Wing‐Shan Lee

885 total citations
12 papers, 506 citations indexed

About

Wing‐Shan Lee is a scholar working on Cancer Research, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wing‐Shan Lee has authored 12 papers receiving a total of 506 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cancer Research, 8 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wing‐Shan Lee's work include Cancer Genomics and Diagnostics (9 papers), Epigenetics and DNA Methylation (5 papers) and Prenatal Screening and Diagnostics (5 papers). Wing‐Shan Lee is often cited by papers focused on Cancer Genomics and Diagnostics (9 papers), Epigenetics and DNA Methylation (5 papers) and Prenatal Screening and Diagnostics (5 papers). Wing‐Shan Lee collaborates with scholars based in Hong Kong, China and United States. Wing‐Shan Lee's co-authors include Rossa W. K. Chiu, Peiyong Jiang, Yuk Ming Dennis Lo, K.C. Allen Chan, Suk Hang Cheng, Wenlei Peng, Tak Yeung Leung, Rebecca W.Y. Chan, Meng Ni and Ali Rashidfarrokhi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genome Research and Clinical Chemistry.

In The Last Decade

Wing‐Shan Lee

12 papers receiving 506 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wing‐Shan Lee Hong Kong	10	328	289	145	103	68	12	506
Wanxia Gai Hong Kong	8	265 0.8×	191 0.7×	48 0.3×	34 0.3×	119 1.8×	13	405
Jasper J.H. Eijsink Netherlands	13	155 0.5×	345 1.2×	50 0.3×	87 0.8×	125 1.8×	19	610
Luc Dehaspe Belgium	11	223 0.7×	189 0.7×	297 2.0×	38 0.4×	114 1.7×	21	593
Fiona S. Togneri United Kingdom	7	96 0.3×	115 0.4×	226 1.6×	120 1.2×	48 0.7×	9	440
Ji Cheng United States	3	80 0.2×	263 0.9×	56 0.4×	50 0.5×	335 4.9×	7	534
Johann Hermann Germany	6	98 0.3×	225 0.8×	57 0.4×	40 0.4×	174 2.6×	8	578
Sabine Weickmann Germany	13	460 1.4×	568 2.0×	28 0.2×	36 0.3×	129 1.9×	17	749
Maniesh van der Vaart South Africa	4	179 0.5×	135 0.5×	27 0.2×	22 0.2×	73 1.1×	4	282
Rachel T. Klein United States	10	205 0.6×	204 0.7×	48 0.3×	55 0.5×	140 2.1×	15	600
Éva Márton Hungary	10	234 0.7×	276 1.0×	17 0.1×	21 0.2×	47 0.7×	28	403

Countries citing papers authored by Wing‐Shan Lee

Since Specialization

Citations

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

Fields of papers citing papers by Wing‐Shan Lee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wing‐Shan Lee

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

All Works

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12 of 12 papers shown

Chan, Rebecca W.Y., Peter Pak‐Hang Cheung, Meng Ni, et al.. (2022). Fragmentomics of urinary cell-free DNA in nuclease knockout mouse models. PLoS Genetics. 18(7). e1010262–e1010262. 11 indexed citations

Xie, Tingting, Guangya Wang, Spencer C Ding, et al.. (2022). High-resolution analysis for urinary DNA jagged ends. npj Genomic Medicine. 7(1). 14–14. 5 indexed citations

Wang, Guangya, W.K. Lam, Lowell Ling, et al.. (2022). Fragment Ends of Circulating Microbial DNA as Signatures for Pathogen Detection in Sepsis. Clinical Chemistry. 69(2). 189–201. 9 indexed citations

Jiang, Peiyong, Tingting Xie, Spencer C Ding, et al.. (2020). Detection and characterization of jagged ends of double-stranded DNA in plasma. Genome Research. 30(8). 1144–1153. 76 indexed citations

Mary-Jane, L, Haiqiang Zhang, Peiyong Jiang, et al.. (2019). Topologic Analysis of Plasma Mitochondrial DNA Reveals the Coexistence of Both Linear and Circular Molecules. Clinical Chemistry. 65(9). 1161–1170. 29 indexed citations

Cheng, Timothy H.T., Peiyong Jiang, Jeremy Yuen‐Chun Teoh, et al.. (2019). Noninvasive Detection of Bladder Cancer by Shallow-Depth Genome-Wide Bisulfite Sequencing of Urinary Cell-Free DNA for Methylation and Copy Number Profiling. Clinical Chemistry. 65(7). 927–936. 42 indexed citations

Serpas, Lee, Rebecca W.Y. Chan, Peiyong Jiang, et al.. (2018). Dnase1l3deletion causes aberrations in length and end-motif frequencies in plasma DNA. Proceedings of the National Academy of Sciences. 116(2). 641–649. 133 indexed citations

Vong, Joaquim S. L., Peiyong Jiang, Suk‐Hang Cheng, et al.. (2018). Enrichment of fetal and maternal long cell‐free DNA fragments from maternal plasma following DNA repair. Prenatal Diagnosis. 39(2). 88–99. 11 indexed citations

Cheng, Timothy H.T., Peiyong Jiang, Wing‐Shan Lee, et al.. (2017). Genomewide bisulfite sequencing reveals the origin and time-dependent fragmentation of urinary cfDNA. Clinical Biochemistry. 50(9). 496–501. 52 indexed citations

10.

Vong, Joaquim S. L., Jason C.H. Tsang, Peiyong Jiang, et al.. (2017). Single-Stranded DNA Library Preparation Preferentially Enriches Short Maternal DNA in Maternal Plasma. Clinical Chemistry. 63(5). 1031–1037. 20 indexed citations

11.

Hui, Winnie W. I., Peiyong Jiang, Tong Yu, et al.. (2016). Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases. Clinical Chemistry. 63(2). 513–524. 72 indexed citations

12.

Garcia-Barceló, Mercè, MH Sham, Wing‐Shan Lee, et al.. (2004). Highly Recurrent RET Mutations and Novel Mutations in Genes of the Receptor Tyrosine Kinase and Endothelin Receptor B Pathways in Chinese Patients with Sporadic Hirschsprung Disease. Clinical Chemistry. 50(1). 93–100. 46 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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