Suse Broyde

7.5k total citations
221 papers, 6.2k citations indexed

About

Suse Broyde is a scholar working on Molecular Biology, Cancer Research and Organic Chemistry. According to data from OpenAlex, Suse Broyde has authored 221 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 208 papers in Molecular Biology, 34 papers in Cancer Research and 29 papers in Organic Chemistry. Recurrent topics in Suse Broyde's work include DNA and Nucleic Acid Chemistry (175 papers), DNA Repair Mechanisms (103 papers) and RNA and protein synthesis mechanisms (45 papers). Suse Broyde is often cited by papers focused on DNA and Nucleic Acid Chemistry (175 papers), DNA Repair Mechanisms (103 papers) and RNA and protein synthesis mechanisms (45 papers). Suse Broyde collaborates with scholars based in United States, United Kingdom and China. Suse Broyde's co-authors include Brian E. Hingerty, Nicholas E. Geacintov, Dinshaw J. Patel, Monique Cosman, Yuqin Cai, Shantu Amin, Robert Shapiro, Lihua Wang, Yingkai Zhang and Seymour Steven Brody and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Suse Broyde

219 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Suse Broyde United States	43	5.6k	1.4k	685	511	501	221	6.2k
Carmelo J. Rizzo United States	35	3.0k 0.5×	859 0.6×	834 1.2×	243 0.5×	255 0.5×	145	4.2k
Brian E. Hingerty United States	35	3.5k 0.6×	790 0.6×	767 1.1×	375 0.7×	201 0.4×	122	4.5k
I.J. Clifton United Kingdom	34	3.8k 0.7×	1.3k 0.9×	378 0.6×	680 1.3×	267 0.5×	79	5.8k
Ziro Yamaizumi United Kingdom	32	3.1k 0.6×	854 0.6×	338 0.5×	614 1.2×	207 0.4×	93	4.4k
P.D. Lawley United Kingdom	44	4.4k 0.8×	2.0k 1.5×	799 1.2×	688 1.3×	339 0.7×	91	6.1k
Ward W. Smith United States	28	2.0k 0.4×	431 0.3×	506 0.7×	583 1.1×	211 0.4×	38	3.4k
Thomas D. Tullius United States	42	5.2k 0.9×	200 0.1×	870 1.3×	1.0k 2.0×	723 1.4×	84	6.6k
Richard N. Armstrong United States	45	5.7k 1.0×	198 0.1×	594 0.9×	497 1.0×	414 0.8×	142	7.4k
I. Goldberg United States	45	5.5k 1.0×	412 0.3×	2.9k 4.2×	898 1.8×	360 0.7×	186	7.7k
Kent S. Gates United States	37	2.9k 0.5×	542 0.4×	1.8k 2.6×	321 0.6×	111 0.2×	154	4.6k

Countries citing papers authored by Suse Broyde

Since Specialization

Citations

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

Fields of papers citing papers by Suse Broyde

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suse Broyde

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Paul, Debamita, Hong Mu, Qing Dai, et al.. (2020). Tethering-facilitated DNA ‘opening’ and complementary roles of β-hairpin motifs in the Rad4/XPC DNA damage sensor protein. Nucleic Acids Research. 48(21). 12348–12364. 11 indexed citations

Cai, Yuqin, Nicholas E. Geacintov, & Suse Broyde. (2019). Variable impact of conformationally distinct DNA lesions on nucleosome structure and dynamics: Implications for nucleotide excision repair. DNA repair. 87. 102768–102768. 9 indexed citations

Steinbach, Peter, Debamita Paul, Hong Mu, et al.. (2017). Enhanced spontaneous DNA twisting/bending fluctuations unveiled by fluorescence lifetime distributions promote mismatch recognition by the Rad4 nucleotide excision repair complex. Nucleic Acids Research. 46(3). 1240–1255. 20 indexed citations

Wickramaratne, Susith, Shaofei Ji, Yan Ru Su, et al.. (2016). Bypass of DNA-Protein Cross-links Conjugated to the 7-Deazaguanine Position of DNA by Translesion Synthesis Polymerases. Journal of Biological Chemistry. 291(45). 23589–23603. 35 indexed citations

Tang, Yijin, Zhi Liu, Shuang Ding, et al.. (2012). Nuclear Magnetic Resonance Solution Structure of an N²-Guanine DNA Adduct Derived from the Potent Tumorigen Dibenzo[a,l]pyrene: Intercalation from the Minor Groove with Ruptured Watson–Crick Base Pairing. Biochemistry. 51(48). 9751–9762. 11 indexed citations

Wang, Lihua, et al.. (2012). Preferred WMSA catalytic mechanism of the nucleotidyl transfer reaction in human DNA polymerase κ elucidates error-free bypass of a bulky DNA lesion. Nucleic Acids Research. 40(18). 9193–9205. 31 indexed citations

Broyde, Suse, et al.. (2009). Influence of local sequence context on damaged base conformation in human DNA polymerase ι: molecular dynamics studies of nucleotide incorporation opposite a benzo[a]pyrene-derived adenine lesion. Nucleic Acids Research. 37(21). 7095–7109. 14 indexed citations

Kropachev, Konstantin, Yuqin Cai, Yang Liu, et al.. (2009). The Sequence Dependence of Human Nucleotide Excision Repair Efficiencies of Benzo[a]pyrene-derived DNA Lesions: Insights into the Structural Factors that Favor Dual Incisions. Journal of Molecular Biology. 386(5). 1193–1203. 57 indexed citations

Ding, Shuang, Alexander Kolbanovskiy, Alexander Durandin, et al.. (2009). Absolute configurations of DNA lesions determined by comparisons of experimental ECD and ORD spectra with DFT calculations. Chirality. 21(1E). E231–41. 20 indexed citations

10.

Rechkoblit, Olga, Lucy Malinina, Yuan Cheng, et al.. (2009). Impact of Conformational Heterogeneity of OxoG Lesions and Their Pairing Partners on Bypass Fidelity by Y Family Polymerases. Structure. 17(5). 725–736. 28 indexed citations

11.

Mocquet, Vincent, Konstantin Kropachev, Marina Kolbanovskiy, et al.. (2007). The human DNA repair factor XPC‐HR23B distinguishes stereoisomeric benzo[a]pyrenyl‐DNA lesions. The EMBO Journal. 26(12). 2923–2932. 80 indexed citations

12.

Goodenough, Angela K., et al.. (2007). Transcription Processing at 1,N2-Ethenoguanine by Human RNA Polymerase II and Bacteriophage T7 RNA Polymerase. Journal of Molecular Biology. 375(2). 353–366. 21 indexed citations

13.

Chen, Dandan, Alexander Kolbanovskiy, Shuang Ding, et al.. (2006). Nucleotide excision repair of DNA adducts derived from the binding of the equine estrogen metabolite 4-OHEN to dC and dA adducts in vitro.. Cancer Research. 66. 1232–1232. 1 indexed citations

14.

Zhang, Na, Xuanwei Huang, Brian E. Hingerty, et al.. (2005). Methylation of Cytosine at C5 in a CpG Sequence Context Causes a Conformational Switch of a Benzo[a]pyrene diol epoxide-N2-guanine Adduct in DNA from a Minor Groove Alignment to Intercalation with Base Displacement. Journal of Molecular Biology. 346(4). 951–965. 46 indexed citations

15.

Wang, Lihua, Brian E. Hingerty, A. R. Srinivasan, Wilma K. Olson, & Suse Broyde. (2002). Accurate Representation of B-DNA Double Helical Structure with Implicit Solvent and Counterions. Biophysical Journal. 83(1). 382–406. 24 indexed citations

16.

Yang, Linjing, William A. Beard, Samuel H. Wilson, et al.. (2002). Local Deformations Revealed by Dynamics Simulations of DNA Polymerase β with DNA Mismatches at the Primer Terminus. Journal of Molecular Biology. 321(3). 459–478. 47 indexed citations

17.

Broyde, Suse. (1996). Setting the stage for predicting RNA thermodynamic properties and their structural components. Biophysical Journal. 70(4). 1571–1572. 2 indexed citations

18.

Cosman, Monique, Radovan Fiala, Brian E. Hingerty, et al.. (1995). Solution Conformation of the (-)-trans-anti-Benzo[c]phenanthrene-dA ([BPh]dA) Adduct opposite dT in a DNA Duplex: Intercalation of the Covalently Attached Benzo[c]phenanthrenyl Ring to the 3'-Side of the Adduct Site and Comparison with the (+)-trans-anti-[BPh]dA opposite dT Stereoisomer. Biochemistry. 34(4). 1295–1307. 56 indexed citations

19.

Jacobson, Michael D., Robert Shapiro, Graham R. Underwood, et al.. (1988). Synthesis and conformation of a dinucleoside monophosphate modified by aniline. Chemical Research in Toxicology. 1(3). 152–159. 17 indexed citations

20.

Hingerty, Brian E. & Suse Broyde. (1986). Energy Minimized Structures of Carcinogen-DNA. Adducts: 2-Acetylaminofluorene and 2-Aminofluorene. Journal of Biomolecular Structure and Dynamics. 4(3). 365–372. 32 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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