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For: Elliott AM, du Souich C, Adam S, Dragojlovic N, van Karnebeek C, Nelson TN, Lehman A, Lynd LD, Friedman JM; CAUSES Study. The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia. Mol Genet Genomic Med 2018. [PMID: 29851296 DOI: 10.1002/mgg3.410] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Neuheuser L, Meyer R, Begemann M, Elbracht M, Eggermann T. Next generation sequencing and imprinting disorders: Current applications and future perspectives: Lessons from Silver-Russell syndrome. Molecular and Cellular Probes 2019;44:1-7. [DOI: 10.1016/j.mcp.2018.12.007] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
2 Elliott AM, du Souich C, Lehman A, Guella I, Evans DM, Candido T, Tooman L, Armstrong L, Clarke L, Gibson W, Gill H, Lavoie PM, Lewis S, Mckinnon ML, Nikkel SM, Patel M, Solimano A, Synnes A, Ting J, van Allen M, Christilaw J, Farrer MJ, Friedman JM, Osiovich H. RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit—successes and challenges. Eur J Pediatr 2019;178:1207-18. [DOI: 10.1007/s00431-019-03399-4] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 7.0] [Reference Citation Analysis]
3 Dragojlovic N, van Karnebeek CDM, Ghani A, Genereaux D, Kim E, Birch P, Elliott AM, Friedman JM, Lynd LD; CAUSES Study. The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders. Genet Med 2020;22:292-300. [DOI: 10.1038/s41436-019-0635-6] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
4 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]
5 Elliott AM, du Souich C, Adam S, Dragojlovic N, van Karnebeek C, Nelson TN, Lehman A, Lynd LD, Friedman JM; CAUSES Study. The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia. Mol Genet Genomic Med 2018. [PMID: 29851296 DOI: 10.1002/mgg3.410] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
6 Cheung F, Birch P, Friedman JM, Elliott AM, Adam S; CAUSES Study, GenCOUNSEL Study. The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing. Journal of Genetic Counseling. [DOI: 10.1002/jgc4.1558] [Reference Citation Analysis]
7 Cook CB, Armstrong L, Boerkoel CF, Clarke LA, du Souich C, Demos MK, Gibson WT, Gill H, Lopez E, Patel MS, Selby K, Abu-Sharar Z, Elliott AM, Friedman JM; CAUSES Study. Somatic mosaicism detected by genome-wide sequencing in 500 parent-child trios with suspected genetic disease: clinical and genetic counseling implications. Cold Spring Harb Mol Case Stud 2021;7:a006125. [PMID: 34697084 DOI: 10.1101/mcs.a006125] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Smith EE, du Souich C, Dragojlovic N, Elliott AM; CAUSES Study, RAPIDOMICS Study. Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit. J Genet Couns 2019;28:263-72. [DOI: 10.1002/jgc4.1074] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
9 Elliott AM, Dragojlovic N, Campbell T, Adam S, Souich CD, Fryer M, Lehman A, Karnebeek CV, Lynd LD, Friedman JM. Utilization of telehealth in paediatric genome-wide sequencing: Health services implementation issues in the CAUSES Study. J Telemed Telecare 2021;:1357633X20982737. [PMID: 33470133 DOI: 10.1177/1357633X20982737] [Reference Citation Analysis]
10 Liang NSY, Adam S, Elliott AM, Siemens A, du Souich C, Friedman JM, Birch P; CAUSES Study., GenCOUNSEL Study. After genomic testing results: Parents' long-term views. J Genet Couns 2021. [PMID: 34165210 DOI: 10.1002/jgc4.1454] [Reference Citation Analysis]
11 Phillips KA, Douglas MP, Wordsworth S, Buchanan J, Marshall DA. Availability and funding of clinical genomic sequencing globally. BMJ Glob Health 2021;6:e004415. [PMID: 33574068 DOI: 10.1136/bmjgh-2020-004415] [Reference Citation Analysis]
12 Cook CB, Dragojlovic N, Siemens A, Adam S, du Souich C, van Karnebeek C, Lehman A, Nelson TN, Friedman J, Lynd LD, Elliott AM; CAUSES Study., GenCOUNSEL Study. Integration of genetic counsellors in genomic testing triage: Outcomes of a genomic consultation service in British Columbia, Canada. Eur J Med Genet 2021;64:104024. [PMID: 32798762 DOI: 10.1016/j.ejmg.2020.104024] [Reference Citation Analysis]
13 Elliott AM. Genetic Counseling and Genome Sequencing in Pediatric Rare Disease. Cold Spring Harb Perspect Med 2020;10:a036632. [PMID: 31501267 DOI: 10.1101/cshperspect.a036632] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Taylor J, Craft J, Blair E, Wordsworth S, Beeson D, Chandratre S, Cossins J, Lester T, Németh AH, Ormondroyd E, Patel SY, Pagnamenta AT, Taylor JC, Thomson KL, Watkins H, Wilkie AOM, Knight JC. Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series. Genome Med 2019;11:46. [PMID: 31345272 DOI: 10.1186/s13073-019-0651-9] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 4.3] [Reference Citation Analysis]
15 Hitchcock EC, Study C, Elliott AM. Shortened consent forms for genome-wide sequencing: Parent and provider perspectives. Mol Genet Genomic Med 2020;8:e1254. [PMID: 32383361 DOI: 10.1002/mgg3.1254] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]