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 54
- Congenital heart defects research 43
- RNA modifications and cancer 29
- Bone Metabolism and Diseases 14
- Genetics 52
- Genomics and Rare Diseases 22
- Co-authors
- Marco Tartaglia (37 shared papers)Robert J. Desnick (17 shared papers)Amy E. Roberts (10 shared papers)Guo‐Ping Shi (5 shared papers)Harold A. Chapman (2 shared papers)Giuseppe Zampino (7 shared papers)Mary Ella Pierpont (6 shared papers)Judith Allanson (2 shared papers)
- Journals
- The American Journal of Human Genetics (14 papers)Circulation (8 papers)Nature Genetics (7 papers)Current Opinion in Cardiology (6 papers)Human Mutation (6 papers)
- Partner nations
- United StatesItalyUnited Kingdom
In The Last Decade
Bruce D. Gelb
215 papers receiving 15.3k citations
Bruce D. Gelb's Hit Papers
Peers
Comparison fields: 5 of 165
- Immunology 3.2k
- Molecular Biology 10.4k
- Oncology 2.3k
- Cardiology and Cardiovascular Medicine 1.8k
- Genetics 2.1k
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
Showing the 20 most-cited of 223 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Hit paper breakdown → | 2001 | 1277 |
| 2 | Pycnodysostosis, a Lysosomal Disease Caused by Cathepsin K Deficiency Hit paper breakdown → | 1996 | 847 |
| 3 | Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia Hit paper breakdown → | 2003 | 766 |
| 4 | Genetic Basis for Congenital Heart Defects: Current Knowledge Hit paper breakdown → | 2007 | 625 |
| 5 | PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity Hit paper breakdown → | 2002 | 576 |
| 6 | Noonan syndrome Hit paper breakdown → | 2013 | 541 |
| 7 | 2010 | 438 | |
| 8 | 1993 | 413 | |
| 9 | Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association Hit paper breakdown → | 2018 | 397 |
| 10 | Enabling Technologies for Personalized and Precision Medicine Hit paper breakdown → | 2020 | 329 |
| 11 | 1994 | 321 | |
| 12 | 2006 | 304 | |
| 13 | 2011 | 283 | |
| 14 | 2005 | 268 | |
| 15 | 2000 | 226 | |
| 16 | 2000 | 210 | |
| 17 | 2002 | 209 | |
| 18 | 2018 | 181 | |
| 19 | 1999 | 180 | |
| 20 | 2006 | 178 |
About Bruce D. Gelb
Bruce D. Gelb is a scholar working on Molecular Biology, Genetics, Immunology, Epidemiology and Cardiology and Cardiovascular Medicine, having authored 223 papers that have together received 16.0k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (54 papers), Congenital heart defects research (43 papers), Galectins and Cancer Biology (38 papers), RNA modifications and cancer (29 papers), Congenital Heart Disease Studies (29 papers), Genomics and Rare Diseases (22 papers), Bone Metabolism and Diseases (14 papers) and Peptidase Inhibition and Analysis (13 papers). The work is most often cited by research in Immunology (3.2k citations), Molecular Biology (10.4k citations), Oncology (2.3k citations), Cardiology and Cardiovascular Medicine (1.8k citations) and Genetics (2.1k 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, Andrew H. Crosby and Michael A. Patton. Their work appears in journals such as The American Journal of Human Genetics, Circulation, Nature Genetics, Current Opinion in Cardiology and Human Mutation.
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.