Hill M - Search Results

1

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. Among authors: hill m. 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.

2

Determination of foetal sex in pregnancies at risk of haemophilia: a qualitative study exploring the clinical practices and attitudes of health professionals in the United Kingdom.

Hill M, Compton C, Lewis C, Skirton H, Chitty LS. Hill M, et al. Haemophilia. 2012 Jul;18(4):575-83. doi: 10.1111/j.1365-2516.2011.02653.x. Epub 2011 Sep 23. Haemophilia. 2012. PMID: 21951674

3

Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users' perspective.

Lewis C, Hill M, Skirton H, Chitty LS. Lewis C, et al. Among authors: hill m. Eur J Hum Genet. 2012 Nov;20(11):1127-33. doi: 10.1038/ejhg.2012.50. Epub 2012 Mar 28. Eur J Hum Genet. 2012. PMID: 22453293 Free PMC article.

4

Implementing noninvasive prenatal fetal sex determination using cell-free fetal DNA in the United Kingdom.

Hill M, Lewis C, Jenkins L, Allen S, Elles RG, Chitty LS. Hill M, et al. Expert Opin Biol Ther. 2012 Jun;12 Suppl 1:S119-26. doi: 10.1517/14712598.2012.666522. Epub 2012 Apr 16. Expert Opin Biol Ther. 2012. PMID: 22500945

5

Fetal sex determination using cell-free fetal DNA: service users' experiences of and preferences for service delivery.

Lewis C, Hill M, Skirton H, Chitty LS. Lewis C, et al. Among authors: hill m. Prenat Diagn. 2012 Aug;32(8):735-41. doi: 10.1002/pd.3893. Epub 2012 May 10. Prenat Diagn. 2012. PMID: 22573474

6

Women's and health professionals' preferences for prenatal tests for Down syndrome: a discrete choice experiment to contrast noninvasive prenatal diagnosis with current invasive tests.

Hill M, Fisher J, Chitty LS, Morris S. Hill M, et al. Genet Med. 2012 Nov;14(11):905-13. doi: 10.1038/gim.2012.68. Epub 2012 Aug 30. Genet Med. 2012. PMID: 22935718 Free article.

7

Non-invasive prenatal testing for single gene disorders: exploring the ethics.

Deans Z, Hill M, Chitty LS, Lewis C. Deans Z, et al. Among authors: hill m. Eur J Hum Genet. 2013 Jul;21(7):713-8. doi: 10.1038/ejhg.2012.250. Epub 2012 Nov 28. Eur J Hum Genet. 2013. PMID: 23188047 Free PMC article.

8

Non-invasive prenatal diagnosis for single gene disorders: experience of patients.

Lewis C, Hill M, Chitty LS. Lewis C, et al. Among authors: hill m. Clin Genet. 2014 Apr;85(4):336-42. doi: 10.1111/cge.12179. Epub 2013 May 27. Clin Genet. 2014. PMID: 23631435

9

Views and preferences for the implementation of non-invasive prenatal diagnosis for single gene disorders from health professionals in the United Kingdom.

Hill M, Karunaratna M, Lewis C, Forya F, Chitty L. Hill M, et al. Am J Med Genet A. 2013 Jul;161A(7):1612-8. doi: 10.1002/ajmg.a.35972. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696422

10

Non-invasive prenatal testing for trisomy 21: a cross-sectional survey of service users' views and likely uptake.

Lewis C, Hill M, Silcock C, Daley R, Chitty LS. Lewis C, et al. Among authors: hill m. BJOG. 2014 Apr;121(5):582-94. doi: 10.1111/1471-0528.12579. Epub 2014 Jan 17. BJOG. 2014. PMID: 24433394

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