Thomas M. Jovin

24.1k total citations · 6 hit papers
298 papers, 19.4k citations indexed

About

Thomas M. Jovin is a scholar working on Molecular Biology, Biomedical Engineering and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Thomas M. Jovin has authored 298 papers receiving a total of 19.4k indexed citations (citations by other indexed papers that have themselves been cited), including 178 papers in Molecular Biology, 38 papers in Biomedical Engineering and 35 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Thomas M. Jovin's work include DNA and Nucleic Acid Chemistry (81 papers), Advanced biosensing and bioanalysis techniques (50 papers) and Monoclonal and Polyclonal Antibodies Research (33 papers). Thomas M. Jovin is often cited by papers focused on DNA and Nucleic Acid Chemistry (81 papers), Advanced biosensing and bioanalysis techniques (50 papers) and Monoclonal and Polyclonal Antibodies Research (33 papers). Thomas M. Jovin collaborates with scholars based in Germany, Argentina and United States. Thomas M. Jovin's co-authors include Fritz M. Pohl, Elizabeth A. Jares‐Erijman, D. J. Arndt‐Jovin, Donna J. Arndt‐Jovin, Wolfgang Hoyer, Vinod Subramaniam, Paul T. Englund, Dmitry Cherny, Carlos W. Bertoncini and Markus Zweckstetter and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Thomas M. Jovin

297 papers receiving 18.5k citations

Hit Papers

Salt-induced co-operative... 1964 2026 1984 2005 1972 1990 2005 2004 1964 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Salt-induced co-operative conformational change of a synthetic DNA: Equilibrium and kinetic studies with poly(dG-dC)
    1972 1.1k citations Thomas M. Jovin et al. profile →
  2. Studying single living cells and chromosomes by confocal Raman microspectroscopy
    1990 718 citations D. J. Arndt‐Jovin, Thomas M. Jovin et al. profile →
  3. Release of long-range tertiary interactions potentiates aggregation of natively unstructured α-synuclein
    2005 668 citations Carlos W. Bertoncini, Young‐Sang Jung et al. Proceedings of the National Academy of Sciences profile →
  4. Quantum dot ligands provide new insights into erbB/HER receptor–mediated signal transduction
    2004 625 citations Diane S. Lidke, Péter Nagy et al. profile →
  5. An apparatus for preparative temperature-regulated polyacrylamide gel electrophoresis
    1964 560 citations Thomas M. Jovin et al. profile →
  6. Enzymatic Synthesis of Deoxyribonucleic Acid
    1969 501 citations Thomas M. Jovin et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas M. Jovin Germany 73 11.8k 2.4k 2.4k 2.3k 2.1k 298 19.4k
Stefan Becker Germany 65 8.3k 0.7× 3.0k 1.3× 1.4k 0.6× 1.8k 0.8× 985 0.5× 357 16.3k
David Klenerman United Kingdom 70 7.3k 0.6× 1.2k 0.5× 1.9k 0.8× 3.8k 1.6× 1.4k 0.7× 320 16.1k
Roland Riek Switzerland 73 17.2k 1.5× 3.3k 1.4× 2.8k 1.2× 8.1k 3.5× 761 0.4× 285 25.1k
Vinod Subramaniam Netherlands 57 4.3k 0.4× 1.1k 0.5× 2.5k 1.0× 2.6k 1.1× 1.7k 0.8× 226 10.2k
Elizabeth D. Getzoff United States 62 7.6k 0.6× 1.5k 0.6× 691 0.3× 2.0k 0.9× 1.1k 0.5× 149 14.4k
Yifan Cheng United States 67 16.6k 1.4× 2.2k 0.9× 501 0.2× 1.5k 0.6× 528 0.2× 213 25.5k
Tuomas P. J. Knowles United Kingdom 88 19.2k 1.6× 4.0k 1.6× 4.0k 1.7× 14.8k 6.4× 791 0.4× 465 32.9k
Nikolay V. Dokholyan United States 66 10.3k 0.9× 2.4k 1.0× 1.2k 0.5× 1.6k 0.7× 325 0.2× 370 14.7k
Anthony L. Fink United States 86 17.8k 1.5× 4.7k 1.9× 7.0k 2.9× 9.1k 4.0× 467 0.2× 231 28.7k
Yuji Goto Japan 79 15.7k 1.3× 4.2k 1.7× 800 0.3× 6.0k 2.6× 319 0.1× 377 21.7k

Countries citing papers authored by Thomas M. Jovin

Since Specialization
Citations

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

Fields of papers citing papers by Thomas M. Jovin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas M. Jovin. 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 Thomas M. Jovin. The network helps show where Thomas M. Jovin may publish in the future.

Co-authorship network of co-authors of Thomas M. Jovin

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas M. Jovin. A scholar is included among the top collaborators of Thomas M. Jovin 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 Thomas M. Jovin. Thomas M. Jovin 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.
Burgess, Antony W., Yoav I. Henis, Nancy E. Hynes, et al.. (2014). EGF receptor family: twisting targets for improved cancer therapies. Growth Factors. 32(2). 74–81. 6 indexed citations
2.
Bharde, Atul, Raghavendra Palankar, Cornelia Fritsch, et al.. (2013). Magnetic Nanoparticles as Mediators of Ligand-Free Activation of EGFR Signaling. PLoS ONE. 8(7). e68879–e68879. 40 indexed citations
3.
Dı́az, Sebastián A., Elizabeth A. Jares‐Erijman, & Thomas M. Jovin. (2011). Small Photostable Photoswitchable Quantum Dots as Nanotools for Live Cell Imaging. TechConnect Briefs. 3(2011). 205–208. 1 indexed citations
4.
Nagy, Péter, Jeroen Claus, Thomas M. Jovin, & Donna J. Arndt‐Jovin. (2010). Distribution of resting and ligand-bound ErbB1 and ErbB2 receptor tyrosine kinases in living cells using number and brightness analysis. Proceedings of the National Academy of Sciences. 107(38). 16524–16529. 129 indexed citations
5.
Bertoncini, Carlos W., Young‐Sang Jung, Claudio O. Fernández, et al.. (2005). Release of long-range tertiary interactions potentiates aggregation of natively unstructured α-synuclein. Proceedings of the National Academy of Sciences. 102(5). 1430–1435. 668 indexed citations breakdown →
6.
Friedländer, Elza, Donna J. Arndt‐Jovin, Péter Nagy, et al.. (2005). Signal transduction of erbB receptors in trastuzumab (Herceptin) sensitive and resistant cell lines: Local stimulation using magnetic microspheres as assessed by quantitative digital microscopy. Cytometry Part A. 67A(2). 161–171. 16 indexed citations
7.
Fernández, Claudio O., Wolfgang Hoyer, Markus Zweckstetter, et al.. (2004). NMR of α‐synuclein–polyamine complexes elucidates the mechanism and kinetics of induced aggregation. The EMBO Journal. 23(10). 2039–2046. 215 indexed citations
8.
Lidke, Diane S., Péter Nagy, Rainer Heintzmann, et al.. (2004). Real-time visualization of transmembrane receptor tyrosine kinase (erbB) dynamics using quantum dot ligands. Max Planck Institute for Plasma Physics. 86(1). 1 indexed citations
9.
Shchyolkina, Anna K., Dmitry N. Kaluzhny, Olga F. Borisova, et al.. (2003). Formation of the parallel recombination-type triplex by human telomeric sequences. Journal of Biomolecular Structure and Dynamics. 20(6). 868–869. 1 indexed citations
10.
Nagy, Péter, Donna J. Arndt‐Jovin, & Thomas M. Jovin. (2003). Small interfering RNAs suppress the expression of endogenous and GFP-fused epidermal growth factor receptor (erbB1) and induce apoptosis in erbB1-overexpressing cells. Experimental Cell Research. 285(1). 39–49. 82 indexed citations
11.
Nagy, Péter, György Vereb, Zsolt Sebestyén, et al.. (2002). Lipid rafts and the local density of ErbB proteins influence the biological role of homo- and heteroassociations of ErbB2. Journal of Cell Science. 115(22). 4251–4262. 150 indexed citations
12.
Shchyolkina, Anna K., L. E. Minchenkova, Elvira E. Minyat, et al.. (1998). Distamycin-stabilized Antiparallel-Parallel Combination (APC) DNA. Journal of Biomolecular Structure and Dynamics. 15(5). 823–839. 3 indexed citations
13.
Paleček, Emil, Veronika Staňková, Václav Brázda, et al.. (1997). Tumor suppressor protein p53 binds preferentially to supercoiled DNA. Oncogene. 15(18). 2201–2209. 74 indexed citations
14.
Pietrasanta, Lı́a I., A. Schaper, Geoffrey Fox, Francisco J. Barrantes, & Thomas M. Jovin. (1996). Imaging the Electrocyte of Torpedo Marmorata by Scanning Force Microscopy. Biophysical Journal. 10(2). 963–974. 1 indexed citations
15.
Rippe, Karsten, et al.. (1994). Parallel-stranded duplex DNA containing blocks of trans purine-purine and purine-pyrimidine base pairs. Nucleic Acids Research. 22(16). 3293–3303. 42 indexed citations
16.
Fritzsche, H., et al.. (1993). Structure and Drug interaction of parellel-stranded DNA studies by infrared spectroscope and fluorence. Nucleic Acids Research. 21(22). 5085–5091. 56 indexed citations
17.
18.
Clegg, Robert M., et al.. (1990). SENSITIVE AND RAPID DETERMINATIONS OF FLUORESCENCE LIFETIMES IN THE FREQUENCY-DOMAIN IN A LIGHT-MICROSCOPE. Biophysical Journal. 57(2). 2 indexed citations
19.
Krakow, Joseph S., Gary Rhodes, & Thomas M. Jovin. (1976). RNA Polymerase: Catalytic Mechanisms and Inhibitors. Cold Spring Harbor Monograph Archive. 6. 127–157. 12 indexed citations
20.
Bähr, Wolfgang, et al.. (1976). Binding of Rifampicin to Escherichia coli RNA Polymerase: Thermodynamic and Kinetic Studies. Cold Spring Harbor Monograph Archive. 6. 369–396. 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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