Anja Weise

5.5k total citations
160 papers, 3.2k citations indexed

About

Anja Weise is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Anja Weise has authored 160 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 116 papers in Genetics, 75 papers in Plant Science and 71 papers in Molecular Biology. Recurrent topics in Anja Weise's work include Genomic variations and chromosomal abnormalities (100 papers), Chromosomal and Genetic Variations (75 papers) and Prenatal Screening and Diagnostics (42 papers). Anja Weise is often cited by papers focused on Genomic variations and chromosomal abnormalities (100 papers), Chromosomal and Genetic Variations (75 papers) and Prenatal Screening and Diagnostics (42 papers). Anja Weise collaborates with scholars based in Germany, United States and Poland. Anja Weise's co-authors include Thomas Liehr, Kristin Mrasek, Nadezda Kosyakova, Heike Starke, Uwe Claussen, U. Claussen, Elisabeth Ewers, Michael Glei, Anita Heller and Vladimir A. Trifonov and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Nano Letters.

In The Last Decade

Anja Weise

153 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anja Weise Germany 30 1.9k 1.4k 1.2k 760 313 160 3.2k
Teresa Costa Canada 27 1.3k 0.7× 1.7k 1.2× 573 0.5× 195 0.3× 666 2.1× 47 3.3k
David S. Cram Australia 40 2.1k 1.1× 1.5k 1.1× 207 0.2× 1.8k 2.3× 837 2.7× 136 4.8k
Susan J. Kimber United Kingdom 42 639 0.3× 2.4k 1.8× 76 0.1× 345 0.5× 590 1.9× 156 5.1k
Guangxiu Lu China 30 848 0.4× 1.6k 1.2× 113 0.1× 606 0.8× 194 0.6× 229 3.2k
John Arne Dahl Norway 23 286 0.1× 1.8k 1.3× 111 0.1× 170 0.2× 201 0.6× 52 2.4k
Ray Kit Ng Hong Kong 19 310 0.2× 1.8k 1.3× 148 0.1× 139 0.2× 90 0.3× 37 2.4k
Joshua Babiarz United States 23 427 0.2× 3.2k 2.4× 204 0.2× 303 0.4× 284 0.9× 38 4.3k
Masahiro Oka Japan 30 398 0.2× 2.9k 2.1× 98 0.1× 70 0.1× 766 2.4× 81 4.2k
Geppino Falco Italy 31 267 0.1× 2.1k 1.5× 158 0.1× 182 0.2× 196 0.6× 87 3.2k
J J Cassiman Belgium 34 573 0.3× 1.9k 1.4× 70 0.1× 60 0.1× 230 0.7× 66 3.4k

Countries citing papers authored by Anja Weise

Since Specialization
Citations

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

Fields of papers citing papers by Anja Weise

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anja Weise

This figure shows the co-authorship network connecting the top 25 collaborators of Anja Weise. A scholar is included among the top collaborators of Anja Weise 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 Anja Weise. Anja Weise 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.
Liehr, Thomas, Anja Weise, Eva Miriam Buhl, et al.. (2025). Decoding HuH-7: a comprehensive genetic and molecular portrait of a widely used hepatocellular carcinoma model. Frontiers in Cell and Developmental Biology. 13. 1648639–1648639.
2.
Bekhite, Mohamed M., et al.. (2024). Generation of a human induced pluripotent stem cell lines (UKJi003-A) from a patient with Fabry disease and healthy donor (UKJi004-A). Stem Cell Research. 82. 103620–103620. 1 indexed citations
3.
4.
Liehr, Thomas, et al.. (2017). Noninvasive Prenatal Testing - When Is It Advantageous to Apply. PubMed. 2(1). 1–11. 20 indexed citations
5.
Loghin, Florin C., Anja Weise, Aniello Falco, et al.. (2016). Scalable spray deposition process for highly uniform and reproducible CNT-TFTs. Flexible and Printed Electronics. 1(4). 45002–45002. 19 indexed citations
6.
Tanomtong, Alongklod, Arunrat Chaveerach, Krit Pinthong, et al.. (2014). High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis). Archives of Biological Sciences. 66(4). 1603–1607. 2 indexed citations
7.
Schüle, Silke, A. Altendorf-Hofmann, Yuan Chen, et al.. (2013). Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases. Journal of Cancer Research and Clinical Oncology. 139(11). 1861–1867. 6 indexed citations
8.
Sheth, Frenny, Joris Andrieux, Elisabeth Ewers, et al.. (2011). Characterization of sSMC by FISH and molecular techniques. European Journal of Medical Genetics. 54(3). 247–255. 14 indexed citations
9.
Liehr, Thomas, Jim Schröder, Monika Ziegler, et al.. (2011). Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements. SHILAP Revista de lepidopterología. 14(2). 13–6. 14 indexed citations
10.
Melo, Joana Barbosa, Liesbeth Backx, Joris Vermeesch, et al.. (2011). Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances. Journal of Applied Genetics. 52(2). 193–200. 12 indexed citations
11.
Mkrtchyan, Hasmik, Sophie Hinreiner, Marina Manvelyan, et al.. (2010). The Human Genome Puzzle — the Role of Copy Number Variation in Somatic Mosaicism. Current Genomics. 11(6). 426–431. 30 indexed citations
12.
Liehr, Thomas, Iris Bartels, Barbara Zoll, et al.. (2010). Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?. Cytogenetic and Genome Research. 132(1-2). 121–123. 3 indexed citations
13.
Wagner, Jasenka, Feodora Stipoljev, Ivana Škrlec, et al.. (2009). Partial monosomy 4q and partial trisomy 13q: phenotype and molecular mapping of the breakpoints. Chromosome Research. 1 indexed citations
14.
Liehr, Thomas, Markus Stümm, Gordana Joksiċ, et al.. (2008). Pallister-Killian Syndrome: Rare Phenotypic Features and Variable Karyotypes. Balkan Journal of Medical Genetics. 11(2). 9 indexed citations
15.
Mrasek, Kristin, Gabriele Krüger, Ingrid Bauer, et al.. (2008). A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences. Cytogenetic and Genome Research. 121(3-4). 286–287. 3 indexed citations
16.
Garwe, F., Andrea Csáki, Arne Bochmann, et al.. (2008). Optically controlled thermal management on the nanometer length scale. Nanotechnology. 19(5). 55207–55207. 33 indexed citations
17.
Glei, Michael, U. Claussen, A. Kuechler, et al.. (2006). Comet Fluorescence in situ Hybridization Analysis for Oxidative Stress-Induced DNA Damage in Colon Cancer Relevant Genes. Toxicological Sciences. 96(2). 279–284. 28 indexed citations
18.
Brečević, Lukrecija, S. Michel, Heike Starke, et al.. (2006). Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenetic and Genome Research. 114(3-4). 319–324. 11 indexed citations
19.
Weise, Anja, Heike Starke, Kristin Mrasek, U. Claussen, & Thomas Liehr. (2004). New insights into the evolution of chromosome 1. Cytogenetic and Genome Research. 108(1-3). 217–222. 17 indexed citations
20.
Weise, Anja, Anita Heller, Heike Starke, et al.. (2003). Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding method. Cytogenetic and Genome Research. 103(1-2). 34–39. 32 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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