L‐C Tsui

557 citations
14 papers · 409 · h-index 9

Impact in

Papers in

L‐C Tsui

13 papers receiving 403 citations

Peers

L‐C Tsui
Comparison fields: 5 of 59
  • Developmental Biology 47
  • Pulmonary and Respiratory Medicine 230
  • Genetics 64
  • Genetics 96
  • Molecular Biology 132
Replace Odile Boute with:
Odile Boute France
Silvia Spena Italy
Toru Udaka Japan
R Hennekam Netherlands
Lidia Pezzani Italy
PER ZETTERQVIST Sweden
Randi Koll Germany
Beate Mitulla Germany
Carole Brewer United Kingdom
Kiyoshi Kikkawa Japan
L‐C Tsui relative to Odile Boute France Odile Boute's profile →
Citations per field
00.5×6.4×
Odile Boute · 1×
Citations per year

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-authors

The 25 scholars most cited alongside L‐C Tsui, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with L‐C Tsui Line = papers co-authored together L‐C Tsui links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 199181
2
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.
199274
3
A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
199167
4 200265
5 200442
6
Novel cystic fibrosis mutation (2215insG) in two adolescent Taiwanese siblings.
200021
7 200219
8 200418
9 200411
10 20045
11
Molecular approaches to the cystic fibrosis gene.
19873
12 19982
13 19971
14 20060

About L‐C Tsui

L‐C Tsui is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Molecular Biology, Surgery and Genetics, having authored 14 papers that have together received 409 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (8 papers), Tracheal and airway disorders (4 papers), Connective tissue disorders research (3 papers), Neonatal Respiratory Health Research (3 papers), Congenital limb and hand anomalies (2 papers), Pancreatic function and diabetes (1 paper), Bone health and treatments (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). The work is most often cited by research in Developmental Biology (47 citations), Pulmonary and Respiratory Medicine (230 citations), Genetics (64 citations), Genetics (96 citations) and Molecular Biology (132 citations). L‐C Tsui has collaborated with scholars based in Canada, United States and Hong Kong. Frequent co-authors include Richard Rozmahel, Julian Zielenski, Muhammad Faiyaz‐Ul‐Haque, D. Markiewicz, Sayedul Haque, Wasim Ahmad, M. Siddique, Frauke Rininsland, Johanna M. Rommens and Mary Corey. Their work appears in journals such as Clinical Genetics, Human Mutation, Journal of Cystic Fibrosis, Journal of Biological Chemistry and Gastroenterology.

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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