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Cited by in F6Publishing
For: Brothers KB, Lynch JA, Aufox SA, Connolly JJ, Gelb BD, Holm IA, Sanderson SC, McCormick JB, Williams JL, Wolf WA, Antommaria AH, Clayton EW. Practical guidance on informed consent for pediatric participants in a biorepository. Mayo Clin Proc 2014;89:1471-80. [PMID: 25264176 DOI: 10.1016/j.mayocp.2014.07.006] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Sabatello M, Appelbaum PS. Raising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings. J Law Med Ethics 2016;44:292-308. [PMID: 27338605 DOI: 10.1177/1073110516654123] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 4.0] [Reference Citation Analysis]
2 Murdoch B, Jandura A, Caulfield T. Reconsenting paediatric research participants for use of identifying data. J Med Ethics. [DOI: 10.1136/medethics-2021-107958] [Reference Citation Analysis]
3 Paquette ED, Derrington SF, Shukla A, Sinha N, Oswald S, Sorce L, Michelson KN. Biobanking in the Pediatric Critical Care Setting: Adolescent/Young Adult Perspectives. J Empir Res Hum Res Ethics 2018;13:391-401. [PMID: 29900801 DOI: 10.1177/1556264618782231] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
4 Brothers KB, Holm IA, Childerhose JE, Antommaria AHM, Bernhardt BA, Clayton EW, Gelb BD, Joffe S, Lynch JA, McCormick JB, McCullough LB, Parsons DW, Sundaresan AS, Wolf WA, Yu JH, Wilfond BS; Pediatrics Workgroup of the Clinical Sequencing Exploratory Research (CSER) Consortium. When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority. J Pediatr 2016;168:226-231.e1. [PMID: 26477867 DOI: 10.1016/j.jpeds.2015.09.020] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis]
5 Patrinos D, Knoppers BM, Kleiderman E, Rahbari N, Laplante DP, Wazana A. Re-contact Following Withdrawal of Minors from Research. Canadian Journal of Bioethics 2022;5:45. [DOI: 10.7202/1087202ar] [Reference Citation Analysis]
6 Goldenberg A, Brothers K. Misplaced Trust: Building Research Relationships in the Age of Biorepository Networks. Am J Bioeth 2018;18:21-3. [PMID: 29621469 DOI: 10.1080/15265161.2018.1431330] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
7 Nguyen MT, Goldblatt J, Isasi R, Jagut M, Jonker AH, Kaufmann P, Ouillade L, Molnar-Gabor F, Shabani M, Sid E, Tassé AM, Wong-Rieger D, Knoppers BM; IRDiRC-GA4GH Model Consent Clauses Task Force. Model consent clauses for rare disease research. BMC Med Ethics 2019;20:55. [PMID: 31370847 DOI: 10.1186/s12910-019-0390-x] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
8 Green RC, Goddard KAB, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. Am J Hum Genet 2016;98:1051-66. [PMID: 27181682 DOI: 10.1016/j.ajhg.2016.04.011] [Cited by in Crossref: 92] [Cited by in F6Publishing: 86] [Article Influence: 15.3] [Reference Citation Analysis]
9 Lynch JA, Zoller H. Recognizing Differences and Commonalities: The Rhetoric of Health and Medicine and Critical-Interpretive Health Communication. Communication Quarterly 2015;63:498-503. [DOI: 10.1080/01463373.2015.1103592] [Cited by in Crossref: 6] [Article Influence: 0.9] [Reference Citation Analysis]
10 Kasperbauer TJ, Halverson C. Adolescent Assent and Reconsent for Biobanking: Recent Developments and Emerging Ethical Issues. Front Med (Lausanne) 2021;8:686264. [PMID: 34307413 DOI: 10.3389/fmed.2021.686264] [Reference Citation Analysis]
11 López E, Thompson R, Gainotti S, Wang CM, Rubinstein Y, Taruscio D, Monaco L, Lochmüller H, Alonso V, Posada de la Paz M. Overview of existing initiatives to develop and improve access and data sharing in rare disease registries and biobanks worldwide. Expert Opinion on Orphan Drugs 2016;4:729-39. [DOI: 10.1080/21678707.2016.1188002] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
12 Garrison NA. Considerations for Returning Research Results to Culturally Diverse Participants and Families of Decedents. J Law Med Ethics 2015;43:569-75. [PMID: 26479567 DOI: 10.1111/jlme.12300] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
13 Garrett JR, Lantos JD, Biesecker LG, Childerhose JE, Chung WK, Holm IA, Koenig BA, McEwen JE, Wilfond BS, Brothers K; Clinical Sequencing Exploratory Research (CSER) Consortium Pediatrics Working Group. Rethinking the "open future" argument against predictive genetic testing of children. Genet Med 2019;21:2190-8. [PMID: 30894702 DOI: 10.1038/s41436-019-0483-4] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 6.3] [Reference Citation Analysis]
14 Wolf SM, Scholtes E, Koenig BA, Petersen GM, Berry SA, Beskow LM, Daly MB, Fernandez CV, Green RC, LeRoy BS, Lindor NM, O'Rourke PP, Breitkopf CR, Rothstein MA, Van Ness B, Wilfond BS. Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants. J Law Med Ethics 2018;46:87-109. [PMID: 30008546 DOI: 10.1177/1073110518766024] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
15 Jose R, Rooney R, Nagisetty N, Davis R, Hains D. Biorepository and integrative genomics initiative: designing and implementing a preliminary platform for predictive, preventive and personalized medicine at a pediatric hospital in a historically disadvantaged community in the USA. EPMA J 2018;9:225-34. [PMID: 30174759 DOI: 10.1007/s13167-018-0141-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
16 Brothers KB, Goldenberg AJ. Ethical and legal considerations for pediatric biobank consent: current and future perspectives. Per Med 2016;13:597-607. [PMID: 29754545 DOI: 10.2217/pme-2016-0028] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
17 Metcalfe RE. Open Science Within Pediatric Medical and Mental Health Systems: Practical Considerations for Behavioral Health Researchers. Front Psychol 2022;13:856949. [PMID: 35310242 DOI: 10.3389/fpsyg.2022.856949] [Reference Citation Analysis]
18 Rothstein MA, Wilbanks JT, Brothers KB. Citizen Science on Your Smartphone: An ELSI Research Agenda. J Law Med Ethics 2015;43:897-903. [PMID: 26711425 DOI: 10.1111/jlme.12327] [Cited by in Crossref: 15] [Cited by in F6Publishing: 17] [Article Influence: 3.0] [Reference Citation Analysis]
19 Berkman BE, Howard D, Wendler D. Reconsidering the Need for Reconsent at 18. Pediatrics 2018;142:e20171202. [PMID: 29980586 DOI: 10.1542/peds.2017-1202] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
20 Kong CC, Tarling TE, Strahlendorf C, Dittrick M, Vercauteren SM. Opinions of Adolescents and Parents About Pediatric Biobanking. Journal of Adolescent Health 2016;58:474-80. [DOI: 10.1016/j.jadohealth.2015.12.015] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 2.5] [Reference Citation Analysis]
21 Hartsock JA, Schwartz PH, Waltz AC, Ott MA. Anticipatory Waivers of Consent for Pediatric Biobanking. Ethics Hum Res 2019;41:14-21. [PMID: 30895753 DOI: 10.1002/eahr.500008] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
22 Fossey R, Kochan D, Winkler E, Pacyna JE, Olson J, Thibodeau S, Connolly JJ, Harr M, Behr MA, Prows CA, Cobb B, Myers MF, Leslie ND, Namjou-Khales B, Milo Rasouly H, Wynn J, Fedotov A, Chung WK, Gharavi A, Williams JL, Pais L, Holm I, Aufox S, Smith ME, Scrol A, Leppig K, Jarvik GP, Wiesner GL, Li R, Stroud M, Smoller JW, Sharp RR, Kullo IJ. Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience. J Pers Med 2018;8:E2. [PMID: 29301385 DOI: 10.3390/jpm8010002] [Cited by in Crossref: 29] [Cited by in F6Publishing: 25] [Article Influence: 7.3] [Reference Citation Analysis]