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List of works by Ainsley J Newson

"What should happen before asymptomatic men decide whether or not to have a PSA test?" A report on three community juries

scientific article published in October 2015

'There is a lot of good in knowing, but there is also a lot of downs': public views on ethical considerations in population genomic screening

scientific article published on 20 May 2020

A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public

scientific article published on 4 October 2016

Australians' knowledge and perceptions of direct-to-consumer personal genome testing

article

Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study

scientific article published on 13 November 2018

Australians' views and experience of personal genomic testing: survey findings from the Genioz study

scientific article published on 21 January 2019

Australians' views on personal genomic testing: focus group findings from the Genioz study

article

Behavioural genetics: why eugenic selection is preferable to enhancement

scientific article published on January 2006

Cascade testing in familial hypercholesterolaemia: how should family members be contacted?

scientific article

Childhood genetic testing for familial cancer: should adoption make a difference?

scientific article

Clinical Genetics and the Problem With Unqualified Confidentiality

article

Commentary: Consent and confidentiality in publishing--the view of the BMJ's ethics committee

scientific article published on 8 September 2008

Compensated transnational surrogacy in Australia: time for a comprehensive review

scientific article

Consent to the publication of patient information: incompetent patients may pose a problem

scientific article published on October 2004

Current Ethical Issues in Synthetic Biology: Where Should We Go from Here? ⬇️

scientific article published on May 1, 2011

Depression under stress: ethical issues in genetic testing

scientific article published in September 2009

Distress, uncertainty, and positive experiences associated with receiving information on personal genomic risk of melanoma

scientific article published in 2018

Do We Need Ethical Theory to Achieve Quality Critical Engagement in Clinical Ethics?

scientific article

Does personalized melanoma genomic risk information trigger conversations about skin cancer prevention and skin examination with family, friends and health professionals?

scientific article published on 19 June 2017

Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challenges

scientific article

Ethical and legal issues in mitochondrial transfer

scientific article published on 21 April 2016

Ethical aspects arising from non-invasive fetal diagnosis

scientific article published on April 2008

Ethical considerations for choosing between possible models for using NIPD for aneuploidy detection

article

Ethical issues in reproductive genetic carrier screening

scientific article published on 27 September 2020

Exploring the Potential Emotional and Behavioural Impact of Providing Personalised Genomic Risk Information to the Public: A Focus Group Study

scientific article published on 22 September 2015

Family communication about genomic sequencing: A qualitative study with cancer patients and relatives

scientific article published on 20 October 2020

For your interest? The ethical acceptability of using non-invasive prenatal testing to test 'purely for information'.

scientific article published on January 2015

From Chance to Choice: Genetics and Justice.

scientific article published in February 2002

From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing

scientific article published on 30 December 2019

Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")

scientific article published on 16 July 2020

Gene structure and sequence analysis of mouse centromere proteins A and C.

scientific article published in January 1998

Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study

scientific article published on 11 February 2019

Genetics and Insurance in Australia: Concerns around a Self-Regulated Industry

scientific article published on 26 October 2017

Genomic Testing in The Paediatric Population: Ethical Considerations in Light of Recent Policy Statements

scientific article published on June 2016

Genomic intensive care: should we perform genome testing in critically ill newborns?

scientific article

Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia

scientific article published on 21 November 2018

Informed choice in prenatal testing: a survey among obstetricians and gynaecologists in Europe and Asia

article

Is Mitochondrial Donation Germ-Line Gene Therapy? Classifications and Ethical Implications

scientific article published in January 2017

Is informed choice in prenatal testing universally valued? A population-based survey in Europe and Asia.

scientific article published on 15 April 2009

Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic.

scientific article published on 25 September 2017

Known unknowns: building an ethics of uncertainty into genomic medicine

scientific article

Obligations and preferences in knowing and not knowing: the importance of context

scientific article published on 29 April 2020

Partially functional Cenpa-GFP fusion protein causes increased chromosome missegregation and apoptosis during mouse embryogenesis

scientific article published on 01 January 2003

Patient perspectives on molecular tumor profiling: "Why wouldn't you?"

scientific article published on 31 July 2019

Personal Genomics as an Interactive Web Broadcast

scientific article published on 01 January 2009

Prenatal diagnosis and abortion for congenital abnormalities: is it ethical to provide one without the other?

scientific article published in August 2009

Public attitudes towards novel reproductive technologies: a citizens’ jury on mitochondrial donation

scientific article published on 01 April 2019

Public preferences for communicating personal genomic risk information: a focus group study

scientific article

Rapid Challenges: Ethics and Genomic Neonatal Intensive Care

scientific article published on 01 January 2019

Reconceptualizing Autonomy for Bioethics

scholarly article by Lisa Dive et al published 2018 in Kennedy Institute of Ethics Journal

Reforming research ethics committees

scientific article published on September 2005

Regulating Risk and the Boundaries of State Conduct: A Relational Perspective on Home Birth in Australia

article

Response to open peer commentaries on "Prenatal diagnosis and abortion for congenital abnormalities: is it ethical to provide one without the other?".

scientific article published in August 2009

Rethinking pediatric ethics consultations

scientific article published in January 2015

Scanning the body, sequencing the genome: Dealing with unsolicited findings

scientific article published on 4 October 2017

Sharing precision medicine data with private industry: Outcomes of a citizens’ jury in Singapore

scientific article published in 2022

Should non-invasiveness change informed consent procedures for prenatal diagnosis?

scientific article

Should parental refusals of newborn screening be respected?

scientific article published in January 2006

Should we undertake genetic research on intelligence?

scientific article

Synthetic Biology for Human Health: Issues for Ethical Discussion and Policy-making

article

Technical Categories and Ethical Justifications: Why Cwik's Approach is the Wrong Way Around for Categorizing Germ-Line Gene Editing

scientific article published on 01 August 2020

The PiGeOn project: protocol for a longitudinal study examining psychosocial, behavioural and ethical issues and outcomes in cancer tumour genomic profiling

scientific article published on 5 April 2018

The PiGeOn project: protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer.

scientific article published on 23 April 2018

The melanoma genomics managing your risk study: A protocol for a randomized controlled trial evaluating the impact of personal genomic risk information on skin cancer prevention behaviors

scientific article published on 23 May 2018

The nature and significance of behavioural genetic information

scientific article published in January 2004

The need for ethics as well as evidence in evidence-based medicine

scientific article published on 31 May 2016

The perils of a broad approach to public interest in health data research: a response to Ballantyne and Schaefer

scientific article published on 15 September 2020

The value of clinical ethics support in Australian health care

scientific article published in June 2015

Whither authenticity?

scientific article published in January 2005

Who should access germline genome sequencing? A mixed methods study of patient views

scientific article published on 26 November 2019

Whole genome sequencing in children: ethics, choice and deliberation

scientific article

Why should ethics approval be required prior to publication of health promotion research?

scientific article published on 9 November 2015

Will the introduction of non-invasive prenatal diagnostic testing erode informed choices? An experimental study of health care professionals

article

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