Vincent W. Coljee

1.3k total citations
29 papers, 1.0k citations indexed

About

Vincent W. Coljee is a scholar working on Molecular Biology, Ecology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Vincent W. Coljee has authored 29 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 11 papers in Ecology and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Vincent W. Coljee's work include DNA and Nucleic Acid Chemistry (19 papers), Bacteriophages and microbial interactions (11 papers) and Advanced biosensing and bioanalysis techniques (9 papers). Vincent W. Coljee is often cited by papers focused on DNA and Nucleic Acid Chemistry (19 papers), Bacteriophages and microbial interactions (11 papers) and Advanced biosensing and bioanalysis techniques (9 papers). Vincent W. Coljee collaborates with scholars based in United States, Denmark and France. Vincent W. Coljee's co-authors include Mara Prentiss, Claudia Danilowicz, David R. Nelson, Cédric Bouzigues, David K. Lubensky, Vincent J. Cristofalo, Nancy Kleckner, Mitch O. Rotenberg, Søren Bregenholt and John S. Haurum and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Physical Review Letters.

In The Last Decade

Vincent W. Coljee

28 papers receiving 971 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent W. Coljee United States 18 785 224 174 154 130 29 1.0k
David Izhaky Israel 13 651 0.8× 499 2.2× 214 1.2× 119 0.8× 64 0.5× 16 1.4k
Wesley P. Wong United States 18 789 1.0× 391 1.7× 557 3.2× 67 0.4× 133 1.0× 41 1.7k
Andrea Holt Netherlands 14 719 0.9× 151 0.7× 157 0.9× 196 1.3× 38 0.3× 15 1.1k
Michael M. Baksh United States 14 451 0.6× 108 0.5× 158 0.9× 64 0.4× 73 0.6× 21 757
Jean‐Marc Victor France 24 1.6k 2.0× 89 0.4× 143 0.8× 73 0.5× 70 0.5× 51 2.0k
David Grünwald United States 25 2.0k 2.6× 130 0.6× 323 1.9× 67 0.4× 40 0.3× 46 2.8k
Christian Zahnd Switzerland 11 1.1k 1.3× 178 0.8× 184 1.1× 849 5.5× 104 0.8× 12 1.5k
Benedict Hébert Canada 9 628 0.8× 197 0.9× 292 1.7× 72 0.5× 47 0.4× 10 1.3k
Bram van den Broek Netherlands 24 1.1k 1.3× 110 0.5× 279 1.6× 24 0.2× 98 0.8× 42 1.6k
Johannes B. Woehrstein United States 11 1.3k 1.7× 87 0.4× 636 3.7× 76 0.5× 147 1.1× 12 1.9k

Countries citing papers authored by Vincent W. Coljee

Since Specialization
Citations

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

Fields of papers citing papers by Vincent W. Coljee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent W. Coljee. 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 Vincent W. Coljee. The network helps show where Vincent W. Coljee may publish in the future.

Co-authorship network of co-authors of Vincent W. Coljee

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent W. Coljee. A scholar is included among the top collaborators of Vincent W. Coljee 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 Vincent W. Coljee. Vincent W. Coljee 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.
Danilowicz, Claudia, et al.. (2017). ATP hydrolysis provides functions that promote rejection of pairings between different copies of long repeated sequences. Nucleic Acids Research. 45(14). 8448–8462. 17 indexed citations
2.
Coljee, Vincent W., et al.. (2015). ssDNA Pairing Accuracy Increases When Abasic Sites Divide Nucleotides into Small Groups. PLoS ONE. 10(6). e0130875–e0130875. 3 indexed citations
3.
Vlassakis, Julea, Efraim Feinstein, Darren Yang, et al.. (2013). Tension on dsDNA bound to ssDNA-RecA filaments may play an important role in driving efficient and accurate homology recognition and strand exchange. Physical Review E. 87(3). 16 indexed citations
4.
Wang, Xianzhe, Vincent W. Coljee, & Jennifer A. Maynard. (2013). Back to the future: recombinant polyclonal antibody therapeutics. Current Opinion in Chemical Engineering. 2(4). 405–415. 28 indexed citations
5.
Yang, Darren, et al.. (2012). Complementary strand relocation may play vital roles in RecA-based homology recognition. Nucleic Acids Research. 40(20). 10441–10451. 22 indexed citations
6.
Danilowicz, Claudia, Efraim Feinstein, Vincent W. Coljee, et al.. (2011). RecA homology search is promoted by mechanical stress along the scanned duplex DNA. Nucleic Acids Research. 40(4). 1717–1727. 26 indexed citations
7.
Danilowicz, Claudia, et al.. (2011). Changes in the tension in dsDNA alter the conformation of RecA bound to dsDNA–RecA filaments. Nucleic Acids Research. 39(20). 8833–8843. 12 indexed citations
8.
Danilowicz, Claudia, et al.. (2010). Study of force induced melting of dsDNA as a function of length and conformation. Journal of Physics Condensed Matter. 22(41). 414106–414106. 6 indexed citations
9.
Danilowicz, Claudia, et al.. (2009). Single molecule detection of direct, homologous, DNA/DNA pairing. Proceedings of the National Academy of Sciences. 106(47). 19824–19829. 60 indexed citations
10.
11.
Danilowicz, Claudia, et al.. (2007). Direct measurements of the stabilization of single-stranded DNA under tension by single-stranded binding proteins. Physical Review E. 76(2). 21916–21916. 13 indexed citations
12.
Danilowicz, Claudia, et al.. (2007). Effects of temperature on the mechanical properties of single stranded DNA. Physical Review E. 75(3). 30902–30902. 17 indexed citations
13.
Danilowicz, Claudia, et al.. (2007). Measurement of the salt-dependent stabilization of partially open DNA by Escherichia coli SSB protein. Nucleic Acids Research. 36(1). 294–299. 24 indexed citations
14.
Meijer, Per‐Johan, Peter S. Andersen, Margit Haahr Hansen, et al.. (2006). Isolation of Human Antibody Repertoires with Preservation of the Natural Heavy and Light Chain Pairing. Journal of Molecular Biology. 358(3). 764–772. 95 indexed citations
15.
Andersen, Peter S., et al.. (2006). Extensive restrictions in the VH sequence usage of the human antibody response against the Rhesus D antigen. Molecular Immunology. 44(4). 412–422. 25 indexed citations
16.
Danilowicz, Claudia, et al.. (2006). Comparison of the measured phase diagrams in the force-temperature plane for the unzipping of two different natural DNA sequences. The European Physical Journal E. 19(3). 339–344. 4 indexed citations
17.
Wiberg, Finn C., Søren K. Rasmussen, Torben P. Frandsen, et al.. (2006). Production of target‐specific recombinant human polyclonal antibodies in mammalian cells. Biotechnology and Bioengineering. 94(2). 396–405. 63 indexed citations
18.
Danilowicz, Claudia, et al.. (2004). Measurement of the Phase Diagram of DNA Unzipping in the Temperature-Force Plane. Physical Review Letters. 93(7). 78101–78101. 80 indexed citations
19.
Murray, Heather L., Svetlana A. Mikheeva, Vincent W. Coljee, et al.. (2001). Excision of Group II Introns as Circles. Molecular Cell. 8(1). 201–211. 49 indexed citations
20.
Coljee, Vincent W., Heather L. Murray, William F. Donahue, & Kevin A. Jarrell. (2000). Seamless gene engineering using RNA- and DNA-overhang cloning. Nature Biotechnology. 18(7). 789–791. 15 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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