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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
1612010
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
1522016
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
1462013
Global perspectives on clinical adoption of NIPT
MA Minear, C Lewis, S Pradhan, S Chandrasekharan
Prenatal diagnosis 35 (10), 959-967, 2015
1362015
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
1112014
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
912014
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
852018
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
852012
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
812016
Living without a diagnosis: the parental experience
C Lewis, H Skirton, R Jones
Genetic testing and molecular biomarkers 14 (6), 807-815, 2010
752010
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
722016
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
692014
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
682018
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
682014
Non‐invasive prenatal diagnosis for single gene disorders: experience of patients
C Lewis, M Hill, LS Chitty
Clinical genetics 85 (4), 336-342, 2014
682014
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
652012
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
622017
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
582013
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
542013
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
492012
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