Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?

por Karampetsou, Evangelia, Morrogh, Deborah, Chitty, Lyn
Publicado 2014

Women’s Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study

por Lewis, Celine, Hill, Melissa, Chitty, Lyn S.
Publicado 2016

A qualitative study looking at informed choice in the context of non‐invasive prenatal testing for aneuploidy

por Lewis, Celine, Hill, Melissa, Chitty, Lyn S.
Publicado 2016

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

por Lewis, Celine, Hill, Melissa, Chitty, Lyn S.
Publicado 2017

Routine testing of fetal Rhesus D status in Rhesus D negative women using cell-free fetal DNA: an investigation into the preferences and information needs of women

por Oxenford, Kerry, Silcock, Caroline, Hill, Melissa, Chitty, Lyn
Publicado 2013

Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy

por Lewis, Celine, Hill, Melissa, Skirton, Heather, Chitty, Lyn S
Publicado 2016

RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy

por Lo, Kitty K., Boustred, Christopher, Chitty, Lyn S., Plagnol, Vincent
Publicado 2014

Non-invasive prenatal diagnosis (NIPD): how analysis of cell-free DNA in maternal plasma has changed prenatal diagnosis for monogenic disorders

por Hanson, Britt, Scotchman, Elizabeth, Chitty, Lyn S., Chandler, Natalie J.
Publicado 2022

Model-Based Analysis of Costs and Outcomes of Non-Invasive Prenatal Testing for Down’s Syndrome Using Cell Free Fetal DNA in the UK National Health Service

por Morris, Stephen, Karlsen, Saffron, Chung, Nancy, Hill, Melissa, Chitty, Lyn S.
Publicado 2014

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

por Oxenford, Kerry, Daley, Rebecca, Lewis, Celine, Hill, Melissa, Chitty, Lyn S.
Publicado 2017

Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed‐methods systematic review

por Harding, Eleanor, Hammond, Jennifer, Chitty, Lyn S., Hill, Melissa, Lewis, Celine
Publicado 2020

Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis

por Mellis, Rhiannon, Oprych, Kathryn, Scotchman, Elizabeth, Hill, Melissa, Chitty, Lyn S
Publicado 2022

Postmortem magnetic resonance appearances of congenital high airway obstruction syndrome

por Arthurs, Owen J., Chitty, Lyn S., Judge-Kronis, Lydia, Sebire, Neil J.
Publicado 2014

Preferences for Prenatal Tests for Cystic Fibrosis: A Discrete Choice Experiment to Compare the Views of Adult Patients, Carriers of Cystic Fibrosis and Health Professionals

por Hill, Melissa, Suri, Ranjan, Nash, Edward F., Morris, Stephen, Chitty, Lyn S.
Publicado 2014

Implementing Prenatal Diagnosis Based on Cell-Free Fetal DNA: Accurate Identification of Factors Affecting Fetal DNA Yield

por Barrett, Angela N., Zimmermann, Bernhard G., Wang, Darrell, Holloway, Andrew, Chitty, Lyn S.
Publicado 2011

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

por Hill, Melissa, Barrett, Angela, Choolani, Mahesh, Lewis, Celine, Fisher, Jane, Chitty, Lyn S.
Publicado 2017

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

por Hill, Melissa, Hammond, Jennifer, Lewis, Celine, Mellis, Rhiannon, Clement, Emma, Chitty, Lyn S.
Publicado 2020

Confined placental mosaicism: implications for fetal chromosomal analysis using microarray comparative genomic hybridization

por Karampetsou, Evangelia, Morrogh, Deborah, Ballard, Terry, Waters, Jonathan J, Lench, Nicholas, Chitty, Lyn S
Publicado 2014

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

por Hill, Melissa, Oteng‐Ntim, Eugene, Forya, Frida, Petrou, Mary, Morris, Stephen, Chitty, Lyn S.
Publicado 2017

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

por Sanderson, Saskia C, Hill, Melissa, Patch, Christine, Searle, Beverly, Lewis, Celine, Chitty, Lyn S
Publicado 2019