Katrin Hoffmann

2.6k total citations
31 papers, 1.7k citations indexed

About

Katrin Hoffmann is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Katrin Hoffmann has authored 31 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Katrin Hoffmann's work include Genetic Associations and Epidemiology (4 papers), Epilepsy research and treatment (4 papers) and Pharmacological Effects and Toxicity Studies (4 papers). Katrin Hoffmann is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Epilepsy research and treatment (4 papers) and Pharmacological Effects and Toxicity Studies (4 papers). Katrin Hoffmann collaborates with scholars based in Germany, United States and Switzerland. Katrin Hoffmann's co-authors include Wolfgang Löscher, Ina Gröticke, Ada L. Olins, Allan J. Morrison, Richard P. Wenzel, Donald E. Olins, Karl Sperling, Stefan Mundlos, Raoul Heller and Tom H. Lindner and has published in prestigious journals such as Nature Genetics, Bioinformatics and Circulation Research.

In The Last Decade

Katrin Hoffmann

29 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrin Hoffmann Germany 19 724 338 327 219 184 31 1.7k
Carlo Fusco Italy 21 565 0.8× 276 0.8× 258 0.8× 353 1.6× 296 1.6× 118 1.8k
Stephen J. Langer United States 23 838 1.2× 598 1.8× 293 0.9× 131 0.6× 91 0.5× 37 2.3k
D. Goossens Belgium 25 797 1.1× 284 0.8× 548 1.7× 248 1.1× 72 0.4× 75 1.9k
Ye Wu China 24 1.2k 1.7× 262 0.8× 501 1.5× 395 1.8× 257 1.4× 173 2.3k
Mitsunobu Shimadzu Japan 22 812 1.1× 452 1.3× 195 0.6× 59 0.3× 83 0.5× 43 1.7k
Lifen Yang China 22 553 0.8× 196 0.6× 315 1.0× 200 0.9× 65 0.4× 82 1.5k
Salmo Raskin Brazil 28 1.5k 2.0× 1.1k 3.2× 578 1.8× 183 0.8× 134 0.7× 147 2.8k
Michael C. Kruer United States 25 746 1.0× 449 1.3× 412 1.3× 342 1.6× 218 1.2× 74 2.2k
Luca Massimino Italy 26 1.2k 1.7× 343 1.0× 408 1.2× 108 0.5× 47 0.3× 73 2.1k
Sara Gil‐Perotín Spain 23 920 1.3× 422 1.2× 154 0.5× 47 0.2× 144 0.8× 44 2.4k

Countries citing papers authored by Katrin Hoffmann

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Hoffmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Hoffmann

This figure shows the co-authorship network connecting the top 25 collaborators of Katrin Hoffmann. A scholar is included among the top collaborators of Katrin Hoffmann 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 Katrin Hoffmann. Katrin Hoffmann 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.
Hoffmann, Katrin, et al.. (2017). CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs’ dystrophy. Graefe s Archive for Clinical and Experimental Ophthalmology. 255(8). 1621–1631. 32 indexed citations
2.
Weichert, Alexander, Karim D. Kalache, Ann Carolin Longardt, et al.. (2016). Familial Gordon syndrome associated with a PIEZO2 mutation. American Journal of Medical Genetics Part A. 173(1). 254–259. 25 indexed citations
3.
4.
Hoffmann, Katrin & Raoul Heller. (2011). Uniparental disomies 7 and 14. Best Practice & Research Clinical Endocrinology & Metabolism. 25(1). 77–100. 43 indexed citations
5.
Jamsheer, Aleksander, Mateusz Kolanczyk, Denise Horn, et al.. (2010). Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family. BMC Medical Genetics. 11(1). 110–110. 19 indexed citations
6.
Stassen, Hans H., Katrin Hoffmann, & Christian Scharfetter. (2009). The difficulties of reproducing conventionally derived results through 500k-chip technology. BMC Proceedings. 3(S7). S66–S66. 1 indexed citations
7.
Seifert, Wenke, Katrin Hoffmann, Tom H. Lindner, et al.. (2009). HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing. European Journal of Human Genetics. 17(12). 1570–1576. 22 indexed citations
8.
Türkmen, Seval, Gao Guo, Masoud Garshasbi, et al.. (2009). CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait. PLoS Genetics. 5(5). e1000487–e1000487. 109 indexed citations
9.
Hoffmann, Katrin, Franz Rüschendorf, Bertram Müller‐Myhsok, et al.. (2009). A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany*. Journal of Hypertension. 27(5). 983–990. 8 indexed citations
10.
Seelow, Dominik, Heike Goehler, & Katrin Hoffmann. (2009). FragIdent – Automatic identification and characterisation of cDNA-fragments. BMC Genomics. 10(1). 95–95.
11.
Gröticke, Ina, Katrin Hoffmann, & Wolfgang Löscher. (2008). Behavioral alterations in a mouse model of temporal lobe epilepsy induced by intrahippocampal injection of kainate. Experimental Neurology. 213(1). 71–83. 119 indexed citations
12.
Bankstahl, Jens P., Katrin Hoffmann, Kerstin Bethmann, & Wolfgang Löscher. (2008). Glutamate is critically involved in seizure-induced overexpression of P-glycoprotein in the brain. Neuropharmacology. 54(6). 1006–1016. 59 indexed citations
13.
Hoffmann, Katrin, Karl Sperling, Ada L. Olins, & Donald E. Olins. (2007). The granulocyte nucleus and lamin B receptor: avoiding the ovoid. Chromosoma. 116(3). 227–235. 94 indexed citations
14.
Gröticke, Ina, Katrin Hoffmann, & Wolfgang Löscher. (2007). Behavioral alterations in the pilocarpine model of temporal lobe epilepsy in mice. Experimental Neurology. 207(2). 329–349. 168 indexed citations
15.
Schwabe, Georg C., Katrin Hoffmann, Niki T. Loges, et al.. (2007). Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. Human Mutation. 29(2). 289–298. 163 indexed citations
16.
Gotfryd, Kamil, Sylwia Owczarek, Katrin Hoffmann, et al.. (2006). Multiple effects of pentyl-4-yn-VPA enantiomers: From toxicity to short-term memory enhancement. Neuropharmacology. 52(3). 764–778. 9 indexed citations
17.
Franke, André, Andreas Wollstein, Markus Teuber, et al.. (2006). GENOMIZER: an integrated analysis system for genome-wide association data. Human Mutation. 27(6). 583–588. 14 indexed citations
18.
Hoffmann, Katrin, Alexandra M. Gastens, Holger A. Volk, & Wolfgang Löscher. (2006). Expression of the multidrug transporter MRP2 in the blood–brain barrier after pilocarpine-induced seizures in rats. Epilepsy Research. 69(1). 1–14. 41 indexed citations
19.
Weber, Stefanie, Katrin Hoffmann, Nikola Jeck, et al.. (2000). Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene. European Journal of Human Genetics. 8(6). 414–422. 78 indexed citations
20.
Browning, Jeffrey L., et al.. (1996). Time-Dependent Variability of Infarct Size and Hemispheric Volume in Experimental Focal Cerebral Ischemia in the Rabbit. Journal of Neurotrauma. 13(10). 583–588. 3 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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