Stephan Imreh

901 total citations
25 papers, 743 citations indexed

About

Stephan Imreh is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Stephan Imreh has authored 25 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Oncology and 7 papers in Cancer Research. Recurrent topics in Stephan Imreh's work include RNA modifications and cancer (6 papers), Cancer Genomics and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Stephan Imreh is often cited by papers focused on RNA modifications and cancer (6 papers), Cancer Genomics and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Stephan Imreh collaborates with scholars based in Sweden, United States and United Kingdom. Stephan Imreh's co-authors include George Klein, Eugene R. Zabarovsky, Jan P. Dumanski, Maria Kost‐Alimova, Anna Szeles, Irina Kholodnyuk, Hajnalka Kiss, Eric J. Stanbridge, Ying Yang and Eyal Seroussi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Virology and International Journal of Cancer.

In The Last Decade

Stephan Imreh

25 papers receiving 733 citations

Peers

Stephan Imreh
Peter Lichter Germany
Anne Fertitta United States
Caroline Braem Belgium
Deborah Nusskern United States
Rut Valgardsdottir Italy
L.L. Deaven United States
Sarah Oikemus United States
Brian Freie United States
J M Parrington United Kingdom
Sal LaForgia United States
Peter Lichter Germany
Stephan Imreh
Citations per year, relative to Stephan Imreh Stephan Imreh (= 1×) peers Peter Lichter

Countries citing papers authored by Stephan Imreh

Since Specialization
Citations

This map shows the geographic impact of Stephan Imreh'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 Stephan Imreh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephan Imreh more than expected).

Fields of papers citing papers by Stephan Imreh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephan Imreh. 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 Stephan Imreh. The network helps show where Stephan Imreh may publish in the future.

Co-authorship network of co-authors of Stephan Imreh

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Imreh. A scholar is included among the top collaborators of Stephan Imreh 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 Stephan Imreh. Stephan Imreh 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
1.
Zhou, Xiaoling, Nicholas C. Popescu, George Klein, & Stephan Imreh. (2007). The interferon-α responsive gene TMEM7 suppresses cell proliferation and is downregulated in human hepatocellular carcinoma. Cancer Genetics and Cytogenetics. 177(1). 6–15. 38 indexed citations
2.
Ståhl, Teresita Díaz de, Johanna Sandgren, Arkadiusz Piotrowski, et al.. (2007). Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array. Human Mutation. 29(3). 398–408. 35 indexed citations
3.
Imreh, Stephan, George Klein, & Eugene R. Zabarovsky. (2003). Search for unknown tumor‐antagonizing genes. Genes Chromosomes and Cancer. 38(4). 307–321. 67 indexed citations
4.
Kiss, Hajnalka, Csaba Kiss, Maria Kost‐Alimova, et al.. (2002). Comparative human/murine sequence analysis of the common eliminated region 1 from human 3p21.3. Mammalian Genome. 13(11). 646–655. 14 indexed citations
5.
Kiss, Hajnalka, Ying Yang, Csaba Kiss, et al.. (2002). The transcriptional map of the common eliminated region 1 (C3CER1) in 3p21.3. European Journal of Human Genetics. 10(1). 52–61. 37 indexed citations
6.
Kiss, Hajnalka, Darek Kedra, Csaba Kiss, et al.. (2001). The LZTFL1 Gene Is a Part of a Transcriptional Map Covering 250 kb within the Common Eliminated Region 1 (C3CER1) in 3p21.3. Genomics. 73(1). 10–19. 32 indexed citations
7.
Tapia‐Páez, Isabel, Kevin P. O'Brien, Maria Kost‐Alimova, et al.. (2000). Fine mapping of the constitutional translocation t(11;22)(q23;q11). Human Genetics. 106(5). 506–516. 18 indexed citations
8.
Yang, Ying, Hajnalka Kiss, Maria Kost‐Alimova, et al.. (1999). A 1-Mb PAC Contig Spanning the Common Eliminated Region 1 (CER1) in Microcell Hybrid-Derived SCID Tumors. Genomics. 62(2). 147–155. 25 indexed citations
9.
Seroussi, Eyal, Darek Kedra, Maria Kost‐Alimova, et al.. (1999). TOM1Genes Map to Human Chromosome 22q13.1 and Mouse Chromosome 8C1 and Encode Proteins Similar to the Endosomal Proteins HGS and STAM. Genomics. 57(3). 380–388. 17 indexed citations
10.
Telenius, Håkan, et al.. (1999). Stability of a Functional Murine Satellite DNA-based Artificial Chromosome Across Mammalian Species. Chromosome Research. 7(1). 3–7. 34 indexed citations
11.
Szeles, Anna, Ying Yang, Irina Kholodnyuk, et al.. (1997). Human/mouse microcell hybrid based elimination test reduces the putative tumor suppressor region at 3p21.3 to 1.6 cM. Genes Chromosomes and Cancer. 20(4). 329–336. 1 indexed citations
12.
Imreh, Stephan, Maria Kost‐Alimova, Irina Kholodnyuk, et al.. (1997). Differential elimination of 3p and retention of 3q segments in human/mouse microcell hybrids during tumor growth. Genes Chromosomes and Cancer. 20(3). 224–233. 26 indexed citations
13.
Kholodnyuk, Irina, В. И. Кашуба, Anna Szeles, et al.. (1997). A 3p21.3 region is preferentially eliminated from human chromosome 3/mouse microcell hybrids during tumor growth in SCID mice. Genes Chromosomes and Cancer. 18(3). 200–211. 34 indexed citations
14.
15.
Imreh, Márta P., Pedro O. de Campos‐Lima, Stephan Imreh, et al.. (1995). Mechanisms of allele‐selective down‐regulation of HLA class I in Burkitt's lymphoma. International Journal of Cancer. 62(1). 90–96. 24 indexed citations
16.
Imreh, Stephan, et al.. (1994). Nonrandom loss of human chromosome 3 fragments from mouse‐human microcell hybrids following progressive growth in SCID mice. Genes Chromosomes and Cancer. 11(4). 237–245. 43 indexed citations
17.
Kubota, Koichi, et al.. (1992). Correlation of myc expression with the growth‐arrested and transformed phenotypes in hybrids between A T lymphoma and an antigen‐responsive T‐cell line. International Journal of Cancer. 51(6). 927–934. 5 indexed citations
18.
Boldog, Ferenc, Kristina Arheden, Stephan Imreh, et al.. (1991). Involvement of 3p Deletions in Sporadic and Hereditary Forms of Renal Cell Carcinoma. Genes Chromosomes and Cancer. 3(5). 403–406. 10 indexed citations
19.
Minárovits, János, Michael Steinitz, Ferenc Boldog, et al.. (1990). Differences in C‐myc and pvt‐1 amplification in sewa sarcoma sublines selected for adherent or non‐adherent growth. International Journal of Cancer. 45(3). 514–520. 11 indexed citations
20.

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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