Search Results - "Tse, Wing Yee"

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  1. 1

    Improved Properties of the Big Five Inventory and the Rosenberg Self-Esteem Scale in the Expanded Format Relative to the Likert Format by Zhang, Xijuan, Tse, Winnie Wing-Yee, Savalei, Victoria

    Published in Frontiers in psychology (04-06-2019)
    “…Previous research by Zhang and Savalei (2015) proposed an alternative scale format to the Likert scale format: the Expanded format. Scale items in the Expanded…”
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    Journal Article
  2. 2

    Does strict invariance matter? Valid group mean comparisons with ordered-categorical items by Tse, Winnie Wing-Yee, Lai, Mark H. C., Zhang, Yichi

    Published in Behavior research methods (01-04-2024)
    “…Measurement invariance (MI) of a psychometric scale is a prerequisite for valid group comparisons of the measured construct. While the invariance of loadings…”
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  3. 3

    Adjusting for partial invariance in latent parameter estimation: Comparing forward specification search and approximate invariance methods by Lai, Mark H. C., Liu, Yuanfang, Tse, Winnie Wing-Yee

    Published in Behavior research methods (01-02-2022)
    “…Measurement invariance is the condition that an instrument measures a target construct in the same way across subgroups, settings, and time. In psychological…”
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  4. 4

    Correcting for Unreliability and Partial Invariance: A Two-Stage Path Analysis Approach by Lai, Mark H. C., Tse, Winnie Wing-Yee, Zhang, Gengrui, Li, Yixiao, Hsiao, Yu-Yu

    Published in Structural equation modeling (04-03-2023)
    “…In path analysis, using composite scores without adjustment for measurement unreliability and violations of factorial invariance across groups lead to biased…”
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  5. 5

    A novel nonsense mutation in the LPL gene in a Chinese neonate with hypertriglyceridemia by Chan, Angel On-kei, But, Wai-man, Lau, Gene Tze-chin, Tse, Wing-yee, Shek, Chi-chung

    Published in Clinica chimica acta (01-06-2006)
    “…Lipoprotein lipase (LPL) deficiency is a rare autosomal recessive disorder characterized by hypertriglyceridemia. The genetic defect lies in a mutation of the…”
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  6. 6

    Diagnosis of 5α-reductase 2 deficiency: is measurement of dihydrotestosterone essential? by Chan, Angel On Kei, But, Betty Wai Man, Lee, Ching Yin, Lam, Yuen Yu, Ng, Kwok Leung, Tung, Joanna Yuet Ling, Kwan, Elaine Yin Wah, Chan, Yuk Kit, Tsui, Teresa Kam Chi, Lam, Almen Lai Na, Tse, Wing Yee, Cheung, Pik To, Shek, Chi Chung

    Published in Clinical chemistry (Baltimore, Md.) (01-05-2013)
    “…5α-Reductase 2 deficiency (5ARD) is a known cause of 46,XY disorders of sex development (DSD). Traditionally, the diagnosis relies on dihydrotestosterone (DHT)…”
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  7. 7

    Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type la by Lam, Ching-Wan, But, Wai-Man, Shek, Chi-Chung, Tong, Sui-Fan, Chan, Yuen-Shan, Choy, Kwong-Wai, Tse, Wing-Yee, Pang, Chi-Pui, Hjelm, Nils Magnus

    Published in Clinical genetics (01-03-1998)
    “…Glycogen storage disease type la (GSD1a) is an autosomal recessive metabolic disorder caused by a deficiency in glucose‐6‐phosphatase (GóPase). We analyzed the…”
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  8. 8
  9. 9

    Diagnosis of 5[alpha]-Reductase 2 Deficiency: Is Measurement of Dihydrotestosterone Essential? by Chan, Angel OnKei, But, Betty Wai Man, Lee, Ching Yin, Lam, Yuen Yu, Ng, Kwok Leung, Tung, Joanna Yuet Ling, Kwan, Elaine Yin Wah, Chan, Yuk Kit, Tsui, Teresa Kam Chi, Lam, Almen Lai Na, Tse, Wing Yee, Cheung, Pik To, Shek, Chi Chung

    Published in Clinical chemistry (Baltimore, Md.) (01-05-2013)
    “…5α-Reductase 2 deficiency (5ARD) is a known cause of 46,XY disorders of sex development (DSD). Traditionally, the diagnosis relies on dihydrotestosterone (DHT)…”
    Get full text
    Journal Article
  10. 10

    Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a by LAM, C.-W, BUT, W.-M, SHEK, C.-C, TONG, S.-F, CHAN, Y.-S, CHOY, K.-W, TSE, W.-Y, PANG, C.-P, HJELM, N. M

    Published in Clinical genetics (01-03-1998)
    “…Glycogen storage disease type la (GSD1a) is an autosomal recessive metabolic disorder caused by a deficiency in glucose-6-phosphatase (G6Pase). We analyzed the…”
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    Journal Article