BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Trier C, Fournous G, Strand JM, Stray-Pedersen A, Pettersen RD, Rowe AD. Next-generation sequencing of newborn screening genes: the accuracy of short-read mapping. NPJ Genom Med 2020;5:36. [PMID: 32944285 DOI: 10.1038/s41525-020-00142-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Bush L, Davidson H, Gelles S, Lea D, Koehly LM. Experiences of Families Caring for Children with Newborn Screening-Related Conditions: Implications for the Expansion of Genomics in Population-Based Neonatal Public Health Programs. IJNS 2022;8:35. [DOI: 10.3390/ijns8020035] [Reference Citation Analysis]
2 Woerner AC, Gallagher RC, Vockley J, Adhikari AN. The Use of Whole Genome and Exome Sequencing for Newborn Screening: Challenges and Opportunities for Population Health. Front Pediatr 2021;9:663752. [PMID: 34350142 DOI: 10.3389/fped.2021.663752] [Reference Citation Analysis]
3 Owen MJ, Lefebvre S, Hansen C, Kunard CM, Dimmock DP, Smith LD, Scharer G, Mardach R, Willis MJ, Feigenbaum A, Niemi AK, Ding Y, Van Der Kraan L, Ellsworth K, Guidugli L, Lajoie BR, McPhail TK, Mehtalia SS, Chau KK, Kwon YH, Zhu Z, Batalov S, Chowdhury S, Rego S, Perry J, Speziale M, Nespeca M, Wright MS, Reese MG, De La Vega FM, Azure J, Frise E, Rigby CS, White S, Hobbs CA, Gilmer S, Knight G, Oriol A, Lenberg J, Nahas SA, Perofsky K, Kim K, Carroll J, Coufal NG, Sanford E, Wigby K, Weir J, Thomson VS, Fraser L, Lazare SS, Shin YH, Grunenwald H, Lee R, Jones D, Tran D, Gross A, Daigle P, Case A, Lue M, Richardson JA, Reynders J, Defay T, Hall KP, Veeraraghavan N, Kingsmore SF. An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases. Nat Commun 2022;13:4057. [PMID: 35882841 DOI: 10.1038/s41467-022-31446-6] [Reference Citation Analysis]
4 Mujamammi AH. Insights into National Laboratory Newborn Screening and Future Prospects. Medicina 2022;58:272. [DOI: 10.3390/medicina58020272] [Reference Citation Analysis]
5 Bick D, Bick SL, Dimmock DP, Fowler TA, Caulfield MJ, Scott RH. An online compendium of treatable genetic disorders. Am J Med Genet C Semin Med Genet 2021;187:48-54. [PMID: 33350578 DOI: 10.1002/ajmg.c.31874] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 King JR, Notarangelo LD, Hammarström L. An appraisal of the Wilson & Jungner criteria in the context of genomic-based newborn screening for inborn errors of immunity. J Allergy Clin Immunol 2021;147:428-38. [PMID: 33551024 DOI: 10.1016/j.jaci.2020.12.633] [Reference Citation Analysis]
7 Tsang KY, Chan TCH, Yeung MCW, Wong TK, Lau WT, Mak CM. Validation of amplicon-based next generation sequencing panel for second-tier test in newborn screening for inborn errors of metabolism. Journal of Laboratory Medicine 2021;45:267-74. [DOI: 10.1515/labmed-2021-0115] [Reference Citation Analysis]