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

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project

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Development and Evaluation of a Telephone Communication Protocol for the Delivery of Personalized Melanoma Genomic Risk to the General Population

(2017) Georgina L. Fenton et al.   Journal of Genetic Counseling

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

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The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis

(2016) Gareth J Hollands et al.   BMJ-British Medical Journal

Lifestyle Advice Combined with Personalized Estimates of Genetic or Phenotypic Risk of Type 2 Diabetes, and Objectively Measured Physical Activity: A Randomized Controlled Trial

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The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis

(2016) Gareth J Hollands et al.   BMJ-British Medical Journal

Psychological distress related to BRCA testing in ovarian cancer patients

(2015) Merete Bjørnslett et al.   Familial Cancer

Participant use and communication of findings from exome sequencing: a mixed-methods study

(2015) Katie L. Lewis et al.   GENETICS IN MEDICINE

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

(2015) Amelia K. Smit et al.   HEALTH EXPECTATIONS

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

(2015) Matthew H Law et al.   NATURE GENETICS

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

A New Approach to Assessing Affect and the Emotional Implications of Personal Genomic Testing for Common Disease Risk

(2015) Suzanne C. O''Neill et al.   Public Health Genomics

Impact of direct-to-consumer genomic testing at long term follow-up

(2013) Cinnamon S Bloss et al.   JOURNAL OF MEDICAL GENETICS

Public health implications from COGS and potential for risk stratification and screening

(2013) Hilary Burton et al.   NATURE GENETICS

Long-Term Psychosocial Outcomes of BRCA1/BRCA2 Testing: Differences across Affected Status and Risk-Reducing Surgery Choice

(2012) K. D. Graves et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

Patients’ understanding of and responses to multiplex genetic susceptibility test results

(2012) Kimberly A. Kaphingst et al.   GENETICS IN MEDICINE

Communicating Genetic Risk Information for Common Disorders in the Era of Genomic Medicine

(2011) Denise M. Lautenbach et al.   Annual Review of Genomics and Human Genetics

Long-Term Reactions to Genetic Testing for BRCA1 and BRCA2 Mutations: Does Time Heal Women's Concerns?

(2011) Chanita Hughes Halbert et al.   JOURNAL OF CLINICAL ONCOLOGY

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

(2011) Satoru Yokoyama et al.   NATURE

Charting a course for genomic medicine from base pairs to bedside

(2011) Eric D. Green et al.   NATURE

The impact of the format of graphical presentation on health-related knowledge and treatment choices

(2008) Sarah T. Hawley et al.   PATIENT EDUCATION AND COUNSELING