Celine Lewis
Celine Lewis
UCL Institute of Child Health and Great Ormond Street Hospital
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe
H Skirton, C Lewis, A Kent, DA Coviello
European Journal of Human Genetics 18 (9), 972-977, 2010
1462010
Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down’s syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units
LS Chitty, D Wright, M Hill, TI Verhoef, R Daley, C Lewis, S Mason, ...
bmj 354, 2016
1432016
Non-invasive prenatal testing for Down's syndrome: pregnant women's views and likely uptake
C Lewis, C Silcock, LS Chitty
Public health genomics 16 (5), 223-232, 2013
1322013
Global perspectives on clinical adoption of NIPT
MA Minear, C Lewis, S Pradhan, S Chandrasekharan
Prenatal diagnosis 35 (10), 959-967, 2015
1192015
Non‐invasive prenatal testing for trisomy 21: a cross‐sectional survey of service users' views and likely uptake
C Lewis, M Hill, C Silcock, R Daley, LS Chitty
BJOG: An International Journal of Obstetrics & Gynaecology 121 (5), 582-594, 2014
1032014
Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol
M Hill, D Wright, R Daley, C Lewis, F McKay, S Mason, N Lench, ...
BMC pregnancy and childbirth 14 (1), 1-10, 2014
892014
Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users’ perspective
C Lewis, M Hill, H Skirton, LS Chitty
European journal of human genetics 20 (11), 1127-1133, 2012
812012
Factors affecting uptake of postmortem examination in the prenatal, perinatal and paediatric setting
C Lewis, M Hill, OJ Arthurs, C Hutchinson, LS Chitty, NJ Sebire
BJOG: An International Journal of Obstetrics & Gynaecology 125 (2), 172-181, 2018
722018
Living without a diagnosis: the parental experience
C Lewis, H Skirton, R Jones
Genetic Testing and Molecular Biomarkers 14 (6), 807-815, 2010
672010
Offering prenatal diagnostic tests: European guidelines for clinical practice
H Skirton, L Goldsmith, L Jackson, C Lewis, L Chitty
European Journal of Human Genetics 22 (5), 580-586, 2014
652014
Women’s experiences and preferences for service delivery of non-invasive prenatal testing for aneuploidy in a public health setting: a mixed methods study
C Lewis, M Hill, LS Chitty
PloS one 11 (4), e0153147, 2016
642016
Non‐invasive prenatal diagnosis for single gene disorders: experience of patients
C Lewis, M Hill, LS Chitty
Clinical genetics 85 (4), 336-342, 2014
632014
Fetal sex determination using cell‐free fetal DNA: service users' experiences of and preferences for service delivery
C Lewis, M Hill, H Skirton, LS Chitty
Prenatal diagnosis 32 (8), 735-741, 2012
632012
What hinders minority ethnic access to cancer genetics services and what may help?
A Allford, N Qureshi, J Barwell, C Lewis, J Kai
European Journal of Human Genetics 22 (7), 866-874, 2014
622014
Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy
C Lewis, M Hill, H Skirton, LS Chitty
European Journal of Human Genetics 24 (6), 809-816, 2016
612016
Delivering an accredited non‐invasive prenatal diagnosis service for monogenic disorders and recommendations for best practice
LA Jenkins, ZC Deans, C Lewis, S Allen
Prenatal diagnosis 38 (1), 44-51, 2018
592018
Views and preferences for the implementation of non‐invasive prenatal diagnosis for single gene disorders from health professionals in the United Kingdom
M Hill, M Karunaratna, C Lewis, F Forya, L Chitty
American Journal of Medical Genetics Part A 161 (7), 1612-1618, 2013
562013
Non-invasive prenatal testing for single gene disorders: exploring the ethics
Z Deans, M Hill, LS Chitty, C Lewis
European Journal of Human Genetics 21 (7), 713-718, 2013
512013
Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?
M Hill, A Barrett, M Choolani, C Lewis, J Fisher, LS Chitty
Prenatal diagnosis 37 (13), 1281-1290, 2017
482017
Implementing noninvasive prenatal fetal sex determination using cell-free fetal DNA in the United Kingdom
M Hill, C Lewis, L Jenkins, S Allen, RG Elles, LS Chitty
Expert opinion on biological therapy 12 (sup1), S119-S126, 2012
472012
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