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Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100, 000 Genomes Project.
Lewis C, Hammond J, Hill M, Searle B, Hunter A, Patch C, Chitty LS, Sanderson SC. Lewis C, et al. Among authors: hammond j. Eur J Med Genet. 2020 Nov;63(11):104043. doi: 10.1016/j.ejmg.2020.104043. Epub 2020 Aug 22. Eur J Med Genet. 2020. PMID: 32835846 Free article.
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals.
Lewis C, Hammond J, Klapwijk JE, Harding E, Lou S, Vogel I, Szepe EJ, Hui L, Ingvoldstad-Malmgren C, Soller MJ, Ormond KE, Choolani M, Hill M, Riedijk S. Lewis C, et al. Among authors: hammond j. Prenat Diagn. 2021 May;41(6):720-732. doi: 10.1002/pd.5932. Epub 2021 Mar 30. Prenat Diagn. 2021. PMID: 33724493 Free PMC article.
Assessing women's preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design.
Hammond J, Klapwijk JE, Riedijk S, Lou S, Ormond KE, Vogel I, Hui L, Sziepe EJ, Buchanan J, Ingvoldstad-Malmgren C, Soller MJ, Harding E, Hill M, Lewis C. Hammond J, et al. PLoS One. 2022 Jan 28;17(1):e0261898. doi: 10.1371/journal.pone.0261898. eCollection 2022. PLoS One. 2022. PMID: 35089945 Free PMC article. Clinical Trial.
1,677 results