L.-C. Tsui

2.4k total citations · 2 hit papers
16 papers, 1.9k citations indexed

About

L.-C. Tsui is a scholar working on Molecular Biology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, L.-C. Tsui has authored 16 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Oncology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in L.-C. Tsui's work include Glycosylation and Glycoproteins Research (2 papers), DNA Repair Mechanisms (2 papers) and Nitric Oxide and Endothelin Effects (2 papers). L.-C. Tsui is often cited by papers focused on Glycosylation and Glycoproteins Research (2 papers), DNA Repair Mechanisms (2 papers) and Nitric Oxide and Endothelin Effects (2 papers). L.-C. Tsui collaborates with scholars based in Canada, United States and Japan. L.-C. Tsui's co-authors include Stephen W. Scherer, Henry H. Heng, Anne V. Hall, Keith Schappert, Robert Stewart, X.-M. Shi, Philip A. Marsden, Gerald H. Thomsen, Bharati Bapat and Hyeja Kim and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

L.-C. Tsui

15 papers receiving 1.9k citations

Hit Papers

MADR2 Maps to 18q21 and Encodes a TGFβ–Regulated MAD–Rela... 1993 2026 2004 2015 1996 1993 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L.-C. Tsui Canada 12 960 537 352 346 308 16 1.9k
David S. Taylor United Kingdom 26 877 0.9× 290 0.5× 104 0.3× 300 0.9× 153 0.5× 58 1.9k
Zheqing Cai United States 14 815 0.8× 270 0.5× 262 0.7× 271 0.8× 459 1.5× 17 2.0k
Izumi Suzuma Japan 26 1.3k 1.3× 248 0.5× 177 0.5× 254 0.7× 87 0.3× 29 2.8k
Jing‐Ping Lin United States 21 788 0.8× 324 0.6× 303 0.9× 233 0.7× 311 1.0× 52 2.1k
Hitoshi Takagi Japan 28 2.2k 2.3× 318 0.6× 342 1.0× 502 1.5× 87 0.3× 43 3.8k
Kyu Youn Ahn South Korea 25 948 1.0× 344 0.6× 201 0.6× 200 0.6× 66 0.2× 58 1.7k
Xiaohua Xin United States 16 1.2k 1.3× 217 0.4× 292 0.8× 139 0.4× 65 0.2× 34 1.8k
Miyo Matsumura Japan 34 1.6k 1.7× 167 0.3× 170 0.5× 159 0.5× 145 0.5× 138 4.1k
Spiegel Am United States 24 1.3k 1.3× 179 0.3× 379 1.1× 164 0.5× 67 0.2× 47 2.2k
Ken‐ichirou Morishige Japan 27 1.2k 1.2× 123 0.2× 344 1.0× 277 0.8× 169 0.5× 90 2.4k

Countries citing papers authored by L.-C. Tsui

Since Specialization
Citations

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

Fields of papers citing papers by L.-C. Tsui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L.-C. Tsui. 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 L.-C. Tsui. The network helps show where L.-C. Tsui may publish in the future.

Co-authorship network of co-authors of L.-C. Tsui

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

All Works

16 of 16 papers shown
1.
Osborne, Lucy R., Martin Li, Barbara R. Pober, et al.. (2001). A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome. Nature Genetics. 29(3). 321–325. 228 indexed citations
2.
Nomiyama, Hisayuki, Lucy R. Osborne, Jun Kusuda, et al.. (1998). Assignment of the Human CC Chemokine MPIF-2/Eotaxin-2 (SCYA24) to Chromosome 7q11.23. Genomics. 49(2). 339–340. 17 indexed citations
3.
Schanen, N. Carolyn, Stephen W. Scherer, L.-C. Tsui, & Uta Francke. (1996). Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1. Cytogenetic and Genome Research. 72(2-3). 187–188. 11 indexed citations
4.
Nakabayashi, Kazuhiko, Toshihiko Ogata, Michihiko Fujii, et al.. (1996). A Panel of Radiation Hybrids Defining the 7q31-q32 Region of Human Chromosome 7. DNA Research. 3(3). 181–183.
5.
Petronis, Artūras, Henry H. Heng, Timothy A. Klempan, et al.. (1996). Direct detection of expanded trinucleotide repeats using PCR and DNA hybridization techniques. American Journal of Medical Genetics. 67(1). 85–91. 18 indexed citations
6.
Takahara, Kazuhiko, Lucy R. Osborne, Rosemary W. Elliott, et al.. (1996). Fine Mapping of the Human and Mouse Genes for the Type I Procollagen COOH-Terminal Proteinase Enhancer Protein. Genomics. 31(2). 253–256. 8 indexed citations
7.
Eppert, Kolja, Stephen W. Scherer, Hilmi Özçelik, et al.. (1996). MADR2 Maps to 18q21 and Encodes a TGFβ–Regulated MAD–Related Protein That Is Functionally Mutated in Colorectal Carcinoma. Cell. 86(4). 543–552. 717 indexed citations breakdown →
8.
Torigoe, K, Seiji Sato, Hitoshi Kusaba, et al.. (1995). A YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines.. Genome Research. 5(3). 233–244. 19 indexed citations
9.
Gray, Brian A., Stephen W. Scherer, L.-C. Tsui, et al.. (1995). Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient.. PubMed. 56(6). 1411–6. 25 indexed citations
10.
Heng, Henry H., et al.. (1994). Localization of the Human Gene for Inducible Nitric Oxide Synthase (NOS2) to Chromosome 17q11.2-q12. Genomics. 19(1). 183–185. 51 indexed citations
11.
Peichel, Catherine L., Stephen W. Scherer, L.-C. Tsui, David R. Beier, & Thomas Vogt. (1993). Mapping the midkine family of developmentally regulated signaling molecules. Mammalian Genome. 4(11). 632–638. 8 indexed citations
12.
Marsden, Philip A., Henry H. Heng, Stephen W. Scherer, et al.. (1993). Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene. Journal of Biological Chemistry. 268(23). 17478–17488. 717 indexed citations breakdown →
13.
Dörk, Thilo, Thomas Neumann, Ulrich Wulbrand, et al.. (1992). Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families. Human Genetics. 88(4). 417–425. 58 indexed citations
14.
Hogg, David, Michael B. Gorin, Camilla Heinzmann, et al.. (1987). Nucleotide Sequence for the cDNA of the Bovine βB2 Crystallin and Assignment of the Orthologous Human Locus to Chromosome 22. Current Eye Research. 6(11). 1335–1342. 30 indexed citations
15.
Cai, Guang-Yun, et al.. (1986). Localization of a β-crystallin gene, HuβA3/A1 (gene symbol: <i>CRYB1</i>), to the long arm of human chromosome 17. Cytogenetic and Genome Research. 42(4). 202–207. 18 indexed citations
16.
Tsui, L.-C., M. Zsiga, Derek Kennedy, et al.. (1985). Cystic fibrosis: progress in mapping the disease locus using polymorphic DNA markers. I.. Cytogenetic and Genome Research. 39(4). 299–301. 6 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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