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Kelly

Dados Biográficos

ID3862
NOMEKelly
SOBRENOMEKelly
ASSINATURAKELLY
AFILIAÇÕESUniversity of Exeter
ORCID0000-0003-1045-4615
VERIFICADOSim
TOTAL DE OBRAS36
TOTAL DE CITAÇÕES171
TOTAL COMO AUTOR36
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO1981
ANO MAIS RECENTE DE PUBLICAÇÃO2020
ÍNDICE H9
  • It’s My Secret Space’

    Open Access•Gail Kinman, Louise Grant et al.•ARTICLE•The British Journal of Social Work•2020•Citada por: 9•Referências: 58

    Social workers are at high risk of job-related stress that can impair their well-being and professional practice. Although organisational support is a fundamental requirement, it has been argued that social workers need to develop emotional resilience to help them manage the demands of the job. This mixed method study examines the effects of an eight-week mindfulness training course on several resources previously found to underpin resilience in …

  • Ceh'eȝteekuu!-Listen-This is Arapaho Land

    Kelly, Kelly Kelly•ARTICLE•The American Indian Quarterly•2020

    We know about the rapid loss of our world's plants, animals and wilderness but few of us are aware of the parallel, perhaps more rapid and equally devastating, extinction of our planet's human cultural diversity and ongoing cultural genocide. The Vision Quest-University of Wyoming (VQ-UWYO) project addresses the physical occupation of Arapaho lands and the concomitant erasure of Arapaho culture as evidenced by the critically endangered status of …

  • As condições genéticas e as Ciências Sociais e Humanas em saúde

    Open Access•Rogério Lima Barbosa, Reni Barsaglini et al.•ARTICLE•Ciência & Saúde Coletiva•2019

    as condies genticas em uma perspectiva dos estudos da deficincia e/ou a pesquisa qualitativa. Os/as autores/as provm de diferentes regies e instituies internacionais e nacionais contribuindo com

  • How to conduct good quality research on violence against children with disabilities

    Open Access•N Kyegombe, Lena Morgon Banks et al.•ARTICLE•BMC Public Health•2019

    With careful planning, challenges in collecting data on disability and violence can be overcome to generate evidence in this neglected area

  • Dimensions of responsibility in medical genetics

    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…

  • Discipline and Craft

    Kelly, Susan Kelly•ARTICLE•African American Review•2017

    1033 African American Review 50.4 (Winter 2017): 1033-1041© 2018 Johns Hopkins University Press and Saint Louis University Kelly_Kelly 2/14/2018 5:45 PM Page 1033 1034 AFRICAN AMERICAN REVIEW Kelly_Kelly 2/14/2018 5:45 PM Page 1034 SUSAN KELLY WITH SONIA SANCHEZ 1035 Kelly_Kelly 2/14/2018 5:45 PM Page 1035 1036 AFRICAN AMERICAN REVIEW Kelly_Kelly 2/14/2018 5:45 PM Page 1036 SUSAN KELLY WITH SONIA SANCHEZ 1037 Kelly_Kelly 2/14/2018 5:45 PM Page 10…

  • Controversy goes online

    Open Access•Sally Wyatt, Anna Harris et al.•ARTICLE•Science & Technology Studies•2016

    Scientific controversy is increasingly played out via the internet, a technology that is simultaneously content, medium and research infrastructure. Here we analyse material from Wikipedia, focusing on schizophrenia genetics. We find that citation and curation of scientific resources follow a negotiated, ad hoc adherence to Wikipedia rules, are based on limited access to scientific literature, and thus lead to a partially constructed ‘review’ of …

  • Families dealing with the uncertainty of genetic disorders

    Open Access•Daniele Carrieri, Hannah Farrimond et al.•ARTICLE•Sociology of Health & Illness•2016•Citada por: 2•Referências: 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 Multisite Accelerated Permanency Project

    Catherine Roller White, Tyler Corwin et al.•ARTICLE•Journal of Social Service Research•2015•Citada por: 1•Referências: 9

    The Multisite Accelerated Permanency Project (MSAPP) implemented permanency roundtables (PRTs) to increase legal permanency rates for older youth in foster care. PRTs are structured meetings intended to expedite legal permanency (defined as adoption, guardianship, or reunification) for youth by involving experts from both inside and outside child welfare agencies in creative and concrete case planning. The target population of this study included…

  • Autobiologies on YouTube

    Open Access•Anna Harris, Kelly et al.•ARTICLE•New Genetics and Society•2014•Citada por: 19•Referências: 14

    Despite a growing personal genomics market, little is known about how people engage with the possibilities offered by direct-to-consumer (DTC) genetic testing. In order to help address this gap, this study deploys narrative analysis of YouTube videos posted by individuals who have purchased DTC genetic testing for disease. Genetic testing is said to be contributing to new states of illness, where individuals may become "patients-in-waiting." In t…

  • Public viewpoints on new non-invasive prenatal genetic tests

    Open Access•Hannah Farrimond, Hannah R Farrimond et al.•ARTICLE•Public Understanding of Science•2013

    Prenatal screening programmes have been critiqued for their routine implementation according to clinical rationale without public debate. A new approach, non-invasive prenatal diagnosis (NIPD), promises diagnosis of fetal genetic disorders from a sample of maternal blood without the miscarriage risk of current invasive prenatal tests (e.g. amniocentesis). Little research has investigated the attitudes of wider publics to NIPD. This study used Q-m…

  • But that was my idea!’ Problems of Authorship and Validation in Contemporary Practices of Creative Dissent

    Kelly, Susan Kelly•ARTICLE•Parallax•2013

  • Illness Online

    Open Access•Sally Wyatt, Anna Harris et al.•ARTICLE•Theory Culture & Society•2013•Citada por: 11•Referências: 11

    Self-reported data are regarded by medical researchers as invalid and less reliable than data produced by experts in clinical settings, yet individuals can increasingly contribute personal information to medical research through a variety of online platforms. In this article we examine this 'participatory turn' in healthcare research, which claims to challenge conventional delineations of what is valid and reliable for medical practice, by using …

  • The Maternal–Foetal Interface and Gestational Chimerism

    Kelly, Susan Elizabeth Kelly•ARTICLE•Science as Culture•2012•Citada por: 9•Referências: 5

    The science of gestational cell transfer—research into the transfer of cells between a pregnant woman and foetus during gestation—and subsequent mingling of transferred cells, or microchimerism, is bringing new attention to the maternal/foetal interface. These findings challenge previous biological understandings of a barrier between the body of a pregnant woman and developing foetus, a barrier maintaining the identity integrity as it were, of tw…

  • The Gift of Spit (And the Obligation to Return It)

    Anna Harris, Sally Wyatt et al.•ARTICLE•Information Communication & Society•2012•Citada por: 26•Referências: 12

    People can now send a sample of their saliva to an internet-based company in order to discover genetic information about themselves. Entering this 'direct-to-consumer' genetic testing (DTC GT) marketplace can result in enticement to engage in various forms of 'participatory' practices, such as taking part in genetic research. In this article, we analyse the research activities of one of the largest and best-known DTC GT companies, 23andMe. 23andM…

  • Diagnosis as a social determinant

    Open Access•Ginny Russell, Kelly et al.•ARTICLE•Social Science & Medicine•2012•Citada por: 4•Referências: 47

  • Looking beyond risk

    Ginny Russell, Kelly et al.•ARTICLE•Health Risk & Society•2011

    Davison, Frankel, and Davey Smith (1989 Davison, C., Frankel, S. and Davey Smith, G. 1989. Inheriting heart trouble: The relevance of common-sense ideas to preventive measures. Health Education Research, 4(3): 329–340. [Crossref] , [Google Scholar]) conceptualised lay epidemiology as the process of interpreting health risks through considering non-traditional sources of information drawn from personal networks and from the public arena. We analys…

  • Assisting Reproduction, Testing Genes

    Open Access•Kelly, Susan E Kelly•ARTICLE•Sociology of Health & Illness•2011

    Birenbaum-Carmeli, D. and Inhorn, M.C. ( eds ) Assisting Reproduction, Testing Genes: Global Encounters with New Biotechnologies . New York : Berghahn Books , 2009 , 304 pp £55 (hbk ) ISBN 978-1-84545-625-2 . Assisted reproductive technologies (ARTs) have proliferated as new biotechnologies and spread widely across the globe. ARTs now include a host of technologies beyond in vitro fertilisation and directed toward different contexts of infertilit…

  • Qualitative Interviewing Techniques and Styles

    Kelly, Susan E Kelly•CHAPTER•The SAGE Handbook of Qualitative…•2010

  • Choosing not to choose

    Open Access•Kelly, Susan E Kelly•ARTICLE•Sociology of Health & Illness•2008•Citada por: 26•Referências: 7

    Parents of children with genetic conditions or impairments stand in a unique position with regard to choices and dilemmas posed by prenatal screening and testing options offered to at‐risk parents as a means to a ‘healthy’ baby. This article reports the results of a qualitative study of parents whose children are clients of a state‐wide rural genetic outreach programme in the US. The analysis seeks to connect the lived experience of parents of ch…

  • Toward an Epistemological Luddism of Bioethics

    Open Access•Kelly, Susan E Kelly•ARTICLE•Science & Technology Studies•2006

    In the decades since its emergence, bioethics has become successfully integrated, institutionally and culturally, into contemporary processes of biotechnological production. Its success is in large part the result of the development within American bioethics of a strong principlist form that has had considerable influence on bioethics developments regarding biotechnology governance internationally. This article presents a critique of bioethics, d…

  • Barriers to Care-Seeking for Children’s Oral Health Among Low-Income Caregivers

    Kelly, Susan E Kelly et al.•ARTICLE•American Journal of Public Health•2005•Citada por: 4•Referências: 14

    Objectives. We identified psychosocial, structural, and cultural barriers to seeking dental care among nonutilizing caregivers of Medicaid-enrolled children. Methods. We used Medicaid utilization records to identify utilizing and nonutilizing African American and White caregivers of Medicaid-enrolled children in Jefferson County, Kentucky. We conducted 8 focus groups (N=76) with a stratified random sample of responding caregivers; transcripts wer…

  • A Different Light

    Open Access•Kelly, Susan E Kelly•ARTICLE•Journal of Contemporary Ethnography•2005•Citada por: 9•Referências: 23

    This article explores narratives of parenting a child with impairments for insight into impairment as both a materially and socially meaningful phenomenon. Drawing from in-depth interviews with parents, a narrative approach is employed to explore the ambiguities of human impairment and embodiment as experienced by an intimate other. Parents'stories illustrate impairment as an intersubjective and intercorporeal accomplishment and illustrate multip…

  • Annie Moore and the archives of displacement

    Kelly, Susan Kelly et al.•ARTICLE•Social & Cultural Geography•2004•Citada por: 6•Referências: 4

    Annie Moore, the first immigrant to enter the USA through the Ellis Island immigrant processing station, stands as an originary figure of the so-called golden age of European immigration to the USA in the late nineteenth century. The contemporary archivization of the Irish immigrant Annie Moore in the Ellis Island Museum, New York and the Cobh Harbour Heritage Centre in County Cork, Ireland repeats the democratic rhetoric of immigration which und…

  • Calling Up Annie Moore

    Kelly, Susan Kelly et al.•ARTICLE•Public Culture•2004•Citada por: 1•Referências: 2

    Susan Kelly lived in New York City from 1998 to 2001 and participated in the Whitney Museum of American Art Independent Study Program,the World Trade Center's studio residency, and the 16 Beaver Group. Currently she is working toward a Ph.D. at Goldsmith's College, London. Stephen Morton is a lecturer in Anglophone literature and culture at the University of Southampton, U.K. He is the author of Gayatri Chakravorty Spivak (2002

Próximo
  • The Gift of Spit (And the Obligation to Return It)

    Anna Harris, Sally Wyatt et al.•ARTICLE•Information Communication & Society•2012•Citada por: 26•Referências: 12

    People can now send a sample of their saliva to an internet-based company in order to discover genetic information about themselves. Entering this 'direct-to-consumer' genetic testing (DTC GT) marketplace can result in enticement to engage in various forms of 'participatory' practices, such as taking part in genetic research. In this article, we analyse the research activities of one of the largest and best-known DTC GT companies, 23andMe. 23andM…

  • Choosing not to choose

    Open Access•Kelly, Susan E Kelly•ARTICLE•Sociology of Health & Illness•2008•Citada por: 26•Referências: 7

    Parents of children with genetic conditions or impairments stand in a unique position with regard to choices and dilemmas posed by prenatal screening and testing options offered to at‐risk parents as a means to a ‘healthy’ baby. This article reports the results of a qualitative study of parents whose children are clients of a state‐wide rural genetic outreach programme in the US. The analysis seeks to connect the lived experience of parents of ch…

  • Public Bioethics and Publics

    Open Access•Kelly, Susan E Kelly•ARTICLE•Science Technology & Human Values•2003•Citada por: 23•Referências: 32

    Public bioethics bodies are used internationally as institutions with the declared aims of facilitating societal debate and providing policy advice in certain areas of scientific inquiry raising questions of values and legitimate science. In the United States, bioethical experts in these institutions use the language of consensus building to justify and define the outcome of the enterprise. However, the implications of public bioethics at science…

  • Autobiologies on YouTube

    Open Access•Anna Harris, Kelly et al.•ARTICLE•New Genetics and Society•2014•Citada por: 19•Referências: 14

    Despite a growing personal genomics market, little is known about how people engage with the possibilities offered by direct-to-consumer (DTC) genetic testing. In order to help address this gap, this study deploys narrative analysis of YouTube videos posted by individuals who have purchased DTC genetic testing for disease. Genetic testing is said to be contributing to new states of illness, where individuals may become "patients-in-waiting." In t…

  • Bioethics and rural health

    Open Access•Kelly, Susan E Kelly•ARTICLE•Social Science & Medicine•2003•Citada por: 15•Referências: 21

  • Illness Online

    Open Access•Sally Wyatt, Anna Harris et al.•ARTICLE•Theory Culture & Society•2013•Citada por: 11•Referências: 11

    Self-reported data are regarded by medical researchers as invalid and less reliable than data produced by experts in clinical settings, yet individuals can increasingly contribute personal information to medical research through a variety of online platforms. In this article we examine this 'participatory turn' in healthcare research, which claims to challenge conventional delineations of what is valid and reliable for medical practice, by using …

  • It’s My Secret Space’

    Open Access•Gail Kinman, Louise Grant et al.•ARTICLE•The British Journal of Social Work•2020•Citada por: 9•Referências: 58

    Social workers are at high risk of job-related stress that can impair their well-being and professional practice. Although organisational support is a fundamental requirement, it has been argued that social workers need to develop emotional resilience to help them manage the demands of the job. This mixed method study examines the effects of an eight-week mindfulness training course on several resources previously found to underpin resilience in …

  • The Maternal–Foetal Interface and Gestational Chimerism

    Kelly, Susan Elizabeth Kelly•ARTICLE•Science as Culture•2012•Citada por: 9•Referências: 5

    The science of gestational cell transfer—research into the transfer of cells between a pregnant woman and foetus during gestation—and subsequent mingling of transferred cells, or microchimerism, is bringing new attention to the maternal/foetal interface. These findings challenge previous biological understandings of a barrier between the body of a pregnant woman and developing foetus, a barrier maintaining the identity integrity as it were, of tw…

  • A Different Light

    Open Access•Kelly, Susan E Kelly•ARTICLE•Journal of Contemporary Ethnography•2005•Citada por: 9•Referências: 23

    This article explores narratives of parenting a child with impairments for insight into impairment as both a materially and socially meaningful phenomenon. Drawing from in-depth interviews with parents, a narrative approach is employed to explore the ambiguities of human impairment and embodiment as experienced by an intimate other. Parents'stories illustrate impairment as an intersubjective and intercorporeal accomplishment and illustrate multip…

  • Annie Moore and the archives of displacement

    Kelly, Susan Kelly et al.•ARTICLE•Social & Cultural Geography•2004•Citada por: 6•Referências: 4

    Annie Moore, the first immigrant to enter the USA through the Ellis Island immigrant processing station, stands as an originary figure of the so-called golden age of European immigration to the USA in the late nineteenth century. The contemporary archivization of the Irish immigrant Annie Moore in the Ellis Island Museum, New York and the Cobh Harbour Heritage Centre in County Cork, Ireland repeats the democratic rhetoric of immigration which und…

  • Trading privileges from eighth‐century England

    Open Access•Kelly, Susan Kelly•ARTICLE•Early Medieval Europe•1992•Citada por: 6

  • Diagnosis as a social determinant

    Open Access•Ginny Russell, Kelly et al.•ARTICLE•Social Science & Medicine•2012•Citada por: 4•Referências: 47

  • Barriers to Care-Seeking for Children’s Oral Health Among Low-Income Caregivers

    Kelly, Susan E Kelly et al.•ARTICLE•American Journal of Public Health•2005•Citada por: 4•Referências: 14

    Objectives. We identified psychosocial, structural, and cultural barriers to seeking dental care among nonutilizing caregivers of Medicaid-enrolled children. Methods. We used Medicaid utilization records to identify utilizing and nonutilizing African American and White caregivers of Medicaid-enrolled children in Jefferson County, Kentucky. We conducted 8 focus groups (N=76) with a stratified random sample of responding caregivers; transcripts wer…

  • Families dealing with the uncertainty of genetic disorders

    Open Access•Daniele Carrieri, Hannah Farrimond et al.•ARTICLE•Sociology of Health & Illness•2016•Citada por: 2•Referências: 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 Multisite Accelerated Permanency Project

    Catherine Roller White, Tyler Corwin et al.•ARTICLE•Journal of Social Service Research•2015•Citada por: 1•Referências: 9

    The Multisite Accelerated Permanency Project (MSAPP) implemented permanency roundtables (PRTs) to increase legal permanency rates for older youth in foster care. PRTs are structured meetings intended to expedite legal permanency (defined as adoption, guardianship, or reunification) for youth by involving experts from both inside and outside child welfare agencies in creative and concrete case planning. The target population of this study included…

  • Calling Up Annie Moore

    Kelly, Susan Kelly et al.•ARTICLE•Public Culture•2004•Citada por: 1•Referências: 2

    Susan Kelly lived in New York City from 1998 to 2001 and participated in the Whitney Museum of American Art Independent Study Program,the World Trade Center's studio residency, and the 16 Beaver Group. Currently she is working toward a Ph.D. at Goldsmith's College, London. Stephen Morton is a lecturer in Anglophone literature and culture at the University of Southampton, U.K. He is the author of Gayatri Chakravorty Spivak (2002

  • A Search for Relevance in Transition from Post-Primary to Secondary

    Open Access•Kelly, Savannah Kelly et al.•ARTICLE•The Australian Journal of…•1981

    At St Therese's Girls School, we have initiated what we believe to be a more meaningful and more relevant utilization of our resources in producing a secondary program that is more appropriate to the needs of our students.During 1980, the program was organized in a similar manner to previous years. Each grade - eight, nine and ten - was in the charge of grade teachers. We were fortunate in having a specialist art teacher, but basically the Post P…

  • The Uses of Literacy in Early Mediaeval Europe

    Jane Stevenson, Kelly et al.•BOOK•The Uses of literacy in early…•1990

    This book investigates the ways in which literacy was important in early mediaeval Europe, and examines the context of literacy, its uses, levels, and distribution, in a number of different early mediaeval societies between c. 400 and c. 1000. The studies, by leading scholars in the field, set out to provide the factual basis from which assessments of the significance of literacy in the early mediaeval world can be made, as well as analysing the …

  • Trading privileges from eighth‐century England

    Open Access•Kelly, Susan Kelly•ARTICLE•Early Medieval Europe•1992•Citada por: 6

  • How can the aps be of more value to its members

    Open Access•Kelly, Susan Kelly•ARTICLE•Australian Psychologist•1994

    The challenges that modern and responsive organisations face include becoming more customer focused, raising the quality of the product and services they market, and improving productivity. This address considers those challenges as they relate to the Australian Psychological Society

  • Inequities in Health Care and Survival After Injury Among Pedestrians

    Open Access•Rebecca Miles-Doan, Rebecca Miles‐doan et al.•ARTICLE•The Journal of Rural Health•1995

    This study investigated whether rural/urban differences in injury mortality and morbidity are primarily due to medical care maldistribution or to other factors such as sociodemographic or environmental characteristics that are highly correlated with location. To separate incidence from case‐fatality rates, the study analyzed the determinants of survival rather than cause‐specific mortality rates. Using information from Florida traffic crash repor…

  • Discipline and Craft

    Sonia Sanchez, Kelly et al.•ARTICLE•African American Review•2000

  • Genetic Maps and Human Imaginations

    Kelly, Susan E Kelly et al.•ARTICLE•Contemporary Sociology A Journal…•2001

    Scientists are racing to unravel the code of life in our DNA sequences. But once we know the code, will we know what life means? Will we know what to do with the powerful information we will have? Barbara Katz Rothman examines the current trends and applications of genetics research on race, illness and procreation. She explores new genetics in the light of her work as a sociologist who has studied motherhood and women's experiences with prenatal…

  • New' genetics meets the old underclass

    Open Access•Kelly, Susan E Kelly•ARTICLE•Critical Public Health•2002

    Ethical and practical issues around genetic research are of major international concern, both in academia and in the public domain. Questions concerning what interventions are possible and appropriate with the increasing amount of genetic information available; challenge our understandings of ourselves, our health and wellbeing, and the role of medical ethics, public health, surveillance and risk. However there has been little reflection on the s…

  • Redesigning Life

    Kelly, Susan E Kelly et al.•ARTICLE•Contemporary Sociology A Journal…•2002

  • Public Bioethics and Publics

    Open Access•Kelly, Susan E Kelly•ARTICLE•Science Technology & Human Values•2003•Citada por: 23•Referências: 32

    Public bioethics bodies are used internationally as institutions with the declared aims of facilitating societal debate and providing policy advice in certain areas of scientific inquiry raising questions of values and legitimate science. In the United States, bioethical experts in these institutions use the language of consensus building to justify and define the outcome of the enterprise. However, the implications of public bioethics at science…

  • Bioethics and rural health

    Open Access•Kelly, Susan E Kelly•ARTICLE•Social Science & Medicine•2003•Citada por: 15•Referências: 21

  • Annie Moore and the archives of displacement

    Kelly, Susan Kelly et al.•ARTICLE•Social & Cultural Geography•2004•Citada por: 6•Referências: 4

    Annie Moore, the first immigrant to enter the USA through the Ellis Island immigrant processing station, stands as an originary figure of the so-called golden age of European immigration to the USA in the late nineteenth century. The contemporary archivization of the Irish immigrant Annie Moore in the Ellis Island Museum, New York and the Cobh Harbour Heritage Centre in County Cork, Ireland repeats the democratic rhetoric of immigration which und…

  • Calling Up Annie Moore

    Kelly, Susan Kelly et al.•ARTICLE•Public Culture•2004•Citada por: 1•Referências: 2

    Susan Kelly lived in New York City from 1998 to 2001 and participated in the Whitney Museum of American Art Independent Study Program,the World Trade Center's studio residency, and the 16 Beaver Group. Currently she is working toward a Ph.D. at Goldsmith's College, London. Stephen Morton is a lecturer in Anglophone literature and culture at the University of Southampton, U.K. He is the author of Gayatri Chakravorty Spivak (2002

  • Barriers to Care-Seeking for Children’s Oral Health Among Low-Income Caregivers

    Kelly, Susan E Kelly et al.•ARTICLE•American Journal of Public Health•2005•Citada por: 4•Referências: 14

    Objectives. We identified psychosocial, structural, and cultural barriers to seeking dental care among nonutilizing caregivers of Medicaid-enrolled children. Methods. We used Medicaid utilization records to identify utilizing and nonutilizing African American and White caregivers of Medicaid-enrolled children in Jefferson County, Kentucky. We conducted 8 focus groups (N=76) with a stratified random sample of responding caregivers; transcripts wer…

  • A Different Light

    Open Access•Kelly, Susan E Kelly•ARTICLE•Journal of Contemporary Ethnography•2005•Citada por: 9•Referências: 23

    This article explores narratives of parenting a child with impairments for insight into impairment as both a materially and socially meaningful phenomenon. Drawing from in-depth interviews with parents, a narrative approach is employed to explore the ambiguities of human impairment and embodiment as experienced by an intimate other. Parents'stories illustrate impairment as an intersubjective and intercorporeal accomplishment and illustrate multip…

  • Toward an Epistemological Luddism of Bioethics

    Open Access•Kelly, Susan E Kelly•ARTICLE•Science & Technology Studies•2006

    In the decades since its emergence, bioethics has become successfully integrated, institutionally and culturally, into contemporary processes of biotechnological production. Its success is in large part the result of the development within American bioethics of a strong principlist form that has had considerable influence on bioethics developments regarding biotechnology governance internationally. This article presents a critique of bioethics, d…

  • Choosing not to choose

    Open Access•Kelly, Susan E Kelly•ARTICLE•Sociology of Health & Illness•2008•Citada por: 26•Referências: 7

    Parents of children with genetic conditions or impairments stand in a unique position with regard to choices and dilemmas posed by prenatal screening and testing options offered to at‐risk parents as a means to a ‘healthy’ baby. This article reports the results of a qualitative study of parents whose children are clients of a state‐wide rural genetic outreach programme in the US. The analysis seeks to connect the lived experience of parents of ch…

  • Qualitative Interviewing Techniques and Styles

    Kelly, Susan E Kelly•CHAPTER•The SAGE Handbook of Qualitative…•2010

  • Looking beyond risk

    Ginny Russell, Kelly et al.•ARTICLE•Health Risk & Society•2011

    Davison, Frankel, and Davey Smith (1989 Davison, C., Frankel, S. and Davey Smith, G. 1989. Inheriting heart trouble: The relevance of common-sense ideas to preventive measures. Health Education Research, 4(3): 329–340. [Crossref] , [Google Scholar]) conceptualised lay epidemiology as the process of interpreting health risks through considering non-traditional sources of information drawn from personal networks and from the public arena. We analys…

  • Assisting Reproduction, Testing Genes

    Open Access•Kelly, Susan E Kelly•ARTICLE•Sociology of Health & Illness•2011

    Birenbaum-Carmeli, D. and Inhorn, M.C. ( eds ) Assisting Reproduction, Testing Genes: Global Encounters with New Biotechnologies . New York : Berghahn Books , 2009 , 304 pp £55 (hbk ) ISBN 978-1-84545-625-2 . Assisted reproductive technologies (ARTs) have proliferated as new biotechnologies and spread widely across the globe. ARTs now include a host of technologies beyond in vitro fertilisation and directed toward different contexts of infertilit…

  • The Maternal–Foetal Interface and Gestational Chimerism

    Kelly, Susan Elizabeth Kelly•ARTICLE•Science as Culture•2012•Citada por: 9•Referências: 5

    The science of gestational cell transfer—research into the transfer of cells between a pregnant woman and foetus during gestation—and subsequent mingling of transferred cells, or microchimerism, is bringing new attention to the maternal/foetal interface. These findings challenge previous biological understandings of a barrier between the body of a pregnant woman and developing foetus, a barrier maintaining the identity integrity as it were, of tw…

  • The Gift of Spit (And the Obligation to Return It)

    Anna Harris, Sally Wyatt et al.•ARTICLE•Information Communication & Society•2012•Citada por: 26•Referências: 12

    People can now send a sample of their saliva to an internet-based company in order to discover genetic information about themselves. Entering this 'direct-to-consumer' genetic testing (DTC GT) marketplace can result in enticement to engage in various forms of 'participatory' practices, such as taking part in genetic research. In this article, we analyse the research activities of one of the largest and best-known DTC GT companies, 23andMe. 23andM…

  • Diagnosis as a social determinant

    Open Access•Ginny Russell, Kelly et al.•ARTICLE•Social Science & Medicine•2012•Citada por: 4•Referências: 47

  • Public viewpoints on new non-invasive prenatal genetic tests

    Open Access•Hannah Farrimond, Hannah R Farrimond et al.•ARTICLE•Public Understanding of Science•2013

    Prenatal screening programmes have been critiqued for their routine implementation according to clinical rationale without public debate. A new approach, non-invasive prenatal diagnosis (NIPD), promises diagnosis of fetal genetic disorders from a sample of maternal blood without the miscarriage risk of current invasive prenatal tests (e.g. amniocentesis). Little research has investigated the attitudes of wider publics to NIPD. This study used Q-m…

  • But that was my idea!’ Problems of Authorship and Validation in Contemporary Practices of Creative Dissent

    Kelly, Susan Kelly•ARTICLE•Parallax•2013

Sociology (19 obras) · Political science (16 obras) · Law (13 obras) · Psychology (11 obras) · Law (9 obras) · Medicine (9 obras) · History (8 obras) · Philosophy (8 obras) · Epistemology (7 obras) · Philosophy (6 obras)

Ethnos_APP • Projeto Open Source • Licença MIT • Frontend v2.0.0 • Privacidade e Cookies • Documentação da API: api.ethnos.app/docs • Código da API: GitHub • DOI: 10.5281/zenodo.17049435 • Código do Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae