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","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.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","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"]]

[["dc.bibliographiccitation.firstpage","15"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Kindheit und Entwicklung"],["dc.bibliographiccitation.lastpage","24"],["dc.bibliographiccitation.volume","30"],["dc.contributor.author","Lang, Sigrun"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Sachse, Steffi"],["dc.contributor.author","Mani, Nivedita"],["dc.contributor.author","Fox-Boyer, Annette V."],["dc.contributor.author","Hartung, Martin"],["dc.contributor.author","Einspieler, Christa"],["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/a000324"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83192"],["dc.language.iso","de"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","2190-6246"],["dc.relation.issn","0942-5403"],["dc.title","Früherkennung von Entwicklungsstörungen: Kanonisches Lallen (k)‌ein diagnostischer Marker‍(!)?"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3"],["dc.bibliographiccitation.journal","Neuroscience & Biobehavioral Reviews"],["dc.bibliographiccitation.lastpage","5"],["dc.bibliographiccitation.volume","107"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Bedogni, Francesco"],["dc.contributor.author","Boterberg, Sofie"],["dc.contributor.author","Camfield, Carol"],["dc.contributor.author","Camfield, Peter"],["dc.contributor.author","Charman, Tony"],["dc.contributor.author","Curfs, Leopold"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Esposito, Gianluca"],["dc.contributor.author","De Filippis, Bianca"],["dc.contributor.author","Goin-Kochel, Robin P."],["dc.contributor.author","Höglinger, Günter U"],["dc.contributor.author","Holzinger, Daniel"],["dc.contributor.author","Iosif, Ana-Maria"],["dc.contributor.author","Lancioni, Giulio E."],["dc.contributor.author","Landsberger, Nicoletta"],["dc.contributor.author","Laviola, Giovanni"],["dc.contributor.author","Marco, Eva M."],["dc.contributor.author","Müller, Michael"],["dc.contributor.author","Neul, Jeffrey L."],["dc.contributor.author","Nielsen-Saines, Karin"],["dc.contributor.author","Nordahl-Hansen, Anders"],["dc.contributor.author","O’Reilly, Mark F."],["dc.contributor.author","Ozonoff, Sally"],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Roeyers, Herbert"],["dc.contributor.author","Rankovic, Marija"],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Tammimies, Kristiina"],["dc.contributor.author","Townend, Gillian S"],["dc.contributor.author","Zwaigenbaum, Lonnie"],["dc.contributor.author","Zweckstetter, Markus"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Marschik, Peter B"],["dc.date.accessioned","2020-12-10T15:20:26Z"],["dc.date.available","2020-12-10T15:20:26Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1016/j.neubiorev.2019.08.014"],["dc.identifier.issn","0149-7634"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/72666"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Towards a consensus on developmental regression"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]