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Wendy Lipworth

Dados Biográficos

ID197626
NOMEWendy Lipworth
PRENOMESWendy
SOBRENOMELipworth
ASSINATURALIPWORTH W
AFILIAÇÕESThe University of Sydney
ORCID0000-0002-0234-657X
VERIFICADOSim
TOTAL DE OBRAS27
TOTAL DE CITAÇÕES20
TOTAL COMO AUTOR27
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2010
ANO MAIS RECENTE DE PUBLICAÇÃO2026
ÍNDICE H3
  • Evolution or erosion? Promissory discourses in ‘accelerated’ regulatory approval of health technologies

    Open Access•Sara Attinger, Ian Kerridge et al.•ARTICLE•BioSocieties•2026

    In recent years, regulatory processes governing the approval of new health technologies have undergone changes aimed at expediting access. Some of these changes involve the adaptation of established standards of evidence for safety and efficacy, which we refer to as evidence-adapted regulatory pathways (EARPs). While EARPs have provided more timely access to potentially beneficial interventions, critics argue that reducing evidentiary thresholds …

  • Stakeholder perspectives regarding single participant research in oncology

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Research Ethics•2026

    The term ‘N-of-1 trial’ has traditionally referred to a specific, well-defined, clinical trial methodology, involving evaluation of an intervention (or interventions) in a single individual, with alternating periods ‘on’ and ‘off’ an intervention. Given methodological constraints, such trials are best suited to the study of chronic, stable conditions, and so have had a limited role in progressive conditions like cancer. According to evidence-base…

  • The ‘power of 1’

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Research Ethics•2026

    Conduct of clinical research involving single patient subjects has a relatively long history. The notion of ‘N-of-1 trials’ first emerged in the 1980s, introducing a method for evaluating the impact of alternately exposing individuals ‘on’ and ‘off’ a particular treatment. In the years since, interest in conventional, randomised, ‘N-of-1 trials’ has fluctuated, though recent advancements in data science, remote monitoring technologies and, more b…

  • Understanding “interests”

    Open Access•Miriam Wiersma, Ian Kerridge et al.•ARTICLE•Medicine Health Care and Philosophy•2025

    Conflicts of interest are widely regarded as being morally, socially, and scientifically problematic in the many sectors, including in the health sector. There has been considerable attention paid to managing conflicts of interest in clinical practice, medical research and health policy through strategies such as recusal, disinvestment, and disclosure. While these efforts have been important, they are often based on a superficial account of “inte…

  • Subconscious value influences on science

    Open Access•Kevin C Elliott, David B Resnik et al.•ARTICLE•Studies in History and Philosophy…•2025•Referências: 84

    Philosophical scholarship on science and values has gradually shifted away from asking whether values have any legitimate role to play in scientific judgment and decision-making and toward considering how to responsibly manage value influences to protect the integrity, rigor, reliability, and trustworthiness of science. This scholarship has focused primarily on helping individual scientists deal with cases in which they are aware of the values at…

  • What moral weight should patient‐led demand have in clinical decisions about assisted reproductive technologies

    Open Access•Melanie R Anderson, Craig Stanbury et al.•ARTICLE•Bioethics•2024

    Evidence suggests that one reason doctors provide certain interventions in assisted reproductive technologies (ART) is because of patient demand. This is particularly the case when it comes to unproven interventions such as ‘add‐ons’ to in vitro fertilisation (IVF) cycles, or providing IVF cycles that are highly unlikely to succeed. Doctors tend to accede to demands for such interventions because patients are willing to do and pay ‘whatever it ta…

  • Therapeutic misunderstandings in modern research

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Bioethics•2024

    Clinical trials play a crucial role in generating evidence about healthcare interventions and improving outcomes for current and future patients. For individual trial participants, however, there are inevitably trade‐offs involved in clinical trial participation, given that trials have traditionally been designed to benefit future patient populations rather than to offer personalised care. Failure to understand the distinction between research an…

  • Clinical innovation ethics frameworks

    Open Access•Miriam Wiersma, Ian Kerridge et al.•ARTICLE•Health Policy•2023

  • Hope and Exploitation in Commercial Provision of Assisted Reproductive Technologies

    Open Access•Anthony Wrigley, Gabriel Watts et al.•ARTICLE•The Hastings Center Report•2023

    Innovation is a key driver of care provision in assisted reproductive technologies (ART). ART providers offer a range of add‐on interventions, aiming to augment standard in vitro fertilization protocols and improve the chances of a live birth. Particularly in the context of commercial provision, an ever‐increasing array of add‐ons are marketed to ART patients, even when evidence to support them is equivocal. A defining feature of ART is hope—hope…

  • The silent world of assisted reproduction

    Open Access•Louis Taffs, Ian Kerridge et al.•ARTICLE•Health Expectations•2023

    CONTEXT: In vitro fertilisation (IVF) is now a common assisted reproductive technology (ART) procedure globally, with 8 million children alive today having been conceived utilising IVF. For many patients, IVF is a difficult experience with many discontinuing treatment because of emotional, relationship and financial stress, or intolerable physical side effects of hormone treatments. DESIGN AND PARTICIPANTS: A qualitative study, in which 31 profes…

  • Are my religious beliefs anyone’s business? A framework for declarations in health and biomedicine

    Narcyz Ghinea, Miriam Wiersma et al.•ARTICLE•Journal of Medical Ethics•2021

    Conflicts of interests (COI) are typically divided into those that are financial and those that are not. While there is general agreement that financial COIs have a significant impact on decisions and need to be declared and managed, the status of non-financial COIs continues to be disputed. In a recent BMJ feature article it was proposed that religious beliefs should be routinely declared as an interest. The article generated over 41 responses f…

  • A survey of Australian public attitudes towards funding of high cost cancer medicines

    Open Access•Narcyz Ghinea, Christine Critchley et al.•ARTICLE•Health Policy•2021

  • Against the use and publication of contemporary unethical research

    Open Access•Wendy C Higgins, William Rogers et al.•ARTICLE•Journal of Medical Ethics•2020

    Recent calls for retraction of a large body of Chinese transplant research and of Dr Jiankui He’s gene editing research has led to renewed interest in the question of publication, retraction and use of unethical biomedical research. In Part 1 of this paper, we briefly review the now well-established consequentialist and deontological arguments for and against the use of unethical research. We argue that, while there are potentially compelling jus…

  • Responding to unethical research

    William Rogers, Wendy C Higgins et al.•ARTICLE•Journal of Medical Ethics•2020

    We thank Goldstein and Peterson, Caplan, and Bramstedt for engaging with our paper on the ethics of publishing and using Chinese transplant research that involves organs procured from executed prisoners.1–4 In that paper, we examine consequentialist and deontological arguments for and against using data from unethical research. Goldstein and Peterson question the relationship between the social and scientific value of the research and the decisio…

  • Examining diversity in public willingness to participate in offshore human biobanking

    Open Access•Christine Critchley, Miriam Wiersma et al.•ARTICLE•Public Understanding of Science•2020

    To ensure their sustainability and scientific utility, human biobanks are networking internationally. Sharing biospecimens and associated data across jurisdictions raise a number of practical, ethical, legal and social challenges that could reduce the publics’ willingness to donate their much needed tissue for research purposes. This research aims to identify the impact of biobank location on willingness to donate through a national quantitative …

  • Limiting religious contributions – a response to Schuklenk

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Developing World Bioethics•2019

  • Treat them into the grave

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Sociology of Health & Illness•2019•Citada por: 2•Referências: 55

    The prescribing of high-cost cancer medicines at the end of life has become a focus of criticism, due primarily to concerns about the safety, efficacy and cost-effectiveness of these medicines in this clinical context. In response to these concerns, a number of interventions have been proposed - frequently focused on improving physician-patient communication at the end of life. Underpinning these strategies is the assumption that the prescribing …

  • Conflicted hope

    C Mayes, Jane Williams et al.•ARTICLE•Health Sociology Review•2018•Citada por: 1•Referências: 30

    Over the past decade ‘social egg freezing’ has emerged as a technology of hope that purports to empower women by enabling them to continue their careers or find the right partner without the fear of jeopardising their fertility. This technology has been promoted and celebrated by fertility companies, bioethicists, clinicians, and multi-national corporations such as Apple and Facebook. While critical questions have been raised, they tend to focus …

  • Conflicts of interest in neoliberal times

    C Mayes, Ian Kerridge et al.•ARTICLE•Health Sociology Review•2016•Referências: 44

    In this paper we report on the findings from six focus groups conducted with Australian medical students. The focus groups discussed students’ perceptions of conflicts of interest and the influence of commercial values in health care and medical education. Our research revealed that students were aware of a number of structural influences that affected the medical education they received and that had the potential to shape their attitudes and pra…

  • Overcoming Entrenched Disagreements

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•Developing World Bioethics•2015

    The debate about whether misoprostol should be distributed to low resource communities to prevent post‐partum haemorrhage ( PPH ), recognised as a major cause of maternal mortality, is deeply polarised. This is in spite of stakeholders having access to the same evidence about the risks and benefits of misoprostol. To understand the disagreement, we conducted a qualitative analysis of the values underpinning debates surrounding community distribut…

  • Ethics & Evidence in Medical Debates

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•The Hastings Center Report•2014

    While ethics and evidence‐based medicine are often viewed as separate domains of inquiry and practice, what we know influences what we can ethically justify doing, and what we see as our moral obligations shapes the way we interpret evidence. The boundaries between the moral and epistemic spheres become particularly blurred when the health of people is at stake and even more so when no “officially” recommended medical intervention is available to…

  • Rules of engagement

    Open Access•Bronwen Morrell, Rowena Forsyth et al.•ARTICLE•Journalism•2014•Citada por: 6•Referências: 18

    Health-related industries use a variety of methods to influence health news, including the formation and maintenance of direct relationships with journalists. These interactions have the potential to subvert news reporting such that it comes to serve the interests of industry in promoting their products, rather than the public interest in critical and accurate news and information. Here, we report the findings of qualitative interviews conducted …

  • Tissue donation to biobanks

    Open Access•Wendy Lipworth, Claudio Corvino et al.•ARTICLE•Sociology of Health & Illness•2011

    Collections of human tissue (biobanks) are thought to be an essential resource for biomedical research. Biobanks have, however, been a source of debate in both bioethics and sociology. In recent years this theorising has been supplemented with empirical research, including a significant body of qualitative research, into donors’ experiences and attitudes. To date, this literature has not been synthesised. We report the findings of a review of qua…

  • Journal peer review in context

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Citada por: 4•Referências: 3

  • Balance, Balancing, and Health

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•Citada por: 7•Referências: 48

    In this article we explore the concept of balance in the context of health. We became interested in balance during a grounded theory study of lay conceptualizations of cancer risk in which participants were concerned with having a good life, which relied heavily on balancing processes. This led us to the qualitative literature about balance in the context of health, which was large and in need of synthesis. We identified 170 relevant studies and …

Próximo
  • Balance, Balancing, and Health

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•Citada por: 7•Referências: 48

    In this article we explore the concept of balance in the context of health. We became interested in balance during a grounded theory study of lay conceptualizations of cancer risk in which participants were concerned with having a good life, which relied heavily on balancing processes. This led us to the qualitative literature about balance in the context of health, which was large and in need of synthesis. We identified 170 relevant studies and …

  • Rules of engagement

    Open Access•Bronwen Morrell, Rowena Forsyth et al.•ARTICLE•Journalism•2014•Citada por: 6•Referências: 18

    Health-related industries use a variety of methods to influence health news, including the formation and maintenance of direct relationships with journalists. These interactions have the potential to subvert news reporting such that it comes to serve the interests of industry in promoting their products, rather than the public interest in critical and accurate news and information. Here, we report the findings of qualitative interviews conducted …

  • Journal peer review in context

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Citada por: 4•Referências: 3

  • Treat them into the grave

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Sociology of Health & Illness•2019•Citada por: 2•Referências: 55

    The prescribing of high-cost cancer medicines at the end of life has become a focus of criticism, due primarily to concerns about the safety, efficacy and cost-effectiveness of these medicines in this clinical context. In response to these concerns, a number of interventions have been proposed - frequently focused on improving physician-patient communication at the end of life. Underpinning these strategies is the assumption that the prescribing …

  • Conflicted hope

    C Mayes, Jane Williams et al.•ARTICLE•Health Sociology Review•2018•Citada por: 1•Referências: 30

    Over the past decade ‘social egg freezing’ has emerged as a technology of hope that purports to empower women by enabling them to continue their careers or find the right partner without the fear of jeopardising their fertility. This technology has been promoted and celebrated by fertility companies, bioethicists, clinicians, and multi-national corporations such as Apple and Facebook. While critical questions have been raised, they tend to focus …

  • Beliefs and beyond

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Health Expectations•2010

    Background Clinicians and public health professionals are centrally concerned with mediating risk. However, people often resist the risk‐related information that is communicated to them by experts, or have their own models of risk that conflict with expert views. Quantitative studies have clearly demonstrated the importance of health beliefs and various cognitive and emotional processes in shaping risk perception. More recently, a growing body of…

  • Tissue donation to biobanks

    Open Access•Wendy Lipworth, Claudio Corvino et al.•ARTICLE•Sociology of Health & Illness•2011

    Collections of human tissue (biobanks) are thought to be an essential resource for biomedical research. Biobanks have, however, been a source of debate in both bioethics and sociology. In recent years this theorising has been supplemented with empirical research, including a significant body of qualitative research, into donors’ experiences and attitudes. To date, this literature has not been synthesised. We report the findings of a review of qua…

  • Journal peer review in context

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Citada por: 4•Referências: 3

  • Balance, Balancing, and Health

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•Citada por: 7•Referências: 48

    In this article we explore the concept of balance in the context of health. We became interested in balance during a grounded theory study of lay conceptualizations of cancer risk in which participants were concerned with having a good life, which relied heavily on balancing processes. This led us to the qualitative literature about balance in the context of health, which was large and in need of synthesis. We identified 170 relevant studies and …

  • Cancer as Rubbish

    Open Access•Bronwen Morrell, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•Referências: 37

    Tissue banking (or biobanking), thought by many to be an essential form of medical research, has raised a number of ethical issues that highlight a need to understand the beliefs and values of tissue donors, including the motivations underlying consent or refusal to donate. Data from our qualitative study of the legal, social, and ethical issues surrounding tumor banking in New South Wales, Australia, show that participants' attitudes to donation…

  • Ethics & Evidence in Medical Debates

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•The Hastings Center Report•2014

    While ethics and evidence‐based medicine are often viewed as separate domains of inquiry and practice, what we know influences what we can ethically justify doing, and what we see as our moral obligations shapes the way we interpret evidence. The boundaries between the moral and epistemic spheres become particularly blurred when the health of people is at stake and even more so when no “officially” recommended medical intervention is available to…

  • Rules of engagement

    Open Access•Bronwen Morrell, Rowena Forsyth et al.•ARTICLE•Journalism•2014•Citada por: 6•Referências: 18

    Health-related industries use a variety of methods to influence health news, including the formation and maintenance of direct relationships with journalists. These interactions have the potential to subvert news reporting such that it comes to serve the interests of industry in promoting their products, rather than the public interest in critical and accurate news and information. Here, we report the findings of qualitative interviews conducted …

  • Overcoming Entrenched Disagreements

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•Developing World Bioethics•2015

    The debate about whether misoprostol should be distributed to low resource communities to prevent post‐partum haemorrhage ( PPH ), recognised as a major cause of maternal mortality, is deeply polarised. This is in spite of stakeholders having access to the same evidence about the risks and benefits of misoprostol. To understand the disagreement, we conducted a qualitative analysis of the values underpinning debates surrounding community distribut…

  • Conflicts of interest in neoliberal times

    C Mayes, Ian Kerridge et al.•ARTICLE•Health Sociology Review•2016•Referências: 44

    In this paper we report on the findings from six focus groups conducted with Australian medical students. The focus groups discussed students’ perceptions of conflicts of interest and the influence of commercial values in health care and medical education. Our research revealed that students were aware of a number of structural influences that affected the medical education they received and that had the potential to shape their attitudes and pra…

  • Conflicted hope

    C Mayes, Jane Williams et al.•ARTICLE•Health Sociology Review•2018•Citada por: 1•Referências: 30

    Over the past decade ‘social egg freezing’ has emerged as a technology of hope that purports to empower women by enabling them to continue their careers or find the right partner without the fear of jeopardising their fertility. This technology has been promoted and celebrated by fertility companies, bioethicists, clinicians, and multi-national corporations such as Apple and Facebook. While critical questions have been raised, they tend to focus …

  • Limiting religious contributions – a response to Schuklenk

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Developing World Bioethics•2019

  • Treat them into the grave

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Sociology of Health & Illness•2019•Citada por: 2•Referências: 55

    The prescribing of high-cost cancer medicines at the end of life has become a focus of criticism, due primarily to concerns about the safety, efficacy and cost-effectiveness of these medicines in this clinical context. In response to these concerns, a number of interventions have been proposed - frequently focused on improving physician-patient communication at the end of life. Underpinning these strategies is the assumption that the prescribing …

  • Against the use and publication of contemporary unethical research

    Open Access•Wendy C Higgins, William Rogers et al.•ARTICLE•Journal of Medical Ethics•2020

    Recent calls for retraction of a large body of Chinese transplant research and of Dr Jiankui He’s gene editing research has led to renewed interest in the question of publication, retraction and use of unethical biomedical research. In Part 1 of this paper, we briefly review the now well-established consequentialist and deontological arguments for and against the use of unethical research. We argue that, while there are potentially compelling jus…

  • Responding to unethical research

    William Rogers, Wendy C Higgins et al.•ARTICLE•Journal of Medical Ethics•2020

    We thank Goldstein and Peterson, Caplan, and Bramstedt for engaging with our paper on the ethics of publishing and using Chinese transplant research that involves organs procured from executed prisoners.1–4 In that paper, we examine consequentialist and deontological arguments for and against using data from unethical research. Goldstein and Peterson question the relationship between the social and scientific value of the research and the decisio…

  • Examining diversity in public willingness to participate in offshore human biobanking

    Open Access•Christine Critchley, Miriam Wiersma et al.•ARTICLE•Public Understanding of Science•2020

    To ensure their sustainability and scientific utility, human biobanks are networking internationally. Sharing biospecimens and associated data across jurisdictions raise a number of practical, ethical, legal and social challenges that could reduce the publics’ willingness to donate their much needed tissue for research purposes. This research aims to identify the impact of biobank location on willingness to donate through a national quantitative …

  • Are my religious beliefs anyone’s business? A framework for declarations in health and biomedicine

    Narcyz Ghinea, Miriam Wiersma et al.•ARTICLE•Journal of Medical Ethics•2021

    Conflicts of interests (COI) are typically divided into those that are financial and those that are not. While there is general agreement that financial COIs have a significant impact on decisions and need to be declared and managed, the status of non-financial COIs continues to be disputed. In a recent BMJ feature article it was proposed that religious beliefs should be routinely declared as an interest. The article generated over 41 responses f…

  • A survey of Australian public attitudes towards funding of high cost cancer medicines

    Open Access•Narcyz Ghinea, Christine Critchley et al.•ARTICLE•Health Policy•2021

  • Clinical innovation ethics frameworks

    Open Access•Miriam Wiersma, Ian Kerridge et al.•ARTICLE•Health Policy•2023

  • Hope and Exploitation in Commercial Provision of Assisted Reproductive Technologies

    Open Access•Anthony Wrigley, Gabriel Watts et al.•ARTICLE•The Hastings Center Report•2023

    Innovation is a key driver of care provision in assisted reproductive technologies (ART). ART providers offer a range of add‐on interventions, aiming to augment standard in vitro fertilization protocols and improve the chances of a live birth. Particularly in the context of commercial provision, an ever‐increasing array of add‐ons are marketed to ART patients, even when evidence to support them is equivocal. A defining feature of ART is hope—hope…

  • The silent world of assisted reproduction

    Open Access•Louis Taffs, Ian Kerridge et al.•ARTICLE•Health Expectations•2023

    CONTEXT: In vitro fertilisation (IVF) is now a common assisted reproductive technology (ART) procedure globally, with 8 million children alive today having been conceived utilising IVF. For many patients, IVF is a difficult experience with many discontinuing treatment because of emotional, relationship and financial stress, or intolerable physical side effects of hormone treatments. DESIGN AND PARTICIPANTS: A qualitative study, in which 31 profes…

  • What moral weight should patient‐led demand have in clinical decisions about assisted reproductive technologies

    Open Access•Melanie R Anderson, Craig Stanbury et al.•ARTICLE•Bioethics•2024

    Evidence suggests that one reason doctors provide certain interventions in assisted reproductive technologies (ART) is because of patient demand. This is particularly the case when it comes to unproven interventions such as ‘add‐ons’ to in vitro fertilisation (IVF) cycles, or providing IVF cycles that are highly unlikely to succeed. Doctors tend to accede to demands for such interventions because patients are willing to do and pay ‘whatever it ta…

  • Therapeutic misunderstandings in modern research

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Bioethics•2024

    Clinical trials play a crucial role in generating evidence about healthcare interventions and improving outcomes for current and future patients. For individual trial participants, however, there are inevitably trade‐offs involved in clinical trial participation, given that trials have traditionally been designed to benefit future patient populations rather than to offer personalised care. Failure to understand the distinction between research an…

  • Understanding “interests”

    Open Access•Miriam Wiersma, Ian Kerridge et al.•ARTICLE•Medicine Health Care and Philosophy•2025

    Conflicts of interest are widely regarded as being morally, socially, and scientifically problematic in the many sectors, including in the health sector. There has been considerable attention paid to managing conflicts of interest in clinical practice, medical research and health policy through strategies such as recusal, disinvestment, and disclosure. While these efforts have been important, they are often based on a superficial account of “inte…

  • Subconscious value influences on science

    Open Access•Kevin C Elliott, David B Resnik et al.•ARTICLE•Studies in History and Philosophy…•2025•Referências: 84

    Philosophical scholarship on science and values has gradually shifted away from asking whether values have any legitimate role to play in scientific judgment and decision-making and toward considering how to responsibly manage value influences to protect the integrity, rigor, reliability, and trustworthiness of science. This scholarship has focused primarily on helping individual scientists deal with cases in which they are aware of the values at…

  • Evolution or erosion? Promissory discourses in ‘accelerated’ regulatory approval of health technologies

    Open Access•Sara Attinger, Ian Kerridge et al.•ARTICLE•BioSocieties•2026

    In recent years, regulatory processes governing the approval of new health technologies have undergone changes aimed at expediting access. Some of these changes involve the adaptation of established standards of evidence for safety and efficacy, which we refer to as evidence-adapted regulatory pathways (EARPs). While EARPs have provided more timely access to potentially beneficial interventions, critics argue that reducing evidentiary thresholds …

Political science (16 obras) · Medicine (13 obras) · Sociology (12 obras) · Psychology (11 obras) · Law (10 obras) · Public relations (10 obras) · Ethics in Clinical Research (8 obras) · Engineering ethics (6 obras) · Qualitative research (6 obras) · Social Psychology (6 obras)

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