Stefan Joos
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Chronic Lymphocytic Leukemia Research
- Glioma Diagnosis and Treatment
- Pathology and Forensic Medicine top 0.5%
- Lymphoma Diagnosis and Treatment
Papers in
-
- Genomics and Chromatin Dynamics 14
-
- Lymphoma Diagnosis and Treatment 18
- Tumors and Oncological Cases 10
- Co-authors
- Peter Lichter (57 shared papers)Martin Bentz (20 shared papers)Martin Zörnig (3 shared papers)Stanislas du Manoir (9 shared papers)Vladimir Kirkin (1 shared paper)Peter Mӧller (6 shared papers)Christof Hofele (14 shared papers)Thomas Cremer (3 shared papers)
- Journals
- Genes Chromosomes and Cancer (12 papers)Blood (8 papers)International Journal of Cancer (5 papers)Journal of Clinical Oncology (3 papers)Seminars in Hematology (2 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Stefan Joos
92 papers receiving 6.2k citations
Peers
Comparison fields: 5 of 126
- Genetics 1.2k
- Pathology and Forensic Medicine 1.6k
- Cancer Research 1.2k
- Oncology 1.5k
- Genetics 1.4k
Countries citing papers authored by Stefan Joos
This map shows the geographic impact of Stefan Joos'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 Stefan Joos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefan Joos more than expected).
Fields of papers citing papers by Stefan Joos
This network shows the impact of papers produced by Stefan Joos. 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 Stefan Joos. The network helps show where Stefan Joos may publish in the future.
Co-authors
The 25 scholars most cited alongside Stefan Joos, 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 94 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 463 | |
| 2 | 1993 | 448 | |
| 3 | 1995 | 266 | |
| 4 | 1996 | 254 | |
| 5 | Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30+ Hodgkin cells. | 2000 | 212 |
| 6 | 2009 | 199 | |
| 7 | 2005 | 181 | |
| 8 | 2002 | 173 | |
| 9 | 2003 | 168 | |
| 10 | Tissue microarray analysis reveals site-specific prevalence of oncogene amplifications in head and neck squamous cell carcinoma. | 2003 | 164 |
| 11 | 2006 | 132 | |
| 12 | 2003 | 130 | |
| 13 | Microarray-based copy number and expression profiling in dedifferentiated and pleomorphic liposarcoma. | 2002 | 129 |
| 14 | 1998 | 125 | |
| 15 | 2004 | 122 | |
| 16 | 1995 | 118 | |
| 17 | 2002 | 115 | |
| 18 | 1998 | 112 | |
| 19 | 1993 | 108 | |
| 20 | 1996 | 106 |
About Stefan Joos
Stefan Joos is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Genetics, Genetics and Oncology, having authored 94 papers that have together received 6.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Lymphoma Diagnosis and Treatment (18 papers), Chronic Lymphocytic Leukemia Research (15 papers), Genomics and Chromatin Dynamics (14 papers), Sarcoma Diagnosis and Treatment (10 papers), Tumors and Oncological Cases (10 papers), Chromosomal and Genetic Variations (8 papers) and Gastrointestinal Tumor Research and Treatment (6 papers). The work is most often cited by research in Genetics (1.2k citations), Pathology and Forensic Medicine (1.6k citations), Cancer Research (1.2k citations), Oncology (1.5k citations) and Genetics (1.4k citations). Stefan Joos has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Peter Lichter, Martin Bentz, Martin Zörnig, Stanislas du Manoir, Vladimir Kirkin, Peter Mӧller, Christof Hofele, Thomas Cremer, Michael R. Speicher and Kolja Freier. Their work appears in journals such as Genes Chromosomes and Cancer, Blood, International Journal of Cancer, Journal of Clinical Oncology and Seminars in Hematology.
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.