Lucy Side

14.8k total citations
50 papers, 1.8k citations indexed

About

Lucy Side is a scholar working on Genetics, Oncology and Reproductive Medicine. According to data from OpenAlex, Lucy Side has authored 50 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 16 papers in Oncology and 11 papers in Reproductive Medicine. Recurrent topics in Lucy Side's work include BRCA gene mutations in cancer (25 papers), Ovarian cancer diagnosis and treatment (11 papers) and Global Cancer Incidence and Screening (7 papers). Lucy Side is often cited by papers focused on BRCA gene mutations in cancer (25 papers), Ovarian cancer diagnosis and treatment (11 papers) and Global Cancer Incidence and Screening (7 papers). Lucy Side collaborates with scholars based in United Kingdom, United States and Australia. Lucy Side's co-authors include Sue Gessler, Jane Wardle, Anne Lanceley, Kevin Shannon, Patricia Thompson, Brigit R. Taylor, Belinda Rahman, Lindsay Fraser, Saskia C. Sanderson and Samuel G. Smith and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Oncology and Blood.

In The Last Decade

Lucy Side

46 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lucy Side United Kingdom	23	956	466	407	286	227	50	1.8k
Jennifer T. Loud United States	19	639 0.7×	430 0.9×	450 1.1×	263 0.9×	127 0.6×	45	1.6k
Hagay Sobol France	33	1.5k 1.6×	733 1.6×	859 2.1×	713 2.5×	154 0.7×	113	2.8k
Judy Kirk Australia	30	1.3k 1.4×	826 1.8×	579 1.4×	554 1.9×	173 0.8×	107	3.1k
Guðríður H. Ólafsdóttir Iceland	18	979 1.0×	537 1.2×	573 1.4×	380 1.3×	124 0.5×	32	1.9k
Wendy Kohlmann United States	28	1.2k 1.2×	982 2.1×	588 1.4×	685 2.4×	124 0.5×	111	3.0k
Agnès Chompret France	20	285 0.3×	541 1.2×	550 1.4×	295 1.0×	38 0.2×	49	1.7k
L. Phuong United States	19	572 0.6×	502 1.1×	360 0.9×	331 1.2×	181 0.8×	42	1.3k
S.D. Fosså Norway	27	181 0.2×	454 1.0×	397 1.0×	142 0.5×	359 1.6×	71	1.9k
Marie Wood United States	25	1.0k 1.1×	848 1.8×	413 1.0×	498 1.7×	100 0.4×	79	2.3k
Alison H. Trainer Australia	22	791 0.8×	400 0.9×	455 1.1×	363 1.3×	113 0.5×	78	1.5k

Countries citing papers authored by Lucy Side

Since Specialization

Citations

This map shows the geographic impact of Lucy Side'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 Lucy Side with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lucy Side more than expected).

Fields of papers citing papers by Lucy Side

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucy Side. 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 Lucy Side. The network helps show where Lucy Side may publish in the future.

Co-authorship network of co-authors of Lucy Side

This figure shows the co-authorship network connecting the top 25 collaborators of Lucy Side. A scholar is included among the top collaborators of Lucy Side 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 Lucy Side. Lucy Side is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Wilson, Nicholas S., et al.. (2025). Multiple early onset atypical cutaneous fibrous histiocytomas in multilocus inherited neoplasia allele syndrome involving TP53 and FLCN genes. Journal of Medical Genetics. 62(12). jmg–2025.

Gaba, Faiza, Xin Yang, Dhivya Chandrasekaran, et al.. (2022). Unselected Population Genetic Testing for Personalised Ovarian Cancer Risk Prediction: A Qualitative Study Using Semi-Structured Interviews. Diagnostics. 12(5). 1028–1028. 5 indexed citations

Pritchard‐Jones, Kathy, Jesper Brok, William Mifsud, et al.. (2021). Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant. Pediatric Nephrology. 37(4). 821–832. 9 indexed citations

Thorneloe, Rachael, Louise Hall, Fiona M Walter, et al.. (2020). Knowledge of Potential Harms and Benefits of Tamoxifen among Women Considering Breast Cancer Preventive Therapy. Cancer Prevention Research. 13(4). 411–422. 11 indexed citations

Rahman, Belinda, Rebecca Kristeleit, Jonathan A. Ledermann, et al.. (2019). Mainstreamed genetic testing in ovarian cancer: patient experience of the testing process. International Journal of Gynecological Cancer. 30(2). 221–226. 14 indexed citations

Taylor, Amy, Angela F. Brady, Ian M. Frayling, et al.. (2018). Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group. Journal of Medical Genetics. 55(6). 372–377. 68 indexed citations

Meisel, Susanne F., Lindsay Fraser, Lucy Side, et al.. (2017). Anticipated health behaviour changes and perceived control in response to disclosure of genetic risk of breast and ovarian cancer: a quantitative survey study among women in the UK. BMJ Open. 7(12). e017675–e017675. 15 indexed citations

Hann, Katie E. J., Lindsay Fraser, Lucy Side, et al.. (2017). Health care professionals’ attitudes towards population-based genetic testing and risk-stratification for ovarian cancer: a cross-sectional survey. BMC Women s Health. 17(1). 132–132. 16 indexed citations

Hann, Katie E. J., Madeleine Freeman, Lindsay Fraser, et al.. (2017). Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review. BMC Public Health. 17(1). 503–503. 220 indexed citations

10.

Meisel, Susanne F., Jo Waller, Lindsay Fraser, et al.. (2017). Impact of a decision aid about stratified ovarian cancer risk-management on women’s knowledge and intentions: a randomised online experimental survey study. BMC Public Health. 17(1). 882–882. 9 indexed citations

11.

Smith, Samuel G., Lucy Side, Susanne F. Meisel, et al.. (2016). Clinician-Reported Barriers to Implementing Breast Cancer Chemoprevention in the UK: A Qualitative Investigation. Public Health Genomics. 19(4). 239–249. 28 indexed citations

12.

Meisel, Susanne F., Belinda Rahman, Lucy Side, et al.. (2016). Genetic testing and personalized ovarian cancer screening: a survey of public attitudes. BMC Women s Health. 16(1). 46–46. 29 indexed citations

13.

Meisel, Susanne F., Nora Pashayan, Belinda Rahman, et al.. (2015). Adjusting the frequency of mammography screening on the basis of genetic risk: Attitudes among women in the UK. The Breast. 24(3). 237–241. 51 indexed citations

14.

Smith, Samuel G., Ivana Šestak, Alice S. Forster, et al.. (2015). Factors affecting uptake and adherence to breast cancer chemoprevention: a systematic review and meta-analysis. Annals of Oncology. 27(4). 575–590. 180 indexed citations

15.

Manchanda, Ranjit, K Loggenberg, Saskia C. Sanderson, et al.. (2014). Population Testing for Cancer Predisposing BRCA1/BRCA2 Mutations in the Ashkenazi-Jewish Community: A Randomized Controlled Trial. JNCI Journal of the National Cancer Institute. 107(1). 379–379. 139 indexed citations

16.

Meisel, Susanne F., Lucy Side, Lindsay Fraser, et al.. (2013). Population-Based, Risk-Stratified Genetic Testing for Ovarian Cancer Risk: A Focus Group Study. Public Health Genomics. 16(4). 184–191. 29 indexed citations

17.

Manchanda, Ranjit, K Loggenberg, Sue Gessler, et al.. (2012). Population based testing for high-penetrance dominant gene mutations: initial results from the pilot phase of GCaPPS. UCL Discovery (University College London). 2 indexed citations

18.

Manchanda, Ranjit, Matthew Burnell, Ahmed R. Abdelraheim, et al.. (2012). Factors influencing uptake and timing of risk reducing salpingo‐oophorectomy in women at risk of familial ovarian cancer: a competing risk time to event analysis. BJOG An International Journal of Obstetrics & Gynaecology. 119(5). 527–536. 58 indexed citations

19.

Lanceley, Anne, et al.. (2012). Family History and Women With Ovarian Cancer:Is it Asked and Does it Matter?. International Journal of Gynecological Cancer. 22(2). 254–259. 22 indexed citations

20.

Side, Lucy, Brigit R. Taylor, Matthew C. Cayouette, et al.. (1997). Homozygous Inactivation of theNF1Gene in Bone Marrow Cells from Children with Neurofibromatosis Type 1 and Malignant Myeloid Disorders. New England Journal of Medicine. 336(24). 1713–1720. 212 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.

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