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

A taxonomy of medical uncertainties in clinical genome sequencing

(2017) Paul K.J. Han et al.   GENETICS IN MEDICINE

A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling

(2017) Barbara A. Athens et al.   Journal of Genetic Counseling

Familial Risk and Heritability of Cancer Among Twins in Nordic Countries

(2016) Lorelei A. Mucci et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Monogenic and polygenic determinants of sarcoma risk: an international genetic study

(2016) Mandy L Ballinger et al.   LANCET ONCOLOGY

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

(2016) Ainsley J. Newson et al.   Molecular Diagnosis & Therapy

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

(2015) Amelia K. Smit et al.   Public Health Genomics

Next-generation sequencing to guide cancer therapy

(2015) Jeffrey Gagan et al.   Genome Medicine

Informed consent for exome sequencing research in families with genetic disease: The emerging issue of incidental findings

(2014) Amanda L. Bergner et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility

(2014) Angela R. Bradbury et al.   GENETICS IN MEDICINE

Guidelines for investigating causality of sequence variants in human disease

(2014) D. G. MacArthur et al.   NATURE

Management of familial cancer: sequencing, surveillance and society

(2014) Nardin Samuel et al.   Nature Reviews Clinical Oncology

Cancer patients acceptance, understanding, and willingness-to-pay for pharmacogenomic testing

(2014) Sinead Cuffe et al.   Pharmacogenetics and Genomics

The Concerns About Recurrence Questionnaire: validation of a brief measure of fear of cancer recurrence amongst Danish and Australian breast cancer survivors

(2014) Belinda Thewes et al.   Journal of Cancer Survivorship

Women’s preferences for selective estrogen reuptake modulators: an investigation using the time trade-off technique

(2014) Angelique F Ralph et al.   SpringerPlus

Perceptions, Knowledge, and Satisfaction With Contralateral Prophylactic Mastectomy Among Young Women With Breast Cancer

(2013) Shoshana M. Rosenberg et al.   ANNALS OF INTERNAL MEDICINE

Lessons from the Cancer Genome

(2013) Levi A. Garraway et al.   CELL

The ‘thousand-dollar genome’: an ethical exploration

(2013) Wybo J Dondorp et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record

(2013) Peter Tarczy-Hornoch et al.   GENETICS IN MEDICINE

Behavioral and psychosocial responses to genomic testing for colorectal cancer risk

(2013) Kristi D. Graves et al.   GENOMICS

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

(2013) J. Savard et al.   INTERNAL MEDICINE JOURNAL

Preventing breast and ovarian cancers in high-risk BRCA1 and BRCA2 mutation carriers

(2013) Ian M Collins et al.   MEDICAL JOURNAL OF AUSTRALIA

High Frequency of Germline TP53 Mutations in a Prospective Adult-Onset Sarcoma Cohort

(2013) Gillian Mitchell et al.   PLoS One

Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms

(2012) Holly K. Tabor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Toward Methodological Innovation in Empirical Ethics Research

(2012) MICHAEL DUNN et al.   CAMBRIDGE QUARTERLY OF HEALTHCARE ETHICS

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

(2012) Flavia M Facio et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals

(2012) Malcolm G Dunlop et al.   GUT

Risky Business: Risk Perception and the Use of Medical Services among Customers of DTC Personal Genetic Testing

(2012) David J. Kaufman et al.   Journal of Genetic Counseling

Attitudes of Patients With Cancer About Personalized Medicine and Somatic Genetic Testing

(2012) Stacy W. Gray et al.   Journal of Oncology Practice

Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics

(2011) JS Roberts et al.   CLINICAL GENETICS

“It’s Not Like Judgment Day”: Public Understanding of and Reactions to Personalized Genomic Risk Information

(2011) Erynn S. Gordon et al.   Journal of Genetic Counseling

Varieties of Uncertainty in Health Care

(2011) Paul K. J. Han et al.   MEDICAL DECISION MAKING

Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease Risk

(2011) Cinnamon S. Bloss et al.   NEW ENGLAND JOURNAL OF MEDICINE

Skin Cancer Concerns and Genetic Risk Information-Seeking in Primary Care

(2011) J. Hay et al.   Public Health Genomics

A Population-Based Survey in Australia of Men’s and Women’s Perceptions of Genetic Risk and Predictive Genetic Testing and Implications for Primary Care

(2011) S. Taylor   Public Health Genomics

What Would You Do?

(2011) J. Couzin-Frankel   SCIENCE

Uptake of Huntington disease predictive testing in a complete population

(2010) PJ Morrison et al.   CLINICAL GENETICS

Impact of communicating personalized genetic risk information on perceived control over the risk: A systematic review

(2010) Ruth E Collins et al.   GENETICS IN MEDICINE

Public Opinion about the Importance of Privacy in Biobank Research

(2009) David J. Kaufman et al.   AMERICAN JOURNAL OF HUMAN GENETICS

‘NOBODY TOSSES A DWARF!’ THE RELATION BETWEEN THE EMPIRICAL AND THE NORMATIVE REEXAMINED

(2009) CARLO LEGET et al.   BIOETHICS

Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families

(2009) Nadine A Kasparian et al.   GENETICS IN MEDICINE

Revisting wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years

(2008) Anne Andermann   BULLETIN OF THE WORLD HEALTH ORGANIZATION

Australian Study on Public Knowledge of Human Genetics and Health

(2008) C. Molster et al.   Public Health Genomics