Vears DF - Search Results

1

Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.

Mulley JC, Scheffer IE, Desai T, Bayly MA, Grinton BE, Vears DF, Berkovic SF, Dibbens LM. Mulley JC, et al. Among authors: vears df. Epilepsia. 2011 Oct;52(10):e139-42. doi: 10.1111/j.1528-1167.2011.03188.x. Epub 2011 Jul 21. Epilepsia. 2011. PMID: 21777232 Free article.

2

What's in a name? Justifying terminology for genomic findings beyond the initial test indication: A scoping review.

White S, Haas M, Laginha KJ, Laurendet K, Gaff C, Vears D, Newson AJ. White S, et al. Genet Med. 2023 Nov;25(11):100936. doi: 10.1016/j.gim.2023.100936. Epub 2023 Jul 13. Genet Med. 2023. PMID: 37454281 Free article. Review.

3

Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography.

Kuiper JML, Borry P, Vears DF, Van Esch H, Cornel MC, Van Hoyweghen I. Kuiper JML, et al. Among authors: vears df. Eur J Hum Genet. 2023 Dec;31(12):1387-1392. doi: 10.1038/s41431-023-01436-3. Epub 2023 Aug 18. Eur J Hum Genet. 2023. PMID: 37592172 Free PMC article.

4

Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?

Vears DF, Savulescu J, Christodoulou J, Wall M, Newson AJ. Vears DF, et al. Pharmgenomics Pers Med. 2023 Jul 1;16:681-691. doi: 10.2147/PGPM.S376083. eCollection 2023. Pharmgenomics Pers Med. 2023. PMID: 37415831 Free PMC article. Review.

5

Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations.

Lynch F, Meng Y, Best S, Goranitis I, Savulescu J, Gyngell C, Vears DF. Lynch F, et al. Among authors: vears df. Eur J Hum Genet. 2024 Mar;32(3):295-301. doi: 10.1038/s41431-023-01381-1. Epub 2023 May 10. Eur J Hum Genet. 2024. PMID: 37165103

6

Storing paediatric genomic data for sequential interrogation across the lifespan.

Gyngell C, Lynch F, Vears D, Bowman-Smart H, Savulescu J, Christodoulou J. Gyngell C, et al. J Med Ethics. 2023 Jun 1:jme-2022-108471. doi: 10.1136/jme-2022-108471. Online ahead of print. J Med Ethics. 2023. PMID: 37263770 Free article.

7

Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation.

Lynch F, Best S, Gaff C, Downie L, Archibald AD, Gyngell C, Goranitis I, Peters R, Savulescu J, Lunke S, Stark Z, Vears DF. Lynch F, et al. Among authors: vears df. Int J Neonatal Screen. 2024 Jan 17;10(1):6. doi: 10.3390/ijns10010006. Int J Neonatal Screen. 2024. PMID: 38248635 Free PMC article.

8

Clinician perspectives on policy approaches to genetic risk disclosure in families.

Phillips A, Vears DF, Van Hoyweghen I, Borry P. Phillips A, et al. Among authors: vears df. Fam Cancer. 2024 Jun;23(2):177-186. doi: 10.1007/s10689-024-00375-2. Epub 2024 Mar 28. Fam Cancer. 2024. PMID: 38548926 Free PMC article.

9

A practical checklist for return of results from genomic research in the European context.

Vears DF, Hallowell N, Bentzen HB, Ellul B, Nøst TH, Kerasidou A, Kerr SM, Th Mayrhofer M, Mežinska S, Ormondroyd E, Solberg B, Sand BW, Budin-Ljøsne I. Vears DF, et al. Eur J Hum Genet. 2023 Jun;31(6):687-695. doi: 10.1038/s41431-023-01328-6. Epub 2023 Mar 22. Eur J Hum Genet. 2023. PMID: 36949262 Free PMC article.

10

Rapid Genomic Testing in Intensive Care: Health Professionals' Perspectives on Ethical Challenges.

Arkell K, Gyngell C, Stark Z, Vears DF. Arkell K, et al. Among authors: vears df. Children (Basel). 2023 May 1;10(5):824. doi: 10.3390/children10050824. Children (Basel). 2023. PMID: 37238372 Free PMC article.

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