Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

(2013) Zoe Lohn et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process

(2013) Carmen Ayuso et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Next-generation sequencing: does the next generation still have a right to an open future?

(2013) Annelien L. Bredenoord et al.   NATURE REVIEWS GENETICS

Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes

(2012) Jennifer J. Johnston et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Incidental findings in genetic research and clinical diagnostic tests: A systematic review

(2012) Leigh Jackson et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Whole-genome sequencing and the physician

(2012) A Thorogood et al.   CLINICAL GENETICS

Effects of informed consent for individual genome sequencing on relevant knowledge

(2012) KA Kaphingst et al.   CLINICAL GENETICS

Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics

(2012) Yvonne Bombard et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Population studies: return of research results and incidental findings Policy Statement

(2012) Bartha Maria Knoppers et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe

(2012) Ros Hastings et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants

(2012) Fiona Alice Miller et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Disease gene identification strategies for exome sequencing

(2012) Christian Gilissen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Taxonomizing, sizing and overcoming the incidentalome

(2012) Isaac S. Kohane et al.   GENETICS IN MEDICINE

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

(2012) Wybo Dondorp et al.   HUMAN MUTATION

Next-generation sequencing demands next-generation phenotyping

(2012) Raoul C.M. Hennekam et al.   HUMAN MUTATION

Genome-wide arrays: Quality criteria and platforms to be used in routine diagnostics

(2012) Joris R. Vermeesch et al.   HUMAN MUTATION

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

(2012) Joep de Ligt et al.   NEW ENGLAND JOURNAL OF MEDICINE

Changing the game with whole exome sequencing

(2011) H Ostrer   CLINICAL GENETICS

Health-care providers’ views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders

(2011) Yvonne Bombard et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Newborn screening for sickle cell disease: whose reproductive benefit?

(2011) Lainie Friedman Ross   EUROPEAN JOURNAL OF HUMAN GENETICS

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

Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy

(2011) Annelien L. Bredenoord et al.   HUMAN MUTATION

Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?

(2011) G. Pichert et al.   JOURNAL OF MEDICAL GENETICS

What can exome sequencing do for you?

(2011) J. Majewski et al.   JOURNAL OF MEDICAL GENETICS

Ethical Considerations Associated with Clinical Use of Next-Generation Sequencing in Children

(2011) John D. Lantos et al.   JOURNAL OF PEDIATRICS

Challenges in the clinical application of whole-genome sequencing

(2010) Kelly E Ormond et al.   LANCET

Managing Incidental Findings on Abdominal CT: White Paper of the ACR Incidental Findings Committee

(2010) Lincoln L. Berland et al.   Journal of the American College of Radiology

Genotype to phenotype—discovery and characterization of novel genomic disorders in a “genotype-first” era

(2009) Heather C Mefford   GENETICS IN MEDICINE

Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screening

(2009) F A Miller et al.   JOURNAL OF MEDICAL ETHICS

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing

(2009) T Schwarzbraun et al.   JOURNAL OF MEDICAL GENETICS

New challenges for informed consent through whole genome array testing

(2009) C Netzer et al.   JOURNAL OF MEDICAL GENETICS

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

(2009) Yvonne Bombard et al.   NATURE REVIEWS GENETICS

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

Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

(2008) Susan M. Wolf et al.   JOURNAL OF LAW MEDICINE & ETHICS

A proposal for a model of informed consent for the collection, storage and use of biological materials for research purposes

(2008) Corinna Porteri et al.   PATIENT EDUCATION AND COUNSELING

Research ethics and the challenge of whole-genome sequencing

(2007) Amy L. McGuire et al.   NATURE REVIEWS GENETICS