Marschik, Peter B.

[["dc.bibliographiccitation.artnumber","104307"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.volume","129"],["dc.contributor.author","Isensee, Corinna"],["dc.contributor.author","Schmid, Benjamin"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Poustka, Luise"],["dc.date.accessioned","2022-09-01T09:49:48Z"],["dc.date.available","2022-09-01T09:49:48Z"],["dc.date.issued","2022"],["dc.identifier.doi","10.1016/j.ridd.2022.104307"],["dc.identifier.pii","S0891422222001378"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/113534"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-597"],["dc.relation.issn","0891-4222"],["dc.rights.uri","https://www.elsevier.com/tdm/userlicense/1.0/"],["dc.title","Impact of COVID-19 pandemic on families living with autism: An online survey"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["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","1053"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Journal of Developmental and Physical Disabilities"],["dc.bibliographiccitation.lastpage","1069"],["dc.bibliographiccitation.volume","34"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Garrido, Dunia"],["dc.contributor.author","Schuller, Björn W."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2022-12-01T08:31:56Z"],["dc.date.available","2022-12-01T08:31:56Z"],["dc.date.issued","2022"],["dc.description.abstract","Abstract\r\n \r\n Rett syndrome (RTT) is a rare, late detected developmental disorder associated with severe deficits in the speech-language domain. Despite a few reports about atypicalities in the speech-language development of infants and toddlers with RTT, a detailed analysis of the pre-linguistic vocalisation repertoire of infants with RTT is yet missing. Based on home video recordings, we analysed the vocalisations between 9 and 11 months of age of three female infants with typical RTT and compared them to three age-matched typically developing (TD) female controls. The video material of the infants had a total duration of 424 min with 1655 infant vocalisations. For each month, we (1) calculated the infants’ canonical babbling ratios with CBR\r\n UTTER\r\n , i.e., the ratio of number of utterances containing canonical syllables to total number of utterances, and (2) classified their pre-linguistic vocalisations in three non-canonical and four canonical vocalisation subtypes. All infants achieved the milestone of canonical babbling at 9 months of age according to their canonical babbling ratios, i.e. CBR\r\n UTTER\r\n  ≥ 0.15. We revealed overall lower CBRs\r\n UTTER\r\n  and a lower proportion of canonical pre-linguistic vocalisations consisting of well-formed sounds that could serve as parts of target-language words for the RTT group compared to the TD group. Further studies with more data from individuals with RTT are needed to study the atypicalities in the pre-linguistic vocalisation repertoire which may portend the later deficits in spoken language that are characteristic features of RTT."],["dc.description.sponsorship"," Austrian Science Fund http://dx.doi.org/10.13039/501100002428"],["dc.description.sponsorship"," Oesterreichische Nationalbank http://dx.doi.org/10.13039/501100004061"],["dc.description.sponsorship"," Rett Deutschland e.V. http://dx.doi.org/10.13039/N/A"],["dc.description.sponsorship"," Medical University of Graz http://dx.doi.org/10.13039/501100010109"],["dc.identifier.doi","10.1007/s10882-022-09837-w"],["dc.identifier.pii","9837"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/118311"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-621"],["dc.relation.eissn","1573-3580"],["dc.relation.issn","1056-263X"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Vocalisation Repertoire at the End of the First Year of Life: An Exploratory Comparison of Rett Syndrome and Typical Development"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","Zeitschrift für Geburtshilfe und Neonatologie"],["dc.contributor.author","Leyener, Uta"],["dc.contributor.author","Kraushaar, Carolin"],["dc.contributor.author","Dathe, Anne-Kathrin"],["dc.contributor.author","Felderhoff-Müser, Ursula"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Hüning, Britta Maria"],["dc.date.accessioned","2022-06-01T09:39:14Z"],["dc.date.available","2022-06-01T09:39:14Z"],["dc.date.issued","2022"],["dc.description.abstract","Zusammenfassung Hintergrund Einheitliche Empfehlungen für stationäre und ambulante Physiotherapie bei Frühgeborenen fehlen in Deutschland. Ziel dieser Studie war die Untersuchung der Verordnungspraxis deutscher Perinatalzentren. Werden standardisierte Assessments zur Indikationsstellung genutzt? Welchen Stellenwert nimmt das General Movements Assessment in der postnatalen Diagnostik ein? Methodik Online-Befragung der deutschen Perinatalzentren mit 21 Fragen zur Indikationsstellung und Verordnungspraxis für stationäre und ambulante Physiotherapie in der Versorgung Frühgeborener, sowie den Kenntnissen zum General Movements Assessment und deren klinische Anwendung via Lime-Survey. Ergebnisse 81% der Teilnehmer empfehlen indikationsbasiert „immer“ oder „häufig“ stationäre Physiotherapie für Frühgeborene, 53% empfehlen „immer“/„häufig“ ambulante Therapie. Die Indikationsstellung erfolgt v. a. bei diesen Symptomen (N=344) und Diagnosen (N=273) (Mehrfachnennungen): Hypotonie (94%), Tonusregulationsstörung (92%), neurologische Auffälligkeiten (97%) und Hirnschädigungen (94%). Standardisierte Testungen nutzen 41% der Teilnehmer. Das General Movements Assessment ist in 87% der Zentren bekannt, 11% setzen sie mehrmals in der Woche, 17% mehrmals im Monat zur Indikationsstellung ein. Schlussfolgerung Physiotherapie wird bei Frühgeborenen häufig verordnet. Die Indikationsstellung erfolgt primär nach Symptom- oder Krankheitsbild, weniger anhand standardisierter Testverfahren. Das General Movements Assessment ist eine weithin bekannte, jedoch klinisch noch nicht allgemein eingesetzte Methode."],["dc.identifier.doi","10.1055/a-1791-5778"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/108421"],["dc.language.iso","de"],["dc.notes.intern","DOI-Import GROB-572"],["dc.relation.eissn","1439-1651"],["dc.relation.issn","0948-2393"],["dc.title","Physiotherapie in Deutschen Perinatalzentren"],["dc.title.alternative","Indikationsstellung und klinische Anwendung des General Movements\n Assessments"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","Journal of Nonverbal Behavior"],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Schuller, Dagmar"],["dc.contributor.author","Schuller, Björn W."],["dc.date.accessioned","2020-06-23T07:47:23Z"],["dc.date.available","2020-06-23T07:47:23Z"],["dc.date.issued","2020"],["dc.description.abstract","Human preverbal development refers to the period of steadily increasing vocal capacities until the emergence of a child’s first meaningful words. Over the last decades, research has intensively focused on preverbal behavior in typical development. Preverbal vocal patterns have been phonetically classified and acoustically characterized. More recently, specific preverbal phenomena were discussed to play a role as early indicators of atypical development. Recent advancements in audio signal processing and machine learning have allowed for novel approaches in preverbal behavior analysis including automatic vocalization-based differentiation of typically and atypically developing individuals. In this paper, we give a methodological overview of current strategies for collecting and acoustically representing preverbal data for intelligent audio analysis paradigms. Efficiency in the context of data collection and data representation is discussed. Following current research trends, we set a special focus on challenges that arise when dealing with preverbal data of individuals with late detected developmental disorders, such as autism spectrum disorder or Rett syndrome."],["dc.identifier.doi","10.1007/s10919-020-00332-4"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66597"],["dc.language.iso","en"],["dc.relation.issn","0191-5886"],["dc.relation.issn","1573-3653"],["dc.title","Efficient Collection and Representation of Preverbal Data in Typical and Atypical Development"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["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.firstpage","1"],["dc.bibliographiccitation.journal","Clinical Linguistics & Phonetics"],["dc.bibliographiccitation.lastpage","16"],["dc.contributor.author","Lang, Sigrun"],["dc.contributor.author","Willmes, Klaus"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Fox-Boyer, Annette"],["dc.date.accessioned","2020-06-23T08:34:41Z"],["dc.date.available","2020-06-23T08:34:41Z"],["dc.date.issued","2020"],["dc.description.abstract","Prelexical phonetic capacities have widely been described to be a precursor for later speech and language development. However, studies so far varied greatly in the measurements used for the detection of canonical babbling onset or the description of infants’ phonetic capacities at one or more set time points. The comparability of results is, therefore, questionable. Thus, the aims of this study were to investigate the associations between (1) different measurements of CBO, (2) different aspects of phonetic capacity at the age of 9 months and (3) age of CBO and phonetic capacities at 9 months. A further aim (4) was to explore whether one of the measures would be suitable to predict the age of word onset (WO) in 20 healthy German-acquiring individuals. The data were derived from monthly recorded spontaneous speech samples between 0 and 18 months. It was found that the different applied prelexical measures equally well serve as valid estimators for the detection of CBO or of infants’ phonetic capacities. Further, age of CBO and phonetic capacities at 9 months were significantly associated even though the age of CBO did not reliably predict phonetic capacities. Prelexical measures and WO were not related. Reasons for no indication of a significant association are discussed."],["dc.identifier.doi","10.1080/02699206.2020.1731606"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66602"],["dc.language.iso","en"],["dc.relation.issn","0269-9206"],["dc.relation.issn","1464-5076"],["dc.title","Prelexical phonetic and early lexical development in German-acquiring infants: canonical babbling and first spoken words"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]