Zhang, Dajie

[["dc.bibliographiccitation.firstpage","95"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.lastpage","108"],["dc.bibliographiccitation.volume","82"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Roche, Laura"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Krieber, Magdalena"],["dc.contributor.author","McLay, Laurie"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Gugatschka, Markus"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2020-06-03T07:28:14Z"],["dc.date.available","2020-06-03T07:28:14Z"],["dc.date.issued","2018"],["dc.description.abstract","ackground Responding to one’s own name (RtN) has been reported as atypical in children with developmental disorders, yet comparative studies on RtN across syndromes are rare. Aims We aim to (a) overview the literature on RtN in different developmental disorders during the first 24 months of life, and (b) report comparative data on RtN across syndromes. Methods and procedures In Part 1, a literature search, focusing on RtN in children during the first 24 months of life with developmental disorders, identified 23 relevant studies. In Part 2, RtN was assessed utilizing retrospective video analysis for infants later diagnosed with ASD, RTT, or FXS, and typically developing peers. Outcomes and results Given a variety of methodologies and instruments applied to assess RtN, 21/23 studies identified RtN as atypical in infants with a developmental disorder. We observed four different developmental trajectories of RtN in ASD, RTT, PSV, and FXS from 9 to 24 months of age. Between-group differences became more distinctive with age. Conclusions and implications RtN may be a potential parameter of interest in a comprehensive early detection model characterising age-specific neurofunctional biomarkers associated with specific disorders, and contribute to early identification."],["dc.identifier.doi","10.1016/j.ridd.2018.04.004"],["dc.identifier.pmid","29655507"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66133"],["dc.language.iso","en"],["dc.relation.issn","0891-4222"],["dc.title","Response to name and its value for the early detection of developmental disorders: Insights from autism spectrum disorder, Rett syndrome, and fragile X syndrome. A perspectives paper"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","6"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Kindheit und Entwicklung"],["dc.bibliographiccitation.lastpage","14"],["dc.bibliographiccitation.volume","30"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2021-04-14T08:30:20Z"],["dc.date.available","2021-04-14T08:30:20Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1026/0942-5403/a000323"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83193"],["dc.language.iso","de"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","2190-6246"],["dc.relation.issn","0942-5403"],["dc.title","Die Bedeutung fötaler und neonataler Motorik für die kindliche Entwicklung und die Früherkennung von Entwicklungsstörungen"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","68"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Developmental Neurorehabilitation"],["dc.bibliographiccitation.lastpage","72"],["dc.bibliographiccitation.volume","21"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Lemcke, Sanne"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Bolte, Sven"],["dc.contributor.author","Townend, Gillian S."],["dc.contributor.author","Briciet Lauritsen, Marlene"],["dc.date.accessioned","2020-06-23T07:54:21Z"],["dc.date.available","2020-06-23T07:54:21Z"],["dc.date.issued","2017"],["dc.description.abstract","Purposes: Typically, early (pre-diagnostic) development in individuals later diagnosed with Rett syndrome (RTT) has been investigated retrospectively using parent reports, medical records and analysis of home videos. In recent years, prospective research designs have been increasingly applied to the investigation of early development in individuals with late phenotypical onset disorders, for example, autism spectrum disorder. Methods: In this study, data collected by the Danish National Birth Cohort lent itself to prospective exploration of the early development of RTT, in particular early motor-, speech-language, and socio-communicative behaviors, mood, and sleep. Results and Conclusions: Despite limitations, this quasi prospective methodology proved promising. In order to add substantially to the body of knowledge, however, specific questions relating to peculiarites in early development could usefully be added to future cohort studies. As this involves considerable work, it may be more realistic to consider a set of indicators which point to a number of developmental disorders rather than to one."],["dc.identifier.doi","10.1080/17518423.2017.1323970"],["dc.identifier.pmid","28534656"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66600"],["dc.language.iso","en"],["dc.relation.eissn","1751-8431"],["dc.relation.issn","1751-8423"],["dc.title","Early development in Rett syndrome - the benefits and difficulties of a birth cohort approach"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","103854"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.volume","110"],["dc.contributor.author","Silva, Nelson"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Kulvicius, Tomas"],["dc.contributor.author","Gail, Alexander"],["dc.contributor.author","Barreiros, Carla"],["dc.contributor.author","Lindstaedt, Stefanie"],["dc.contributor.author","Kraft, Marc"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Nielsen-Saines, Karin"],["dc.contributor.author","Wörgötter, Florentin"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2021-04-14T08:28:50Z"],["dc.date.available","2021-04-14T08:28:50Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1016/j.ridd.2021.103854"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82720"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.issn","0891-4222"],["dc.title","The future of General Movement Assessment: The role of computer vision and machine learning – A scoping review"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","166"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Klinische Neurophysiologie"],["dc.bibliographiccitation.lastpage","171"],["dc.bibliographiccitation.volume","42"],["dc.contributor.author","Bartl-Pokorny, K. D."],["dc.contributor.author","Landerl, K."],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Enzinger, C."],["dc.contributor.author","Gebauer, D."],["dc.contributor.author","Fink, A."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Kozel, N."],["dc.contributor.author","Kargl, R."],["dc.contributor.author","Seither Preisler, A."],["dc.contributor.author","Vollmann, R."],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2020-05-19T11:17:05Z"],["dc.date.available","2020-05-19T11:17:05Z"],["dc.date.issued","2011"],["dc.description.abstract","Dyslexie, als eine der häufigsten umschriebenen Entwicklungsstörungen, ist eine schwerwiegende und persistierende Problematik schriftsprachlicher Verarbeitungsprozesse. Ursächlich für Dyslexie werden phonologische, auditive oder visuelle Defizite, Schwierigkeiten beim schnellen Benennen sowie Automatisierungsdefizite diskutiert. Aufgrund der familiären Häufung der Dyslexie gilt eine genetische Grundlage für diese Störung als gesichert. Post-mortem Untersuchungen fanden bei Dyslektikern Ektopien und Dysplasien im sprachassoziierten perisylvischen Cortex. Ob die Plana temporalia bei Dyslektikern im Vergleich zu Nicht-Dyslektikern symmetrisch sind, wird noch kontroversiell diskutiert. Neben neuroanatomischen Auffälligkeiten wurden mittels funktioneller bildgebender Verfahren auch neurofunktionelle Abweichungen bei Dyslektikern nachgewiesen: Teile der parieto-temporalen und okzipito-temporalen Strukturen der linken Hemisphäre sind bei spezifischen Aufgaben vermindert aktiviert, während linker und rechter Gyrus frontalis inferior und rechtshemisphärische okzipito-temporale Strukturen eine vermehrte Aktivierung aufweisen. Eye-Tracking Studien zeigten bei Dyslektikern häufig längere Fixationen, kleinere Sakkaden und mehr Regressionen als bei normal entwickelten Lesern. Noch immer sind neurofunktionelle und -strukturelle Ergebnisse inkonsistent, was unter anderem mit unterschiedlichen Messverfahren, Altersunterschieden der Probanden, geringer Sample-Größe, uneinheitlicher Definition der Dyslexie und der Heterogenität der Störung selbst zusammenhängt."],["dc.description.abstract","Dyslexia is one of the most common specific developmental disorders. Dyslexics exhibit a profound and persistent reading disorder, frequently accompanied by spelling difficulties. Current theories assume dyslexia to be caused by phonological, auditory or visual deficits, or by deficits in rapid naming and automatisation. Due to the familial risk of this developmental disorder, a genetic origin is being discussed as well. Post-mortem studies revealed ectopias and dysplasias in the language-associated perisylvian cortex of dyslexics. Whether the plana temporalia are symmetrically distributed or asymmetric as in non-dyslexics is still the subject of controversial discussion. In neurofunctional studies dyslexics showed underactivated left-hemispheric parieto-temporal and occipito-temporal structures. However, there was an overactivation of the left and right inferior frontal gyri and of the right-hemispheric occipito-temporal structures. Various eye-tracking studies revealed longer fixations, shorter saccades and more frequent regressions in dyslexics than in normal readers. Neuroanatomic and neurophysiological results are still inconsistent, which is certainly due to the diversity of methodological approaches, to age differences between the participants, small sample sizes, heterogeneous definitions of dyslexia, and to the phenotypic heterogeneity of the disorder itself."],["dc.identifier.doi","10.1055/s-0031-1285905"],["dc.identifier.isi","WOS:000294854000004"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65600"],["dc.identifier.url","http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000294854000004&KeyUID=WOS:000294854000004"],["dc.language.iso","de"],["dc.relation.eissn","1439-4081"],["dc.relation.issn","1434-0275"],["dc.title","Dyslexie und ihre neuronale Signatur"],["dc.title.alternative","Dyslexia and its Neural Signature"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Current Neurology and Neuroscience Reports"],["dc.bibliographiccitation.volume","17"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Peharz, Robert"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","O'Muircheartaigh, Jonathan"],["dc.contributor.author","Roeyers, Herbert"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Spittle, Alicia J."],["dc.contributor.author","Urlesberger, Berndt"],["dc.contributor.author","Schuller, Björn W."],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Ozonoff, Sally"],["dc.contributor.author","Pernkopf, Franz"],["dc.contributor.author","Pock, Thomas"],["dc.contributor.author","Tammimies, Kristiina"],["dc.contributor.author","Enzinger, Christian"],["dc.contributor.author","Krieber, Magdalena"],["dc.contributor.author","Tomantschger, Iris"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Roche, Laura"],["dc.contributor.author","Esposito, Gianluca"],["dc.contributor.author","Gugatschka, Markus"],["dc.contributor.author","Nielsen-Saines, Karin"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Kaufmann, Walter E."],["dc.date.accessioned","2017-09-07T11:52:07Z"],["dc.date.accessioned","2020-06-23T06:57:05Z"],["dc.date.available","2017-09-07T11:52:07Z"],["dc.date.available","2020-06-23T06:57:05Z"],["dc.date.issued","2017"],["dc.description.abstract","PURPOSE OF REVIEW: Substantial research exists focusing on the various aspects and domains of early human development. However, there is a clear blind spot in early postnatal development when dealing with neurodevelopmental disorders, especially those that manifest themselves clinically only in late infancy or even in childhood.; RECENT FINDINGS: This early developmental period may represent an important timeframe to study these disorders but has historically received far less research attention. We believe that only a comprehensive interdisciplinary approach will enable us to detect and delineate specific parameters for specific neurodevelopmental disorders at a very early age to improve early detection/diagnosis, enable prospective studies and eventually facilitate randomised trials of early intervention. In this article, we propose a dynamic framework for characterising neurofunctional biomarkers associated with specific disorders in the development of infants and children. We have named this automated detection 'Fingerprint Model', suggesting one possible approach to accurately and early identify neurodevelopmental disorders."],["dc.identifier.doi","10.1007/s11910-017-0748-8"],["dc.identifier.gro","3151185"],["dc.identifier.pmid","28390033"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/7961"],["dc.language.iso","en"],["dc.notes.intern","WoS Import 2017-07-25"],["dc.notes.status","final"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.eissn","1534-6293"],["dc.relation.issn","1528-4042"],["dc.title","A Novel Way to Measure and Predict Development: A Heuristic Approach to Facilitate the Early Detection of Neurodevelopmental Disorders"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","49"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Advances in Neurodevelopmental Disorders"],["dc.bibliographiccitation.lastpage","61"],["dc.bibliographiccitation.volume","2"],["dc.contributor.author","Roche, Laura"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Schuller, Björn W."],["dc.contributor.author","Esposito, Gianluca"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Roeyers, Herbert"],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Gugatschka, Markus"],["dc.contributor.author","Waddington, Hannah"],["dc.contributor.author","Vollmann, Ralf"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2018-02-22T10:52:33Z"],["dc.date.accessioned","2020-06-03T09:13:15Z"],["dc.date.available","2018-02-22T10:52:33Z"],["dc.date.available","2020-06-03T09:13:15Z"],["dc.date.issued","2018"],["dc.description.abstract","This article provides an overview of studies assessing the early vocalisations of children with autism spectrum disorder (ASD), Rett syndrome (RTT), and fragile X syndrome (FXS) using retrospective video analysis (RVA) during the first 2 years of life. Electronic databases were systematically searched and a total of 23 studies were selected. These studies were then categorised according to whether children were later diagnosed with ASD (13 studies), RTT (8 studies), or FXS (2 studies) and then described in terms of (a) participant characteristics, (b) control group characteristics, (c) video footage, (d) behaviours analysed, and (e) main findings. This overview supports the use of RVA in analysing the early development of vocalisations in children later diagnosed with ASD, RTT, or FXS and provides an in-depth analysis of vocalisation presentation, complex vocalisation production, and the rate and/or frequency of vocalisation production across the three disorders. Implications are discussed in terms of extending crude vocal analyses to more precise methods that might provide more powerful means by which to discriminate between disorders during early development. A greater understanding of the early manifestation of these disorders may then lead to improvements in earlier detection."],["dc.identifier.doi","10.1007/s41252-017-0051-3"],["dc.identifier.pmid","29774230"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/12415"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.relation.eissn","2366-7540"],["dc.relation.issn","2366-7532"],["dc.title","Early Vocal Development in Autism Spectrum Disorder, Rett Syndrome, and Fragile X Syndrome: Insights from Studies using Retrospective Video Analysis"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","Behavioral and Brain Sciences"],["dc.bibliographiccitation.volume","40"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Esposito, Gianluca"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Sigafoos, Jeff"],["dc.date.accessioned","2020-06-23T07:31:36Z"],["dc.date.available","2020-06-23T07:31:36Z"],["dc.date.issued","2017"],["dc.description.abstract","The extent to which early motor patterns represent antecedents to later communicative functions, and the emergence of gesture and/or sign as potential communicative acts in neurodevelopmental disorders (NDDs), are research questions that have received recent attention. It is important to keep in mind that different NDDs have different neurological underpinnings, with correspondingly different implications for their conceptualization, detection, and treatment."],["dc.identifier.doi","10.1017/s0140525x1500299x"],["dc.identifier.pmid","29342523"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66593"],["dc.language.iso","en"],["dc.relation.eissn","1469-1825"],["dc.relation.issn","0140-525X"],["dc.title","Same or different: Common pathways of behavioral biomarkers in infants and children with neurodevelopmental disorders?"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1236"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.lastpage","1239"],["dc.bibliographiccitation.volume","34"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Kaufmann, Walter E."],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Wolin, Thomas"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Pini, Giorgio"],["dc.contributor.author","Zappella, Michele"],["dc.contributor.author","Tager-Flusberg, Helen"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Johnston, Michael V."],["dc.date.accessioned","2020-06-04T06:51:00Z"],["dc.date.available","2020-06-04T06:51:00Z"],["dc.date.issued","2013"],["dc.description.abstract","We delineated the achievement of early speech-language milestones in 15 young children with Rett syndrome (MECP2 positive) in the first two years of life using retrospective video analysis. By contrast to the commonly accepted concept that these children are normal in the pre-regression period, we found markedly atypical development of speech-language capacities, suggesting a paradigm shift in the pathogenesis of Rett syndrome and a possible approach to its early detection."],["dc.identifier.doi","10.1016/j.ridd.2013.01.014"],["dc.identifier.pmid","23400005"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66144"],["dc.language.iso","en"],["dc.relation.issn","0891-4222"],["dc.title","Changing the perspective on early development of Rett syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","109"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.lastpage","119"],["dc.bibliographiccitation.volume","82"],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Vollmann, Ralf"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Gugatschka, Markus"],["dc.contributor.author","Schuller, Björn W."],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2020-05-19T11:14:13Z"],["dc.date.available","2020-05-19T11:14:13Z"],["dc.date.issued","2018"],["dc.description.abstract","Background Early speech-language development of individuals with Rett syndrome (RTT) has been repeatedly characterised by a co-occurrence of apparently typical and atypical vocalisations. Aims To describe specific features of this intermittent character of typical versus atypical early RTT-associated vocalisations by combining auditory Gestalt perception and acoustic vocalisation analysis. Methods and procedures We extracted N = 363 (pre-)linguistic vocalisations from home video recordings of an infant later diagnosed with RTT. In a listening experiment, all vocalisations were assessed for (a)typicality by five experts on early human development. Listeners’ auditory concepts of (a)typicality were investigated in context of a comprehensive set of acoustic time-, spectral- and/or energy-related higher-order features extracted from the vocalisations. Outcomes and results More than half of the vocalisations were rated as ‘atypical’ by at least one listener. Atypicality was mainly related to the auditory attribute ‘timbre’, and to prosodic, spectral, and voice quality features in the acoustic domain. Conclusions and implications Knowledge gained in our study shall contribute to the generation of an objective model of early vocalisation atypicality. Such a model might be used for increasing caregivers’ and healthcare professionals’ sensitivity to identify atypical vocalisation patterns, or even for a probabilistic approach to automatically detect RTT based on early vocalisations."],["dc.identifier.doi","10.1016/j.ridd.2018.02.019"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65584"],["dc.language.iso","en"],["dc.relation.issn","0891-4222"],["dc.title","Typical vs. atypical: Combining auditory Gestalt perception and acoustic analysis of early vocalisations in Rett syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]