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Article: Crossing Boundaries in Schizotypy Research: An Introduction to the Special Supplement

TitleCrossing Boundaries in Schizotypy Research: An Introduction to the Special Supplement
Authors
Keywordsconsortium
psychosis
schizophrenia
schizotypy
Issue Date2018
Citation
Schizophrenia Bulletin, 2018, v. 44, p. S457-S459 How to Cite?
AbstractFor nearly 6 decades, the schizotypy construct has served as a conceptual guide for understanding the phenotypic and clinical variability associated with schizophrenia-spectrum vulnerability. Despite the impact of schizotypy on academic research, the public burden of schizophrenia-spectrum pathology has not diminished over time, and it remains poorly understood with no cures, few treatments, and heavy stigma from the lay public. Following on the success of the 2013 Lemanic Workshop on Schizotypy, the International Consortium on Schizotypy Research (ICSR) was formed to address these needs by accelerating scientific discovery of schizophrenia-spectrum pathology. The ICSR convened its 2017 meeting in Beijing China with the theme of "Crossing Borders". This included a focus on expanding schizotypy research across 5 domains across: Academic disciplinary borders (promoting brain and genetics/genomics research), clinical borders (promoting clinical and non-clinical applications), geographic borders (promoting cross-cultural research), laboratory borders (promoting "big" and "small" data collaborations), and methodology borders (promoting emotion, cognition and behavior research using novel methods). This special supplement provides the highlights from this meeting and related work, including 3 theoretical and position articles, 7 research articles, and 1 invited commentary.
Persistent Identifierhttp://hdl.handle.net/10722/367792
ISSN
2023 Impact Factor: 5.3
2023 SCImago Journal Rankings: 2.249

 

DC FieldValueLanguage
dc.contributor.authorCohen, Alex S.-
dc.contributor.authorChan, Raymond C.K.-
dc.contributor.authorDebbané, Martin-
dc.date.accessioned2025-12-19T07:59:18Z-
dc.date.available2025-12-19T07:59:18Z-
dc.date.issued2018-
dc.identifier.citationSchizophrenia Bulletin, 2018, v. 44, p. S457-S459-
dc.identifier.issn0586-7614-
dc.identifier.urihttp://hdl.handle.net/10722/367792-
dc.description.abstractFor nearly 6 decades, the schizotypy construct has served as a conceptual guide for understanding the phenotypic and clinical variability associated with schizophrenia-spectrum vulnerability. Despite the impact of schizotypy on academic research, the public burden of schizophrenia-spectrum pathology has not diminished over time, and it remains poorly understood with no cures, few treatments, and heavy stigma from the lay public. Following on the success of the 2013 Lemanic Workshop on Schizotypy, the International Consortium on Schizotypy Research (ICSR) was formed to address these needs by accelerating scientific discovery of schizophrenia-spectrum pathology. The ICSR convened its 2017 meeting in Beijing China with the theme of "Crossing Borders". This included a focus on expanding schizotypy research across 5 domains across: Academic disciplinary borders (promoting brain and genetics/genomics research), clinical borders (promoting clinical and non-clinical applications), geographic borders (promoting cross-cultural research), laboratory borders (promoting "big" and "small" data collaborations), and methodology borders (promoting emotion, cognition and behavior research using novel methods). This special supplement provides the highlights from this meeting and related work, including 3 theoretical and position articles, 7 research articles, and 1 invited commentary.-
dc.languageeng-
dc.relation.ispartofSchizophrenia Bulletin-
dc.subjectconsortium-
dc.subjectpsychosis-
dc.subjectschizophrenia-
dc.subjectschizotypy-
dc.titleCrossing Boundaries in Schizotypy Research: An Introduction to the Special Supplement-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1093/schbul/sby089-
dc.identifier.scopuseid_2-s2.0-85055432412-
dc.identifier.volume44-
dc.identifier.spageS457-
dc.identifier.epageS459-
dc.identifier.eissn1745-1701-

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