressions (Volkova, Mohler, Dodds, Tesch, & Bülthoff, 2014b), and even psychological traits (Thoresen et ...of emotional body movements expressed during naturalistic narrative ... See full document

... She initially had no feeding problems, however following weaning to solids she developed a large appetite. At 13 months, following surgery for the correction of patent ductus arteriosus, she started gaining weight. By ... See full document

... Further evidence for di ff erences in the BBB in ASD comes from di- rect examination of the BBB itself. The endothelial adhesion molecules platelet endothelial adhesion molecule-1 and P-selectin have been shown to be ... See full document

... Prevention Study (WOSCOPS) found that the risk of CVD and diabetes increased with the number of MS risk factors. 2 However, there exists complex interaction process among various components and their role to the ... See full document

... Phelan-McDermid syndrome is a microdeletion syn- drome resulting from loss of 22q13 by simple deletion, unbalanced translocation, ring chromosome formation, or other unbalanced structural change ...with ... See full document

... of neural place code, however, is insufficient to explain other aspects of ...this neural-place coding ...of neural populations with temporally coherent ...active neural population(s) would ... See full document

... Using a combination of probabilistic tractography and a regularized multiple regression model from machine learning, known as the elastic net, the current study is the first to demonstrate that the pattern of amygdala ... See full document

... In summary, there is mounting evidence that children and adolescents with 22q11DS may have significant differences in the development and ‘connectivity’ of specific brain regions; however relatively few studies have ... See full document

... 22q11DS deletion might face include learning and educational problems relating to attention difficulties, problems with maths, reading and social relationships as they mature, or autism (Campbell and Swillen, ... See full document

... Recent work indicates that social and communication difficulties may increase the risk for developing social anxiety disorder [48], which may well be the case in 22q11.2DS. However, despite evidence for a relationship ... See full document

... genetically heterogeneous populations, many researchers have sacrificed: (1) detailed phenotyping of the probands, (2) the ability to return to individual participants after analyses, and (3) the familial context ... See full document

... The neuropsychological assessment forms an important part of the total clinical workup. Many children with ASDs present with co-occurring low general cognitive function and may be diagnosed with borderline intelligence ... See full document

... genetic syndrome of coloboma, congenital heart disease, choanal atresia, mental and growth retar- dation, genital anomalies, and ear malformations and hearing loss 22 ; unexpectedly, no associations ... See full document