Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

C. Lewis · SciRah

Researcher profile · Semantic Scholar

C. Lewis

Share profile

C. Lewis — researcher profile on SciRah

h-index: 33
Works: 105
Citations: 3,115

Most-cited papers

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
L. Chitty, D. Wright, M. Hill, T. Verhoef +11 more
2016British medical journal141 citations Open access
Semantic Scholar
Global perspectives on clinical adoption of NIPT
Mollie A. Minear, C. Lewis, S. Pradhan, S. Chandrasekharan
2015Prenatal Diagnosis133 citations Open access
Semantic Scholar
Non-Invasive Prenatal Testing for Down's Syndrome: Pregnant Women's Views and Likely Uptake
C. Lewis, C. Silcock, L. Chitty
2013Public Health Genomics126 citations
Semantic Scholar
Factors affecting uptake of postmortem examination in the prenatal, perinatal and paediatric setting
C. Lewis, M. Hill, O. Arthurs, C. Hutchinson +2 more
2017BJOG: an International Journal of Obstetrics and Gynaecology105 citations Open access
Semantic Scholar
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 +1 more
2014BJOG: an International Journal of Obstetrics and Gynaecology96 citations
Semantic Scholar
Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy
C. Lewis, M. Hill, H. Skirton, L. Chitty
2015European Journal of Human Genetics85 citations Open access
Semantic Scholar
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, L. Chitty
2016PLoS ONE84 citations Open access
Semantic Scholar
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 +12 more
2014BMC Pregnancy and Childbirth80 citations Open access
Semantic Scholar
Living Without a Diagnosis: The Parental Experience
C. Lewis, H. Skirton, Ray B. Jones
2010Genetic Testing and Molecular Biomarkers79 citations Open access
Semantic Scholar
Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users’ perspective
C. Lewis, M. Hill, H. Skirton, L. Chitty
2012European Journal of Human Genetics78 citations Open access
Semantic Scholar
Delivering an accredited non‐invasive prenatal diagnosis service for monogenic disorders and recommendations for best practice
L. Jenkins, Z. Deans, C. Lewis, S. Allen
2018Prenatal Diagnosis76 citations Open access
Semantic Scholar
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 +2 more
2017Prenatal Diagnosis66 citations Open access
Semantic Scholar
Non‐invasive prenatal diagnosis for single gene disorders: experience of patients
C. Lewis, M. Hill, L. Chitty
2014Clinical Genetics61 citations
Semantic Scholar
Offering prenatal diagnostic tests: European guidelines for clinical practice
H. Skirton, L. Goldsmith, Leigh Jackson, C. Lewis +1 more
2013European Journal of Human Genetics58 citations Open access
Semantic Scholar
Fetal sex determination using cell‐free fetal DNA: service users' experiences of and preferences for service delivery
C. Lewis, M. Hill, H. Skirton, L. Chitty
2012Prenatal Diagnosis58 citations
Semantic Scholar
“We might get a lot more families who will agree”: Muslim and Jewish perspectives on less invasive perinatal and paediatric autopsy
C. Lewis, Z. Latif, M. Hill, M. Riddington +5 more
2018PLoS ONE56 citations Open access
Semantic Scholar
Views and preferences for the implementation of non‐invasive prenatal diagnosis for single gene disorders from health professionals in the united kingdom
M. Hill, Madhavi Karunaratna, C. Lewis, F. Forya +1 more
2013American Journal of Medical Genetics. Part A53 citations
Semantic Scholar
Can We Make Assumptions About the Psychosocial Impact of Living as a Carrier, Based on Studies Assessing the Effects of Carrier Testing?
C. Lewis, H. Skirton, Ray B. Jones
2011Journal of Genetic Counseling50 citations
Semantic Scholar
A qualitative study looking at informed choice in the context of non‐invasive prenatal testing for aneuploidy
C. Lewis, M. Hill, L. Chitty
2016Prenatal Diagnosis49 citations Open access
Semantic Scholar
Public views on the donation and use of human biological samples in biomedical research: a mixed methods study
C. Lewis, Margaret Clotworthy, S. Hilton, Caroline Magee +3 more
2013BMJ Open48 citations Open access
Semantic Scholar
Non-invasive prenatal testing for single gene disorders: exploring the ethics
Z. Deans, M. Hill, L. Chitty, C. Lewis
2012European Journal of Human Genetics48 citations Open access
Semantic Scholar
Offering non‐invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
C. Lewis, M. Hill, L. Chitty
2017Prenatal Diagnosis47 citations Open access
Semantic Scholar
Client Views and Attitudes to Non-Invasive Prenatal Diagnosis for Sickle Cell Disease, Thalassaemia and Cystic Fibrosis
M. Hill, C. Compton, Madhavi Karunaratna, C. Lewis +1 more
2014Journal of Genetic Counseling47 citations
Semantic Scholar
Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed‐methods systematic review
Eleanor Harding, Jennifer Hammond, L. Chitty, M. Hill +1 more
2020Prenatal Diagnosis45 citations Open access
Semantic Scholar
Implementing noninvasive prenatal fetal sex determination using cell-free fetal DNA in the United Kingdom
M. Hill, C. Lewis, L. Jenkins, S. Allen +2 more
2012Expert Opinion on Biological Therapy44 citations
Semantic Scholar
Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study
C. Lewis, S. Sanderson, M. Hill, C. Patch +3 more
2020European Journal of Human Genetics43 citations Open access
Semantic Scholar
Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges
M. Hill, Jennifer Hammond, C. Lewis, Rhiannon Mellis +2 more
2020European Journal of Human Genetics39 citations Open access
Semantic Scholar
Health professionals’ and coroners’ views on less invasive perinatal and paediatric autopsy: a qualitative study
C. Lewis, M. Hill, O. Arthurs, J. Hutchinson +2 more
2018Archives of Disease in Childhood38 citations Open access
Semantic Scholar
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness
Franziska Severin, P. Borry, M. Cornel, N. Daniels +18 more
2014European Journal of Human Genetics37 citations Open access
Semantic Scholar
Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed‐methods study with bereaved parents
C. Lewis, M. Riddington, M. Hill, O. Arthurs +6 more
2019BJOG: an International Journal of Obstetrics and Gynaecology36 citations Open access
Semantic Scholar
Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty
Jennifer Hammond, J. E. Klapwijk, M. Hill, Stina Lou +4 more
2020Journal of Genetic Counseling35 citations Open access
Semantic Scholar
Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project
S. Sanderson, M. Hill, C. Patch, Beverly Searle +2 more
2019BMJ Open34 citations Open access
Semantic Scholar
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: A mixed methods study
Michelle Peter, Jennifer Hammond, S. Sanderson, J. Gurasashvili +6 more
2022European Journal of Human Genetics33 citations Open access
Semantic Scholar
Minimally invasive perinatal and pediatric autopsy with laparoscopically assisted tissue sampling: feasibility and experience of the MinImAL procedure
J. Hutchinson, S. Shelmerdine, C. Lewis, J. Parmenter +6 more
2019Ultrasound in Obstetrics and Gynecology33 citations Open access
Semantic Scholar
Determination of foetal sex in pregnancies at risk of haemophilia: a qualitative study exploring the clinical practices and attitudes of health professionals in the United Kingdom
M. Hill, C. Compton, C. Lewis, H. Skirton +1 more
2012Haemophilia33 citations
Semantic Scholar
How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies
J. E. Klapwijk, M. Srebniak, A. Go, L. Govaerts +9 more
2021Clinical Genetics31 citations Open access
Semantic Scholar
Genomics and autism spectrum disorder.
Norah L. Johnson, E. Giarelli, C. Lewis, C. Rice
2013Journal of Nursing Scholarship31 citations Open access
Semantic Scholar
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals
C. Lewis, Jennifer Hammond, J. E. Klapwijk, Eleanor Harding +10 more
2021Prenatal Diagnosis30 citations Open access
Semantic Scholar
Living with Osteogenesis Imperfecta: A qualitative study exploring experiences and psychosocial impact from the perspective of patients, parents and professionals.
M. Hill, Jennifer Hammond, Mithila Sharmin, C. Lewis +5 more
2021Disability and Health Journal30 citations Open access
Semantic Scholar
"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result
Stina Lou, K. Lomborg, C. Lewis, S. Riedijk +2 more
2020Acta Obstetricia et Gynecologica Scandinavica29 citations Open access
Semantic Scholar
Non‐invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers
H. Skirton, L. Goldsmith, Leigh Jackson, C. Lewis +1 more
2015Prenatal Diagnosis29 citations
Semantic Scholar
A pragmatic evidence-based approach to post-mortem perinatal imaging
S. Shelmerdine, J. Hutchinson, C. Lewis, I. Simcock +3 more
2021Insights into Imaging26 citations Open access
Semantic Scholar
Clinical, social and ethical issues associated with non-invasive prenatal testing for aneuploidy
Blanche Griffin, S. Edwards, L. Chitty, C. Lewis
2017Journal of Psychosomatic Obstetrics and Gynaecology26 citations
Semantic Scholar
Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study
Kerry Oxenford, R. Daley, C. Lewis, M. Hill +1 more
2017BMC Pregnancy and Childbirth26 citations Open access
Semantic Scholar
Consent for the use of human biological samples for biomedical research: a mixed methods study exploring the UK public's preferences
C. Lewis, Margaret Clotworthy, S. Hilton, Caroline Magee +3 more
2013BMJ Open26 citations Open access
Semantic Scholar
Minimally invasive autopsy for fetuses and children based on a combination of post-mortem MRI and endoscopic examination: a feasibility study.
C. Lewis, J. Hutchinson, M. Riddington, M. Hill +6 more
2019Health Technology Assessment25 citations Open access
Semantic Scholar
Exploring the impact of Osteogenesis Imperfecta on families: A mixed-methods systematic review.
M. Hill, C. Lewis, M. Riddington, B. Crowe +3 more
2019Disability and Health Journal25 citations Open access
Semantic Scholar
Opening the “black box” of informed consent appointments for genome sequencing: a multisite observational study
S. Sanderson, C. Lewis, C. Patch, M. Hill +2 more
2018Genetics in Medicine24 citations Open access
Semantic Scholar
Reproductive empowerment: The main motivator and outcome of carrier testing
C. Lewis, H. Skirton, Ray B. Jones
2012Journal of Health Psychology22 citations
Semantic Scholar
Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100,000 genomes project.
C. Lewis, Jennifer Hammond, M. Hill, Beverly Searle +4 more
2020European Journal of Medical Genetics21 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

M. Hill×34
Invite
M. Hill — researcher profile on SciRah
L. Chitty×32
Invite
L. Chitty — researcher profile on SciRah
H. Skirton×10
Invite
H. Skirton — researcher profile on SciRah
Jennifer Hammond×8
Invite
Jennifer Hammond — researcher profile on SciRah

×6

Invite

O. Arthurs — researcher profile on SciRah

Invite

N. Sebire — researcher profile on SciRah

S. Sanderson×5

Invite

S. Sanderson — researcher profile on SciRah

Invite

C. Patch — researcher profile on SciRah

Invite

R. Daley — researcher profile on SciRah

Invite

J. Fisher — researcher profile on SciRah

M. Riddington×4

Invite

M. Riddington — researcher profile on SciRah

J. Hutchinson×4

Invite

J. Hutchinson — researcher profile on SciRah