Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings

Quality of life drives patients’ preferences for secondary findings from genomic sequencing

(2020) Chloe Mighton et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes

(2020) Elizabeth Ormondroyd et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review

(2020) Nick Dragojlovic et al.   GENETICS IN MEDICINE

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings

(2020) Emma Reble et al.   HUMAN GENETICS

Integrating Genomics into Healthcare: A Global Responsibility

(2019) Zornitza Stark et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Current conditions in medical genetics practice

(2019) Deborah R. Maiese et al.   GENETICS IN MEDICINE

Development of patient “profiles” to tailor counseling for incidental genomic sequencing results

(2019) Chloe Mighton et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial

(2019) Salma Shickh et al.   BMJ Open

Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources

(2019) June C. Carroll et al.   Frontiers in Genetics

Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

(2019) Yvonne Bombard et al.   GENETICS IN MEDICINE

Whole genome sequencing in the clinic: empowerment or too much information?

(2018) Amanda J. Berberich et al.   CANADIAN MEDICAL ASSOCIATION JOURNAL

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results

(2018) Yvonne Bombard et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Diagnostic Utility of Exome Sequencing for Kidney Disease

(2018) Emily E. Groopman et al.   NEW ENGLAND JOURNAL OF MEDICINE

Personal utility in genomic testing: a systematic literature review

(2017) Jennefer N Kohler et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The Language of Stewardship: Is the “Low-Value” Label Overused?

(2017) Kevin R. Riggs et al.   MAYO CLINIC PROCEEDINGS

Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy

(2017) Maie Walsh et al.   Annals of Clinical and Translational Neurology

Clinical genome sequencing and population preferences for information about ‘incidental’ findings—From medically actionable genes (MAGs) to patient actionable genes (PAGs)

(2017) Thomas Ploug et al.   PLoS One

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

(2016) Sarah S. Kalia et al.   GENETICS IN MEDICINE

The Gene Messenger Impact Project

(2016) June C. Carroll et al.   JOURNAL OF CONTINUING EDUCATION IN THE HEALTH PROFESSIONS

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

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

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment

(2015) Dean A. Regier et al.   CANADIAN MEDICAL ASSOCIATION JOURNAL

Clinical application of whole-exome sequencing across clinical indications

(2015) Kyle Retterer et al.   GENETICS IN MEDICINE

Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature

(2014) Natalie A. Mikat-Stevens et al.   GENETICS IN MEDICINE

Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time

(2011) Jonathan S Berg et al.   GENETICS IN MEDICINE