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Authors whose works are in public domain in at least one jurisdiction

List of works by Melissa Hill

"The communication and support from the health professional is incredibly important": A qualitative study exploring the processes and practices that support parental decision-making about postmortem examination

scientific article published on 04 November 2019

Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing; a mixed-methods systematic review

scientific article published on 02 May 2020

Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges

scientific article published on 19 June 2020

Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project

scientific article published on 03 November 2019

Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study

scientific article

Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?

scientific article published on 7 November 2017

Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study

scientific article published on 01 August 2019

Offering non-invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?

scientific article published on 11 September 2017

Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service

scientific article published on 18 July 2022

Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han's taxonomy of uncertainty

scientific article published on 07 July 2020

Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study

scientific article published on 30 January 2020

Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study

scientific article published in 2022

Preferences for prenatal diagnosis of sickle-cell disorder: A discrete choice experiment comparing potential service users and health-care providers.

scientific article published on 15 May 2017

Special Measures for Quality and Challenged Providers: Study Protocol for Evaluating the Impact of Improvement Interventions in NHS Trusts

scientific article published on 01 April 2020

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