Thorsten Henrich

1.6k total citations
22 papers, 859 citations indexed

About

Thorsten Henrich is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Thorsten Henrich has authored 22 papers receiving a total of 859 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Thorsten Henrich's work include Animal Genetics and Reproduction (7 papers), Developmental Biology and Gene Regulation (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Thorsten Henrich is often cited by papers focused on Animal Genetics and Reproduction (7 papers), Developmental Biology and Gene Regulation (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Thorsten Henrich collaborates with scholars based in Germany, Japan and United States. Thorsten Henrich's co-authors include Joachim Wittbrodt, Detlev Arendt, Antje Fischer, Felix Loosli, Sylke Winkler, Michael Carl, Clemens Grabher, Mirana Ramialison, Makoto Furutani‐Seiki and Carola Burgtorf and has published in prestigious journals such as Nucleic Acids Research, Development and Oncogene.

In The Last Decade

Thorsten Henrich

22 papers receiving 843 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thorsten Henrich Germany 16 621 238 131 82 74 22 859
Alexander Brandt Switzerland 9 685 1.1× 325 1.4× 101 0.8× 58 0.7× 98 1.3× 13 977
Violette Thermes France 12 515 0.8× 214 0.9× 185 1.4× 54 0.7× 77 1.0× 21 873
Laura L. Poling United States 9 800 1.3× 164 0.7× 66 0.5× 61 0.7× 40 0.5× 16 1.2k
Ernesto Maldonado Mexico 16 705 1.1× 157 0.7× 296 2.3× 78 1.0× 57 0.8× 38 1.2k
Mark C. Alliegro United States 18 481 0.8× 97 0.4× 146 1.1× 65 0.8× 40 0.5× 42 775
Carine Barreau France 12 1.1k 1.8× 136 0.6× 87 0.7× 118 1.4× 64 0.9× 14 1.4k
Flavio Garoia Italy 18 506 0.8× 180 0.8× 393 3.0× 73 0.9× 66 0.9× 31 953
Ryutaro Murakami Japan 16 571 0.9× 186 0.8× 100 0.8× 112 1.4× 119 1.6× 34 837
Elad Chomsky Israel 11 903 1.5× 121 0.5× 67 0.5× 108 1.3× 59 0.8× 15 1.2k
Derek Lemons United States 9 1.2k 2.0× 321 1.3× 112 0.9× 103 1.3× 179 2.4× 9 1.5k

Countries citing papers authored by Thorsten Henrich

Since Specialization
Citations

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

Fields of papers citing papers by Thorsten Henrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thorsten Henrich

This figure shows the co-authorship network connecting the top 25 collaborators of Thorsten Henrich. A scholar is included among the top collaborators of Thorsten Henrich 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 Thorsten Henrich. Thorsten Henrich 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.
Zhang, Ping, Stefanie Hammer, Valeria Solozobova, et al.. (2015). TRIM25 has a dual function in the p53/Mdm2 circuit. Oncogene. 34(46). 5729–5738. 74 indexed citations
2.
Shinya, Minori, et al.. (2014). Evolutionary diversification ofMCM3genes inXenopus laevisandDanio rerio. Cell Cycle. 13(20). 3271–3281. 8 indexed citations
3.
Fischer, Antje, Thorsten Henrich, & Detlev Arendt. (2010). The normal development of Platynereis dumerilii (Nereididae, Annelida). Frontiers in Zoology. 7(1). 31–31. 144 indexed citations
4.
Martínez‐Morales, Juan Ramón, Thorsten Henrich, Mirana Ramialison, & Joachim Wittbrodt. (2007). New genes in the evolution of the neural crest differentiation program. Genome biology. 8(3). R36–R36. 39 indexed citations
5.
Bérubé, Hugo, Ivica Letunić, Julien Gagneur, et al.. (2007). 4DXpress: a database for cross-species expression pattern comparisons. Nucleic Acids Research. 36(Database). D847–D853. 26 indexed citations
6.
Henrich, Thorsten, Mirana Ramialison, Beate Wittbrodt, et al.. (2005). MEPD: a resource for medaka gene expression patterns. Computer applications in the biosciences. 21(14). 3195–3197. 21 indexed citations
7.
Quiring, Rebecca, Beate Wittbrodt, Thorsten Henrich, et al.. (2004). Large-scale expression screening by automated whole-mount in situ hybridization. Mechanisms of Development. 121(7-8). 971–976. 45 indexed citations
8.
Henrich, Thorsten, Mirana Ramialison, Erik Segerdell, et al.. (2004). GSD: a genetic screen database. Mechanisms of Development. 121(7-8). 959–963. 4 indexed citations
9.
Iwanami, Norimasa, Yousuke Takahama, Sanae Kunimatsu, et al.. (2004). Mutations affecting thymus organogenesis in Medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 779–789. 23 indexed citations
10.
Yasuoka, Akihito, Yukihiro Hirose, Hiroki Yoda, et al.. (2004). Mutations affecting the formation of posterior lateral line system in Medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 729–738. 23 indexed citations
11.
Schartl, Manfred, Indrajit Nanda, Mariko Kondo, et al.. (2004). Current Status of Medaka Genetics and Genomics. Methods in cell biology. 77. 173–199. 7 indexed citations
12.
Morinaga, Chikako, Takeshi Tomonaga, Takao Sasado, et al.. (2004). Mutations affecting gonadal development in Medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 829–839. 21 indexed citations
13.
Sasado, Takao, Chikako Morinaga, Katsutoshi Niwa, et al.. (2004). Mutations affecting early distribution of primordial germ cells in Medaka (Oryzias latipes) embryo. Mechanisms of Development. 121(7-8). 817–828. 16 indexed citations
14.
Yoda, Hiroki, Yukihiro Hirose, Akihito Yasuoka, et al.. (2004). Mutations affecting retinotectal axonal pathfinding in Medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 715–728. 11 indexed citations
15.
Henrich, Thorsten. (2003). MEPD: a Medaka gene expression pattern database. Nucleic Acids Research. 31(1). 72–74. 20 indexed citations
16.
Grabher, Clemens, et al.. (2003). Transposon-mediated enhancer trapping in medaka. Gene. 322. 57–66. 64 indexed citations
17.
Loosli, Felix, Sylke Winkler, Carola Burgtorf, et al.. (2001). Medakaeyelessis the key factor linking retinal determination and eye growth. Development. 128(20). 4035–4044. 108 indexed citations
18.
Henrich, Thorsten & Joachim Wittbrodt. (2000). An in situ hybridization screen for the rapid isolation of differentially expressed genes. Development Genes and Evolution. 210(1). 28–33. 20 indexed citations
19.
Loosli, Felix, Reinhard W. Köster, Michael Carl, et al.. (2000). A genetic screen for mutations affecting embryonic development in medaka fish ( Oryzias latipes ). Mechanisms of Development. 97(1-2). 133–139. 99 indexed citations
20.
Henrich, Thorsten, Carola Burgtorf, Hans Lehrach, & Joachim Wittbrodt. (1998). Generation of two spotted plasmid cDNA-libraries of the head region of stage 20 and whole stage 17 Medaka embryos.. Max Planck Institute for Plasma Physics. 9. 41–45. 1 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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