Melissa Hill

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 33

Top Topics

Hematopoietic Stem Cell

Systematic Review

Minimally Invasive

Top Venues

Prenatal diagnosis

European journal of human genetics : EJHG

NIHR open research

This page only lists publications with an associated author ORCID identifier.

Publications

Rachel L Sagar, Eva Åström, Lyn S Chitty, Belinda Crowe, Anna L David, Catherine DeVile, Annabelle Forsmark, Vera Franzen, Göran Hermeren, Melissa Hill, Mats Johansson, Caroline Lindemans, Peter Lindgren, Wouter Nijhuis, Dick Oepkes, Mirko Rehberg, Nils-Eric Sahlin, Ralph Sakkers, O Semler, Mikael Sundin, Lilian Walther-Jallow, E J T Joanne Verweij, Magnus Westgren, Cecilia Götherström
An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol. BMJ open 14 (6) (2024)
Hannah McInnes-Dean, Rhiannon Mellis, Morgan Daniel, Holly Walton, Emma L Baple, Marta Bertoli, Jane Fisher, Katarzyna Gajewska-Knapik, Muriel Holder-Espinasse, Caroline Lafarge, Kerry Leeson-Beevers, Alec McEwan, Pranav Pandya, Michael Parker, Sophie Peet, Lauren Roberts, Srividhya Sankaran, Audrey Smith, Dagmar Tapon, Wing Han Wu, Sarah L Wynn, Lyn S Chitty, Melissa Hill, Michelle Peter
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service. Prenatal diagnosis 44 (4) (2024)
Rachel L Sagar, Eva Åström, Lyn S Chitty, Belinda Crowe, Anna L David, Catherine DeVile, Annabelle Forsmark, Vera Franzen, Göran Hermeren, Melissa Hill, Mats Johansson, Caroline Lindemans, Peter Lindgren, Wouter Nijhuis, Dick Oepkes, Mirko Rehberg, Nils-Eric Sahlin, Ralph Sakkers, O Semler, Mikael Sundin, Lilian Walther-Jallow, E J T Joanne Verweij, Magnus Westgren, Cecilia Götherström
An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol. BMJ open 14 (6) (2024)
Hannah McInnes-Dean, Rhiannon Mellis, Morgan Daniel, Holly Walton, Emma L Baple, Marta Bertoli, Jane Fisher, Katarzyna Gajewska-Knapik, Muriel Holder-Espinasse, Caroline Lafarge, Kerry Leeson-Beevers, Alec McEwan, Pranav Pandya, Michael Parker, Sophie Peet, Lauren Roberts, Srividhya Sankaran, Audrey Smith, Dagmar Tapon, Wing Han Wu, Sarah L Wynn, Lyn S Chitty, Melissa Hill, Michelle Peter
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service. Prenatal diagnosis 44 (4) (2024)
Hannah McInnes-Dean, Rhiannon Mellis, Morgan Daniel, Holly Walton, Emma L Baple, Marta Bertoli, Jane Fisher, Katarzyna Gajewska-Knapik, Muriel Holder-Espinasse, Caroline Lafarge, Kerry Leeson-Beevers, Alec McEwan, Pranav Pandya, Michael Parker, Sophie Peet, Lauren Roberts, Srividhya Sankaran, Audrey Smith, Dagmar Tapon, Wing Han Wu, Sarah L Wynn, Lyn S Chitty, Melissa Hill, Michelle Peter
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service. Prenatal diagnosis (2024)
Hannah McInnes-Dean, Rhiannon Mellis, Morgan Daniel, Holly Walton, Emma L Baple, Marta Bertoli, Jane Fisher, Katarzyna Gajewska-Knapik, Muriel Holder-Espinasse, Caroline Lafarge, Kerry Leeson-Beevers, Alec McEwan, Pranav Pandya, Michael Parker, Sophie Peet, Lauren Roberts, Srividhya Sankaran, Audrey Smith, Dagmar Tapon, Wing Han Wu, Sarah L Wynn, Lyn S Chitty, Melissa Hill, Michelle Peter
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service. Prenatal diagnosis 44 (4) (2024)
Rachel L Sagar, Eva Åström, Lyn S Chitty, Belinda Crowe, Anna L David, Catherine DeVile, Annabelle Forsmark, Vera Franzen, Göran Hermeren, Melissa Hill, Mats Johansson, Caroline Lindemans, Peter Lindgren, Wouter Nijhuis, Dick Oepkes, Mirko Rehberg, Nils-Eric Sahlin, Ralph Sakkers, O Semler, Mikael Sundin, Lilian Walther-Jallow, E J T Joanne Verweij, Magnus Westgren, Cecilia Götherström
An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol. BMJ open 14 (6) (2024)
Rachel L Sagar, Eva Åström, Lyn S Chitty, Belinda Crowe, Anna L David, Catherine DeVile, Annabelle Forsmark, Vera Franzen, Göran Hermeren, Melissa Hill, Mats Johansson, Caroline Lindemans, Peter Lindgren, Wouter Nijhuis, Dick Oepkes, Mirko Rehberg, Nils-Eric Sahlin, Ralph Sakkers, O Semler, Mikael Sundin, Lilian Walther-Jallow, E J T Joanne Verweij, Magnus Westgren, Cecilia Götherström
An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol. BMJ open 14 (6) (2024)
Michelle Peter, Jennifer Hammond, Saskia C Sanderson, Jana Gurasashvili, Amy Hunter, Beverly Searle, Christine Patch, Lyn S Chitty, Melissa Hill, Celine Lewis
Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project. European journal of human genetics : EJHG (2023)
Jennifer Siranosian, Celine Lewis, Melissa Hill, Kelly E Ormond
Exploring prenatal testing preferences among US pregnant individuals: A discrete choice experiment. Journal of genetic counseling (2023)
Naomi J Fulop, Estela Capelas Barbosa, Melissa Hill, Jean Ledger, Pei Li Ng, Christopher Sherlaw-Johnson, Lucina Rolewicz, Laura Schlepper, Jonathan Spencer, Sonila M Tomini, Cecilia Vindrola-Padros, Stephen Morris
Rapid evaluation of the Special Measures for Quality and challenged provider regimes: a mixed-methods study. Health and social care delivery research 11 (19) (2023)
Rhiannon Mellis, Dagmar Tapon, Nora Shannon, Esther Dempsey, Pranav Pandya, Lyn S Chitty, Melissa Hill
Implementing a rapid fetal exome sequencing service: What do parents and health professionals think? Prenatal diagnosis 42 (6) (2022)
Michelle Peter, Jennifer Hammond, Saskia C Sanderson, Jana Gurasashvili, Amy Hunter, Beverly Searle, Christine Patch, Lyn S Chitty, Melissa Hill, Celine Lewis
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study. European journal of human genetics : EJHG 30 (5) (2022)
Melissa Hill, Sian Ellard, Jane Fisher, Naomi Fulop, Marian Knight, Mark Kroese, Jean Ledger, Kerry Leeson-Beevers, Alec McEwan, Dominic McMullan, Rhiannon Mellis, Stephen Morris, Michael J Parker, Dagmar Tapon, Emma Baple, Laura Blackburn, Asya Choudry, Caroline Lafarge, Hannah McInnes-Dean, Michelle Peter, Rema Ramakrishnan, Lauren Roberts, Beverly Searle, Emma Smith, Holly Walton, Sarah L Wynn, Wing Han Wu, Lyn S Chitty
Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service. NIHR open research 2 (2022)
James Buchanan, Melissa Hill, Caroline M Vass, Jennifer Hammond, Sam R Riedijk, Jasmijn E Klapwijk, Eleanor Harding, Stina Lou, Ida Vogel, Lisa Hui, Charlotta Ingvoldstad-Malmgren, Maria Johansson Soller, Kelly E Ormond, Mahesh Arjandas Choolani, Qian Zheng, Lyn S Chitty, Celine Lewis
Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice survey. Prenatal diagnosis 42 (7) (2022)
Cecilia Vindrola-Padros, Jean Ledger, Melissa Hill, Sonila M Tomini, Jonathan Spencer, Naomi J Fulop
The Special Measures for Quality and Challenged Provider Regimes in the English NHS: A Rapid Evaluation of a National Improvement Initiative for Failing Healthcare Organisations. International journal of health policy and management (2022)
Rhiannon Mellis, Kathryn Oprych, Elizabeth Scotchman, Melissa Hill, Lyn S Chitty
Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta-analysis. Prenatal diagnosis 42 (6) (2022)
Jasmijn E Klapwijk, Malgorzata Ilona Srebniak, Attie T J I Go, Lutgarde C P Govaerts, Celine Lewis, Jennifer Hammond, Melissa Hill, Stina Lou, Ida Vogel, Kelly E Ormond, Karin E M Diderich, Hennie T Brüggenwirth, Sam R Riedijk
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies. Clinical genetics 100 (6) (2021)
Celine Lewis, Jennifer Hammond, Jasmijn E Klapwijk, Eleanor Harding, Stina Lou, Ida Vogel, Emma J Szepe, Lisa Hui, Charlotta Ingvoldstad-Malmgren, Maria J Soller, Kelly E Ormond, Mahesh Arjandas Choolani, Melissa Hill, Sam Riedijk
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals. Prenatal diagnosis 41 (6) (2021)
Celine Lewis, James Buchanan, Angus John Clarke, Emma Clement, Bettina Friedrich, Jillian Hastings-Ward, Melissa Hill, Ruth Horn, Anneke M Lucassen, Christine Patch, Alexandra Pickard, Lauren Roberts, Saskia C Sanderson, Sarah L Wynn, Cecilia Vindrola-Padros, Monica Lakhanpaul
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol. NIHR open research 1 (2021)
Michelle Peter, Hannah McInnes-Dean, Jane Fisher, Dagmar Tapon, Lyn S Chitty, Melissa Hill
What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing. Prenatal diagnosis (2021)
Naomi J Fulop, Estela Capelas Barbosa, Melissa Hill, Jean Ledger, Christopher Sherlaw-Johnson, Jonathan Spencer, Cecilia Vindrola-Padros, Steve Morris
Special Measures for Quality and Challenged Providers: Study Protocol for Evaluating the Impact of Improvement Interventions in NHS Trusts. International journal of health policy and management 9 (4) (2020)
Celine Lewis, Saskia Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Amy Hunter, Lyn S Chitty
Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study. European journal of human genetics : EJHG 28 (7) (2020)
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, Melissa Hill, Celine Lewis
Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review. Prenatal diagnosis 40 (8) (2020)
Jennifer Hammond, Jasmijn E Klapwijk, Melissa Hill, Stina Lou, Kelly E Ormond, Karin E M Diderich, Sam Riedijk, Celine Lewis
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han's taxonomy of uncertainty. Journal of genetic counseling 30 (1) (2020)
Celine Lewis, John Ciaran Hutchinson, Megan Riddington, Melissa Hill, Owen John Arthurs, Jane Fisher, Angie Wade, Caroline J Doré, Lyn S Chitty, Neil J Sebire
Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study. Health technology assessment (Winchester, England) 23 (46) (2020)
Melissa Hill, Jennifer Hammond, Celine Lewis, Rhiannon Mellis, Emma Clement, Lyn S Chitty
Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges. European journal of human genetics : EJHG 28 (11) (2020)
Celine Lewis, Megan Riddington, Melissa Hill, Charlotte Bevan, Jane Fisher, Lucy Lyas, Ann Chalmers, Owen J Arthurs, John C Hutchinson, Lyn S Chitty, Neil Sebire
"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. Prenatal diagnosis 39 (13) (2019)
Saskia C Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S Chitty
Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project. BMJ open 9 (11) (2019)
Melissa Hill, Angela N Barrett, Mahesh Arjandas Choolani, Celine Lewis, Jane Fisher, Lyn S Chitty
Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome? Prenatal diagnosis 37 (13) (2018)
Celine Lewis, Melissa Hill, Lyn S Chitty
Offering non-invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained? Prenatal diagnosis 37 (11) (2017)
Kerry Oxenford, Rebecca Daley, Celine Lewis, Melissa Hill, Lyn S Chitty
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. BMC pregnancy and childbirth 17 (1) (2017)
Melissa Hill, Eugene Oteng-Ntim, Frida Forya, Mary Petrou, Stephen Morris, Lyn S Chitty
Preferences for prenatal diagnosis of sickle-cell disorder: A discrete choice experiment comparing potential service users and health-care providers. Health expectations : an international journal of public participation in health care and health policy 20 (6) (2017)