Michelle Peter

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 11

Top Topics

Decision Making

Palliative Care

Cross Sectional

Top Venues

Prenatal diagnosis

Orphanet journal of rare diseases

European journal of human genetics : EJHG

NIHR open research

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

Publications

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)
Jennifer Jones, Marie Cruddas, Amy Simpson, Nick Meade, Daphnee Pushparajah, Michelle Peter, Amy Hunter
Factors affecting overall care experience for people living with rare conditions in the UK: exploratory analysis of a quantitative patient experience survey. Orphanet journal of rare diseases 19 (1) (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)
Jennifer Jones, Marie Cruddas, Amy Simpson, Nick Meade, Daphnee Pushparajah, Michelle Peter, Amy Hunter
Factors affecting overall care experience for people living with rare conditions in the UK: exploratory analysis of a quantitative patient experience survey. Orphanet journal of rare diseases 19 (1) (2024)
Jennifer Jones, Marie Cruddas, Amy Simpson, Nick Meade, Daphnee Pushparajah, Michelle Peter, Amy Hunter
Factors affecting overall care experience for people living with rare conditions in the UK: exploratory analysis of a quantitative patient experience survey. Orphanet journal of rare diseases 19 (1) (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)
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)
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)
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)