Felix Mitelman

41.7k total citations · 6 hit papers
611 papers, 30.0k citations indexed

About

Felix Mitelman is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Felix Mitelman has authored 611 papers receiving a total of 30.0k indexed citations (citations by other indexed papers that have themselves been cited), including 180 papers in Molecular Biology, 173 papers in Genetics and 164 papers in Hematology. Recurrent topics in Felix Mitelman's work include Genomic variations and chromosomal abnormalities (146 papers), Acute Myeloid Leukemia Research (127 papers) and Cancer Genomics and Diagnostics (98 papers). Felix Mitelman is often cited by papers focused on Genomic variations and chromosomal abnormalities (146 papers), Acute Myeloid Leukemia Research (127 papers) and Cancer Genomics and Diagnostics (98 papers). Felix Mitelman collaborates with scholars based in Sweden, Denmark and Switzerland. Felix Mitelman's co-authors include Fredrik Mertens, Bertil Johansson, Nils Mandahl, Sverre Heim, Mattias Höglund, Helena Willén, Anders Rydholm, Thoas Fioretos, L. Brandt and Sverre Heim and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Felix Mitelman

603 papers receiving 29.1k citations

Hit Papers

ISCN 1995 An international system for human cytogenetic n... 1985 2026 1998 2012 1995 1985 2007 1996 1997 500 1000 1.5k

Peers

Felix Mitelman
Comparison fields: 5 of 166
  • Molecular Biology 11.8k
  • Hematology 7.3k
  • Cancer Research 6.7k
  • Pulmonary and Respiratory Medicine 6.6k
  • Genetics 6.2k
Replace Michelle M. Le Beau with:
Michelle M. Le Beau United States
Janet D. Rowley United States
L. Jeffrey Medeiros United States
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James D. Griffin United States
Clara D. Bloomfield United States
Anthony D. Ho Germany
Brunangelo Falini Italy
William G. Stetler‐Stevenson United States
Connie J. Eaves Canada
Michelle M. Le Beau United States View profile →
Citations per field, relative to Felix Mitelman
Felix Mitelman · 1×
Citations per year, relative to Felix Mitelman
Felix Mitelman · 1×

Countries citing papers authored by Felix Mitelman

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Felix Mitelman

This figure shows the co-authorship network connecting the top 25 collaborators of Felix Mitelman. A scholar is included among the top collaborators of Felix Mitelman 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 Felix Mitelman. Felix Mitelman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
# Work Indexed citations
1 0
2 3
3 47
4 10
5 191
6 41
7 78
8 52
9 46
10
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.
59
11 28
12 7
13 38
14 33
15
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
282
16
Cytogenetic analysis of 33 basal cell carcinomas.
32
17 64
18 53
19 51
20 9

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.

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