Hans‐Dieter Rott

1.8k total citations
19 papers, 841 citations indexed

About

Hans‐Dieter Rott is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Hans‐Dieter Rott has authored 19 papers receiving a total of 841 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Hans‐Dieter Rott's work include Tuberous Sclerosis Complex Research (4 papers), Genetic and rare skin diseases. (4 papers) and Ultrasound and Hyperthermia Applications (4 papers). Hans‐Dieter Rott is often cited by papers focused on Tuberous Sclerosis Complex Research (4 papers), Genetic and rare skin diseases. (4 papers) and Ultrasound and Hyperthermia Applications (4 papers). Hans‐Dieter Rott collaborates with scholars based in Germany, Australia and United States. Hans‐Dieter Rott's co-authors include Кazuo Maeda, Gail ter Haar, Marvin C. Ziskin, Francis Duck, Stanley B Barnett, Karin Mayer, Wolfgang G. Ballhausen, Anita Rauch, Eckart Haneke and Jaime L. Frías and has published in prestigious journals such as The Lancet, The American Journal of Human Genetics and Journal of the American Academy of Dermatology.

In The Last Decade

Hans‐Dieter Rott

19 papers receiving 798 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hans‐Dieter Rott Germany 14 276 209 195 139 113 19 841
Alexander J. Gougoutas United States 13 309 1.1× 188 0.9× 42 0.2× 244 1.8× 397 3.5× 15 1.1k
Ji Hyun Kim South Korea 13 57 0.2× 115 0.6× 137 0.7× 117 0.8× 192 1.7× 97 780
Massimo Marenzana United Kingdom 17 217 0.8× 108 0.5× 340 1.7× 62 0.4× 223 2.0× 31 1.1k
Eun‐Hae Cho South Korea 18 96 0.3× 209 1.0× 328 1.7× 28 0.2× 80 0.7× 94 1.1k
Dominik Paul Germany 16 135 0.5× 42 0.2× 92 0.5× 375 2.7× 192 1.7× 39 955
Manuel Fischer Germany 18 106 0.4× 148 0.7× 476 2.4× 206 1.5× 84 0.7× 75 1.1k
Yating Yi China 19 254 0.9× 69 0.3× 387 2.0× 69 0.5× 81 0.7× 57 1.3k
Takeo Fukushima Japan 21 175 0.6× 40 0.2× 168 0.9× 69 0.5× 348 3.1× 94 1.2k
Keiko Kudoh Japan 12 122 0.4× 51 0.2× 136 0.7× 179 1.3× 109 1.0× 36 732
Juliane Gust United States 17 842 3.1× 626 3.0× 1.0k 5.3× 124 0.9× 28 0.2× 31 3.3k

Countries citing papers authored by Hans‐Dieter Rott

Since Specialization
Citations

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

Fields of papers citing papers by Hans‐Dieter Rott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans‐Dieter Rott. 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 Hans‐Dieter Rott. The network helps show where Hans‐Dieter Rott may publish in the future.

Co-authorship network of co-authors of Hans‐Dieter Rott

This figure shows the co-authorship network connecting the top 25 collaborators of Hans‐Dieter Rott. A scholar is included among the top collaborators of Hans‐Dieter Rott 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 Hans‐Dieter Rott. Hans‐Dieter Rott is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Shoichet, Sarah A., Kirsten Hoffmann, Corinna Menzel, et al.. (2003). Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation. The American Journal of Human Genetics. 73(6). 1341–1354. 65 indexed citations
2.
Rott, Hans‐Dieter, Beate Lemcke, Martin Zenker, et al.. (2002). Cyst‐like cerebral lesions in tuberous sclerosis. American Journal of Medical Genetics. 111(4). 435–439. 20 indexed citations
3.
Zweier, Christiane, Beate Albrecht, Beate Mitulla, et al.. (2002). “Mowat-Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene. American Journal of Medical Genetics. 108(3). 177–177. 6 indexed citations
4.
Zweier, Christiane, Beate Albrecht, Beate Mitulla, et al.. (2002). “Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene. American Journal of Medical Genetics. 108(3). 177–181. 89 indexed citations
5.
Mayer, Karin, et al.. (2000). Tuberous sclerosis type 1: Three novel mutations detected in exon 15 by a combination of HDA and TGGE. Human Mutation. 16(1). 88–88. 2 indexed citations
6.
Barnett, Stanley B, Gail ter Haar, Marvin C. Ziskin, et al.. (2000). International recommendations and guidelines for the safe use of diagnostic ultrasound in medicine. Ultrasound in Medicine & Biology. 26(3). 355–366. 275 indexed citations
7.
8.
Rott, Hans‐Dieter. (1999). Safety of Ultrasonic Contrast Agents. European Journal of Ultrasound. 9(2). 195–197. 4 indexed citations
9.
Mayer, Karin, Wolfgang G. Ballhausen, & Hans‐Dieter Rott. (1999). Mutation screening of the entire coding regions of theTSC1 and theTSC2 gene with the protein truncation test (PTT) identifies frequent splicing defects. Human Mutation. 14(5). 401–411. 32 indexed citations
10.
Rott, Hans‐Dieter. (1999). Extracutaneous analogies of Blaschko lines. American Journal of Medical Genetics. 85(4). 338–341. 22 indexed citations
11.
Rott, Hans‐Dieter. (1999). Acoustic cavitation and capillary bleeding. European Journal of Ultrasound. 9(3). 277–280. 5 indexed citations
12.
Ziskin, Marvin C., Кazuo Maeda, Wesley L. Nyborg, et al.. (1998). World Federation for Ultrasound in Medicine and Biology, task group report for safety committee of the WFUMB: conclusions and recommendations on thermal and non-thermal mechanisms for biological effects of ultrasound. ePrints Soton (University of Southampton). 17 indexed citations
13.
Rott, Hans‐Dieter, et al.. (1997). The sensitivity of biological tissue to ultrasound. Ultrasound in Medicine & Biology. 23(6). 805–812. 133 indexed citations
14.
Liehr, Thomas, Bernd Rautenstrauß, H. Grehl, et al.. (1996). Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion. Human Genetics. 98(1). 22–28. 33 indexed citations
15.
Claussen, Uwe, et al.. (1994). Chromosomal mosaicism in two patients with epidermal verrucous nevus. Journal of the American Academy of Dermatology. 30(4). 622–625. 17 indexed citations
16.
Kotzot, Dieter, Josef Weigl, W. Huk, & Hans‐Dieter Rott. (1993). Hydantoin syndrome with holoprosencephaly: A possible rare teratogenic effect. Teratology. 48(1). 15–19. 13 indexed citations
17.
Rott, Hans‐Dieter, et al.. (1986). Hypomelanosis of Ito and chromosomal mosaicism in fibroblasts.. PubMed. 2(8502). 343–343. 35 indexed citations
18.
Rott, Hans‐Dieter, et al.. (1986). HYPOMELANOSIS OF ITO AND CHROMOSOMAL MOSAICISM IN FIBROBLASTS. The Lancet. 328(8502). 343–343. 30 indexed citations
19.
Rott, Hans‐Dieter, et al.. (1984). DUCHENNE MUSCULAR DYSTROPHY: CARRIER DETECTION BY ULTRASOUND AND COMPUTERISED TOMOGRAPHY. The Lancet. 323(8368). 111–111. 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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