ArticleFrontiers in genetics2022
Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.
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Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.
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46citing papers in PubMed, 1 pooled it
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What it found
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Who cites it
46 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022.Orphanet journal of rare diseases · 2026Pooled it
- Maternal perspectives on sharing newborn genomic data.European journal of human genetics : EJHG · 2026Article
- Sequencing for a Lifetime: Professional Perspectives on the Value and Feasibility of Lifelong Genomic Medicine.medRxiv : the preprint server for health sciences · 2026Article
- Who and how we engage: A systemic mapping of stakeholder perspectives on genomic newborn screening.European journal of human genetics : EJHG · 2026Article
- Australian parents' perspectives on extended genomic screening: what information to return and when?European journal of human genetics : EJHG · 2026Article
- Parent/caregiver needs during pediatric genome-wide sequencing: A scoping literature review.Journal of genetic counseling · 2026Article
- Missing … presumed well? Legal and ethical aspects of 'missed cases' in genomic newborn screening.European journal of human genetics : EJHG · 2026Article
- A Survey of Current Australasian Practices in the Use of Residual Bloodspots for the Addition of a New Disorder to the Screening Panel.International journal of neonatal screening · 2026Article
- A multi-dimensional framework for establishing and managing a genomic newborn screening program.European journal of human genetics : EJHG · 2026Article
- Public and parent perspectives on genomic sequencing in newborn screening: a scoping review.European journal of human genetics : EJHG · 2026Review
- Designing inclusive newborn sequencing research: insights from parents in underrepresented communities.BMC medical genomics · 2026Article
- Young adult perspectives regarding receiving medically actionable gene testing results for newborns: A qualitative investigation.Journal of community genetics · 2026Article
- Parent Experience and Attitudes Towards Newborn Bloodspot Screening in Ireland.International journal of neonatal screening · 2026Article
- A population-representative survey on attitudes toward genomic newborn screening in Germany.Genetics in medicine open · 2026Article
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- Article
- What Is at Stake in Genetic Newborn Screening for Rare Diseases? An Exploratory Qualitative Study of Parents' and Expectant Parents' Concerns in the Screen4Care Project.Public health genomics · 2026Article
- Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study.Nature medicine · 2025Article
- Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia.American journal of human genetics · 2025Article
- Parents' perspectives on expanded newborn genomic screening in Abu Dhabi, United Arab Emirates.Human genomics · 2025Article
Corrections and comments
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Authors and funding
14 authors.
Brittan ArmstrongCenter for Medical Ethics and Heath Policy, Baylor College of Medicine, Houston, TX, United States.
Kurt D ChristensenPRecisiOn Medicine Translational Research (PROMoTeR) Center, Department of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, United States.
Casie A GenettiDivision of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, United States.
Richard B ParadHarvard Medical School, Boston, MA, United States.
Jill Oliver RobinsonCenter for Medical Ethics and Heath Policy, Baylor College of Medicine, Houston, TX, United States.
Carrie L Blout ZawatskyDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, United States.
Bethany ZettlerDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, United States.
Alan H BeggsHarvard Medical School, Boston, MA, United States.
Ingrid A HolmHarvard Medical School, Boston, MA, United States.
Robert C GreenHarvard Medical School, Boston, MA, United States.
Amy L McGuireCenter for Medical Ethics and Heath Policy, Baylor College of Medicine, Houston, TX, United States.
Hadley Stevens SmithCenter for Medical Ethics and Heath Policy, Baylor College of Medicine, Houston, TX, United States.
Stacey PereiraCenter for Medical Ethics and Heath Policy, Baylor College of Medicine, Houston, TX, United States.
BabySeq Project Team
Funding
Genome Sequence-Based Screening for Childhood Risk and Newborn IllnessU19HD077671 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI BEGGS, ALAN H., GREEN, ROBERT C. · 2013 to 2018
$6.1MPrecision Medicine Policy and Treatment (PreEMPT) Model IIR01HD090019 · NICHD · HARVARD PILGRIM HEALTH CARE, INC. · PI Kurt Derek Christensen · 2017 to 2026
$5.7MExperiences and Outcomes in Early Adopters of Predispositional SequencingR01HG009922 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI GREEN, ROBERT C. · 2018 to 2020
$2.6MCost-effectiveness of Whole Genome Sequencing of Healthy AdultsK01HG009173 · NHGRI · HARVARD PILGRIM HEALTH CARE, INC. · PI CHRISTENSEN, KURT DEREK · 2016 to 2020
$626kAn ELSI-Integrated Evaluation of the Family-Level Utility of Pediatric Genomic SequencingK99HG011491 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI SMITH, HADLEY STEVENS · 2021 to 2022
$164kNHGRI NIH HHS K01 HG009173NHGRI NIH HHS K99 HG011491NHGRI NIH HHS R01 HG009922NICHD NIH HHS R01 HD090019NICHD NIH HHS U19 HD077671
Abstract
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Indexed as
ELSIethicsexome sequencinggenomic sequencingnewborn genomic sequencingnewborn screening (NBS)newborn sequencing
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.