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For: Johnson SB, Slade I, Giubilini A, Graham M. Rethinking the ethical principles of genomic medicine services. Eur J Hum Genet 2020;28:147-54. [PMID: 31534213 DOI: 10.1038/s41431-019-0507-1] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
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1 Eikemo H, Roten LT, Vaaler AE. Research based on existing clinical data and biospecimens: a systematic study of patients' opinions. BMC Med Ethics 2022;23:60. [PMID: 35710552 DOI: 10.1186/s12910-022-00799-4] [Reference Citation Analysis]
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3 Pysar R, Wallingford CK, Boyle J, Campbell SB, Eckstein L, McWhirter R, Terrill B, Jacobs C, McInerney-Leo AM. Australian human research ethics committee members' confidence in reviewing genomic research applications. Eur J Hum Genet 2021. [PMID: 34446835 DOI: 10.1038/s41431-021-00951-5] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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5 Carress H, Lawson DJ, Elhaik E. Population genetic considerations for using biobanks as international resources in the pandemic era and beyond. BMC Genomics 2021;22:351. [PMID: 34001009 DOI: 10.1186/s12864-021-07618-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
6 de Vries JJC, Brown JR, Couto N, Beer M, Le Mercier P, Sidorov I, Papa A, Fischer N, Oude Munnink BB, Rodriquez C, Zaheri M, Sayiner A, Hönemann M, Cataluna AP, Carbo EC, Bachofen C, Kubacki J, Schmitz D, Tsioka K, Matamoros S, Höper D, Hernandez M, Puchhammer-Stöckl E, Lebrand A, Huber M, Simmonds P, Claas ECJ, López-Labrador FX; ESCV Network on Next-Generation Sequencing. Recommendations for the introduction of metagenomic next-generation sequencing in clinical virology, part II: bioinformatic analysis and reporting. J Clin Virol 2021;138:104812. [PMID: 33819811 DOI: 10.1016/j.jcv.2021.104812] [Cited by in Crossref: 4] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
7 Newson AJ. The promise of public health ethics for precision medicine: the case of newborn preventive genomic sequencing. Hum Genet 2021. [PMID: 33715055 DOI: 10.1007/s00439-021-02269-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Adashi EY, Cohen IG. CRISPR immunity: a case study for justified somatic genetic modification? J Med Ethics 2021:medethics-2020-106838. [PMID: 33658335 DOI: 10.1136/medethics-2020-106838] [Reference Citation Analysis]
9 Mann SP, Treit PV, Geyer PE, Omenn GS, Mann M. Ethical Principles, Constraints and Opportunities in Clinical Proteomics. Mol Cell Proteomics 2021;:100046. [PMID: 33453411 DOI: 10.1016/j.mcpro.2021.100046] [Cited by in Crossref: 3] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
10 Vidgen ME, Kaladharan S, Malacova E, Hurst C, Waddell N. Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia. BMC Med Ethics 2020;21:119. [PMID: 33213438 DOI: 10.1186/s12910-020-00563-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
11 Díaz-Peña R, Quiñones LA, Castro-Santos P, Durán J, Lucia A. Latin American Genes: The Great Forgotten in Rheumatoid Arthritis. J Pers Med 2020;10:E196. [PMID: 33114702 DOI: 10.3390/jpm10040196] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Hudson M, Garrison NA, Sterling R, Caron NR, Fox K, Yracheta J, Anderson J, Wilcox P, Arbour L, Brown A, Taualii M, Kukutai T, Haring R, Te Aika B, Baynam GS, Dearden PK, Chagné D, Malhi RS, Garba I, Tiffin N, Bolnick D, Stott M, Rolleston AK, Ballantyne LL, Lovett R, David-chavez D, Martinez A, Sporle A, Walter M, Reading J, Carroll SR. Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data. Nat Rev Genet 2020;21:377-84. [DOI: 10.1038/s41576-020-0228-x] [Cited by in Crossref: 29] [Cited by in F6Publishing: 63] [Article Influence: 14.5] [Reference Citation Analysis]
13 Wright CF, Ware JS, Lucassen AM, Hall A, Middleton A, Rahman N, Ellard S, Firth HV. Genomic variant sharing: a position statement. Wellcome Open Res 2019;4:22. [PMID: 31886409 DOI: 10.12688/wellcomeopenres.15090.2] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]