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For: Remec ZI, Trebusak Podkrajsek K, Repic Lampret B, Kovac J, Groselj U, Tesovnik T, Battelino T, Debeljak M. Next-Generation Sequencing in Newborn Screening: A Review of Current State. Front Genet 2021;12:662254. [PMID: 34122514 DOI: 10.3389/fgene.2021.662254] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Lund AM, Wibrand F, Skogstrand K, Bækvad-Hansen M, Gregersen N, Andresen BS, Hougaard DM, Dunø M, Olsen RKJ. Use of Molecular Genetic Analyses in Danish Routine Newborn Screening. Int J Neonatal Screen 2021;7:50. [PMID: 34449524 DOI: 10.3390/ijns7030050] [Reference Citation Analysis]
2 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] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Korotkov E, Zaytsev K, Fedorov A. Use of 6 Nucleotide Length Words to Study the Complexity of Gene Sequences from Different Organisms. Entropy 2022;24:632. [DOI: 10.3390/e24050632] [Reference Citation Analysis]
4 Shibuya Y, Kumar KK, Mader MM, Yoo Y, Ayala LA, Zhou M, Mohr MA, Neumayer G, Kumar I, Yamamoto R, Marcoux P, Liou B, Bennett FC, Nakauchi H, Sun Y, Chen X, Heppner FL, Wyss-Coray T, Südhof TC, Wernig M. Treatment of a genetic brain disease by CNS-wide microglia replacement. Sci Transl Med 2022;14:eabl9945. [PMID: 35294256 DOI: 10.1126/scitranslmed.abl9945] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 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]
6 Scarpa M, Bonham JR, Dionisi-vici C, Prevot J, Pergent M, Meyts I, Mahlaoui N, Schielen PC. Newborn screening as a fully integrated system to stimulate equity in neonatal screening in Europe. The Lancet Regional Health - Europe 2022. [DOI: 10.1016/j.lanepe.2022.100311] [Reference Citation Analysis]
7 Kalkman S, Dondorp W. The case for screening in early life for 'non-treatable' disorders: ethics, evidence and proportionality. A report from the Health Council of the Netherlands. Eur J Hum Genet 2022. [PMID: 35132176 DOI: 10.1038/s41431-022-01055-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]