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Wendy K Chung

Biographic Data

ID5506036
NAMEWendy K Chung
GIVEN NAMESWendy K
FAMILY NAMEChung
SIGNATURECHUNG W K
VERIFIEDNo
TOTAL WORKS5
TOTAL CITATIONS6
AUTHOR COUNT5
EDITOR COUNT0
FIRST PUBLICATION YEAR2014
LATEST PUBLICATION YEAR2025
H-INDEX1
  • Understanding individualised genetic interventions as research-treatment hybrids

    Josephine Johnston, Kathryn Tabb et al.•ARTICLE•Journal of Medical Ethics•2025

    Until recently, medicine has had little to offer most of the millions of patients suffering from rare and ultrarare genetic conditions. But the development in 2019 of Milasen, the first genetic intervention developed for and administered to a single patient suffering from an ultrarare genetic disorder, has offered hope to patients and families. In addition, Milasen raised a series of conceptual and ethical questions about how individualised genet…

  • Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals

    Open Access•Anne Reed‐Weston, Anne E Reed-Weston et al.•ARTICLE•Journal of Community Genetics•2020

  • Assessing patient readiness for personalized genomic medicine

    Open Access•Christopher J Frost, Irene L Andrulis et al.•ARTICLE•Journal of Community Genetics•2018

  • Models of Consent to Return of Incidental Findings in Genomic Research

    Open Access•Paul S Appelbaum, Peter Appelbaum et al.•ARTICLE•The Hastings Center Report•2014

    Genomic research-including whole genome sequencing and whole exome sequencing-has a growing presence in contemporary biomedical investigation. The capacity of sequencing techniques to generate results that go beyond the primary aims of the research-historically referred to as "incidental findings"-has generated considerable discussion as to how this information should be handled-that is, whether incidental results should be returned, and if so, w…

  • Bitter taste phenotype and body weight predict children's selection of sweet and savory foods at a palatable test-meal

    Open Access•Kathleen L Keller, Annemarie Olsen et al.•ARTICLE•Appetite•2014•Cited by: 6•References: 64

  • Bitter taste phenotype and body weight predict children's selection of sweet and savory foods at a palatable test-meal

    Open Access•Kathleen L Keller, Annemarie Olsen et al.•ARTICLE•Appetite•2014•Cited by: 6•References: 64

  • Models of Consent to Return of Incidental Findings in Genomic Research

    Open Access•Paul S Appelbaum, Peter Appelbaum et al.•ARTICLE•The Hastings Center Report•2014

    Genomic research-including whole genome sequencing and whole exome sequencing-has a growing presence in contemporary biomedical investigation. The capacity of sequencing techniques to generate results that go beyond the primary aims of the research-historically referred to as "incidental findings"-has generated considerable discussion as to how this information should be handled-that is, whether incidental results should be returned, and if so, w…

  • Bitter taste phenotype and body weight predict children's selection of sweet and savory foods at a palatable test-meal

    Open Access•Kathleen L Keller, Annemarie Olsen et al.•ARTICLE•Appetite•2014•Cited by: 6•References: 64

  • Assessing patient readiness for personalized genomic medicine

    Open Access•Christopher J Frost, Irene L Andrulis et al.•ARTICLE•Journal of Community Genetics•2018

  • Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals

    Open Access•Anne Reed‐Weston, Anne E Reed-Weston et al.•ARTICLE•Journal of Community Genetics•2020

  • Understanding individualised genetic interventions as research-treatment hybrids

    Josephine Johnston, Kathryn Tabb et al.•ARTICLE•Journal of Medical Ethics•2025

    Until recently, medicine has had little to offer most of the millions of patients suffering from rare and ultrarare genetic conditions. But the development in 2019 of Milasen, the first genetic intervention developed for and administered to a single patient suffering from an ultrarare genetic disorder, has offered hope to patients and families. In addition, Milasen raised a series of conceptual and ethical questions about how individualised genet…

Biology (4 works) · Genomics and Rare Diseases (4 works) · Medicine (4 works) · Ethics in Clinical Research (3 works) · Genetic testing (3 works) · Bioinformatics (2 works) · BRCA gene mutations in cancer (2 works) · Computer Science (2 works) · Confidentiality (2 works) · Family medicine (2 works)

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