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For: Knoppers BM, Zawati MH, Sénécal K. Return of genetic testing results in the era of whole-genome sequencing. Nat Rev Genet 2015;16:553-9. [PMID: 26239711 DOI: 10.1038/nrg3960] [Cited by in Crossref: 98] [Cited by in F6Publishing: 88] [Article Influence: 14.0] [Reference Citation Analysis]
Number Citing Articles
1 Elliott AM, Friedman JM. The importance of genetic counselling in genome-wide sequencing. Nat Rev Genet 2018;19:735-6. [DOI: 10.1038/s41576-018-0057-3] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 5.3] [Reference Citation Analysis]
2 Hofstatter E, Mehra K, Yushak M, Pusztai L. Tumor profiling and the incidentalome: patient decisions and risks. Future Oncology 2015;11:3299-305. [DOI: 10.2217/fon.15.260] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
3 Horiuchi Y, Matsubayashi H, Kiyozumi Y, Nishimura S, Higashigawa S, Kado N, Nagashima T, Mizuguchi M, Ohnami S, Arai M, Urakami K, Kusuhara M, Yamaguchi K. Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients. Hum Genet 2021;140:321-31. [PMID: 32710294 DOI: 10.1007/s00439-020-02207-6] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Blasimme A, Brall C, Vayena E. Reporting Genetic Findings to Individual Research Participants: Guidelines From the Swiss Personalized Health Network. Front Genet 2020;11:585820. [PMID: 33362850 DOI: 10.3389/fgene.2020.585820] [Reference Citation Analysis]
5 Borle K, Dey A, Carrion P, Austin J, Elliott AM; GenCOUNSEL Study. Genetic counseling research and COVID-19: A lesson in resiliency. J Genet Couns 2021. [PMID: 34510629 DOI: 10.1002/jgc4.1502] [Reference Citation Analysis]
6 Liu J, Zhou Y, Qi X, Chen J, Chen W, Qiu G, Wu Z, Wu N. CRISPR/Cas9 in zebrafish: an efficient combination for human genetic diseases modeling. Hum Genet 2017;136:1-12. [PMID: 27807677 DOI: 10.1007/s00439-016-1739-6] [Cited by in Crossref: 51] [Cited by in F6Publishing: 40] [Article Influence: 8.5] [Reference Citation Analysis]
7 Staunton C, Kösters M, Pramstaller PP, Mascalzoni D. Return of research results (RoRR) to the healthy CHRIS cohort: designing a policy with the participants. J Community Genet 2021. [PMID: 34241790 DOI: 10.1007/s12687-021-00536-1] [Reference Citation Analysis]
8 Hylind R, Smith M, Rasmussen-Torvik L, Aufox S. Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results. J Community Genet 2018;9:19-26. [PMID: 28656483 DOI: 10.1007/s12687-017-0314-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
9 Huang K, Yang M, Pan Z, Heidel FH, Scherr M, Eder M, Fischer T, Büsche G, Welte K, von Neuhoff N, Ganser A, Li Z. Leukemogenic potency of the novel FLT3-N676K mutant. Ann Hematol 2016;95:783-91. [DOI: 10.1007/s00277-016-2616-z] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
10 Mackley M, McGuire K, Taylor J, Watkins H, Ormondroyd E. From Genotype to Phenotype. Circ Genom Precis Med 2018;11:e002316. [PMID: 30354302 DOI: 10.1161/CIRCGEN.118.002316] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 1.3] [Reference Citation Analysis]
11 Boeldt DL, Cheung C, Ariniello L, Darst BF, Topol S, Schork NJ, Philis-Tsimikas A, Torkamani A, Fortmann AL, Bloss CS. Patient perspectives on whole-genome sequencing for undiagnosed diseases. Per Med 2017;14:17-25. [PMID: 29749824 DOI: 10.2217/pme-2016-0050] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
12 Winkler EC, Wiemann S. Findings made in gene panel to whole genome sequencing: data, knowledge, ethics – and consequences? Expert Review of Molecular Diagnostics 2016;16:1259-70. [DOI: 10.1080/14737159.2016.1212662] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 1.2] [Reference Citation Analysis]
13 Kelly MA, Leader JB, Wain KE, Bodian D, Oetjens MT, Ledbetter DH, Martin CL, Strande NT. Leveraging population-based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project. Am J Med Genet C Semin Med Genet 2021;187:83-94. [PMID: 33576083 DOI: 10.1002/ajmg.c.31887] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Lázaro-Muñoz G, Farrell MS, Crowley JJ, Filmyer DM, Shaughnessy RA, Josiassen RC, Sullivan PF. Improved ethical guidance for the return of results from psychiatric genomics research. Mol Psychiatry 2018;23:15-23. [PMID: 29158581 DOI: 10.1038/mp.2017.228] [Cited by in Crossref: 22] [Cited by in F6Publishing: 20] [Article Influence: 4.4] [Reference Citation Analysis]
15 Hurlimann T, Jaitovich Groisman I, Godard B. Exploring neurologists' perspectives on the return of next generation sequencing results to their patients: a needed step in the development of guidelines. BMC Med Ethics 2018;19:81. [PMID: 30268121 DOI: 10.1186/s12910-018-0320-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
16 Wu N, Liu B, Du H, Zhao S, Li Y, Cheng X, Wang S, Lin J, Zhou J, Qiu G, Wu Z, Zhang J; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study. The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases. Comput Struct Biotechnol J 2019;17:954-62. [PMID: 31360334 DOI: 10.1016/j.csbj.2019.06.006] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 3.7] [Reference Citation Analysis]
17 Liu Z, Chai T, Zhang Y, Chu A, Liang B, Guo X, Guo Z, Song R, Hou G, Yuan J, Liu Y, Zhang Y. Identification of abnormal nuclear and mitochondrial genes in esophageal cancer cells. Mol Med Rep 2018;17:2817-26. [PMID: 29257265 DOI: 10.3892/mmr.2017.8228] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
18 Elliott AM, Guimond C. Genetic counseling considerations in cerebral palsy. Mol Genet Metab 2021:S1096-7192(21)00755-1. [PMID: 34389249 DOI: 10.1016/j.ymgme.2021.07.004] [Reference Citation Analysis]
19 Bradbury AR, Patrick-Miller L, Egleston BL, Maxwell KN, DiGiovanni L, Brower J, Fetzer D, Bennett Gaieski J, Brandt A, McKenna D, Long J, Powers J, Stopfer JE, Nathanson KL, Domchek SM. Returning Individual Genetic Research Results to Research Participants: Uptake and Outcomes Among Patients With Breast Cancer. JCO Precis Oncol 2018;2. [PMID: 32095738 DOI: 10.1200/po.17.00250] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
20 Arora NS, Davis JK, Kirby C, McGuire AL, Green RC, Blumenthal-Barby JS, Ubel PA; MedSeq Project. Communication challenges for nongeneticist physicians relaying clinical genomic results. Per Med 2016;14:423-31. [PMID: 29181085 DOI: 10.2217/pme-2017-0008] [Cited by in Crossref: 22] [Cited by in F6Publishing: 18] [Article Influence: 4.4] [Reference Citation Analysis]
21 Pulford DJ, Harter P, Floquet A, Barrett C, Suh DH, Friedlander M, Arranz JA, Hasegawa K, Tada H, Vuylsteke P, Mirza MR, Donadello N, Scambia G, Johnson T, Cox C, Chan JK, Imhof M, Herzog TJ, Calvert P, Wimberger P, Berton-Rigaud D, Lim MC, Elser G, Xu CF, du Bois A. Communicating BRCA research results to patients enrolled in international clinical trials: lessons learnt from the AGO-OVAR 16 study. BMC Med Ethics 2016;17:63. [PMID: 27769273 DOI: 10.1186/s12910-016-0144-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
22 Bertier G, Hétu M, Joly Y. Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users' views. BMC Med Genomics 2016;9:52. [PMID: 27514372 DOI: 10.1186/s12920-016-0213-6] [Cited by in Crossref: 34] [Cited by in F6Publishing: 33] [Article Influence: 5.7] [Reference Citation Analysis]
23 Umbach N, Beißbarth T, Bleckmann A, Duttge G, Flatau L, König A, Kuhn J, Perera-bel J, Roschauer J, Schulze T, Schweda M, Urban A, Zimmermann A, Sax U. Clinical application of genomic high-throughput data: Infrastructural, ethical, legal and psychosocial aspects. European Neuropsychopharmacology 2020;31:1-15. [DOI: 10.1016/j.euroneuro.2019.09.008] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
24 Fleming J, Terrill B, Dziadek M, Kirk EP, Roscioli T, Barlow-stewart K. Personal genomic screening: How best to facilitate preparedness of future clients. European Journal of Medical Genetics 2019;62:397-404. [DOI: 10.1016/j.ejmg.2019.05.006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
25 Brunfeldt M, Teare H, Soini S, Kääriäinen H. Perceptions of legislation relating to the sharing of genomic biobank results with donors-a survey of BBMRI-ERIC biobanks. Eur J Hum Genet 2018;26:324-9. [PMID: 29330544 DOI: 10.1038/s41431-017-0049-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
26 Du L, Wang M. Genetic Privacy and Data Protection: A Review of Chinese Direct-to-Consumer Genetic Test Services. Front Genet 2020;11:416. [PMID: 32425986 DOI: 10.3389/fgene.2020.00416] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
27 Teare HJA, Prictor M, Kaye J. Reflections on dynamic consent in biomedical research: the story so far. Eur J Hum Genet 2021;29:649-56. [PMID: 33249421 DOI: 10.1038/s41431-020-00771-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
28 Newey PJ. Clinical genetic testing in endocrinology: Current concepts and contemporary challenges. Clin Endocrinol 2019;91:587-607. [DOI: 10.1111/cen.14053] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
29 Mwaka E, Horn L. Researchers' Perspectives on Informed Consent and Ethical Review of Biobank Research in South Africa: A Cross-Sectional Study. J Empir Res Hum Res Ethics 2019;14:307-17. [PMID: 31378129 DOI: 10.1177/1556264619866991] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
30 Nestor JG, Groopman EE, Gharavi AG. Towards precision nephrology: the opportunities and challenges of genomic medicine. J Nephrol 2018;31:47-60. [PMID: 29043570 DOI: 10.1007/s40620-017-0448-0] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
31 Ralefala D, Kasule M, Matshabane OP, Wonkam A, Matshaba M, de Vries J. Participants' Preferences and Reasons for Wanting Feedback of Individual Genetic Research Results From an HIV-TB Genomic Study: A Case Study From Botswana. J Empir Res Hum Res Ethics 2021;16:525-36. [PMID: 34662218 DOI: 10.1177/15562646211043985] [Reference Citation Analysis]
32 Olgiati S, Quadri M, Bonifati V. Genetics of movement disorders in the next-generation sequencing era: NGS in Movement Disorders. Mov Disord 2016;31:458-70. [DOI: 10.1002/mds.26521] [Cited by in Crossref: 28] [Cited by in F6Publishing: 18] [Article Influence: 4.7] [Reference Citation Analysis]
33 Clarke AJ, Wallgren-Pettersson C. Ethics in genetic counselling. J Community Genet 2019;10:3-33. [PMID: 29949066 DOI: 10.1007/s12687-018-0371-7] [Cited by in Crossref: 21] [Cited by in F6Publishing: 14] [Article Influence: 5.3] [Reference Citation Analysis]
34 Mackley MP, Capps B. Expect the unexpected: screening for secondary findings in clinical genomics research. Br Med Bull 2017;122:109-22. [PMID: 28398474 DOI: 10.1093/bmb/ldx009] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
35 Khan M, Fadaie Z, Cornelis SS, Cremers FPM, Roosing S. Identification and Analysis of Genes Associated with Inherited Retinal Diseases. Methods Mol Biol 2019;1834:3-27. [PMID: 30324433 DOI: 10.1007/978-1-4939-8669-9_1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
36 Schickhardt C, Fleischer H, Winkler EC. Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysis. BMC Med Ethics 2020;21:7. [PMID: 31948449 DOI: 10.1186/s12910-020-0446-y] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
37 Matsen CB, Lyons S, Goodman MS, Biesecker BB, Kaphingst KA. Decision role preferences for return of results from genome sequencing amongst young breast cancer patients. Patient Educ Couns 2019;102:155-61. [PMID: 30098907 DOI: 10.1016/j.pec.2018.08.004] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
38 Beauvais MJS, Thorogood AM, Szego MJ, Sénécal K, Zawati MH, Knoppers BM. Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility. Front Genet 2021;12:535340. [PMID: 33868358 DOI: 10.3389/fgene.2021.535340] [Reference Citation Analysis]
39 Chalmers D, Nicol D, Kaye J, Bell J, Campbell AV, Ho CW, Kato K, Minari J, Ho CH, Mitchell C, Molnár-Gábor F, Otlowski M, Thiel D, Fullerton SM, Whitton T. Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era. BMC Med Ethics 2016;17:39. [PMID: 27405974 DOI: 10.1186/s12910-016-0124-2] [Cited by in Crossref: 56] [Cited by in F6Publishing: 53] [Article Influence: 9.3] [Reference Citation Analysis]
40 Stoeklé HC, Mamzer-Bruneel MF, Vogt G, Hervé C. 23andMe: a new two-sided data-banking market model. BMC Med Ethics 2016;17:19. [PMID: 27059184 DOI: 10.1186/s12910-016-0101-9] [Cited by in Crossref: 36] [Cited by in F6Publishing: 27] [Article Influence: 6.0] [Reference Citation Analysis]
41 Torrorey-Sawe R, van der Merwe N, Mining SK, Kotze MJ. Pioneering Informed Consent for Return of Research Results to Breast Cancer Patients Facing Barriers to Implementation of Genomic Medicine: The Kenyan BRCA1/2 Testing Experience Using Whole Exome Sequencing. Front Genet 2020;11:170. [PMID: 32231682 DOI: 10.3389/fgene.2020.00170] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
42 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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44 Liu GH, Xu MJ, Chang QC, Gao JF, Wang CR, Zhu XQ. De novo transcriptomic analysis of the female and male adults of the blood fluke Schistosoma turkestanicum. Parasit Vectors 2016;9:143. [PMID: 26968659 DOI: 10.1186/s13071-016-1436-2] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
45 Wei X, Qiu J, Yong K, Fan J, Zhang Q, Hua H, Liu J, Wang Q, Olsen KM, Han B, Huang X. A quantitative genomics map of rice provides genetic insights and guides breeding. Nat Genet 2021;53:243-53. [PMID: 33526925 DOI: 10.1038/s41588-020-00769-9] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 13.0] [Reference Citation Analysis]
46 Feliubadaló L, Tonda R, Gausachs M, Trotta JR, Castellanos E, López-Doriga A, Teulé À, Tornero E, Del Valle J, Gel B, Gut M, Pineda M, González S, Menéndez M, Navarro M, Capellá G, Gut I, Serra E, Brunet J, Beltran S, Lázaro C. Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer. Sci Rep 2017;7:37984. [PMID: 28050010 DOI: 10.1038/srep37984] [Cited by in Crossref: 28] [Cited by in F6Publishing: 26] [Article Influence: 5.6] [Reference Citation Analysis]
47 Zhang XX, Cong W, Elsheikha HM, Liu GH, Ma JG, Huang WY, Zhao Q, Zhu XQ. De novo transcriptome sequencing and analysis of the juvenile and adult stages of Fasciola gigantica. Infect Genet Evol 2017;51:33-40. [PMID: 28286139 DOI: 10.1016/j.meegid.2017.03.007] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
48 Leitsalu L, Alavere H, Jacquemont S, Kolk A, Maillard AM, Reigo A, Nõukas M, Reymond A, Männik K, Ng PC, Metspalu A. Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants. Per Med 2016;13:303-14. [PMID: 29749813 DOI: 10.2217/pme-2016-0009] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
49 Vadaparampil ST, Cragun D. Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing. Transl Behav Med 2018;8:80-4. [PMID: 29385585 DOI: 10.1093/tbm/ibx048] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
50 Groopman EE, Rasouly HM, Gharavi AG. Genomic medicine for kidney disease. Nat Rev Nephrol 2018;14:83-104. [PMID: 29307893 DOI: 10.1038/nrneph.2017.167] [Cited by in Crossref: 50] [Cited by in F6Publishing: 44] [Article Influence: 12.5] [Reference Citation Analysis]
51 Martyn M, Kanga-parabia A, Lynch E, James PA, Macciocca I, Trainer AH, Halliday J, Keogh L, Wale J, Winship I, Bogwitz M, Valente G, Walsh M, Downie L, Amor D, Wallis M, Cunningham F, Burgess M, Brown NJ, Jarmolowicz A, Lunke S, Goranitis I, Gaff CL; Melbourne Genomics Health Alliance. A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system. J Genet Couns 2019;28:388-97. [DOI: 10.1002/jgc4.1102] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
52 Tamayo LI, Lin H, Ahmed A, Shahriar H, Hasan R, Sarwar G, Eunus HM, Ahsan H, Pierce BL. Research Participants' Attitudes towards Receiving Information on Genetic Susceptibility to Arsenic Toxicity in Rural Bangladesh. Public Health Genomics 2020;23:69-76. [PMID: 32069464 DOI: 10.1159/000505632] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
53 Young AL, Butow PN, Tucker KM, Wakefield CE, Healey E, Williams R. Challenges and strategies proposed by genetic health professionals to assist with family communication. Eur J Hum Genet 2019;27:1630-8. [PMID: 31189929 DOI: 10.1038/s41431-019-0447-9] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
54 Turner H, Jackson L. Evidence for penetrance in patients without a family history of disease: a systematic review. Eur J Hum Genet 2020;28:539-50. [PMID: 31937893 DOI: 10.1038/s41431-019-0556-5] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 4.5] [Reference Citation Analysis]
55 Hallowell N, Parker M, Nellåker C. Big data phenotyping in rare diseases: some ethical issues. Genet Med 2019;21:272-4. [PMID: 29907800 DOI: 10.1038/s41436-018-0067-8] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
56 Holm IA. Pediatric Issues in Return of Results and Incidental Findings: Weighing Autonomy and Best Interests. Genet Test Mol Biomarkers 2017;21:155-8. [PMID: 28140662 DOI: 10.1089/gtmb.2016.0414] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
57 Kawame H, Fukushima A, Fuse N, Nagami F, Suzuki Y, Sakurai-Yageta M, Yasuda J, Yamaguchi-Kabata Y, Kinoshita K, Ogishima S, Takai T, Kuriyama S, Hozawa A, Nakaya N, Nakamura T, Minegishi N, Sugawara J, Suzuki K, Tomita H, Uruno A, Kobayashi T, Aizawa Y, Tokutomi T, Yamamoto K, Ohneda K, Kure S, Aoki Y, Katagiri H, Ishigaki Y, Sawada S, Sasaki M, Yamamoto M. The return of individual genomic results to research participants: design and pilot study of Tohoku Medical Megabank Project. J Hum Genet 2021. [PMID: 34234266 DOI: 10.1038/s10038-021-00952-8] [Reference Citation Analysis]
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59 Chad L, Szego MJ. Please give me a copy of my child's raw genomic data. NPJ Genom Med 2021;6:15. [PMID: 33597540 DOI: 10.1038/s41525-021-00175-y] [Reference Citation Analysis]
60 Korngiebel DM, West KM, Burke W. Clinician-Stakeholders' Perspectives on Using Patient Portals to Return Lynch Syndrome Screening Results. J Genet Couns 2018;27:349-57. [PMID: 29159545 DOI: 10.1007/s10897-017-0179-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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62 Vornanen M, Aktan-Collan K, Hallowell N, Konttinen H, Kääriäinen H, Haukkala A. "I would like to discuss it further with an expert": a focus group study of Finnish adults' perspectives on genetic secondary findings. J Community Genet 2018;9:305-14. [PMID: 29340884 DOI: 10.1007/s12687-018-0356-6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
63 Ottman R, Freyer C, Mefford HC, Poduri A, Lowenstein DH; Epilepsy Return of Results Workshop Participants. Return of individual results in epilepsy genomic research: A view from the field. Epilepsia 2018;59:1635-42. [PMID: 30098010 DOI: 10.1111/epi.14530] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
64 Caenazzo L, Tozzo P, Dierickx K. New Frontiers and Old Challenges: How to Manage Incidental Findings When Forensic Diagnosis Goes Beyond. Diagnostics (Basel) 2020;10:E731. [PMID: 32971910 DOI: 10.3390/diagnostics10090731] [Reference Citation Analysis]
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