Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project

The BabySeq project: implementing genomic sequencing in newborns

(2018) Ingrid A. Holm et al.   BMC Pediatrics

Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium

(2018) Laura M. Amendola et al.   Journal of Genetic Counseling

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants

(2018) Josh E. Petrikin et al.   npj Genomic Medicine

A curated gene list for reporting results of newborn genomic sequencing

(2017) Ozge Ceyhan-Birsoy et al.   GENETICS IN MEDICINE

Newborn Sequencing in Genomic Medicine and Public Health

(2017) Jonathan S. Berg et al.   PEDIATRICS

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

(2016) Zornitza Stark et al.   GENETICS IN MEDICINE

Participants and Study Decliners’ Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing

(2016) Jill Oliver Robinson et al.   Journal of Empirical Research on Human Research Ethics

Psychosocial Factors Influencing Parental Interest in Genomic Sequencing of Newborns

(2016) S. E. Waisbren et al.   PEDIATRICS

Potential Psychosocial Risks of Sequencing Newborns

(2016) L. A. Frankel et al.   PEDIATRICS

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

(2015) Jeffrey R. Botkin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates

(2015) Dale L. Bodian et al.   GENETICS IN MEDICINE

Short-term Outcomes of Infants Enrolled in Randomized Clinical Trials vs Those Eligible but Not Enrolled

(2015) Elizabeth E. Foglia et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

GINA, Genetic Discrimination, and Genomic Medicine

(2015) Robert C. Green et al.   NEW ENGLAND JOURNAL OF MEDICINE

Parents are interested in newborn genomic testing during the early postpartum period

(2014) Susan E. Waisbren et al.   GENETICS IN MEDICINE

Resistance to Therapy in Acute Promyelocytic Leukemia

(2014) Jacqueline Lehmann-Che et al.   NEW ENGLAND JOURNAL OF MEDICINE

Parents’ interest in whole-genome sequencing of newborns

(2013) Aaron J. Goldenberg et al.   GENETICS IN MEDICINE

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

Enrollment of Extremely Low Birth Weight Infants in a Clinical Research Study May Not Be Representative

(2012) W. Rich et al.   PEDIATRICS

Enrollment experiences in a pediatric longitudinal observational study: The Environmental Determinants of Diabetes in the Young (TEDDY) study

(2011) Barbro Lernmark et al.   Contemporary Clinical Trials

Parents' Decisions to Screen Newborns for FMR1 Gene Expansions in a Pilot Research Project

(2011) D. Skinner et al.   PEDIATRICS

Motivations of Mothers to Enroll Their Newborn Infants in General Clinical Research on Well-Infant Care and Development

(2008) A. Maayan-Metzger et al.   PEDIATRICS