| 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 | 178 | 2010 |
| 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 | 171 | 2016 |
| Global perspectives on clinical adoption of NIPT MA Minear, C Lewis, S Pradhan, S Chandrasekharan Prenatal diagnosis 35 (10), 959-967, 2015 | 160 | 2015 |
| 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 | 157 | 2013 |
| 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 | 122 | 2014 |
| 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 | 101 | 2018 |
| 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, 1-10, 2014 | 97 | 2014 |
| 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 | 95 | 2012 |
| 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 | 90 | 2016 |
| Living without a diagnosis: the parental experience C Lewis, H Skirton, R Jones Genetic testing and molecular biomarkers 14 (6), 807-815, 2010 | 85 | 2010 |
| 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 | 83 | 2018 |
| 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 | 82 | 2017 |
| 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 | 82 | 2014 |
| 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 | 80 | 2016 |
| 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 | 76 | 2014 |
| Non‐invasive prenatal diagnosis for single gene disorders: experience of patients C Lewis, M Hill, LS Chitty Clinical genetics 85 (4), 336-342, 2014 | 75 | 2014 |
| 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 | 68 | 2012 |
| 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 | 62 | 2013 |
| 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 | 57 | 2013 |
| 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 | 56 | 2012 |
Melissa HillGreat Ormond Street Hospital NHS Foundation TrustZweryfikowany adres z ucl.ac.uk
