A. Zimber

1.6k total citations
52 papers, 1.4k citations indexed

About

A. Zimber is a scholar working on Molecular Biology, Animal Science and Zoology and Oncology. According to data from OpenAlex, A. Zimber has authored 52 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Animal Science and Zoology and 12 papers in Oncology. Recurrent topics in A. Zimber's work include Animal Virus Infections Studies (10 papers), Drug Transport and Resistance Mechanisms (9 papers) and Herpesvirus Infections and Treatments (9 papers). A. Zimber is often cited by papers focused on Animal Virus Infections Studies (10 papers), Drug Transport and Resistance Mechanisms (9 papers) and Herpesvirus Infections and Treatments (9 papers). A. Zimber collaborates with scholars based in Israel, France and United States. A. Zimber's co-authors include Christian Gespach, A. Yaniv, Quang‐Dé Nguyen, Arnona Gazit, Erik Bruyneel, Philip R. Debruyne, Eric Chastre, K. Perk, Olivier De Wever and Gérard Redeuilh and has published in prestigious journals such as JNCI Journal of the National Cancer Institute, Oncogene and Journal of Virology.

In The Last Decade

A. Zimber

51 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
A. Zimber Israel 18 701 461 220 189 172 52 1.4k
Osamu Takeda Japan 20 571 0.8× 199 0.4× 218 1.0× 88 0.5× 105 0.6× 46 1.3k
Takehiko Koide Japan 27 968 1.4× 175 0.4× 242 1.1× 96 0.5× 83 0.5× 77 2.1k
Michel Lacasa France 20 659 0.9× 366 0.8× 92 0.4× 326 1.7× 189 1.1× 37 1.4k
L. I. Huschtscha Australia 13 884 1.3× 417 0.9× 206 0.9× 77 0.4× 56 0.3× 16 1.4k
Wayne L. Ryan United States 18 727 1.0× 149 0.3× 303 1.4× 78 0.4× 87 0.5× 64 1.5k
Gudrun Totzke Germany 19 565 0.8× 236 0.5× 217 1.0× 72 0.4× 132 0.8× 29 1.2k
Ramesh B. Batchu United States 25 1.0k 1.5× 446 1.0× 199 0.9× 77 0.4× 137 0.8× 55 1.7k
Chia‐Huei Lee Taiwan 19 548 0.8× 306 0.7× 214 1.0× 56 0.3× 221 1.3× 34 1.2k
Gian G. Re United States 19 1.2k 1.6× 173 0.4× 117 0.5× 52 0.3× 137 0.8× 35 1.7k
Chunyan Tian China 24 1.2k 1.6× 374 0.8× 256 1.2× 151 0.8× 197 1.1× 76 1.8k

Countries citing papers authored by A. Zimber

Since Specialization
Citations

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

Fields of papers citing papers by A. Zimber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Zimber

This figure shows the co-authorship network connecting the top 25 collaborators of A. Zimber. A scholar is included among the top collaborators of A. Zimber 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 A. Zimber. A. Zimber 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.
Zimber, A. & Christian Gespach. (2008). Bile Acids and Derivatives, Their Nuclear Receptors FXR, PXR and Ligands: Role in Health and Disease and Their Therapeutic Potential. Anti-Cancer Agents in Medicinal Chemistry. 8(5). 540–563. 45 indexed citations
2.
Sabbah, Michèle, Shahin Emami, Gérard Redeuilh, et al.. (2008). Molecular signature and therapeutic perspective of the epithelial-to-mesenchymal transitions in epithelial cancers. Drug Resistance Updates. 11(4-5). 123–151. 255 indexed citations
3.
Maurin, Nicole, Marie‐Elisabeth Forgue‐Lafitte, Pierre Lévy, A. Zimber, & Jacques Bara. (2006). Progression of tumors arising from large ACF is associated with the MUC5AC expression during rat colon MNNG carcinogenis. International Journal of Cancer. 120(3). 477–483. 15 indexed citations
4.
Zimber, A., Quang‐Dé Nguyen, & Christian Gespach. (2004). Nuclear bodies and compartments: functional roles and cellular signalling in health and disease. Cellular Signalling. 16(10). 1085–1104. 129 indexed citations
5.
Bara, Jacques, et al.. (2003). Abnormal Expression of Gastric Mucin in Human and Rat Aberrant Crypt Foci during Colon Carcinogenesis. Tumor Biology. 24(3). 109–115. 27 indexed citations
6.
Debruyne, Philip R., Erik Bruyneel, Xiaodong Li, et al.. (2002). Bile acids stimulate invasion and haptotaxis in human colorectal cancer cells through activation of multiple oncogenic signaling pathways. Oncogene. 21(44). 6740–6750. 68 indexed citations
7.
Debruyne, Philip R., Erik Bruyneel, Xuedong Li, et al.. (2001). The role of bile acids in carcinogenesis. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 480-481. 359–369. 143 indexed citations
8.
Zimber, A., Dania Hirsch, Eric Chastre, et al.. (1997). Human Colorectal Carcinogenesis Is Associated with Deregulation of Homeobox Gene Expression. Biochemical and Biophysical Research Communications. 232(3). 742–748. 92 indexed citations
9.
Zimber, A., et al.. (1994). Inhibition of proliferation and induction of monocytic differentiation in HL60 human promyelocytic leukemia cells treated with bile acids In vitro. International Journal of Cancer. 59(1). 71–77. 19 indexed citations
10.
Louvet, Christophe, Dominique Fagot, Eric Chastre, et al.. (1994). The arotinoid Ro 40-8757 has antiproliferative effects in drug-resistant human colon and breast cancer cell lines in vitro. Cancer Letters. 85(1). 83–86. 5 indexed citations
11.
Zusman, I., A. Zimber, Zecharia Madar, & Abraham Nyska. (1992). Morphological, Histochemical and Immunohistochemical Differences between Tumorous and Adjacent Tissues in Chemically Induced Colon Cancer in Rats. Cells Tissues Organs. 145(1). 29–34. 4 indexed citations
12.
Zimber, A., et al.. (1991). Effects of lithocholic acid exposure throughout pregnancy on late prenatal and early postnatal development in rats. Teratology. 43(4). 355–361. 12 indexed citations
13.
Zusman, Itshak, A. Zimber, & Abraham Nyska. (1991). Role of Morphological Methods in the Analysis of Chemically Induced Colon Cancer in Rats. Cells Tissues Organs. 142(4). 351–356. 10 indexed citations
14.
Zusman, Itshak, et al.. (1991). Effects of N-Methyl-N’-Nitro-N-Nitrosoguanidine and Deoxycholic Acid on Processes of Tumorous Transformation of Rat Visceral Yolk Sac. Cells Tissues Organs. 140(4). 362–368. 2 indexed citations
15.
Zusman, I., et al.. (1991). Nuclear polymorphism and nuclear size in precarcinomatous and carcinomatous lesions in rat colon and liver. Cytometry. 12(4). 302–307. 12 indexed citations
16.
Zusman, I. & A. Zimber. (1990). Effects of Secondary Bile Acids on the in vitro Development of Early Somite Rat Embryos. Cells Tissues Organs. 138(2). 144–149. 5 indexed citations
18.
Zimber, A., et al.. (1983). Lymphoproliferative disease of turkeys: Pathogenesis, Viraemia and serum protein analysis following infection1. Avian Pathology. 12(1). 101–116. 10 indexed citations
19.
Ianconescu, M., A. Yaniv, Arnona Gazit, K. Perk, & A. Zimber. (1983). Susceptibility of domestic birds to Lymphoproliferative disease virus (LPDV) of Turkeys1. Avian Pathology. 12(3). 291–302. 13 indexed citations
20.
Yaniv, A., et al.. (1980). A reverse transcriptase assay for the diagnosis of lymphoproliferative disease (LPD) of Turkeys. Avian Pathology. 9(4). 481–487. 14 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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