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For: Ayres S, Gallacher L, Stark Z, Brett GR. Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates. J Genet Couns 2019;28:273-82. [DOI: 10.1002/jgc4.1086] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Aldridge CE, Osiovich H, Hal Siden H, Elliott AM; RAPIDOMICS Study., GenCOUNSEL Study. Rapid genome-wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences. J Genet Couns 2021;30:616-29. [PMID: 33131147 DOI: 10.1002/jgc4.1353] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Au MG. Partners in care. Am J Med Genet A 2021;185:2630-2. [PMID: 33666328 DOI: 10.1002/ajmg.a.62149] [Reference Citation Analysis]
4 Demarest S, Marsh R, Treat L, Fisher MP, Dempsey A, Junaid M, Downs J, Leonard H, Benke T, Morris MA. The Lived Experience of Parents' Receiving the Diagnosis of CDKL5 Deficiency Disorder for Their Child. J Child Neurol 2022;:8830738221076285. [PMID: 35196159 DOI: 10.1177/08830738221076285] [Reference Citation Analysis]
5 Best S, Brown H, Lunke S, Patel C, Pinner J, Barnett CP, Wilson M, Sandaradura SA, McClaren B, Brett GR, Braithwaite J, Stark Z. Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level. NPJ Genom Med 2021;6:5. [PMID: 33510162 DOI: 10.1038/s41525-020-00168-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Lynch F, Nisselle A, Stark Z, Gaff CL, McClaren B. Parents' experiences of decision making for rapid genomic sequencing in intensive care. Eur J Hum Genet 2021. [PMID: 34426661 DOI: 10.1038/s41431-021-00950-6] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Van Bergen NJ, Linster CL, Christodoulou J. Reply: NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness. Brain 2020;143:e55. [PMID: 32462208 DOI: 10.1093/brain/awaa131] [Reference Citation Analysis]
8 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]
9 Forbes TA, Wallace J, Kumble S, Delatycki MB, Stark Z. Neonatal Bartter syndrome diagnosed by rapid genomics following low risk pre‐conception carrier screening. J Paediatrics Child Health. [DOI: 10.1111/jpc.15955] [Reference Citation Analysis]
10 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]
11 Brett GR, Martyn M, Lynch F, de Silva MG, Ayres S, Gallacher L, Boggs K, Baxendale A, Schenscher S, King-Smith S, Fowles L, Springer A, Lunke S, Vasudevan A, Krzesinski E, Pinner J, Sandaradura SA, Barnett C, Patel C, Wilson M, Stark Z. Parental experiences of ultrarapid genomic testing for their critically unwell infants and children. Genet Med 2020;22:1976-85. [PMID: 32719395 DOI: 10.1038/s41436-020-0912-4] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
12 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]
13 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]
14 Nevin SM, Wakefield CE, Barlow‐stewart K, Mcgill BC, Bye A, Palmer EE, Dale RC, Gill D, Kothur K, Boggs K, Le Marne F, Beavis E, Macintosh R, Sachdev R; Children's Hospital At Westmead Neurology Group, Cogenes Group. Psychosocial impact of genetic testing on parents of children with developmental and epileptic encephalopathy. Dev Med Child Neurol 2022;64:95-104. [DOI: 10.1111/dmcn.14971] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
15 Álvaro-Sánchez S, Abreu-Rodríguez I, Abulí A, Serra-Juhe C, Garrido-Navas MDC. Current Status of Genetic Counselling for Rare Diseases in Spain. Diagnostics (Basel) 2021;11:2320. [PMID: 34943558 DOI: 10.3390/diagnostics11122320] [Reference Citation Analysis]
16 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]
17 Kohut K, Limb S, Crawford G. The Changing Role of the Genetic Counsellor in the Genomics Era. Curr Genet Med Rep 2019;7:75-84. [DOI: 10.1007/s40142-019-00163-w] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]