Bruce D. Gelb
Impact in
- Immunology top 0.5%
- Galectins and Cancer Biology
- Molecular Biology top 0.2%
- Protein Tyrosine Phosphatases
- Congenital heart defects research
- RNA modifications and cancer
- Bone Metabolism and Diseases
Papers in
-
- Protein Tyrosine Phosphatases 53
- Congenital heart defects research 46
- RNA modifications and cancer 30
- Immunology 40
- Galectins and Cancer Biology 36
- Co-authors
- Marco TartagliaRobert J. DesnickAmy E. RobertsGuo‐Ping ShiHarold A. ChapmanGiuseppe ZampinoMary Ella PierpontJudith Allanson
- Journals
- The American Journal of Human Genetics (14 papers)Circulation (8 papers)Human Molecular Genetics (6 papers)Current Opinion in Cardiology (6 papers)Nature Genetics (6 papers)
- Partner nations
- United StatesItalyUnited Kingdom
In The Last Decade
Bruce D. Gelb
209 papers receiving 14.3k citations
Hit Papers
Peers
Comparison fields: 5 of 166
- Immunology 3.7k
- Molecular Biology 10.2k
- Oncology 2.5k
- Cardiology and Cardiovascular Medicine 1.9k
- Genetics 2.0k
Countries citing papers authored by Bruce D. Gelb
This map shows the geographic impact of Bruce D. Gelb'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 Bruce D. Gelb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruce D. Gelb more than expected).
Fields of papers citing papers by Bruce D. Gelb
This network shows the impact of papers produced by Bruce D. Gelb. 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 Bruce D. Gelb. The network helps show where Bruce D. Gelb may publish in the future.
Co-authors
The 25 scholars most cited alongside Bruce D. Gelb, 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 | 2025 | 1 | |
| 2 | 2025 | 2 | |
| 3 | 2024 | 3 | |
| 4 | 2024 | 2 | |
| 5 | 2023 | 6 | |
| 6 | 2023 | 2 | |
| 7 | 2023 | 9 | |
| 8 | 2023 | 8 | |
| 9 | 2022 | 7 | |
| 10 | 2022 | 9 | |
| 11 | 2021 | 12 | |
| 12 | 2019 | 29 | |
| 13 | 2019 | 49 | |
| 14 | Abstract 18206: Fatal Myocarditis is Associated With Rare Cardiomyopathy Gene Variants | 2017 | 1 |
| 15 | 2017 | 22 | |
| 16 | 2010 | 64 | |
| 17 | 2003 | 70 | |
| 18 | Mutation of a tubulin folding gene, TCFE, causes the autosomal recessive Kenny-Caffey syndrome | 2002 | 1 |
| 19 | 2001 | 74 | |
| 20 | 1995 | 5 |
About Bruce D. Gelb
Bruce D. Gelb is a scholar working on Molecular Biology, Immunology, Genetics, Cancer Research and Health Informatics, having authored 210 papers that have together received 14.6k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (53 papers), Congenital heart defects research (46 papers), Galectins and Cancer Biology (36 papers), Congenital Heart Disease Studies (32 papers), RNA modifications and cancer (30 papers), Genomics and Rare Diseases (22 papers), Genomic variations and chromosomal abnormalities (17 papers) and Cardiomyopathy and Myosin Studies (16 papers). The work is most often cited by research in Immunology (3.7k citations), Molecular Biology (10.2k citations), Oncology (2.5k citations), Cardiology and Cardiovascular Medicine (1.9k citations) and Genetics (2.0k citations). Bruce D. Gelb has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include Marco Tartaglia, Robert J. Desnick, Amy E. Roberts, Guo‐Ping Shi, Harold A. Chapman, Giuseppe Zampino, Mary Ella Pierpont, Judith Allanson, Kamini Kalidas and Steve Jeffery. Their work appears in journals such as The American Journal of Human Genetics, Circulation, Human Molecular Genetics, Current Opinion in Cardiology and Nature Genetics.
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.