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Y H Chang

Biographic Data

ID30659
NAMEY H Chang
GIVEN NAMESY H
FAMILY NAMEChang
SIGNATURECHANG Y H
AFFILIATIONSMackay Memorial Hospital
ORCID0000-0003-3321-0357
VERIFIEDYes
TOTAL WORKS8
TOTAL CITATIONS1
AUTHOR COUNT8
EDITOR COUNT0
FIRST PUBLICATION YEAR2012
LATEST PUBLICATION YEAR2025
H-INDEX1
  • Nonzero-Sum Time Perception Is Associated with Greater Willingness to Help

    Open Access•Yu Niiya, Syamil Yakin et al.•ARTICLE•European Journal of Investigation…•2025

    People are less likely to help others when they view time as a scarce resource. Does changing people’s perception of time influence their willingness to help? We hypothesized that people would be more willing to help and would allocate more time to helping others when they view time as a nonzero-sum resource (i.e., as a resource that merely exists or that can be created moment-by-moment with their interactions with others) versus a zero-sum resou…

  • From Overgrowth to Complex Malformations: A Novel EZH2 Variant Reveals the Expanding Clinical Spectrum of Weaver Syndrome

    Open Access•Chung‐Lin Lee, Chih‐Kuang Chuang et al.•ARTICLE•Children•2025

    Weaver syndrome is a rare congenital overgrowth disorder caused by pathogenic EZH2 variants. This study reports a novel EZH2 variant associated with atypical manifestations, including severe bilateral camptodactyly and complex brain malformations. A 4-year-old Taiwanese female exhibited classical Weaver syndrome features including macrosomia, macrocephaly, hypertelorism, and developmental delay, plus atypical findings of severe bilateral camptoda…

  • Del Signo a La Semiótica. La Seducción De Los Pies Femeninos: From the Sign to Semiotics. The Seduction of Female Feet

    Open Access•Y H Chang, Ya-Hui Chang et al.•ARTICLE•Signa Revista de la Asociación…•2025

    El objetivo de este artículo es indagar acerca de los pies femeninos como un signo en la semiótica y explorar la convergencia de las ideas semióticas en la seducción corporal. Partiendo del concepto del cuerpo de Mary Douglas y de las nociones de seducción de Jean Baudrillard y George Bataille, se observa la seducción a través de los pies femeninos en el óleo Les hasards heureux de l’escarpolette de Jean-Honoré Fragonard y en la obra erótica Jin …

  • The past that ties us together: Nostalgia Strengthens Social Networks

    Kuan‐ju Huang, Y H Chang•ARTICLE•Cognition & Emotion•2025•References: 75

    1,467), we found that trait-like nostalgia was associated with increased motivation to maintain social networks, which in turn predicted the number of close social ties. In other words, those who value nostalgia and experience it more frequently are more motivated to strengthen important relationships, which helps mitigate the loss of these bonds over the life span. These findings contribute to our understanding of the social nature of nostalgia …

  • Examining the evolution of research on grandparent caregiving

    Open Access•Y H Chang, Yaqing Chang et al.•ARTICLE•Children and Youth Services Review•2025•Cited by: 1•References: 1

  • Rapid Weight Loss and Severe Failure to Thrive Mimicking Lipodystrophy Syndrome in a 1-Year-Old Taiwanese Girl with Costello Syndrome

    Open Access•Yu-Min Syu, Hung‐Chang Lee et al.•ARTICLE•Children•2022

    Costello syndrome (CS) is a type of RASopathy caused mainly by de-novo heterozygous pathogenic variants in the HRAS gene located on chromosome 11p15.5. The phenotype of CS is characterized by prenatal overgrowth, postnatal failure to thrive, curly or sparse fine hair, coarse facial features, and multisystem involvement, including cardiovascular, endocrine, and gastroenterological disorders. We present a one-year-old girl with rapid weight loss an…

  • Wiedemann–Steiner Syndrome with a Pathogenic Variant in KMT2A from Taiwan

    Open Access•Chung‐Lin Lee, Chih‐Kuang Chuang et al.•ARTICLE•Children•2021

    Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder. Patients with WSS have characteristics of growth retardation, facial dysmorphism, hypertrichosis cubiti (HC), and neurodevelopmental delays. WSS is in an autosomal dominant inherited pattern caused by a mutation of the KMT2A gene (NM_001197104.2). In this article, we discuss a 5-year-old boy who has mild intellectual disability (ID), hypotonia, HC, hypertrichosis on the back, dysmorphic…

  • Adolescents and Leisure Activities: The Impact of Expectation and Experience on Service Satisfaction

    Open Access•Cheng-Hsui Chen, Y H Chang et al.•ARTICLE•Social Behavior and Personality…•2012

    Although service quality has been found to be a key concept for organizations, it has rarely been applied to the leisure activities of adolescents. Therefore, in this research we examined the relationships among adolescents' expectations of quality, perceptions of quality of actual experiences, and satisfaction with those experiences. We also examined the relationship between expectation and actual experience in terms of the adolescents' satisfac…

  • Examining the evolution of research on grandparent caregiving

    Open Access•Y H Chang, Yaqing Chang et al.•ARTICLE•Children and Youth Services Review•2025•Cited by: 1•References: 1

  • Adolescents and Leisure Activities: The Impact of Expectation and Experience on Service Satisfaction

    Open Access•Cheng-Hsui Chen, Y H Chang et al.•ARTICLE•Social Behavior and Personality…•2012

    Although service quality has been found to be a key concept for organizations, it has rarely been applied to the leisure activities of adolescents. Therefore, in this research we examined the relationships among adolescents' expectations of quality, perceptions of quality of actual experiences, and satisfaction with those experiences. We also examined the relationship between expectation and actual experience in terms of the adolescents' satisfac…

  • Wiedemann–Steiner Syndrome with a Pathogenic Variant in KMT2A from Taiwan

    Open Access•Chung‐Lin Lee, Chih‐Kuang Chuang et al.•ARTICLE•Children•2021

    Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder. Patients with WSS have characteristics of growth retardation, facial dysmorphism, hypertrichosis cubiti (HC), and neurodevelopmental delays. WSS is in an autosomal dominant inherited pattern caused by a mutation of the KMT2A gene (NM_001197104.2). In this article, we discuss a 5-year-old boy who has mild intellectual disability (ID), hypotonia, HC, hypertrichosis on the back, dysmorphic…

  • Rapid Weight Loss and Severe Failure to Thrive Mimicking Lipodystrophy Syndrome in a 1-Year-Old Taiwanese Girl with Costello Syndrome

    Open Access•Yu-Min Syu, Hung‐Chang Lee et al.•ARTICLE•Children•2022

    Costello syndrome (CS) is a type of RASopathy caused mainly by de-novo heterozygous pathogenic variants in the HRAS gene located on chromosome 11p15.5. The phenotype of CS is characterized by prenatal overgrowth, postnatal failure to thrive, curly or sparse fine hair, coarse facial features, and multisystem involvement, including cardiovascular, endocrine, and gastroenterological disorders. We present a one-year-old girl with rapid weight loss an…

  • Nonzero-Sum Time Perception Is Associated with Greater Willingness to Help

    Open Access•Yu Niiya, Syamil Yakin et al.•ARTICLE•European Journal of Investigation…•2025

    People are less likely to help others when they view time as a scarce resource. Does changing people’s perception of time influence their willingness to help? We hypothesized that people would be more willing to help and would allocate more time to helping others when they view time as a nonzero-sum resource (i.e., as a resource that merely exists or that can be created moment-by-moment with their interactions with others) versus a zero-sum resou…

  • From Overgrowth to Complex Malformations: A Novel EZH2 Variant Reveals the Expanding Clinical Spectrum of Weaver Syndrome

    Open Access•Chung‐Lin Lee, Chih‐Kuang Chuang et al.•ARTICLE•Children•2025

    Weaver syndrome is a rare congenital overgrowth disorder caused by pathogenic EZH2 variants. This study reports a novel EZH2 variant associated with atypical manifestations, including severe bilateral camptodactyly and complex brain malformations. A 4-year-old Taiwanese female exhibited classical Weaver syndrome features including macrosomia, macrocephaly, hypertelorism, and developmental delay, plus atypical findings of severe bilateral camptoda…

  • Del Signo a La Semiótica. La Seducción De Los Pies Femeninos: From the Sign to Semiotics. The Seduction of Female Feet

    Open Access•Y H Chang, Ya-Hui Chang et al.•ARTICLE•Signa Revista de la Asociación…•2025

    El objetivo de este artículo es indagar acerca de los pies femeninos como un signo en la semiótica y explorar la convergencia de las ideas semióticas en la seducción corporal. Partiendo del concepto del cuerpo de Mary Douglas y de las nociones de seducción de Jean Baudrillard y George Bataille, se observa la seducción a través de los pies femeninos en el óleo Les hasards heureux de l’escarpolette de Jean-Honoré Fragonard y en la obra erótica Jin …

  • The past that ties us together: Nostalgia Strengthens Social Networks

    Kuan‐ju Huang, Y H Chang•ARTICLE•Cognition & Emotion•2025•References: 75

    1,467), we found that trait-like nostalgia was associated with increased motivation to maintain social networks, which in turn predicted the number of close social ties. In other words, those who value nostalgia and experience it more frequently are more motivated to strengthen important relationships, which helps mitigate the loss of these bonds over the life span. These findings contribute to our understanding of the social nature of nostalgia …

  • Examining the evolution of research on grandparent caregiving

    Open Access•Y H Chang, Yaqing Chang et al.•ARTICLE•Children and Youth Services Review•2025•Cited by: 1•References: 1

Psychology (4 works) · Social Psychology (3 works) · Genomics and Rare Diseases (2 works) · Perception (2 works) · Advertising and Communication Studies (1 works) · Affect (linguistics (1 works) · Agenesis (1 works) · Agenesis of the corpus callosum (1 works) · Aging, Elder Care, and Social Issues (1 works) · Applied Psychology (1 works)

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