Hsiao‐Mei Lu

1.7k total citations
22 papers, 651 citations indexed

About

Hsiao‐Mei Lu is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Hsiao‐Mei Lu has authored 22 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Hsiao‐Mei Lu's work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cancer Genomics and Diagnostics (5 papers). Hsiao‐Mei Lu is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cancer Genomics and Diagnostics (5 papers). Hsiao‐Mei Lu collaborates with scholars based in United States, China and Taiwan. Hsiao‐Mei Lu's co-authors include Jefferey Chen, Shuwei Li, Wenbo Mu, Aaron Elliott, Elizabeth Chao, Mary Helen Black, Kelly D. Farwell, Yuan Tian, Hong Lu and Wenqi Zeng and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Journal of Neurophysiology.

In The Last Decade

Hsiao‐Mei Lu

21 papers receiving 646 citations

Peers

Hsiao‐Mei Lu
Tymor Hamamsy United States
Nicola Whiffin United Kingdom
Christopher DeBoever United States
Salma Ben‐Salem United Arab Emirates
Katri Pylkäs Finland
Duncan B. Johnstone United States
Praveen F. Cherukuri United States
Maartje van de Vorst Netherlands
Lídia Feliubadaló Spain
Megan R. Vanstone Canada
Tymor Hamamsy United States
Hsiao‐Mei Lu
Citations per year, relative to Hsiao‐Mei Lu Hsiao‐Mei Lu (= 1×) peers Tymor Hamamsy

Countries citing papers authored by Hsiao‐Mei Lu

Since Specialization
Citations

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

Fields of papers citing papers by Hsiao‐Mei Lu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hsiao‐Mei Lu. 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 Hsiao‐Mei Lu. The network helps show where Hsiao‐Mei Lu may publish in the future.

Co-authorship network of co-authors of Hsiao‐Mei Lu

This figure shows the co-authorship network connecting the top 25 collaborators of Hsiao‐Mei Lu. A scholar is included among the top collaborators of Hsiao‐Mei Lu 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 Hsiao‐Mei Lu. Hsiao‐Mei Lu 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.
Shih, Andrew, Tomi Jun, Andrew D. Skol, et al.. (2022). Inherited cancer predisposing mutations in patients with therapy‐related myeloid neoplasms. British Journal of Haematology. 200(4). 489–493. 3 indexed citations
2.
Black, Mary Helen, Shuwei Li, Holly LaDuca, et al.. (2020). Validation of a prostate cancer polygenic risk score. The Prostate. 80(15). 1314–1321. 19 indexed citations
3.
Tian, Yuan, Tina Pesaran, Adam Chamberlin, et al.. (2019). REVEL and BayesDel outperform other in silico meta-predictors for clinical variant classification. Scientific Reports. 9(1). 12752–12752. 58 indexed citations
4.
Qian, Dajun, Shuwei Li, Yuan Tian, et al.. (2018). A Bayesian framework for efficient and accurate variant prediction. PLoS ONE. 13(9). e0203553–e0203553. 10 indexed citations
5.
Mu, Wenbo, Bing Li, Sitao Wu, et al.. (2018). Detection of structural variation using target captured next-generation sequencing data for genetic diagnostic testing. Genetics in Medicine. 21(7). 1603–1610. 24 indexed citations
6.
Lu, Hsiao‐Mei, Shuwei Li, Mary Helen Black, et al.. (2018). Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing. JAMA Oncology. 5(1). 51–51. 116 indexed citations
7.
Black, Mary Helen, Shuwei Li, Holly LaDuca, et al.. (2018). Polygenic risk score for breast cancer in high-risk women.. Journal of Clinical Oncology. 36(15_suppl). 1508–1508. 9 indexed citations
8.
LaDuca, Holly, Kelly D. Farwell, Huy Gia Vuong, et al.. (2017). Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels. PLoS ONE. 12(2). e0170843–e0170843. 79 indexed citations
9.
Hagman, Kelly D. Farwell, Deepali N. Shinde, Cameron Mroske, et al.. (2016). Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine. 19(2). 224–235. 34 indexed citations
10.
Mu, Wenbo, Hsiao‐Mei Lu, Jefferey Chen, Shuwei Li, & Aaron Elliott. (2016). Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing. Journal of Molecular Diagnostics. 18(6). 923–932. 121 indexed citations
11.
Cohen, Julie S., Siddharth Srivastava, Kelly D. Farwell, et al.. (2015). ELP2 is a novel gene implicated in neurodevelopmental disabilities. American Journal of Medical Genetics Part A. 167(6). 1391–1395. 58 indexed citations
12.
Mroske, Cameron, Kristen Rasmussen, Deepali N. Shinde, et al.. (2015). Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalities. BMC Medical Genetics. 16(1). 102–102. 21 indexed citations
13.
14.
Yu, Lan, Wenqi Zeng, Xiang Li, et al.. (2013). A human de novo mutation inMYH10phenocopies the loss of function mutation in mice. PubMed. 1(1). e26144–e26144. 32 indexed citations
15.
16.
Lu, Hsiao‐Mei & Jie Liang. (2007). A model study of protein nascent chain and cotranslational folding using hydrophobic‐polar residues. Proteins Structure Function and Bioinformatics. 70(2). 442–449. 15 indexed citations
17.
Lu, Hsiao‐Mei & Jie Liang. (2007). Perturbation-based Markovian Transmission Model for Macromolecular Machinery in Cell. Conference proceedings. 388. 5029–5034. 2 indexed citations
18.
Li, Yiming & Hsiao‐Mei Lu. (2004). Electron energy state spin-splitting in nanoscale InAs/GaAs semiconductor quantum dots and rings. 2. 885–888. 1 indexed citations
19.
Huang, Lei, Hsiao‐Mei Lu, & Yang Dai. (2003). Feature Selection of Support Vector Regression for Quantitative Structure-Activity Relationships (QSAR).. 88–93.
20.
Li, Yiming, Hsiao‐Mei Lu, Ting-wei Tang, & Simon M. Sze. (2003). A novel parallel adaptive Monte Carlo method for nonlinear Poisson equation in semiconductor devices. Mathematics and Computers in Simulation. 62(3-6). 413–420. 23 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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