Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results

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

(2017) Saskia C Sanderson et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

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

How do providers discuss the results of pediatric exome sequencing with families?

(2017) Sarah A Walser et al.   Personalized Medicine

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

(2016) Robert C. Green et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Whole-exome sequencing in pediatrics: parents’ considerations toward return of unsolicited findings for their child

(2016) Candice Cornelis et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical exome sequencing: results from 2819 samples reflecting 1000 families

(2016) Daniel Trujillano et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?

(2016) Deborah Cragun et al.   Genetic Testing and Molecular Biomarkers

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

Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing

(2016) Allison Werner-Lin 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

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

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

Effects of racial and ethnic group and health literacy on responses to genomic risk information in a medically underserved population.

(2015) Kimberly A. Kaphingst et al.   HEALTH PSYCHOLOGY

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

(2015) Laurel K Willig et al.   Lancet Respiratory Medicine

How do research participants perceive “uncertainty” in genome sequencing?

(2014) Barbara B. Biesecker et al.   GENETICS IN MEDICINE

The usefulness of whole-exome sequencing in routine clinical practice

(2014) Alejandro Iglesias et al.   GENETICS IN MEDICINE

ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing

(2014)   GENETICS IN MEDICINE

Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

(2014) Yaping Yang et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children

(2013) J.C. Sapp et al.   CLINICAL GENETICS

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

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

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

Intrapersonal and interpersonal consequences of protective buffering among cancer patients and caregivers

(2010) Shelby L. Langer et al.   CANCER