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For: Machini K, Douglas J, Braxton A, Tsipis J, Kramer K. Genetic counselors' views and experiences with the clinical integration of genome sequencing. J Genet Couns 2014;23:496-505. [PMID: 24671342 DOI: 10.1007/s10897-014-9709-4] [Cited by in Crossref: 37] [Cited by in F6Publishing: 32] [Article Influence: 4.6] [Reference Citation Analysis]
Number Citing Articles
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17 Li KC, Birch PH, Garrett BM, MacPhee M, Adam S, Friedman JM. Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing. J Nurs Scholarsh 2016;48:265-75. [PMID: 27061758 DOI: 10.1111/jnu.12207] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 2.3] [Reference Citation Analysis]
18 Ashton-Prolla P, Goldim JR, Vairo FP, da Silveira Matte U, Sequeiros J. Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil. J Community Genet 2015;6:275-83. [PMID: 26040235 DOI: 10.1007/s12687-015-0238-0] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 1.4] [Reference Citation Analysis]
19 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]
20 Hernan R, Cho MT, Wilson AL, Ahimaz P, Au C, Berger SM, Guzman E, Primiano M, Shaw JE, Ross M, Tabanfar L, Chilton I, Griffin E, Ratner C, Anyane-yeboa K, Iglesias A, Pisani L, Roohi J, Duong J, Martinez J, Appelbaum P, Klitzman R, Ottman R, Chung WK, Wynn J. Impact of patient education videos on genetic counseling outcomes after exome sequencing. Patient Education and Counseling 2020;103:127-35. [DOI: 10.1016/j.pec.2019.08.018] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
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23 Hurlimann T, Jaitovich Groisman I, Godard B. The elusive ideal of inclusiveness: lessons from a worldwide survey of neurologists on the ethical issues raised by whole-genome sequencing. BMC Med Ethics 2017;18:28. [PMID: 28399922 DOI: 10.1186/s12910-017-0187-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
24 Westerfield LE, Stover SR, Mathur VS, Nassef SA, Carter TG, Yang Y, Eng CM, Van den Veyver IB. Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice. Prenat Diagn 2015;35:1022-9. [PMID: 26275793 DOI: 10.1002/pd.4674] [Cited by in Crossref: 37] [Cited by in F6Publishing: 29] [Article Influence: 5.3] [Reference Citation Analysis]
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27 Chiang J(, Gorin MB. Challenges confronting precision medicine in the context of inherited retinal disorders. Expert Review of Precision Medicine and Drug Development 2016;1:195-205. [DOI: 10.1080/23808993.2016.1152159] [Cited by in Crossref: 4] [Article Influence: 0.7] [Reference Citation Analysis]
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29 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]
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32 Gourna EG, Armstrong N, Wallace SE. Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing. Eur J Hum Genet 2016;24:344-9. [PMID: 26059844 DOI: 10.1038/ejhg.2015.132] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
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