Robert C. Lin
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Gastroenterology top 2%
- Gastrointestinal motility and disorders
Papers in
-
- Congenital heart defects research 4
- Bioactive natural compounds 3
-
- Neurotransmitter Receptor Influence on Behavior 3
- Neuroscience and Neural Engineering 1
- Co-authors
- Edith Bülbring (2 shared papers)Christine E. Seidman (4 shared papers)Craig T. Basson (2 shared papers)David R. Bachinsky (2 shared papers)Thomas A. Traill (1 shared paper)David M. Grayzel (1 shared paper)Janine LeBlanc-Straceski (1 shared paper)Tatjana Levi (1 shared paper)
- Journals
- Nature Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)The American Journal of Human Genetics (1 paper)Transfusion (1 paper)Science (1 paper)
- Partner nations
- United StatesSingaporeSwitzerland
In The Last Decade
Robert C. Lin
16 papers receiving 2.4k citations
Hit Papers
Peers
Comparison fields: 5 of 114
- Developmental Biology 109
- Gastroenterology 250
- Molecular Biology 1.6k
- Genetics 598
- Cellular and Molecular Neuroscience 261
Countries citing papers authored by Robert C. Lin
This map shows the geographic impact of Robert C. Lin'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 Robert C. Lin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert C. Lin more than expected).
Fields of papers citing papers by Robert C. Lin
This network shows the impact of papers produced by Robert C. Lin. 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 Robert C. Lin. The network helps show where Robert C. Lin may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert C. Lin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome Hit paper breakdown → | 1997 | 787 |
| 2 | 1997 | 421 | |
| 3 | The effect of intraluminal application of 5‐hydroxytryptamine and 5‐hydroxytryptophan on peristalsis; the local production of 5‐HT and its release in relation to intraluminal pressure and propulsive activity Hit paper breakdown → | 1958 | 350 |
| 4 | 1999 | 250 | |
| 5 | 1999 | 146 | |
| 6 | 1958 | 124 | |
| 7 | 1994 | 108 | |
| 8 | 1969 | 67 | |
| 9 | 1993 | 65 | |
| 10 | 1969 | 47 | |
| 11 | 1969 | 37 | |
| 12 | 1988 | 35 | |
| 13 | 1996 | 19 | |
| 14 | 1955 | 7 | |
| 15 | 1957 | 6 | |
| 16 | 1952 | 2 |
About Robert C. Lin
Robert C. Lin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Genetics and Plant Science, having authored 16 papers that have together received 2.5k indexed citations. Recurring topics across this work include Congenital heart defects research (4 papers), Neurotransmitter Receptor Influence on Behavior (3 papers), Bioactive natural compounds (3 papers), Psychedelics and Drug Studies (1 paper), Plant Molecular Biology Research (1 paper), Neural dynamics and brain function (1 paper), Neuroscience and Neural Engineering (1 paper) and GABA and Rice Research (1 paper). The work is most often cited by research in Developmental Biology (109 citations), Gastroenterology (250 citations), Molecular Biology (1.6k citations), Genetics (598 citations) and Cellular and Molecular Neuroscience (261 citations). Robert C. Lin has collaborated with scholars based in United States, Singapore and Switzerland. Frequent co-authors include Edith Bülbring, Christine E. Seidman, Craig T. Basson, David R. Bachinsky, Thomas A. Traill, David M. Grayzel, Janine LeBlanc-Straceski, Tatjana Levi, Raju Kucherlapati and Beatrice Renault. Their work appears in journals such as Nature Genetics, Proceedings of the National Academy of Sciences, The American Journal of Human Genetics, Transfusion and Science.
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.