Publications by authors named "Lyn Chitty"

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Evaluating the return of additional findings from the 100,000 Genomes Project: A mixed-methods study exploring participant experiences of receiving secondary findings from genomic sequencing.
Bethany Stafford-Smith, Morgan Daniel, Michelle Peter, Jana Gurasashvili, Rashida Baptiste, Lyn S Chitty

Genet Med· December 2025

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Are People From Black Communities Proportionately Represented in UK and US Studies Examining Views on Screening and Diagnostic Genetic Testing in Pregnancy? A Scoping Review.
Michelle Peter, Rashida Baptiste, Celine Lewis, Lyn S Chitty, Melissa Hill

BJOG· December 2025

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Delivering effective genome sequencing in pediatric care: From research in the 100,000 Genomes Project to routine clinical practice.
Emma Wakeling, Rashida Baptiste, Clarissa Rocca, Bethan Hoskins, Christopher Clarkson, Lyn S Chitty

Genet Med· December 2025

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The Importance of Clinical Acumen for Prenatal Diagnosis in an Increasingly Technological World.
Teresa N Sparks, Lyn S Chitty

Prenat Diagn· December 2025

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Costs and cost-effectiveness of returning secondary findings from genomic sequencing based on the return of additional findings in the 100,000 Genomes Project.
Emma J Smith, Melissa Hill, Lyn S Chitty, Stephen Morris

Genet Med· September 2025

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"I'm quite proud of how we've handled it": health professionals' experiences of returning additional findings from the 100,000 genomes project.
Bethany Stafford-Smith, Jana Gurasashvili, Michelle Peter, Morgan Daniel, Meena Balasubramanian, Lyn S Chitty

Eur J Hum Genet· August 2025

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'I Have my Beliefs, but Then I Have my Reality': Reflections of Black and South Asian Parents Living in England on Screening and Genetic Diagnosis in Pregnancy.
Michelle Peter, Rashida Baptiste, Rachael Buabeng, Lily Islam, Jane Fisher, Lyn S Chitty

Prenat Diagn· June 2025

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Can an Animation Improve Parents' Knowledge and How Does It Compare to Written Information? Development and Survey Evaluation of an Animation for Parents About Prenatal Sequencing.
Morgan Daniel, Hannah McInnes-Dean, Wing Han Wu, Jane Fisher, Caroline Lafarge, Lyn S Chitty

Prenat Diagn· April 2025

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Equity and timeliness as factors in the effectiveness of an ethical prenatal sequencing service: reflections from parents and professionals.
Michelle Peter, Melissa Hill, Jane Fisher, Morgan Daniel, Hannah McInnes-Dean, Lyn S Chitty

Eur J Hum Genet· March 2025

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Implementation of a National Prenatal Exome Sequencing Service in England: Cost-Effectiveness Analysis.
Emma J Smith, Melissa Hill, Michelle Peter, Wing Han Wu, Corinne Mallinson, Lyn S Chitty

BJOG· March 2025

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Navigating the Challenges of Exome Sequencing in Structurally Normal Fetuses.
Sylvie Langlois, Lyn S Chitty

Prenat Diagn· March 2025

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Parental Somatic Mosaicism Detected During Prenatal Diagnosis.
Natalie J Chandler, Elizabeth Scotchman, Fiona McKay, Vijaya Ramachandran, Lyn S Chitty

Prenat Diagn· February 2025

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International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease.
Katherine B Howell, Susan M White, Amy McTague, Alissa M D'Gama, Gregory Costain, Lyn S Chitty

NPJ Genom Med· February 2025

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Evaluating the Implementation of the Rapid Prenatal Exome Sequencing Service in England.
Holly Walton, Morgan Daniel, Michelle Peter, Hannah McInnes-Dean, Rhiannon Mellis, Lyn S Chitty

Public Health Genomics· January 2025

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Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use".
Neeta L Vora, Sylvie Langlois, Lyn S Chitty

Prenat Diagn· November 2024

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Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation.
Rema Ramakrishnan, Corinne Mallinson, Steven Hardy, Jennifer Broughan, Maisie Blyth, Lyn S Chitty

Front Genet· November 2024

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Preferences for coordinated care for rare diseases: discrete choice experiment.
Stephen Morris, Holly Walton, Amy Simpson, Kerry Leeson-Beevers, Lara Bloom, Lyn S Chitty

Orphanet J Rare Dis· September 2024

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Benefits for children with suspected cancer from routine whole-genome sequencing.
Angus Hodder, Sarah M Leiter, Jonathan Kennedy, Dilys Addy, Munaza Ahmed, Lyn S Chitty

Nat Med· July 2024

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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.
Rachel L Sagar, Eva Åström, Lyn S Chitty, Belinda Crowe, Anna L David

BMJ Open· June 2024

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Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals' views and experiences.
Michelle Peter, Rhiannon Mellis, Hannah McInnes-Dean, Morgan Daniel, Holly Walton, Lyn S Chitty

Front Genet· June 2024

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Expanding Access to Noninvasive Prenatal Diagnosis for Monogenic Conditions to Consanguineous Families.
Britt Hanson, Joe Shaw, Nikita Povarnitsyn, Benjamin Bowns, Elizabeth Young, Lyn S Chitty

Clin Chem· May 2024

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Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.
Gillian V Blayney, Eoghan Laffan, Preethi A Jacob, Caitlin D Baptiste, Heinz Gabriel, Lyn S Chitty

Prenat Diagn· April 2024

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'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service.
Hannah McInnes-Dean, Rhiannon Mellis, Morgan Daniel, Holly Walton, Emma L Baple, Lyn S Chitty

Prenat Diagn· April 2024

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Twenty years of progress in the diagnosis and management of foetal urinary tract conditions.
Karin Blakemore, Lyn S Chitty

Prenat Diagn· February 2024

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Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals.
Holly Walton, Pei Li Ng, Amy Simpson, Lara Bloom, Lyn S Chitty

Orphanet J Rare Dis· November 2023

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