Gene selection for genomic newborn screening: Moving toward consensus?-Reference-Cited by-同舟云学术

Gene selection for genomic newborn screening: Moving toward consensus?

Published:2024-05 Issue:5 Volume:26 Page:101077
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Downie Lilian,Bouffler Sophie E.,Amor David J.,Christodoulou John,Yeung Alison,Horton Ari E.,Macciocca Ivan,Archibald Alison D.,Wall Meghan,Caruana Jade,Lunke Sebastian,Stark Zornitza^ORCID

Publisher

Elsevier BV

Reference21 articles.

1. Genomic newborn screening for rare diseases;Stark;Nat Rev Genet,2023

2. Principles of genomic newborn screening programs: a systematic review;Downie;JAMA Netw Open,2021

3. Principles and Practices of Screening for Disease;Wilson,1968

4. A curated gene list for reporting results of newborn genomic sequencing;Ceyhan-Birsoy;Genet Med,2017

5. An age-based framework for evaluating genome-scale sequencing results in newborn screening;Milko;J Pediatr,2019

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1. Wilson and Jungner Revisited: Are Screening Criteria Fit for the 21st Century?;International Journal of Neonatal Screening;2024-09-13

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4. Genomic sequencing in newborn screening: balancing consent with the right of the asymptomatic at-risk child to be found;European Journal of Human Genetics;2024-08-12

5. The Multi-Omic Approach to Newborn Screening: Opportunities and Challenges;International Journal of Neonatal Screening;2024-06-21