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Author Details
Full Name
Ainsley J Newson
Affiliation
Sydney Health Ethics, Sydney School of Public Health, The University of Sydney
ORCID
Career Start Year
1997
Papers
120
H Index
20
Expertise
CM4AI Collaborator
Vardit Ravitsky (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37929870
What moral weight should patient-led demand have in clinical decisions about assisted reproductive technologies?
Bioethics
2024
36065020
Views of the Australian public on the delivery of risk-stratified cancer screening in the population: a qualitative study.
Public Health Res Pract
2023
37963135
Hope and Exploitation in Commercial Provision of Assisted Reproductive Technologies.
Hastings Cent Rep
2023
37802639
Reconsidering reinterpretation: response to commentaries.
J Med Ethics
2023
37640686
Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia - CORRIGENDUM.
Twin Res Hum Genet
2023
36950972
Human Genetics Society of Australasia Position Statement: Use of Polygenic Scores in Clinical Practice and Population Health.
Twin Res Hum Genet
2023
37454281
What's in a name? Justifying terminology for genomic findings beyond the initial test indication: A scoping review.
Genet Med
2023
37415831
Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?
Pharmgenomics Pers Med
2023
37208157
Is there a duty to routinely reinterpret genomic variant classifications?
J Med Ethics
2023
37171853
Is It Just for a Screening Program to Give People All the Information They Want?
Am J Bioeth
2023
37226803
Human Genetics Society of Australasia Position Statement: Genetic Carrier Testing for Recessive Conditions.
Twin Res Hum Genet
2023
36919553
Consistency of What? Appropriately Contextualizing Ethical Analysis of Non-Invasive Prenatal Testing.
Am J Bioeth
2023
36744627
How should severity be understood in the context of reproductive genetic carrier screening?
Bioethics
2023
36868206
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Am J Hum Genet
2023
34244346
Reproductive carrier screening: responding to the eugenics critique.
J Med Ethics
2022
35581418
Ethically robust reproductive genetic carrier screening needs to measure outcomes that matter to patients.
Eur J Hum Genet
2022
35538635
Clinician views and experiences of non-invasive prenatal genetic screening tests in Australia.
Aust N Z J Obstet Gynaecol
2022
36478695
Situating commercialization of assisted reproduction in its socio-political context: a critical interpretive synthesis.
Hum Reprod Open
2022
36579509
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
J Pers Med
2022
36294843
Motivations and Barriers to Participation in a Randomized Trial on Melanoma Genomic Risk: A Mixed-Methods Analysis.
J Pers Med
2022
33715055
The promise of public health ethics for precision medicine: the case of newborn preventive genomic sequencing.
Hum Genet
2022
33855648
"I wish that there was more info": characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variants.
Fam Cancer
2022
35224577
Ethical aspects of the changing landscape for spinal muscular atrophy management in Australia.
Aust J Gen Pract
2022
35277654
Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting.
Eur J Hum Genet
2022
35089837
Intertwined Interests in Expanded Prenatal Genetic Testing: The State's Role in Facilitating Equitable Access.
Am J Bioeth
2022
35168887
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et al.
Genet Med
2022
34426854
Ethical considerations in gene selection for reproductive carrier screening.
Hum Genet
2022
34782753
Taking seriousness seriously in genomic health.
Eur J Hum Genet
2022
34725472
Development and use of the Australian reproductive genetic carrier screening decision aid.
Eur J Hum Genet
2022
32981044
Ethical issues in reproductive genetic carrier screening.
Med J Aust
2021
33848430
The Emergence and Global Spread of Noninvasive Prenatal Testing.
Annu Rev Genomics Hum Genet
2021
33635607
The expectations and realities of nutrigenomic testing in australia: A qualitative study.
Health Expect
2021
35074040
Human Genetics Society of Australasia Position Statement: Use of Human Genetic and Genomic Information in Healthcare Settings.
Twin Res Hum Genet
2021
34650621
Ethics of Reproductive Genetic Carrier Screening: From the Clinic to the Population.
Public Health Ethics
2021
34415629
To offer or request? Disclosing variants of uncertain significance in prenatal testing.
Bioethics
2021
34385669
Impact of personal genomic risk information on melanoma prevention behaviors and psychological outcomes: a randomized controlled trial.
Genet Med
2021
34216141
Knowledge, views and expectations for cancer polygenic risk testing in clinical practice: A cross-sectional survey of health professionals.
Clin Genet
2021
34196500
Enrolling Children in Clinical Trials for Genetic Neurodevelopmental Conditions: Ethics, Parental Decisions, and Children's Identities.
Ethics Hum Res
2021
33974726
Acceptability of risk-stratified population screening across cancer types: Qualitative interviews with the Australian public.
Health Expect
2021
33129629
Family communication about genomic sequencing: A qualitative study with cancer patients and relatives.
Patient Educ Couns
2021
32934111
The perils of a broad approach to public interest in health data research: a response to Ballantyne and Schaefer.
J Med Ethics
2021
32678339
Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission").
Eur J Hum Genet
2021
32350032
Obligations and preferences in knowing and not knowing: the importance of context.
J Med Ethics
2020
31674008
Who should access germline genome sequencing? A mixed methods study of patient views.
Clin Genet
2020
32019532
Disclosure to genetic relatives without consent - Australian genetic professionals' awareness of the health privacy law.
BMC Med Ethics
2020
31980566
Cancer patients' views and understanding of genome sequencing: a qualitative study.
J Med Genet
2020
31885332
From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing.
AJOB Empir Bioeth
2020
33213433
"Who is watching the watchdog?": ethical perspectives of sharing health-related data for precision medicine in Singapore.
BMC Med Ethics
2020
32635964
Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.
Twin Res Hum Genet
2020
32600382
Implementation considerations for offering personal genomic risk information to the public: a qualitative study.
BMC Public Health
2020
1 - 50 of 120
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