Similar articles for PMID: 30964583

Year	Number of Results
1981	1
1998	1
2001	1
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2006	1
2007	1
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2014	10
2015	9
2016	19
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2018	19
2019	30
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2022	24
2023	7
2024	0

1

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. J Genet Couns. 2019 Apr;28(2):263-272. doi: 10.1002/jgc4.1074. Epub 2018 Dec 31. J Genet Couns. 2019. PMID: 30964583

2

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

3

The long-term impact of receiving incidental findings on parents undergoing genome-wide sequencing.

Cheung F, Birch P, Friedman JM; CAUSES Study; GenCOUNSEL Study; Elliott AM, Adam S. Cheung F, et al. J Genet Couns. 2022 Aug;31(4):887-900. doi: 10.1002/jgc4.1558. Epub 2022 Feb 6. J Genet Couns. 2022. PMID: 35128755

4

Rapid genome-wide sequencing in a neonatal intensive care unit: A retrospective qualitative exploration of parental experiences.

Aldridge CE, Osiovich H, Hal Siden H; RAPIDOMICS Study; GenCOUNSEL Study; Elliott AM. Aldridge CE, et al. J Genet Couns. 2021 Apr;30(2):616-629. doi: 10.1002/jgc4.1353. Epub 2020 Nov 1. J Genet Couns. 2021. PMID: 33131147

5

Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates.

Ayres S, Gallacher L, Stark Z, Brett GR. Ayres S, et al. J Genet Couns. 2019 Apr;28(2):273-282. doi: 10.1002/jgc4.1086. Epub 2019 Jan 21. J Genet Couns. 2019. PMID: 30663825

6

Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.

Hitchcock EC, Study C, Elliott AM. Hitchcock EC, et al. Mol Genet Genomic Med. 2020 Jul;8(7):e1254. doi: 10.1002/mgg3.1254. Epub 2020 May 8. Mol Genet Genomic Med. 2020. PMID: 32383361 Free PMC article.

7

A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.

Cakici JA, Dimmock DP, Caylor SA, Gaughran M, Clarke C, Triplett C, Clark MM, Kingsmore SF, Bloss CS. Cakici JA, et al. Am J Hum Genet. 2020 Nov 5;107(5):953-962. doi: 10.1016/j.ajhg.2020.10.004. Am J Hum Genet. 2020. PMID: 33157008 Free PMC article. Clinical Trial.

8

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.

Li KC, Birch PH, Garrett BM, MacPhee M, Adam S, Friedman JM. Li KC, et al. J Nurs Scholarsh. 2016 May;48(3):265-75. doi: 10.1111/jnu.12207. Epub 2016 Apr 7. J Nurs Scholarsh. 2016. PMID: 27061758

9

Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety.

Wainstein T, Campbell T, Stojkova BJ, Lavoie PM, Elliott AM. Wainstein T, et al. J Genet Couns. 2022 Dec;31(6):1306-1316. doi: 10.1002/jgc4.1605. Epub 2022 Jun 22. J Genet Couns. 2022. PMID: 35733279

10

Putting genome-wide sequencing in neonates into perspective.

van der Sluijs PJ, Aten E, Barge-Schaapveld DQCM, Bijlsma EK, Bökenkamp-Gramann R, Donker Kaat L, van Doorn R, van de Putte DF, van Haeringen A, Ten Harkel ADJ, Hilhorst-Hofstee Y, Hoffer MJV, den Hollander NS, van Ierland Y, Koopmans M, Kriek M, Moghadasi S, Nibbeling EAR, Peeters-Scholte CMPCD, Potjer TP, van Rij M, Ruivenkamp CAL, Rutten JW, Steggerda SJ, Suerink M, Tan RNGB, van der Tuin K, Visser R, van der Werf-'t Lam AS, Williams M, Witlox R, Santen GWE. van der Sluijs PJ, et al. Genet Med. 2019 May;21(5):1074-1082. doi: 10.1038/s41436-018-0293-0. Epub 2018 Oct 5. Genet Med. 2019. PMID: 30287924 Free article.

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