Elliott AM - Search Results

1

The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.

Dragojlovic N, Elliott AM, Adam S, van Karnebeek C, Lehman A, Mwenifumbo JC, Nelson TN, du Souich C, Friedman JM, Lynd LD. Dragojlovic N, et al. Among authors: elliott am. Genet Med. 2018 Sep;20(9):1013-1021. doi: 10.1038/gim.2017.226. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300375 Free article. Review.

2

Recommendations for the integration of genomics into clinical practice.

Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, Glass IA, Herman G, Hindorff L, Hisama F, Hudgins L, Innes AM, Jackson L, Jarvik G, Kim R, Korf B, Ledbetter DH, Li M, Liston E, Marshall C, Medne L, Meyn MS, Monfared N, Morton C, Mulvihill JJ, Plon SE, Rehm H, Roberts A, Shuman C, Spinner NB, Stavropoulos DJ, Valverde K, Waggoner DJ, Wilkens A, Cohn RD, Krantz ID. Bowdin S, et al. Among authors: elliott a. Genet Med. 2016 Nov;18(11):1075-1084. doi: 10.1038/gim.2016.17. Epub 2016 May 12. Genet Med. 2016. PMID: 27171546 Free PMC article. Review.

3

Evaluating the use of parental reports to estimate health care resource utilization in children with suspected genetic disorders.

Dragojlovic N, Kim E, Elliott AM; CAUSES Study; Friedman JM, Lynd LD. Dragojlovic N, et al. Among authors: elliott am. J Eval Clin Pract. 2018 Apr;24(2):416-422. doi: 10.1111/jep.12876. J Eval Clin Pract. 2018. PMID: 29603523

4

The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia.

Elliott AM, du Souich C, Adam S, Dragojlovic N, van Karnebeek C, Nelson TN, Lehman A; CAUSES Study; Lynd LD, Friedman JM. Elliott AM, et al. Mol Genet Genomic Med. 2018 May 30;6(4):592-600. doi: 10.1002/mgg3.410. Online ahead of print. Mol Genet Genomic Med. 2018. PMID: 29851296 Free PMC article.

5

The importance of genetic counselling in genome-wide sequencing.

Elliott AM, Friedman JM. Elliott AM, et al. Nat Rev Genet. 2018 Dec;19(12):735-736. doi: 10.1038/s41576-018-0057-3. Nat Rev Genet. 2018. PMID: 30283055 Review. No abstract available.

6

Atypical cerebral palsy: genomics analysis enables precision medicine.

Matthews AM, Blydt-Hansen I, Al-Jabri B, Andersen J, Tarailo-Graovac M, Price M, Selby K, Demos M, Connolly M, Drögemoller B, Shyr C, Mwenifumbo J, Elliott AM, Lee J, Ghani A, Stöckler S, Salvarinova R, Vallance H, Sinclair G, Ross CJ, Wasserman WW, McKinnon ML, Horvath GA, Goez H, van Karnebeek CD; TIDE BC, United for Metabolic Diseases and the CAUSES Study. Matthews AM, et al. Among authors: elliott am. Genet Med. 2019 Jul;21(7):1621-1628. doi: 10.1038/s41436-018-0376-y. Epub 2018 Dec 13. Genet Med. 2019. PMID: 30542205 Free article.

7

New developmental syndromes: Understanding the family experience.

Inglese CN, Elliott AM; CAUSES Study; Lehman A. Inglese CN, et al. Among authors: elliott am. J Genet Couns. 2019 Apr;28(2):202-212. doi: 10.1002/jgc4.1121. Epub 2019 Apr 2. J Genet Couns. 2019. PMID: 30938469

8

Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.

Smith EE, du Souich C, Dragojlovic N; CAUSES Study; RAPIDOMICS Study; Elliott AM. Smith EE, et al. Among authors: elliott am. J Genet Couns. 2019 Apr;28(2):263-272. doi: 10.1002/jgc4.1074. Epub 2018 Dec 31. J Genet Couns. 2019. PMID: 30964583

9

RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.

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. Elliott AM, et al. Eur J Pediatr. 2019 Aug;178(8):1207-1218. doi: 10.1007/s00431-019-03399-4. Epub 2019 Jun 7. Eur J Pediatr. 2019. PMID: 31172278

10

The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders.

Dragojlovic N, van Karnebeek CDM, Ghani A, Genereaux D, Kim E, Birch P; CAUSES Study; Elliott AM, Friedman JM, Lynd LD. Dragojlovic N, et al. Among authors: elliott am. Genet Med. 2020 Feb;22(2):292-300. doi: 10.1038/s41436-019-0635-6. Epub 2019 Aug 29. Genet Med. 2020. PMID: 31462755 Free article.

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