J. Stamberg
- Genetics
- Molecular Biology
- Plant Science
- Pediatrics, Perinatology and Child Health
- Public Health, Environmental and Occupational Health
- Co-authors
- Emilie H. MulesY. KoltinPaul A. LemkeStefán HreiðarssonS PanL T HuHarry OstrerJohn M. Opitz
- Topics
- Genomic variations and chromosomal abnormalities (7 papers)Chromosomal and Genetic Variations (6 papers)Prenatal Screening and Diagnostics (5 papers)
- Partner nations
- United StatesDenmark
In The Last Decade
J. Stamberg
16 papers receiving 302 citations
Peers
Comparison fields: 5 of 68
- Genetics 158
- Molecular Biology 151
- Plant Science 78
- Pediatrics, Perinatology and Child Health 65
- Public Health, Environmental and Occupational Health 49
Countries citing papers authored by J. Stamberg
This map shows the geographic impact of J. Stamberg'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 J. Stamberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Stamberg more than expected).
Fields of papers citing papers by J. Stamberg
This network shows the impact of papers produced by J. Stamberg. 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 J. Stamberg. The network helps show where J. Stamberg may publish in the future.
Co-authorship network of co-authors of J. Stamberg
This figure shows the co-authorship network connecting the top 25 collaborators of J. Stamberg. A scholar is included among the top collaborators of J. Stamberg 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 J. Stamberg. J. Stamberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | 10 | |
| 3 | 29 | |
| 4 | 19 | |
| 5 | 1 | |
| 6 | 0 | |
| 7 | 15 | |
| 8 | The NAD(P)H:quinone oxidoreductase locus in human colon carcinoma HCT 116 cells resistant to mitomycin C. | 30 |
| 9 | 4 | |
| 10 | 19 | |
| 11 | 32 | |
| 12 | 49 | |
| 13 | 15 | |
| 14 | 28 | |
| 15 | The marker Xq28 syndrome ("Fragile-X SYndrome") in a retarded man with mitral valve prolapse. | 12 |
| 16 | 17 | |
| 17 | 44 |
About J. Stamberg
J. Stamberg is a scholar working on Genetics, Toxicology and Pediatrics, Perinatology and Child Health, having authored 17 papers that have together received 329 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Genetics (158 citations), Toxicology (19 citations) and Pediatrics, Perinatology and Child Health (65 citations). J. Stamberg has collaborated with scholars based in United States and Denmark. Frequent co-authors include Emilie H. Mules, Y. Koltin, Paul A. Lemke, Stefán Hreiðarsson, S Pan, L T Hu, Harry Ostrer, John M. Opitz, Lewis Waber and Jeffrey Strovel. Their work appears in journals such as Gene, British Journal of Haematology and Journal of Medical 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.