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Cited by in F6Publishing
For: Marwaha S, Knowles JW, Ashley EA. A guide for the diagnosis of rare and undiagnosed disease: beyond the exome. Genome Med 2022;14. [DOI: 10.1186/s13073-022-01026-w] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Halley MC, Ashley EA, Tabor HK. Supporting undiagnosed participants when clinical genomics studies end. Nat Genet 2022. [PMID: 35902745 DOI: 10.1038/s41588-022-01150-8] [Reference Citation Analysis]
2 Baker EK, Ulm EA, Belonis A, Brightman DS, Hallinan BE, Leslie ND, Miethke AG, Vawter-lee M, Wu Y, Pena LDM. Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center. Front Genet 2022;13:887698. [DOI: 10.3389/fgene.2022.887698] [Reference Citation Analysis]
3 Soraru J, Chakera A, Isbel N, Mallawaarachichi A, Rogers N, Trnka P, Patel C, Mallett A. The evolving role of diagnostic genomics in kidney transplantation. Kidney International Reports 2022. [DOI: 10.1016/j.ekir.2022.05.019] [Reference Citation Analysis]
4 Kerr K, Mckenna C, Heggarty S, Bailie C, Mcmullan J, Crowe A, Kilner J, Donnelly M, Boyle S, Rea G, Flanagan C, Mckee S, Mcknight AJ. A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland. Genes 2022;13:1104. [DOI: 10.3390/genes13071104] [Reference Citation Analysis]