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For: 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]
Number Citing Articles
1 Alston CL, Stenton SL, Hudson G, Prokisch H, Taylor RW. The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines. J Pathol 2021;254:430-42. [PMID: 33586140 DOI: 10.1002/path.5641] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
2 Wainstein T, Campbell T, Stojkova BJ, Lavoie PM, Elliott AM. Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety. J Genet Couns 2022. [PMID: 35733279 DOI: 10.1002/jgc4.1605] [Reference Citation Analysis]
3 Yang Y, Wang Y, Zhou L, Long W, Yu B, Wang H. Molecular Genetic Screening of Neonatal Intensive Care Units: Hyperbilirubinemia as an Example. TACG 2022;Volume 15:39-48. [DOI: 10.2147/tacg.s362148] [Reference Citation Analysis]
4 Palmquist R, Jenkins SM, Bentley D, Miller C, Mao R, Meibos B, Bayrak-Toydemir P, Tvrdik T, Nadauld LD, Bleyl SB, Chowdhury S, Ostrander B, Flores-Daboub J, Longo N, Tristani-Firouzi M, Hobbs C, Bonkowsky JL, Brunelli L. Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics. Pediatr Res 2022. [PMID: 35115709 DOI: 10.1038/s41390-022-01965-5] [Reference Citation Analysis]