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

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

ISCN 1995 An international system for human cytogenetic nomenclature

1995 1.5k citations Felix Mitelman profile →
Catalog of chromosome aberrations in cancer

1985 1.3k citations Felix Mitelman profile →
The impact of translocations and gene fusions on cancer causation

2007 998 citations Felix Mitelman, Bertil Johansson et al. profile →
The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

1996 603 citations Felix Mitelman et al. profile →
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

1997 558 citations Felix Mitelman, Fredrik Mertens et al. profile →
The emerging complexity of gene fusions in cancer

2015 464 citations Fredrik Mertens, Bertil Johansson et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Felix Mitelman	11.8k	7.3k	6.7k	6.6k	6.2k	611	30.0k
Michelle M. Le Beau	16.9k 1.4×	15.6k 2.1×	3.5k 0.5×	1.8k 0.3×	3.5k 0.6×	347	35.2k
Janet D. Rowley	13.1k 1.1×	13.8k 1.9×	3.1k 0.5×	1.1k 0.2×	3.3k 0.5×	298	25.8k
L. Jeffrey Medeiros	9.2k 0.8×	7.7k 1.1×	5.2k 0.8×	5.0k 0.8×	1.2k 0.2×	1.3k	40.1k
Jon C. Aster	20.4k 1.7×	5.2k 0.7×	3.8k 0.6×	2.2k 0.3×	1.4k 0.2×	278	32.0k
James D. Griffin	12.8k 1.1×	12.4k 1.7×	1.9k 0.3×	1.9k 0.3×	1.5k 0.2×	354	29.7k
Clara D. Bloomfield	17.7k 1.5×	28.5k 3.9×	5.3k 0.8×	1.9k 0.3×	1.9k 0.3×	406	42.9k
Anthony D. Ho	9.6k 0.8×	7.6k 1.0×	1.8k 0.3×	2.3k 0.3×	1.5k 0.2×	687	27.5k
Brunangelo Falini	9.3k 0.8×	7.3k 1.0×	2.1k 0.3×	2.7k 0.4×	1.1k 0.2×	390	32.9k
William G. Stetler‐Stevenson	14.4k 1.2×	5.2k 0.7×	19.1k 2.9×	2.7k 0.4×	1.9k 0.3×	282	35.7k
Connie J. Eaves	14.1k 1.2×	11.5k 1.6×	3.8k 0.6×	1.9k 0.3×	3.4k 0.6×	395	29.2k

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

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20 of 20 papers shown

Mertens, Fredrik, Jakob Hofvander, Nils Mandahl, & Felix Mitelman. (2024). Aneuploidy in neoplasia: Single‐cell data on 83,862 tumors. International Journal of Cancer. 156(1). 34–39.

Mandahl, Nils, Fredrik Mertens, & Felix Mitelman. (2023). Gene amplification in neoplasia: A cytogenetic survey of 80 131 cases. Genes Chromosomes and Cancer. 63(1). e23214–e23214. 3 indexed citations

Bruford, Elspeth A., Cristina R. Antonescu, Andrew J. Carroll, et al.. (2021). HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia. 35(11). 3040–3043. 47 indexed citations

Persson, Helena, Rolf Søkilde, Jari Häkkinen, et al.. (2020). Analysis of fusion transcripts indicates widespread deregulation of snoRNAs and their host genes in breast cancer. International Journal of Cancer. 146(12). 3343–3353. 10 indexed citations

Lilljebjörn, Henrik, Rasmus Henningsson, Axel Hyrenius‐Wittsten, et al.. (2016). Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia. Nature Communications. 7(1). 11790–11790. 191 indexed citations

Heim, Sverre & Felix Mitelman. (2015). Cancer cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Lund University Publications (Lund University). 41 indexed citations

Mitelman, Felix, et al.. (2009). Prophase analysis of ring chromosome 13-an attempt at phenotypekaryotype correlation. Hereditas. 93(2). 231–233. 1 indexed citations

Andersson, Anna, Tor Olofsson, David Lindgren, et al.. (2005). Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations. Proceedings of the National Academy of Sciences. 102(52). 19069–19074. 78 indexed citations

Wever, Ivo De, Paola Dal Cin, Christopher D.�M. Fletcher, et al.. (2000). Cytogenetic, Clinical, and Morphologic Correlations in 78 Cases of Fibromatosis: A Report from the CHAMP Study Group. Modern Pathology. 13(10). 1080–1085. 56 indexed citations

10.

Jin, Yuesheng, Fredrik Mertens, Bertil Persson, et al.. (1998). Nonrandom Numerical Chromosome Abnormalities in Basal Cell Carcinomas. Cancer Genetics and Cytogenetics. 103(1). 35–42. 15 indexed citations

11.

Sciot, Raf, Måns Åkerman, Paola Dal Cin, et al.. (1997). Cytogenetic Analysis of Subcutaneous Angiolipoma: Further Evidence Supporting Its Difference from Ordinary Pure Lipomas. The American Journal of Surgical Pathology. 21(4). 441–444. 46 indexed citations

12.

Jin, Y., Bertil Persson, Hans Petter Gullestad, et al.. (1997). The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinomas.. PubMed. 57(3). 404–6. 19 indexed citations

13.

Panagopoulos, Ioannis, Nikos Pandis, Carl Petersson, et al.. (1996). The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.. PubMed. 56(21). 4871–5. 59 indexed citations

14.

Mertens, Fredrik, Helena Willén, Anders Rydholm, et al.. (1995). Trisomy 20 is a primary chromosome aberration in desmoid tumors. International Journal of Cancer. 63(4). 527–529. 21 indexed citations

15.

Jin, Y., Fredrik Mertens, Janusz Limon, et al.. (1994). Characteristic karyotypic features in lacrimal and salivary gland carcinomas. British Journal of Cancer. 70(1). 42–47. 38 indexed citations

16.

Mitelman, Felix. (1992). 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. KARGER eBooks. 282 indexed citations

17.

Mertens, Fredrik, Stephanie Heim, Nils Mandahl, et al.. (1991). Cytogenetic analysis of 33 basal cell carcinomas.. PubMed. 51(3). 954–7. 32 indexed citations

18.

Nilbert, Mef, Sverre Heim, Nils Mandahl, et al.. (1988). Karyotypic rearrangements in 20 uterine leiomyomas. Cytogenetic and Genome Research. 49(4). 300–304. 53 indexed citations

19.

Borgström, Georg, Lasse Teerenhovi, P Vuopio, et al.. (1980). Clinical implications of monosomy 7 in acute nonlymphocytic leukemia. Cancer Genetics and Cytogenetics. 2(2). 115–126. 51 indexed citations

20.

Gustavii, Björn, et al.. (1980). Prenatal chromosomal analysis of fetal blood obtained at fetoscopy.. BMJ. 280(6222). 1107.1–1107. 9 indexed citations

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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