Celine Lewis

3.5k total citations
102 papers, 2.4k citations indexed

About

Celine Lewis is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Celine Lewis has authored 102 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Pediatrics, Perinatology and Child Health, 42 papers in Genetics and 26 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Celine Lewis's work include Prenatal Screening and Diagnostics (46 papers), Genomics and Rare Diseases (26 papers) and BRCA gene mutations in cancer (26 papers). Celine Lewis is often cited by papers focused on Prenatal Screening and Diagnostics (46 papers), Genomics and Rare Diseases (26 papers) and BRCA gene mutations in cancer (26 papers). Celine Lewis collaborates with scholars based in United Kingdom, United States and Singapore. Celine Lewis's co-authors include Lyn S. Chitty, Melissa Hill, Heather Skirton, Owen J. Arthurs, Ray Jones, Domenico Coviello, Alastair Kent, Rebecca Daley, Neil J. Sebire and J. Ciaran Hutchinson and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Celine Lewis

98 papers receiving 2.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Celine Lewis United Kingdom	30	1.5k	763	448	338	241	102	2.4k
Melissa Hill United Kingdom	34	2.0k 1.3×	802 1.1×	350 0.8×	591 1.7×	462 1.9×	113	2.9k
Bernadette Modell United Kingdom	25	1.3k 0.8×	573 0.8×	272 0.6×	167 0.5×	314 1.3×	50	4.0k
Olav Bjørn Petersen Denmark	32	2.0k 1.3×	578 0.8×	440 1.0×	439 1.3×	331 1.4×	185	3.4k
Susan Klugman United States	19	1.6k 1.0×	549 0.7×	326 0.7×	299 0.9×	241 1.0×	57	2.2k
J. M. M. van Lith Netherlands	25	1.4k 0.9×	196 0.3×	448 1.0×	395 1.2×	154 0.6×	104	2.1k
J. M. G. van Vugt Netherlands	37	2.5k 1.7×	359 0.5×	441 1.0×	469 1.4×	530 2.2×	142	3.8k
Devereux N. Saller United States	19	1.1k 0.7×	233 0.3×	198 0.4×	373 1.1×	141 0.6×	51	1.4k
Mireille N. Bekker Netherlands	25	1.2k 0.8×	195 0.3×	383 0.9×	204 0.6×	169 0.7×	120	1.9k
B. Modell United Kingdom	32	1.4k 0.9×	755 1.0×	267 0.6×	168 0.5×	383 1.6×	81	3.7k
Lorraine Dugoff United States	35	4.4k 2.9×	540 0.7×	925 2.1×	1.3k 3.7×	398 1.7×	97	5.3k

Countries citing papers authored by Celine Lewis

Since Specialization

Citations

This map shows the geographic impact of Celine Lewis's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Celine Lewis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Celine Lewis more than expected).

Fields of papers citing papers by Celine Lewis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Celine Lewis. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Celine Lewis. The network helps show where Celine Lewis may publish in the future.

Co-authorship network of co-authors of Celine Lewis

This figure shows the co-authorship network connecting the top 25 collaborators of Celine Lewis. A scholar is included among the top collaborators of Celine Lewis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Celine Lewis. Celine Lewis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sanderson, Saskia C., et al.. (2025). Parental knowledge, attitudes, satisfaction and decisional conflict regarding whole genome sequencing in the Genomic Medicine Service: a multisite survey study in England. Journal of Medical Genetics. 62(4). 289–297. 2 indexed citations

Peter, Michelle, et al.. (2025). Are People From Black Communities Proportionately Represented in UK and US Studies Examining Views on Screening and Diagnostic Genetic Testing in Pregnancy? A Scoping Review. BJOG An International Journal of Obstetrics & Gynaecology. 132(13). 1956–1965. 1 indexed citations

Sanderson, Saskia C., et al.. (2025). Anxiety and quality‐of‐life for parents of children with undiagnosed rare conditions: A multi‐site quantitative survey study. Journal of Genetic Counseling. 34(4). e70085–e70085. 1 indexed citations

Sanderson, Saskia C., et al.. (2024). What does a consent conversation for whole genome sequencing look like in the NHS Genomic Medicine Service? An observational study. European Journal of Human Genetics. 33(4). 504–512. 2 indexed citations

Clarke, Angus, et al.. (2024). Written communication of whole genome sequencing results in the NHS Genomic Medicine Service: a multi-centre service evaluation. European Journal of Human Genetics. 32(11). 1436–1445.

Gurasashvili, Jana, et al.. (2023). The disequilibrium of hope: A grounded theory analysis of parents' experiences of receiving a “no primary finding” result from genome sequencing. Journal of Genetic Counseling. 33(5). 1089–1102. 7 indexed citations

Rosenthal, Diana Margot, Antoinette Schoenthaler, Michelle Heys, et al.. (2023). How Does Living in Temporary Accommodation and the COVID-19 Pandemic Impact under 5s’ Healthcare Access and Health Outcomes? A Qualitative Study of Key Professionals in a Socially and Ethnically Diverse and Deprived Area of London. International Journal of Environmental Research and Public Health. 20(2). 1300–1300. 1 indexed citations

Skirrow, Helen, Kimberley Foley, Céire Costelloe, et al.. (2023). Maternal predictors of timeliness & uptake of Measles, Mumps & Rubella vaccine: A birth cohort study. European Journal of Public Health. 33(Supplement_2).

Lewis, Celine. (2023). Genomic testing for rare disease diagnosis—where are we now, and where should we be heading? The reflections of a behavioural scientist. European Journal of Human Genetics. 31(11). 1204–1206.

10.

Rosenthal, Diana Margot, Marcella Ucci, Michelle Heys, et al.. (2022). A Citizen Science Approach to Identifying Indoor Environmental Barriers to Optimal Health for under 5s Experiencing Homelessness in Temporary Accommodation. International Journal of Environmental Research and Public Health. 19(7). 3976–3976. 5 indexed citations

11.

Hammond, Jennifer, Sam Riedijk, Stina Lou, et al.. (2022). Assessing women’s preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design. PLoS ONE. 17(1). e0261898–e0261898. 12 indexed citations

12.

Srebniak, Malgorzata I., Attie T. J. I. Go, Lutgarde Govaerts, et al.. (2021). How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies. Clinical Genetics. 100(6). 647–658. 19 indexed citations

13.

Lewis, Celine, James Buchanan, Angus Clarke, et al.. (2021). Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol. SHILAP Revista de lepidopterología. 1. 23–23. 4 indexed citations

14.

Shelmerdine, Susan C., J. Ciaran Hutchinson, Celine Lewis, et al.. (2021). A pragmatic evidence-based approach to post-mortem perinatal imaging. Insights into Imaging. 12(1). 101–101. 17 indexed citations

15.

Lewis, Celine, Bao Sheng Loe, Chris Sidey‐Gibbons, et al.. (2019). Development of a measure of genome sequencing knowledge for young people: The kids‐KOGS. Clinical Genetics. 96(5). 411–417. 4 indexed citations

16.

Sanderson, Saskia C., Melissa Hill, Christine Patch, et al.. (2019). Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project. BMJ Open. 9(11). e029699–e029699. 29 indexed citations

17.

Sanderson, Saskia C., Bao Sheng Loe, Camila Pires Cremasco Gabriel, et al.. (2018). Development of the Knowledge of Genome Sequencing (KOGS) questionnaire. Patient Education and Counseling. 101(11). 1966–1972. 14 indexed citations

18.

Chitty, Lyn S., D. Wright, Melissa Hill, et al.. (2016). Uptake, Outcomes, and Costs of Implementing Non-invasive Prenatal Testing for Down Syndrome Into NHS Maternity Care: Prospective Cohort Study in Eight Diverse Maternity Units. Obstetrical & Gynecological Survey. 71(11). 637–639. 5 indexed citations

19.

Lewis, Celine, et al.. (2013). Non-Invasive Prenatal Testing for Down's Syndrome: Pregnant Women's Views and Likely Uptake. Public Health Genomics. 16(5). 223–232. 105 indexed citations

20.

Hill, Melissa, Celine Lewis, Lucy Jenkins, et al.. (2012). Implementing noninvasive prenatal fetal sex determination using cell-free fetal DNA in the United Kingdom. Expert Opinion on Biological Therapy. 12(sup1). S119–S126. 30 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact