H. Zankl

1.8k total citations
78 papers, 1.5k citations indexed

About

H. Zankl is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, H. Zankl has authored 78 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 27 papers in Genetics and 16 papers in Cancer Research. Recurrent topics in H. Zankl's work include Genomic variations and chromosomal abnormalities (15 papers), Carcinogens and Genotoxicity Assessment (13 papers) and Chromosomal and Genetic Variations (10 papers). H. Zankl is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Carcinogens and Genotoxicity Assessment (13 papers) and Chromosomal and Genetic Variations (10 papers). H. Zankl collaborates with scholars based in Germany, Poland and United States. H. Zankl's co-authors include K. D. Zang, Gerhard Eisenbrand, Harry Scherthan, Doris Marko, Laurent Meijer, Anna Maria Friedel, G. Eisenbrand, A. Rodewald, Heide Seidel and Matthias Schneider and has published in prestigious journals such as Nature, The Lancet and Cancer Research.

In The Last Decade

H. Zankl

78 papers receiving 1.4k citations

Peers

H. Zankl

GENET

EPIDE

Yoshiyuki Kobayashi Japan

Or Kakhlon Israel

Gazi S. Hossain United States

Hideto Hoshino Japan

Lauren Diebold United States

Richard R. Vaillancourt United States

Filiberto Cimino Italy

Tomonori Hosoya Japan

Jiying Sun Japan

Bin Ye China

Yoshiyuki Kobayashi Japan

H. Zankl

747 ×1.2

196 ×0.7

GENET

127 ×0.5

79 ×0.3

132 ×0.7

EPIDE

Citations per year, relative to H. Zankl H. Zankl (= 1×) peers Yoshiyuki Kobayashi

Countries citing papers authored by H. Zankl

Since Specialization

Citations

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

Fields of papers citing papers by H. Zankl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Zankl

This figure shows the co-authorship network connecting the top 25 collaborators of H. Zankl. A scholar is included among the top collaborators of H. Zankl 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 H. Zankl. H. Zankl 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

Baum, Matthias, et al.. (2006). Acrylamide and Glycidamide: Approach towards Risk Assessment Based on Biomarker Guided Dosimetry of Genotoxic/Mutagenic Effects in Human Blood. Advances in experimental medicine and biology. 561. 77–88. 16 indexed citations

Baum, Matthias, et al.. (2004). Genotoxic and mutagenic properties of acrylamide and glycidamide in human lymphocytes and V79-cells.. Cancer Research. 64. 740–740. 1 indexed citations

Zankl, H., et al.. (2004). In vitro evaluation of the cytotoxic and mutagenic potential of the 5-aminolevulinic acid hexylester-mediated photodynamic therapy. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 561(1-2). 91–100. 12 indexed citations

Baum, Matthias, et al.. (2004). Acrylamide and glycidamide: genotoxic effects in V79-cells and human blood. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 580(1-2). 61–69. 60 indexed citations

Zankl, H., et al.. (2001). Mutagenic and cytotoxic effectiveness of zinc dimethyl and zinc diisononyldithiocarbamate in human lymphocyte cultures. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 497(1-2). 89–99. 11 indexed citations

Kappler, Roland, et al.. (2000). Double Minutes and c-MYC Amplification in Acute Myelogenous Leukemia. Cancer Genetics and Cytogenetics. 120(1). 73–79. 40 indexed citations

Marko, Doris, et al.. (1998). Induction of apoptosis by an inhibitor of cAMP-specific PDE in malignant murine carcinoma cells overexpressing PDE activity in comparison to their nonmalignant counterparts. Cell Biochemistry and Biophysics. 28(2-3). 75–101. 51 indexed citations

Eisenbrand, G., et al.. (1997). Genotoxic effects of 2-trans-hexenal in human buccal mucosa cells in vivo. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 390(1-2). 161–165. 30 indexed citations

Zankl, H., et al.. (1997). Exhaustive physical exercise increases frequency of micronuclei. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 389(2-3). 243–246. 38 indexed citations

10.

Eisenbrand, G., et al.. (1995). Genotoxic effects of the α, β-unsaturated aldehydes 2-trans-butenal,2-trans-hexenal and 2-trans, 6-cis-rmnonadienal. Mutation Research/Environmental Mutagenesis and Related Subjects. 335(3). 259–265. 38 indexed citations

11.

Schmitt, Holger, Nikolaus Blin, H. Zankl, & Harry Scherthan. (1994). Telomere length variation in normal and malignant human tissues. Genes Chromosomes and Cancer. 11(3). 171–177. 36 indexed citations

12.

Zankl, H., et al.. (1991). Characterization of Marker Chromosomes in Namalva Cells by Chromosomal In Situ Suppression (CISS) Hybridization and R‐Banding. Genes Chromosomes and Cancer. 3(5). 394–399. 1 indexed citations

13.

Gadhia, Pankaj, et al.. (1991). Adriamycin-induced sister chromatid exchange and chromosomal aberrations in Down's syndrome lymphocytes. Mutagenesis. 6(1). 31–33. 1 indexed citations

14.

Scherthan, Harry, et al.. (1990). Use of a centromere‐specific DNA probe (p82H) in nonisotopic in situ hybridization for classification of micronuclei. Genes Chromosomes and Cancer. 2(1). 59–62. 62 indexed citations

15.

Pees, H.W., et al.. (1988). Tetraploidy and Y chromosome loss in acute mixed-lineage leukemia. Cancer Genetics and Cytogenetics. 33(2). 185–191. 5 indexed citations

16.

Gadhia, Pankaj, et al.. (1988). Effects of bleomycin on Down's syndrome lymphocytes in culture. Mutation Research Letters. 207(3-4). 153–158. 5 indexed citations

17.

Eisenbrand, Gerhard, et al.. (1988). Cytogenetic effects of N-nitrosodiethanolamine (NDELA) and NDELA-monoacetate in human lymphocytes. Journal of Cancer Research and Clinical Oncology. 114(6). 575–578. 6 indexed citations

18.

Rodewald, A., et al.. (1981). Dermatoglyphic Peculiarities in Down’s Syndrome Detection of Mosaicism and Balanced Translocation Carriers. PubMed. 2. 41–56. 2 indexed citations

19.

Zankl, H.. (1970). Differences between species in sperm resorption in the epididymis.. 5. 32–36. 1 indexed citations

20.

Zankl, H. & W. Leidl. (1969). Effect of vasoligation and a sympatholytic agent on the number of sperm cells in the epididymis in rabbit. Reproduction. 18(1). 181–182. 10 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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