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For: Ross LF, Clayton EW. Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq. Pediatrics 2019;144:e20191031. [PMID: 31719124 DOI: 10.1542/peds.2019-1031] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Dondorp W, Bolt I, Tibben A, De Wert G, Van Summeren M. 'We Should View Him as an Individual': The Role of the Child's Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing. Health Care Anal 2021;29:249-61. [PMID: 33389383 DOI: 10.1007/s10728-020-00425-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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4 Powell SN, Byfield G, Bennetone A, Frantz AM, Harrison LK, James-crook ER, Osborne H, Owens TH, Shaw JL, O’daniel J, Milko LV. Parental Guidance Suggested: Engaging Parents as Partners in Research Studies of Genomic Screening for a Pediatric Population. Front Genet 2022;13:867030. [DOI: 10.3389/fgene.2022.867030] [Reference Citation Analysis]
5 Burdon KP. The utility of genomic testing in the ophthalmology clinic: A review. Clin Exp Ophthalmol 2021;49:615-25. [PMID: 34231298 DOI: 10.1111/ceo.13970] [Reference Citation Analysis]
6 Raymond FL. Clinical Genomics in Critically Ill Infants and Children. JAMA 2020;323:2480-2. [PMID: 32573653 DOI: 10.1001/jama.2020.8112] [Reference Citation Analysis]
7 Bailey DB. Early Intervention and Newborn Screening: Parallel Roads or Divergent Highways? Infants & Young Children 2021;34:3-16. [DOI: 10.1097/iyc.0000000000000181] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Zimmer KP. Newborn Screening: Still Room for Improvement. Dtsch Arztebl Int 2021;118:99-100. [PMID: 33835004 DOI: 10.3238/arztebl.m2021.0008] [Reference Citation Analysis]
9 Newson AJ. The promise of public health ethics for precision medicine: the case of newborn preventive genomic sequencing. Hum Genet 2021. [PMID: 33715055 DOI: 10.1007/s00439-021-02269-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 de Castro MJ, González-Vioque E, Barbosa-Gouveia S, Salguero E, Rite S, López-Suárez O, Pérez-Muñuzuri A, Couce ML. Rapid Phenotype-Driven Gene Sequencing with the NeoSeq Panel: A Diagnostic Tool for Critically Ill Newborns with Suspected Genetic Disease. J Clin Med 2020;9:E2362. [PMID: 32718099 DOI: 10.3390/jcm9082362] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
11 Wu X, Yang Y, Zhou L, Long W, Yu B. Are We Ready for Newborn Genetic Screening? A Cross-Sectional Survey of Healthcare Professionals in Southeast China. Front Pediatr 2022;10:875229. [DOI: 10.3389/fped.2022.875229] [Reference Citation Analysis]
12 Snir M, Nazareth S, Simmons E, Hayward L, Ashcraft K, Bristow SL, Esplin ED, Aradhya S. Democratizing genomics: Leveraging software to make genetics an integral part of routine care. Am J Med Genet C Semin Med Genet 2021;187:14-27. [PMID: 33296144 DOI: 10.1002/ajmg.c.31866] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 . The Fraught Reality of Genomic Sequencing. Am J Nurs 2020;120:14. [PMID: 32079781 DOI: 10.1097/01.NAJ.0000656268.80006.1b] [Reference Citation Analysis]
14 Tarini BA. The Effect of BabySeq on Pediatric and Genomic Research-More Than Baby Steps. JAMA Pediatr 2021;175:1107-8. [PMID: 34424259 DOI: 10.1001/jamapediatrics.2021.2826] [Reference Citation Analysis]