L‐C Tsui

557 total citations
14 papers, 409 citations indexed

About

L‐C Tsui is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, L‐C Tsui has authored 14 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pulmonary and Respiratory Medicine, 4 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in L‐C Tsui's work include Cystic Fibrosis Research Advances (8 papers), Tracheal and airway disorders (4 papers) and Connective tissue disorders research (3 papers). L‐C Tsui is often cited by papers focused on Cystic Fibrosis Research Advances (8 papers), Tracheal and airway disorders (4 papers) and Connective tissue disorders research (3 papers). L‐C Tsui collaborates with scholars based in Canada, United States and Hong Kong. L‐C Tsui's co-authors include Richard Rozmahel, Julian Zielenski, Muhammad Faiyaz‐Ul‐Haque, M. Siddique, Wasim Ahmad, D. Markiewicz, Sayedul Haque, Johanna M. Rommens, Frauke Rininsland and Mary Corey and has published in prestigious journals such as Journal of Biological Chemistry, Gastroenterology and Human Mutation.

In The Last Decade

L‐C Tsui

13 papers receiving 403 citations

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 9 230 132 96 64 47 14 409
Silvia Spena Italy 13 178 0.8× 185 1.4× 117 1.2× 45 0.7× 112 2.4× 25 527
Toru Udaka Japan 9 152 0.7× 138 1.0× 84 0.9× 167 2.6× 24 0.5× 14 338
Odile Boute France 13 36 0.2× 162 1.2× 222 2.3× 47 0.7× 35 0.7× 31 471
Randi Koll Germany 9 26 0.1× 206 1.6× 152 1.6× 65 1.0× 22 0.5× 13 346
Kiyoshi Kikkawa Japan 12 32 0.1× 182 1.4× 211 2.2× 44 0.7× 14 0.3× 27 378
R Hennekam Netherlands 10 40 0.2× 94 0.7× 164 1.7× 23 0.4× 14 0.3× 14 318
PER ZETTERQVIST Sweden 12 101 0.4× 114 0.9× 85 0.9× 12 0.2× 31 0.7× 24 360
Lidia Pezzani Italy 12 28 0.1× 161 1.2× 174 1.8× 24 0.4× 49 1.0× 33 426
Darya Gorbenko del Blanco Spain 11 117 0.5× 185 1.4× 276 2.9× 16 0.3× 5 0.1× 15 439
Christine A. Oley Australia 9 76 0.3× 205 1.6× 93 1.0× 80 1.3× 4 0.1× 10 416

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

14 of 14 papers shown
1.
Dorfman, Ruslan, Andrew J. Sandford, Mary Corey, et al.. (2006). 15 Analysis of candidate genes as modifiers of Cystic Fibrosis. Journal of Cystic Fibrosis. 5. S4–S4.
2.
Lindinger, Angelika, et al.. (2004). A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13. Clinical Genetics. 67(2). 183–188. 18 indexed citations
3.
Lo, Bernard, Muhammad Faiyaz‐Ul‐Haque, Brenda Banwell, et al.. (2004). The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9‐cM region on chromosome 11q23. Clinical Genetics. 65(2). 137–142. 5 indexed citations
4.
Faiyaz‐Ul‐Haque, Muhammad, Sayedul Haque, M. PATEL, et al.. (2004). Fine mapping of the X‐linked split‐hand/split‐foot malformation (SHFM2) locus to a 5.1‐Mb region on Xq26.3 and analysis of candidate genes. Clinical Genetics. 67(1). 93–97. 42 indexed citations
5.
Faiyaz‐Ul‐Haque, Muhammad, Wasim Ahmad, Syed A. Hussain, et al.. (2004). Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis). Clinical Genetics. 66(2). 144–151. 11 indexed citations
6.
7.
Zielenski, Julian, et al.. (2002). Complete screening of the CFTR gene in Argentine cystic fibrosis patients. Clinical Genetics. 61(3). 207–213. 19 indexed citations
8.
Zielenski, Julian, et al.. (2000). Novel cystic fibrosis mutation (2215insG) in two adolescent Taiwanese siblings.. PubMed. 99(7). 564–7. 21 indexed citations
9.
Ahmed, Najma N., Mary Corey, Julian Zielenski, et al.. (1998). Molecular consequences of CFTR gene mutations in the exocrine pancreas. Gastroenterology. 114. A437–A437. 2 indexed citations
10.
11.
Hamosh, Ada, Beryl J. Rosenstein, Mary Corey, et al.. (1992). Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus.. PubMed. 51(2). 245–50. 74 indexed citations
12.
Rozmahel, Richard, et al.. (1991). Characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene.. Journal of Biological Chemistry. 266(36). 24471–24476. 81 indexed citations
13.
Zielenski, Julian, D. Markiewicz, Frauke Rininsland, Johanna M. Rommens, & L‐C Tsui. (1991). A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.. PubMed. 49(6). 1256–62. 67 indexed citations
14.
Tsui, L‐C, N. Plavsic, D. Markiewicz, et al.. (1987). Molecular approaches to the cystic fibrosis gene.. PubMed. 254. 73–87. 3 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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