Wan‐Ping Lee

3.5k total citations
31 papers, 407 citations indexed

About

Wan‐Ping Lee is a scholar working on Molecular Biology, Genetics and Electrical and Electronic Engineering. According to data from OpenAlex, Wan‐Ping Lee has authored 31 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Electrical and Electronic Engineering. Recurrent topics in Wan‐Ping Lee's work include VLSI and FPGA Design Techniques (8 papers), Low-power high-performance VLSI design (8 papers) and Genomics and Rare Diseases (7 papers). Wan‐Ping Lee is often cited by papers focused on VLSI and FPGA Design Techniques (8 papers), Low-power high-performance VLSI design (8 papers) and Genomics and Rare Diseases (7 papers). Wan‐Ping Lee collaborates with scholars based in United States, Taiwan and Australia. Wan‐Ping Lee's co-authors include Yao‐Wen Chang, Hung‐Yi Liu, Charles Lee, Kai Ye, Xiaofei Yang, Li‐San Wang, Yuk Yee Leung, Christy Pu, Yueh‐Ching Chou and Jennifer Lingard and has published in prestigious journals such as Nature Communications, Human Molecular Genetics and Genome biology.

In The Last Decade

Wan‐Ping Lee

29 papers receiving 396 citations

Peers

Wan‐Ping Lee
Qing Yu China
Shun Yao China
Paul Quinn United Kingdom
Réka Nagy United Kingdom
Wan‐Ping Lee
Citations per year, relative to Wan‐Ping Lee Wan‐Ping Lee (= 1×) peers Ali Nazari

Countries citing papers authored by Wan‐Ping Lee

Since Specialization
Citations

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

Fields of papers citing papers by Wan‐Ping Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wan‐Ping Lee

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

All Works

20 of 20 papers shown
1.
Guo, Michael H., et al.. (2025). Polygenic burden of short tandem repeat expansions promotes risk for Alzheimer’s disease. Nature Communications. 16(1). 1126–1126. 4 indexed citations
2.
Wang, Hui, Beth A. Dombroski, Yaqin Si, et al.. (2025). Structural variation detection and association analysis of whole‐genome‐sequence data from 16,543 Alzheimer's disease sequencing project subjects. Alzheimer s & Dementia. 21(6). e70277–e70277. 1 indexed citations
3.
Wang, Li‐San, Yuk Yee Leung, Wan‐Ping Lee, et al.. (2024). Genomic Frontiers in Alzheimer’s Research: A Primer on the Alzheimer’s Disease Sequencing Project (ADSP) and its AI/ML Opportunities. Alzheimer s & Dementia. 20(S1). e087888–e087888. 1 indexed citations
4.
Wang, Hui, Timothy S. Chang, Beth A. Dombroski, et al.. (2024). Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub‐haplotypes. Alzheimer s & Dementia. 20(S1). e086923–e086923.
5.
Malamon, John, John J. Farrell, Beth A. Dombroski, et al.. (2024). A comparative study of structural variant calling in WGS from Alzheimer’s disease families. Life Science Alliance. 7(5). e202302181–e202302181. 3 indexed citations
6.
Greenfest‐Allen, Emily, Otto Valladares, Pavel P. Kuksa, et al.. (2023). NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge. Alzheimer s & Dementia. 20(2). 1123–1136. 11 indexed citations
7.
Wang, Hui, Li‐San Wang, Gerard D. Schellenberg, & Wan‐Ping Lee. (2023). The role of structural variations in Alzheimer’s disease and other neurodegenerative diseases. Frontiers in Aging Neuroscience. 14. 1073905–1073905. 12 indexed citations
8.
Ho, Pei‐Chuan, Hui Wang, Wan‐Ping Lee, et al.. (2023). The prediction of Alzheimer’s disease through multi-trait genetic modeling. Frontiers in Aging Neuroscience. 15. 1168638–1168638. 3 indexed citations
9.
Lee, Wan‐Ping, Qihui Zhu, Xiaofei Yang, et al.. (2022). JAX-CNV: A Whole-Genome Sequencing-Based Algorithm for Copy Number Detection at Clinical Grade Level. Genomics Proteomics & Bioinformatics. 20(6). 1197–1206. 4 indexed citations
10.
Leung, Yuk Yee, et al.. (2022). Polygenic Risk Scores in Alzheimer’s Disease Genetics: Methodology, Applications, Inclusion, and Diversity. Journal of Alzheimer s Disease. 89(1). 1–12. 23 indexed citations
11.
Lee, Wan‐Ping, Mitchell Conery, Yuk Yee Leung, et al.. (2021). Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project. Frontiers in Genetics. 12. 752390–752390. 6 indexed citations
12.
Ipsen, Ilse C. F., Tzu‐Hung Hsiao, Ching‐Heng Lin, et al.. (2021). SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data. Frontiers in Genetics. 12. 710055–710055. 2 indexed citations
13.
Yang, Xiaofei, Wan‐Ping Lee, Kai Ye, & Charles Lee. (2019). One reference genome is not enough. Genome biology. 20(1). 104–104. 48 indexed citations
14.
Lee, Wan‐Ping, Joseph F. Leone, Qihui Zhu, et al.. (2018). FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods. Genome biology. 19(1). 38–38. 38 indexed citations
15.
Lee, Wan‐Ping, Jiantao Wu, & Gábor Marth. (2015). Toolbox for Mobile-Element Insertion Detection on Cancer Genomes. Cancer Informatics. 14s1. CIN.S24657–CIN.S24657. 3 indexed citations
16.
Lee, Wan‐Ping, Hung‐Yi Liu, & Yao‐Wen Chang. (2009). Voltage-Island Partitioning and Floorplanning Under Timing Constraints. IEEE Transactions on Computer-Aided Design of Integrated Circuits and Systems. 28(5). 690–702. 13 indexed citations
17.
Lee, Wan‐Ping, et al.. (2008). Sensitivity-based multiple-Vt cell swapping for leakage power reduction. 168–171. 1 indexed citations
18.
Lee, Wan‐Ping, Hung‐Yi Liu, & Yao‐Wen Chang. (2007). An ILP algorithm for post-floorplanning voltage-island generation considering power-network planning. International Conference on Computer Aided Design. 650–655. 50 indexed citations
19.
Liu, Hung‐Yi, Wan‐Ping Lee, & Yao‐Wen Chang. (2007). A Provably Good Approximation Algorithm for Power Optimization Using Multiple Supply Voltages. Proceedings - ACM IEEE Design Automation Conference. 887–890.
20.
Lee, Wan‐Ping, et al.. (2002). Correlations Among Serum Calcium, Vitamin D and Parathyroid Hormone Levels in the Elderly in Southern Taiwan. Journal of Nursing Research. 10(1). 65–72. 8 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

Rankless by CCL
2026