Lee Silcock

403 total citations
14 papers, 239 citations indexed

About

Lee Silcock is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Lee Silcock has authored 14 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Lee Silcock's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Lee Silcock is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Lee Silcock collaborates with scholars based in United Kingdom, Qatar and United States. Lee Silcock's co-authors include Dominic McMullan, Chirag Patel, Louise Brueton, Helen Cox, Mark D. Kilby, Christopher Kent, Joanna Jarvis, Rachel Harrison, Sarah Hillman and Esther L. Moss and has published in prestigious journals such as Blood, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Lee Silcock

13 papers receiving 227 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lee Silcock United Kingdom	8	103	67	66	57	53	14	239
Wilfred Wu United States	6	53 0.5×	89 1.3×	21 0.3×	32 0.6×	76 1.4×	7	297
Niklas Pal Sweden	8	61 0.6×	17 0.3×	29 0.4×	32 0.6×	46 0.9×	15	210
Pei‐Chi Kao United States	8	75 0.7×	15 0.2×	41 0.6×	28 0.5×	22 0.4×	28	230
Lixian Chang China	11	134 1.3×	31 0.5×	13 0.2×	51 0.9×	36 0.7×	58	348
Seon Kyung Lee South Korea	11	99 1.0×	45 0.7×	57 0.9×	12 0.2×	47 0.9×	31	314
Jiang‐Feng Ye China	10	123 1.2×	15 0.2×	20 0.3×	37 0.6×	63 1.2×	16	395
J Stříteský Czechia	8	54 0.5×	41 0.6×	43 0.7×	21 0.4×	14 0.3×	28	247
Klaus Strathmann Germany	7	131 1.3×	40 0.6×	14 0.2×	20 0.4×	34 0.6×	8	286
Masaya Uno Japan	10	70 0.7×	9 0.1×	63 1.0×	33 0.6×	42 0.8×	47	334
Philip Twiss United Kingdom	9	149 1.4×	90 1.3×	21 0.3×	86 1.5×	47 0.9×	10	309

Countries citing papers authored by Lee Silcock

Since Specialization

Citations

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

Fields of papers citing papers by Lee Silcock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lee Silcock

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

All Works

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14 of 14 papers shown

Silcock, Lee, et al.. (2025). BTN2A1 and BTN3A1 as Novel Coeliac Disease Risk Loci: An In Silico Analysis. International Journal of Molecular Sciences. 26(21). 10697–10697.

Ward, Douglas G., Laura Baxter, Sascha Ott, et al.. (2022). Highly Sensitive and Specific Detection of Bladder Cancer via Targeted Ultra-deep Sequencing of Urinary DNA. European Urology Oncology. 6(1). 67–75. 19 indexed citations

James, Nicola, Rebecca Mathew, Lee Silcock, et al.. (2021). Human sample authentication in biomedical research: comparison of two platforms. Scientific Reports. 11(1). 13982–13982. 4 indexed citations

Moss, Esther L., et al.. (2020). Utility of Circulating Tumor DNA for Detection and Monitoring of Endometrial Cancer Recurrence and Progression. Cancers. 12(8). 2231–2231. 41 indexed citations

Sastry, Konduru S., Lee Silcock, Lotfi Chouchane, et al.. (2020). Differential responsiveness to BRAF inhibitors of melanoma cell lines BRAF V600E-mutated. Journal of Translational Medicine. 18(1). 192–192. 8 indexed citations

Silcock, Lee, Shu Yau, Yvonne Daniel, et al.. (2020). A novel non‐invasive prenatal sickle cell disease test for all at‐risk pregnancies. British Journal of Haematology. 190(1). 119–124. 24 indexed citations

Silcock, Lee, Hakeem Almabrazi, Younes Mokrab, et al.. (2019). Monoallelic expression in melanoma. Journal of Translational Medicine. 17(1). 112–112. 4 indexed citations

Ward, Douglas G., Naheema S. Gordon, Rebecca H. Boucher, et al.. (2019). Targeted deep sequencing of urothelial bladder cancers and associated urinary DNA : a 23‐gene panel with utility for non‐invasive diagnosis and risk stratification. British Journal of Urology. 124(3). 532–544. 37 indexed citations

Daniel, Yvonne, Lee Silcock, Joo Wook Ahn, et al.. (2019). Non-Invasive Prenatal Diagnosis (NIPD) of Sickle-Cell Disease By Massively Parallel Sequencing of Cell-Free Fetal DNA in Maternal Serum. Blood. 134(Supplement_1). 2085–2085. 3 indexed citations

10.

Terranegra, Annalisa, Teresa Arcidiacono, Caterina Brasacchio, et al.. (2019). Glucagon-like peptide-1 receptor and sarcoglycan delta genetic variants can affect cardiovascular risk in chronic kidney disease patients under hemodialysis. Clinical Kidney Journal. 13(4). 666–673. 3 indexed citations

11.

Sastry, Konduru S., Lee Silcock, Lotfi Chouchane, et al.. (2016). Differential Responsiveness to Braf Inhibitors of Melanoma Cell Lines Braf V600e-Mutated. 1 indexed citations

12.

Hillman, Sarah, Dominic McMullan, Lee Silcock, Eamonn R. Maher, & Mark D. Kilby. (2013). How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?. The Journal of Maternal-Fetal & Neonatal Medicine. 27(7). 649–657. 19 indexed citations

13.

Patel, Chirag, Lee Silcock, Dominic McMullan, Louise Brueton, & Helen Cox. (2012). TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype. European Journal of Human Genetics. 20(8). 863–869. 39 indexed citations

14.

Dixit, Abhijit, Chirag Patel, Rachel Harrison, et al.. (2012). 17q12 microdeletion syndrome: Three patients illustrating the phenotypic spectrum. American Journal of Medical Genetics Part A. 158A(9). 2317–2321. 37 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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