Anna Szeles

1.8k citations

33 papers · 1.5k indexed · h-index 21

Impact in

Cancer Research top 5%
- MicroRNA in disease regulation
- Cancer Genomics and Diagnostics
Molecular Biology top 10%
- Extracellular vesicles in disease
- RNA Interference and Gene Delivery
- CRISPR and Genetic Engineering

Papers in

Pathology and Forensic Medicine 9
- Genetic factors in colorectal cancer 5
Cancer Research 7
- Cancer Genomics and Diagnostics 6

Co-authors: Lars Holmgren Anna‐Lena Spetz Anna Bergsmedh Marie Arsenian‐Henriksson M. Judah Folkman Anders Bratt Kerstin I. Falk Judah Folkman
Journals: Chromosome Research (4 papers)Genes Chromosomes and Cancer (4 papers)Proceedings of the National Academy of Sciences (3 papers)Blood (2 papers)Stem Cells and Development (2 papers)
Partner nations: Sweden United States Hungary

In The Last Decade

Anna Szeles

33 papers receiving 1.5k citations

Peers

Countries citing papers authored by Anna Szeles

Since Specialization

Citations

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

Fields of papers citing papers by Anna Szeles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Anna Szeles, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Szeles Line = papers co-authored together Anna Szeles links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Epstein–Barr virus promotes genomic instability in Burkitt's lymphoma Oncogene ·Siamak A. Kamranvar, Antal A. Sarkady, Anna Szeles, Maria G. Masucci	2007	79
2	Rad51-related changes in global gene expression Biochemical and Biophysical Research Communications ·Lukas M. Orre, Susann Fält, Anna Szeles, Rolf Lewensohn, Anders Wennborg, Jenny Flygare	2006	7
3	Evaluation of spectral karyotyping (SKY) in biodosimetry for the triage situation following gamma irradiation International Journal of Radiation Biology ·Anna Szeles, Embaixada Arquitectura, Rolf Lewensohn, Svetlana Bajalica‐Lagercrantz, Catharina Larsson	2006	10
4	Culture and Expansion of the Human Embryonic Stem Cell Line HS181, Evaluated in a Double-Color System Stem Cells and Development ·Márta P. Imreh, Susanne Wolbank, Christian Unger, Karin Gertow, Alar Aints, Anna Szeles, Stefan Imreh, Outi Hovatta, Gabriel Fried, Huili, Lars Ährlund‐Richter	2004	22
5	Mouse euchromatin specific “genome-painting” with a LINE probe: A rapid method for identification and mapping of human chromosomes in mouse-human microcell hybrids by two-color FISH Hereditas ·Róbert L. Katona, Anna Szeles, Gyula Hadlaczky	2004	1
6	Consistent downregulation of human lactoferrin gene, in the common eliminated region 1 on 3p21.3, following tumor growth in severe combined immunodeficient (SCID) mice Cancer Letters ·Ying Yang, Jingfeng Li, Anna Szeles, Márta P. Imreh, Maria Kost‐Alimova, Hajnalka Kiss, Irina Kholodnyuk, Park A. Wiseman, A. Zhebrowsky, George Klein, Stefan Imreh	2003	16
7	Inactivation of the human fragile histidine triad gene at 3p14.2 in monochromosomal human/mouse microcell hybrid-derived severe combined immunodeficient mouse tumors. PubMed ·Josephine Peyton Marsh, Anna Szeles, Ying Yang, George Klein, Stefan Imreh	2000	12
8	A 1-Mb PAC Contig Spanning the Common Eliminated Region 1 (CER1) in Microcell Hybrid-Derived SCID Tumors Genomics ·Ying Yang, Hajnalka Kiss, Maria Kost‐Alimova, Darek Kedra, Ingegerd Fransson, Eyal Seroussi, Jingfeng Li, Anna Szeles, Irina Kholodnyuk, Márta P. Imreh, Katalin Fodor, Gyula Hadlaczky, George Klein, Jan P. Dumanski, Stephan Imreh	1999	25
9	Horizontal Transfer of DNA by the Uptake of Apoptotic Bodies Blood ·Lars Holmgren, Anna Szeles, Éva Rajnavölgyi, Judah Folkman, Georg Klein, Ingemar Ernberg, Kerstin I. Falk	1999	63
10	Restricted expression of Epstein-Barr virus (EBV)-encoded, growth transformation-associated antigens in an EBV- and human herpesvirus type 8-carrying body cavity lymphoma line. Journal of General Virology ·László Székely, Gunnar O. Klein, Norihiro Teramoto, Rakshan P, Sweta Priyadarshni, Chen Fu, Anna Szeles, 竹司岡本, Katja Pokrovskaja Tamm, Barbro Ehlin‐Henriksson	1998	76
11	B-CLL cells with unusual properties International Journal of Cancer ·Javier Avila‐Cariño, Nongnit Lewin, Yoshihiko Tomita, Anna Szeles, З.Р. Ахметшина, Szilvia Mosolits, Håkan Mellstedt, George Klein, Eva Klein	1997	19
12	Assignment of the ARHA and GPX1 genes to human chromosome bands 3p21.3 by in situ hybridization and with somatic cell hybrids Cytogenetic and Genome Research ·Csaba Kiss, J. Li, Anna Szeles, Rinat Gizatullin, В. И. Кашуба, Tamara Lushnikova, Alexei Protopopov, Hữu Phước Lê, Hajnalka Kiss, Josephine Peyton Marsh, Stefan Imreh, George Klein, Eugene R. Zabarovsky	1997	33
13	Human/mouse microcell hybrid based elimination test reduces the putative tumor suppressor region at 3p21.3 to 1.6 cM Genes Chromosomes and Cancer ·Anna Szeles, Ying Yang, З.Р. Ахметшина, Irina Kholodnyuk, Hajnalka Kiss, Maria Kost‐Alimova, Eugene R. Zabarovsky, Eric J. Stanbridge, George Klein, Stephan Imreh	1997	1
14	Differential elimination of 3p and retention of 3q segments in human/mouse microcell hybrids during tumor growth Genes Chromosomes and Cancer ·Stephan Imreh, Maria Kost‐Alimova, Irina Kholodnyuk, Ying Yang, Anna Szeles, Hajnalka Kiss, Yie Liu, Karen Polinger Foster, Eugene R. Zabarovsky, Eric J. Stanbridge, George Klein	1997	26
15	A 3p21.3 region is preferentially eliminated from human chromosome 3/mouse microcell hybrids during tumor growth in SCID mice Genes Chromosomes and Cancer ·Irina Kholodnyuk, Morton H. Jones, В. И. Кашуба, Zixuan Teng, Anna Szeles, Eric J. Stanbridge, Eugene R. Zabarovsky, George Klein, Stephan Imreh	1997	34
16	Evidence for a megareplicon covering megabases of centromeric chromosome segments Chromosome Research ·Kristoffel Castelein, Mariana Di Domenico, Steve Diller, Imre Cserpán, Katalin Fodor, Róbert L. Katona, J. R. Haddow, Károly Fátyol, Anna Szeles, Aladar A. Szalay, Gy. Hadlaczky	1996	27
17	Mapping of a new MAP kinase activated protein kinase gene (3PK) to human chromosome band 3p21.2 and ordering of 3PK and two cosmid markers in the 3p22–p21 tumour-suppressor region by two-colour fluorescencein situ hybridization Chromosome Research ·Anna Szeles, Svetlana Bajalica‐Lagercrantz, Annika Lindblom, Tamara Lushnikova, В. И. Кашуба, Stephan Imreh, Magnus Nordenskjöld, Cécile Michel, Tatsuya Fujinaka	1996	11
18	De novo chromosome formations by large-scale amplification of the centromeric region of mouse chromosomes Chromosome Research ·Mariana Di Domenico, Steve Diller, Imre Cserpán, Katalin Fodor, Róbert L. Katona, J. R. Haddow, Károly Fátyol, Kristoffel Castelein, Anna Szeles, Andrew R. S. Ross, A. T. Sumner, Aladar A. Szalay, Gy. Hadlaczky	1996	43
19	A group of notI jumping and linking clones cover 2.5 Mb in the 3p21–p22 region suspected to contain a tumor suppressor gene Cancer Genetics and Cytogenetics ·В. И. Кашуба, Anna Szeles, Anjali Jindia, Ann-Sofie Nilsson, Ulf S.R. Bergerheim, William S. Modi, Klaus Aringer, Michael Dean, Eric J. Stanbridge, Gösta Winberg, George Klein, Eugene R. Zabarovsky	1995	25
20	Hypersomy of chromosome 15 with retrovirally rearranged c-myc, loss of germline c-myc and IgK/c-myc juxtaposition in a macrophage-monocytic tumour line European Journal of Cancer ·Stefan Imreh, Kshyanaprava Mohanty, Chinmay Kumar Panda, Magda Babonits, Håkan Axelson, M. T. Silva, Anna Szeles, F. Wiener, George Klein	1994	2

About Anna Szeles

Anna Szeles is a scholar working on Pathology and Forensic Medicine, Cancer Research, Oncology, Genetics and Molecular Biology, having authored 33 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Viral-associated cancers and disorders (7 papers), Cancer Genomics and Diagnostics (6 papers), Genetic factors in colorectal cancer (5 papers), Chromosomal and Genetic Variations (5 papers), Phagocytosis and Immune Regulation (4 papers), RNA and protein synthesis mechanisms (4 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Cancer Research (408 citations), Molecular Biology (1.0k citations), Immunology (306 citations), Oncology (359 citations) and Genetics (256 citations). Anna Szeles has collaborated with scholars based in Sweden, United States and Hungary. Frequent co-authors include Lars Holmgren, Anna‐Lena Spetz, Anna Bergsmedh, Marie Arsenian‐Henriksson, M. Judah Folkman, Anders Bratt, Kerstin I. Falk, Judah Folkman, Georg Klein and Éva Rajnavölgyi. Their work appears in journals such as Chromosome Research, Genes Chromosomes and Cancer, Proceedings of the National Academy of Sciences, Blood and Stem Cells and Development.

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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