Research graph
References from Caregiver's perspectives toward genome sequencing in children with neurodevelopmental disorders: Integrating genomic information into pediatric care. Local targets link to admitted publications; unresolved targets remain external evidence.
Unresolved reference
2013 · External reference
Health, functionality, and social support in families with a child with a neurodevelopmental disorder - a pilot study
10.2147/ndt.s195722 · 2019 · External reference
Understanding the psychosocial effects of WES test results on parents of children with rare diseases
10.1007/s10897-016-9958-5 · 2016 · External reference
Genetic testing in neurodevelopmental disorders
10.3389/fped.2021.526779 · 2021 · External reference
Paediatricians underuse recommended genetic tests in children with global developmental delay
10.1093/pch/pxy033 · 2018 · External reference
Newborn screening for neurodevelopmental disorders may exacerbate health disparities
10.1542/peds.2023-061727 · 2023 · External reference
The psychological impact of genetic information on children: a systematic review
10.1038/gim.2015.181 · 2016 · External reference
Promoting optimal development: identifying infants and young children with developmental disorders through developmental surveillance and screening
10.1542/peds.2019-3449 · 2020 · External reference
Unresolved reference
2018 · External reference
Committee on Children With Disabilities. Developmental surveillance and screening in infants and young children
10.1542/peds.108.1.192 · 2001 · External reference
Neurodevelopmental disorders and genetic testing: current approaches and future advances
10.1002/ana.23950 · 2013 · External reference
Committee on Children With Disabilities. Developmental surveillance and screening in infants and young children
10.1542/peds.108.1.192 · 2001 · External reference
Genetic testing in patients with neurodevelopmental disorders: experience of 511 patients at Cincinnati Children’s Hospital Medical Center
10.1007/s10803-021-05337-6 · 2022 · External reference
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
10.1038/s41436-021-01242-6 · 2021 · External reference
How do parents decide on genetic testing in pediatrics? A systematic review
10.1016/j.gim.2025.101390 · 2025 · External reference
Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research
10.1038/s41431-022-01245-0 · 2023 · External reference
Knowledge, attitudes and experiences of genetic testing for autism spectrum disorders among caregivers, patients, and health providers: a systematic review
10.5498/wjp.v13.i5.247 · 2023 · External reference
The social value of genomic sequencing for disadvantaged families facing rare disease
10.1016/j.socscimed.2022.115465 · 2022 · External reference
Parents' perceptions of personal utility of exome sequencing results
10.1038/s41436-019-0730-8 · 2020 · External reference
Not the end of the odyssey: parental perceptions of whole exome sequencing (WES) in pediatric undiagnosed disorders
10.1007/s10897-016-9933-1 · 2016 · External reference
Genomic sequencing in diverse and underserved pediatric populations: parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results
10.1016/j.gim.2025.101363 · 2025 · External reference
Clinical exome sequencing for genetic identification of rare mendelian disorders
10.1001/jama.2014.14604 · 2014 · External reference
Parental attitudes and beliefs regarding the genetic testing of children
2005 · External reference
Assessing the psychological impact of genetic susceptibility testing
2019 · External reference
Perceived utility and disutility of genomic sequencing for pediatric patients: perspectives from parents with diverse sociodemographic characteristics
10.1002/ajmg.a.62619 · 2022 · External reference
Children with genetic conditions in the United States: prevalence estimates from the 2016-2017 National Survey of Children’s Health
10.1016/j.gim.2021.09.004 · 2022 · External reference
Neurodevelopmental disorders—the history and future of a diagnostic concept
10.31887/dcns.2020.22.1/macrocq · 2020 · External reference
Parental experiences of genetic testing
10.1542/neo.25-3-e151 · 2024 · External reference
Possibly positive or certainly uncertain?”: participants’ responses to uncertain diagnostic results from exome sequencing
10.1038/gim.2017.135 · 2018 · External reference
What does it mean?”: uncertainties in understanding results of chromosomal microarray testing
10.1038/gim.2011.52 · 2012 · External reference
Pitfalls and challenges in genetic test interpretation: an exploration of genetic professionals' experience with interpretation of results
10.1111/cge.13917 · 2021 · External reference
Is that something that should concern me?”: a qualitative exploration of parent understanding of their child’s genomic test results
2021 · External reference
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
10.1038/s41431-022-01065-2 · 2022 · External reference
Council on Children With Disabilities, Section on Developmental and Behavioral Pediatrics. Patient- and family-centered care coordination: a framework for integrating care for children and youth across multiple systems
2014 · External reference
American Academy of Pediatrics Committee on Genetics. Clinical genetic evaluation of the child with mental retardation or developmental delays
10.1542/peds.2006-1006 · 2006 · External reference
The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing
2023 · External reference
GUÍA: a digital platform to facilitate result disclosure in genetic counseling
10.1038/s41436-020-01063-z · 2021 · External reference
The clinical sequencing evidence-generating research consortium: integrating genomic sequencing in diverse and medically underserved populations
10.1016/j.ajhg.2018.08.007 · 2018 · External reference
Variant reclassification and recontact research: a scoping review
2024 · External reference
Systematic reanalysis of genomic data improves quality of variant interpretation
10.1111/cge.13259 · 2018 · External reference
Developing and using a codebook for the analysis of interview data: an example from a professional development research project
10.1177/1525822x10388468 · 2011 · External reference
Known unknowns: building an ethics of uncertainty into genomic medicine
10.1186/s12920-016-0219-0 · 2016 · External reference
Defining and achieving health equity in genomic medicine
10.18865/ed.29.s1.173 · 2019 · External reference
The impact of climate change on global biodiversity
2022 · External reference
A unique service: how an embedded psychology team can help patients and genetics clinicians within a clinical genetics service
10.1038/s41431-022-01112-y · 2022 · External reference
Infant and maternal mental health in primary care: a guide for pediatricians and residency training programs
2026 · External reference
