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Attitudes of people with inherited retinal conditions toward gene editing technology.
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Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families.
PLoS One. 2015 Jul 6;10(7):e0131679. doi: 10.1371/journal.pone.0131679. eCollection 2015.
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Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier alleles.
Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3052-9. doi: 10.1167/iovs.05-0111.
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Strategies for Interdisciplinary Human Gene Editing Research: Insights from a Swiss Project.
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Experts' perspectives on human gene editing in Switzerland.
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A decade of public engagement regarding human germline gene editing: a systematic scoping review.
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Whether Whole Eye Transplant is a Benefit or Harm Depends on More Than the Observer.
Am J Bioeth. 2024 May;24(5):87-90. doi: 10.1080/15265161.2024.2328281. Epub 2024 Apr 18.
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"What if" should precede "whether" and "how" in the social conversation around human germline gene editing.
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A Q methodology study on divergent perspectives on CRISPR-Cas9 in the Netherlands.
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1
Genome-edited baby claim provokes international outcry.
Nature. 2018 Nov;563(7733):607-608. doi: 10.1038/d41586-018-07545-0.
2
How do genetically disabled adults view selective reproduction? Impairment, identity, and genetic screening.
Mol Genet Genomic Med. 2018 Nov;6(6):941-956. doi: 10.1002/mgg3.463. Epub 2018 Sep 9.
3
Correction of the Marfan Syndrome Pathogenic FBN1 Mutation by Base Editing in Human Cells and Heterozygous Embryos.
Mol Ther. 2018 Nov 7;26(11):2631-2637. doi: 10.1016/j.ymthe.2018.08.007. Epub 2018 Aug 14.
4
Saturation in qualitative research: exploring its conceptualization and operationalization.
Qual Quant. 2018;52(4):1893-1907. doi: 10.1007/s11135-017-0574-8. Epub 2017 Sep 14.
6
Correction of a pathogenic gene mutation in human embryos.
Nature. 2017 Aug 24;548(7668):413-419. doi: 10.1038/nature23305. Epub 2017 Aug 2.
7
Impairment Experiences, Identity and Attitudes Towards Genetic Screening: the Views of People with Spinal Muscular Atrophy.
J Genet Couns. 2018 Feb;27(1):69-84. doi: 10.1007/s10897-017-0122-7. Epub 2017 Jun 30.
8
Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors.
Cell Res. 2017 Jun;27(6):830-833. doi: 10.1038/cr.2017.57. Epub 2017 Apr 21.
9
A Global Social Media Survey of Attitudes to Human Genome Editing.
Cell Stem Cell. 2016 May 5;18(5):569-72. doi: 10.1016/j.stem.2016.04.011.
10
Should you edit your children's genes?
Nature. 2016 Feb 25;530(7591):402-5. doi: 10.1038/530402a.

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