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Peter D Turnpenny

Biographic Data

ID6463760
NAMEPeter D Turnpenny
GIVEN NAMESPeter D
FAMILY NAMETurnpenny
SIGNATURETURNPENNY P D
AFFILIATIONSExeter Hospital
ORCID0000-0002-5947-0897
VERIFIEDYes
TOTAL WORKS4
TOTAL CITATIONS2
AUTHOR COUNT4
EDITOR COUNT0
FIRST PUBLICATION YEAR1993
LATEST PUBLICATION YEAR2018
H-INDEX1
  • Dimensions of responsibility in medical genetics: Exploring the complexity of the “duty to recontact”

    Open Access•Sharon Doheny, A Clarke et al.•ARTICLE•New Genetics and Society•2018

    Discussion of a “duty to recontact” emerged as technological advances left professionals considering getting back in touch with patients they had seen in the past. While there has been much discussion of the duty to recontact as a matter of theory and ethics, there has been rather little empirically based analysis of what this “duty” consists of. Drawing on interviews with 34 professionals working in, or closely with, genetics services, this pape…

  • Families dealing with the uncertainty of genetic disorders: The case of Neurofibromatosis Type 1

    Open Access•Daniele Carrieri, Hannah Farrimond et al.•ARTICLE•Sociology of Health & Illness•2016•Cited by: 2•References: 54

    Some scholars contend that genetic medicine is transforming the experience of illness and the social category of the family - bringing future risks into the present, and potentially strengthening familial biological bonds in light of these shared genetic risks. However, research has shown that genetic information is interpreted and acted upon through a rich repertoire of adaptable social, cultural and familial factors which pre-exist and interact…

  • Genes, Identity and Adoption

    Open Access•Peter Turnpenny, Peter D Turnpenny•ARTICLE•Adoption & Fostering•1995

  • The Fragile-X Syndrome and Adoption

    Open Access•Peter Turnpenny, Peter D Turnpenny•ARTICLE•Adoption & Fostering•1993•References: 1

  • Families dealing with the uncertainty of genetic disorders: The case of Neurofibromatosis Type 1

    Open Access•Daniele Carrieri, Hannah Farrimond et al.•ARTICLE•Sociology of Health & Illness•2016•Cited by: 2•References: 54

    Some scholars contend that genetic medicine is transforming the experience of illness and the social category of the family - bringing future risks into the present, and potentially strengthening familial biological bonds in light of these shared genetic risks. However, research has shown that genetic information is interpreted and acted upon through a rich repertoire of adaptable social, cultural and familial factors which pre-exist and interact…

  • The Fragile-X Syndrome and Adoption

    Open Access•Peter Turnpenny, Peter D Turnpenny•ARTICLE•Adoption & Fostering•1993•References: 1

  • Genes, Identity and Adoption

    Open Access•Peter Turnpenny, Peter D Turnpenny•ARTICLE•Adoption & Fostering•1995

  • Families dealing with the uncertainty of genetic disorders: The case of Neurofibromatosis Type 1

    Open Access•Daniele Carrieri, Hannah Farrimond et al.•ARTICLE•Sociology of Health & Illness•2016•Cited by: 2•References: 54

    Some scholars contend that genetic medicine is transforming the experience of illness and the social category of the family - bringing future risks into the present, and potentially strengthening familial biological bonds in light of these shared genetic risks. However, research has shown that genetic information is interpreted and acted upon through a rich repertoire of adaptable social, cultural and familial factors which pre-exist and interact…

  • Dimensions of responsibility in medical genetics: Exploring the complexity of the “duty to recontact”

    Open Access•Sharon Doheny, A Clarke et al.•ARTICLE•New Genetics and Society•2018

    Discussion of a “duty to recontact” emerged as technological advances left professionals considering getting back in touch with patients they had seen in the past. While there has been much discussion of the duty to recontact as a matter of theory and ethics, there has been rather little empirically based analysis of what this “duty” consists of. Drawing on interviews with 34 professionals working in, or closely with, genetics services, this pape…

Psychology (3 works) · Biology (2 works) · Business (2 works) · Sociology (2 works) · Aesthetics (1 works) · Art (1 works) · Autism Spectrum Disorder Research (1 works) · Biomedical Ethics and Regulation (1 works) · BRCA gene mutations in cancer (1 works) · Congenital heart defects research (1 works)

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