Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

Author:

Marathe Priya N.ORCID,Suckiel Sabrina A.,Bonini Katherine E.,Kelly Nicole R.,Scarimbolo Laura,Insel Beverly J.,Odgis Jacqueline A.,Sebastin Monisha,Ramos Michelle A.,Di Biase Miranda,Gallagher Katie M.,Brown Kaitlyn,Rodriguez Jessica E.,Yelton Nicole,Aguiñiga Karla Lopez,Rodriguez Michelle A.,Maria Estefany,Lopez Jessenia,Zinberg Randi E.,Diaz George A.,Greally John M.,Abul-Husn Noura S.,Bauman Laurie J.,Gelb Bruce D.,Wasserstein Melissa P.,Kenny Eimear E.,Horowitz Carol R.

Funder

National Human Genome Research Institute

Icahn School of Medicine at Mount Sinai

National Institute on Minority Health and Health Disparities

National Institutes of Health

National Center for Advancing Translational Sciences

Publisher

Elsevier BV

Reference45 articles.

1. Recent developments in genetic/genomic medicine;Horton;Clin. Sci.,2019

2. Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases;Clark;NPJ Genom. Med.,2018

3. Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients;Abul-Husn;medRxiv,2023

4. Utility of Genetic Testing from the Perspective of Parents/Caregivers: A Scoping Review;Hayeems;Children,2021

5. Personal utility in genomic testing: a systematic literature review;Kohler;Eur. J. Hum. Genet.,2017

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