Felix Mitelman
Impact in
- Hematology top 0.05%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics
Papers in
-
- Genomics and Chromatin Dynamics 48
- Genetics 172
- Genomic variations and chromosomal abnormalities 146
- Chronic Lymphocytic Leukemia Research 58
- Co-authors
- Fredrik Mertens (128 shared papers)Bertil Johansson (107 shared papers)Nils Mandahl (216 shared papers)Sverre Heim (172 shared papers)Mattias Höglund (70 shared papers)Helena Willén (74 shared papers)Anders Rydholm (70 shared papers)Thoas Fioretos (42 shared papers)
- Journals
- Genes Chromosomes and Cancer (98 papers)Hereditas (55 papers)International Journal of Cancer (31 papers)Cancer Genetics and Cytogenetics (142 papers)European Journal Of Haematology (14 papers)
- Partner nations
- SwedenDenmarkSwitzerland
In The Last Decade
Felix Mitelman
599 papers receiving 28.1k citations
Felix Mitelman's Hit Papers
Peers
Comparison fields: 5 of 165
- Hematology 6.9k
- Cancer Research 6.0k
- Genetics 3.4k
- Pathology and Forensic Medicine 4.9k
- Rheumatology 3.2k
Countries citing papers authored by Felix Mitelman
This map shows the geographic impact of Felix Mitelman'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 Felix Mitelman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Felix Mitelman more than expected).
Fields of papers citing papers by Felix Mitelman
This network shows the impact of papers produced by Felix Mitelman. 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 Felix Mitelman. The network helps show where Felix Mitelman may publish in the future.
Co-authors
The 25 scholars most cited alongside Felix Mitelman, 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 612 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ISCN 1995 An international system for human cytogenetic nomenclature Hit paper breakdown → | 1995 | 1547 |
| 2 | Catalog of chromosome aberrations in cancer Hit paper breakdown → | 1985 | 1314 |
| 3 | The impact of translocations and gene fusions on cancer causation Hit paper breakdown → | 2007 | 1004 |
| 4 | The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein Hit paper breakdown → | 1996 | 608 |
| 5 | A breakpoint map of recurrent chromosomal rearrangements in human neoplasia Hit paper breakdown → | 1997 | 557 |
| 6 | The emerging complexity of gene fusions in cancer Hit paper breakdown → | 2015 | 468 |
| 7 | Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage. | 1994 | 419 |
| 8 | Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. | 1997 | 377 |
| 9 | 2001 | 329 | |
| 10 | 2000 | 326 | |
| 11 | 2002 | 316 | |
| 12 | ISCN 1991 : guidelines for cancer cytogenetics : supplement to An international system for human cytogenetic nomenclature : recommendations of the Standing Committee on Human Cytogenetic Nomenclature, Subcommittee on Cancer Cytogenetics | 1992 | 282 |
| 13 | Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. | 1996 | 270 |
| 14 | 2004 | 268 | |
| 15 | 2000 | 246 | |
| 16 | 1992 | 238 | |
| 17 | Fusion of the EWS and CHOP genes in myxoid liposarcoma. | 1996 | 225 |
| 18 | 1981 | 209 | |
| 19 | 1988 | 208 | |
| 20 | 1978 | 196 |
About Felix Mitelman
Felix Mitelman is a scholar working on Molecular Biology, Genetics, Hematology, Cancer Research and Pathology and Forensic Medicine, having authored 612 papers that have together received 29.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (146 papers), Acute Myeloid Leukemia Research (126 papers), Cancer Genomics and Diagnostics (97 papers), Sarcoma Diagnosis and Treatment (95 papers), Acute Lymphoblastic Leukemia research (75 papers), Chronic Myeloid Leukemia Treatments (71 papers), Chronic Lymphocytic Leukemia Research (58 papers) and Genomics and Chromatin Dynamics (48 papers). The work is most often cited by research in Hematology (6.9k citations), Cancer Research (6.0k citations), Genetics (3.4k citations), Pathology and Forensic Medicine (4.9k citations) and Rheumatology (3.2k citations). Felix Mitelman has collaborated with scholars based in Sweden, Denmark and Switzerland. Frequent co-authors include Fredrik Mertens, Bertil Johansson, Nils Mandahl, Sverre Heim, Mattias Höglund, Helena Willén, Anders Rydholm, Thoas Fioretos, L. Brandt and Sverre Heim. Their work appears in journals such as Genes Chromosomes and Cancer, Hereditas, International Journal of Cancer, Cancer Genetics and Cytogenetics and European Journal Of Haematology.
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.