Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study

Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project

(2019) Saskia C Sanderson et al.   BMJ Open

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

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study

(2018) Michael P Mackley et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

(2018) Kelly E. Ormond et al.   GENETICS IN MEDICINE

Paediatric genomics: diagnosing rare disease in children

(2018) Caroline F. Wright et al.   NATURE REVIEWS GENETICS

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial

(2018) Salma Shickh et al.   BMJ Open

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

(2018) Clare Turnbull et al.   BMJ-British Medical Journal

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

(2018) Clare Turnbull et al.   BMJ-British Medical Journal

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature

(2018) J. Delanne et al.   European Journal of Medical Genetics

Opening the “black box” of informed consent appointments for genome sequencing: a multisite observational study

(2018) Saskia C. Sanderson et al.   GENETICS IN MEDICINE

Fostering trust in healthcare: Participants’ experiences, views, and concerns about the 100,000 genomes project

(2018) Sandi Dheensa et al.   European Journal of Medical Genetics

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

(2017) Anath C Lionel et al.   GENETICS IN MEDICINE

Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results

(2017) Courtney Berrios et al.   Journal of Genetic Counseling

Diagnostic needs for rare diseases and shared prediagnostic phenomena: Results of a German-wide expert Delphi survey

(2017) Susanne Blöß et al.   PLoS One

The 100 000 Genomes Project: What it means for paediatrics

(2016) Blanche H Griffin et al.   Archives of Disease in Childhood-Education and Practice Edition

My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings

(2016) Holly K. Tabor et al.   GENETICS IN MEDICINE

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies

(2016) Michael P. Mackley et al.   GENETICS IN MEDICINE

Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders

(2016) Allyn McConkie Rosell et al.   Journal of Genetic Counseling

Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases

(2016) Lotte Krabbenborg et al.   Journal of Genetic Counseling

Pediatric Whole Exome Sequencing: an Assessment of Parents’ Perceived and Actual Understanding.

(2016) Leandra K. Tolusso et al.   Journal of Genetic Counseling

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?

(2016) J A Anderson et al.   JOURNAL OF MEDICAL ETHICS

Experiences with obtaining informed consent for genomic sequencing

(2015) Barbara A. Bernhardt et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project

(2015) Saskia C Sanderson et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

“Not Tied Up Neatly with a Bow”: Professionals’ Challenging Cases in Informed Consent for Genomic Sequencing

(2015) Ashley N. Tomlinson et al.   Journal of Genetic Counseling

Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice

(2014) Anya E. R. Prince et al.   Journal of Genetic Counseling

Informed consent for return of incidental findings in genomic research

(2013) Paul S. Appelbaum et al.   GENETICS IN MEDICINE