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For: Clowes Candadai SV, Sikes MC, Thies JM, Freed AS, Bennett JT. Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges. J Genet Couns 2019;28:283-91. [PMID: 30964580 DOI: 10.1002/jgc4.1116] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Lynch F, Nisselle A, Stark Z, Gaff CL, McClaren B. Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery. Eur J Hum Genet 2022. [PMID: 35953518 DOI: 10.1038/s41431-022-01168-w] [Reference Citation Analysis]
2 Stark Z, Ellard S. Rapid genomic testing for critically ill children: time to become standard of care? Eur J Hum Genet 2021. [PMID: 34744166 DOI: 10.1038/s41431-021-00990-y] [Reference Citation Analysis]
3 Clark CR, Reyes K, Ormond KE, Caleshu C, Moscarello T. U.S. Genetic counselors' perceptions of inpatient genetic counseling: A valuable model for medically complex patients. J Genet Couns 2021. [PMID: 34124811 DOI: 10.1002/jgc4.1435] [Reference Citation Analysis]
4 Magness E, Magoulas P, Moscarello T, Ma D, Helm BM, Mizerik E. Characterization of genetic counselor practices in inpatient care settings. J Genet Couns 2021;30:1181-90. [PMID: 33713511 DOI: 10.1002/jgc4.1401] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Lu P, Ma L, Sun J, Gong X, Cai C. A Chinese newborn with Zellweger syndrome and compound heterozygous mutations novel in the PEX1 gene: a case report and literature review. Transl Pediatr 2021;10:446-53. [PMID: 33708531 DOI: 10.21037/tp-20-167] [Reference Citation Analysis]
6 Lynch F, Nisselle A, Gaff CL, McClaren B. Rapid acute care genomics: Challenges and opportunities for genetic counselors. J Genet Couns 2021;30:30-41. [PMID: 33238072 DOI: 10.1002/jgc4.1362] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Hill M, Hammond J, Lewis C, Mellis R, Clement E, Chitty LS. Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges. Eur J Hum Genet 2020;28:1529-40. [PMID: 32561901 DOI: 10.1038/s41431-020-0667-z] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
8 Freed AS, Clowes Candadai SV, Sikes MC, Thies J, Byers HM, Dines JN, Ndugga-Kabuye MK, Smith MB, Fogus K, Mefford HC, Lam C, Adam MP, Sun A, McGuire JK, DiGeronimo R, Dipple KM, Deutsch GH, Billimoria ZC, Bennett JT. The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children. J Pediatr 2020:S0022-3476(20)30721-6. [PMID: 32553838 DOI: 10.1016/j.jpeds.2020.06.020] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
9 Deuitch N, Soo-Jin Lee S, Char D. Translating genomic testing results for pediatric critical care: Opportunities for genetic counselors. J Genet Couns 2020;29:78-87. [PMID: 31701594 DOI: 10.1002/jgc4.1182] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
10 Conta JH. Laboratory Stewardship for Clinical Genetic Testing. Curr Genet Med Rep 2019;7:180-6. [DOI: 10.1007/s40142-019-00175-6] [Reference Citation Analysis]