Mary Sopta

1.8k total citations
24 papers, 1.5k citations indexed

About

Mary Sopta is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Mary Sopta has authored 24 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Oncology. Recurrent topics in Mary Sopta's work include Genomics and Chromatin Dynamics (8 papers), Fungal and yeast genetics research (7 papers) and RNA and protein synthesis mechanisms (5 papers). Mary Sopta is often cited by papers focused on Genomics and Chromatin Dynamics (8 papers), Fungal and yeast genetics research (7 papers) and RNA and protein synthesis mechanisms (5 papers). Mary Sopta collaborates with scholars based in Croatia, Canada and United States. Mary Sopta's co-authors include Jack Greenblatt, Ana Traven, Zachary F. Burton, Branka Jeličić, Richard W. Carthew, C. James Ingles, Ivica Rubelj, Deming Xu, Johnson M. S. Wong and Robert A. Phillips and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Mary Sopta

23 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary Sopta Croatia 15 1.2k 244 233 99 98 24 1.5k
Joachim Schnier United States 20 1.3k 1.1× 174 0.7× 228 1.0× 26 0.3× 70 0.7× 40 1.5k
Yoshiki Ohba Japan 21 868 0.7× 260 1.1× 121 0.5× 54 0.5× 51 0.5× 36 1.2k
Susan E. Conrad United States 26 934 0.8× 521 2.1× 345 1.5× 92 0.9× 55 0.6× 41 1.4k
Patrick H. Thibodeau United States 19 823 0.7× 126 0.5× 195 0.8× 67 0.7× 132 1.3× 32 1.3k
Linda J. Wheeler United States 17 1.1k 0.9× 201 0.8× 178 0.8× 77 0.8× 67 0.7× 30 1.3k
Kinichiro Oda Japan 21 898 0.7× 381 1.6× 345 1.5× 157 1.6× 73 0.7× 42 1.4k
Qi Hu United States 17 1.0k 0.9× 142 0.6× 121 0.5× 31 0.3× 99 1.0× 29 1.3k
Amy J. Malhowski United States 9 800 0.7× 216 0.9× 215 0.9× 69 0.7× 80 0.8× 9 1.1k
Hugo Würtele Canada 18 1.2k 1.0× 155 0.6× 131 0.6× 34 0.3× 163 1.7× 40 1.4k
Monica Hirsch‐Kauffmann Austria 23 1.1k 0.9× 321 1.3× 276 1.2× 102 1.0× 106 1.1× 70 1.4k

Countries citing papers authored by Mary Sopta

Since Specialization
Citations

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

Fields of papers citing papers by Mary Sopta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mary Sopta

This figure shows the co-authorship network connecting the top 25 collaborators of Mary Sopta. A scholar is included among the top collaborators of Mary Sopta 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 Mary Sopta. Mary Sopta 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.
Wang, Qi, Jiyoti Verma, Yanan Wang, et al.. (2020). The YEATS Domain Histone Crotonylation Readers Control Virulence-Related Biology of a Major Human Pathogen. Cell Reports. 31(3). 107528–107528. 21 indexed citations
2.
Sopta, Mary, et al.. (2017). Telomeres, Nutrition, and Longevity: Can We Really Navigate Our Aging?. The Journals of Gerontology Series A. 73(1). 39–47. 59 indexed citations
3.
Sopta, Mary, et al.. (2017). A meta-analysis reveals complex regulatory properties at Taf14-repressed genes. BMC Genomics. 18(1). 175–175. 5 indexed citations
4.
Šimatović, Ana, et al.. (2016). The Walker A motif mutation recA4159 abolishes the SOS response and recombination in a recA730 mutant of Escherichia coli. Research in Microbiology. 167(6). 462–471. 2 indexed citations
5.
Jeličić, Branka, et al.. (2013). The two faces of Cdk8, a positive/negative regulator of transcription. Biochimie. 97. 22–27. 94 indexed citations
6.
Jeličić, Branka, et al.. (2013). Solvent-exposed serines in the Gal4 DNA-binding domain are required for promoter occupancy and transcriptional activationin vivo. FEMS Yeast Research. 14(2). 302–309. 2 indexed citations
7.
Sopta, Mary, et al.. (2008). Telomerase regulation at the crossroads of cell fate. Cytogenetic and Genome Research. 122(3-4). 263–272. 58 indexed citations
8.
Matulić, Maja, Mary Sopta, & Ivica Rubelj. (2007). Telomere dynamics: the means to an end. Cell Proliferation. 40(4). 462–474. 6 indexed citations
9.
Saint‐Ruf, Claude, et al.. (2007). Causes and Consequences of DNA Repair Activity Modulation During Stationary Phase inEscherichia coli. Critical Reviews in Biochemistry and Molecular Biology. 42(4). 259–270. 27 indexed citations
10.
Traven, Ana, Branka Jeličić, & Mary Sopta. (2006). review Yeast Gal4: a transcriptional paradigm revisited.
11.
Traven, Ana, et al.. (2005). Mitochondrial dysfunction enhances Gal4-dependent transcription. FEMS Microbiology Letters. 253(2). 207–213. 2 indexed citations
12.
Arnerić, Milica, et al.. (2002). The Retinoblastoma Family of Proteins Directly Represses Transcription in Saccharomyces cerevisiae. Journal of Biological Chemistry. 277(11). 8797–8801. 2 indexed citations
13.
Traven, Ana, Johnson M. S. Wong, Deming Xu, Mary Sopta, & C. James Ingles. (2001). Interorganellar Communication. Journal of Biological Chemistry. 276(6). 4020–4027. 179 indexed citations
14.
Winegarden, Neil, Ken Wong, Mary Sopta, & J. Timothy Westwood. (1996). Sodium Salicylate Decreases Intracellular ATP, Induces Both Heat Shock Factor Binding and Chromosomal Puffing, but Does Not Induce hsp 70 Gene Transcription in Drosophila. Journal of Biological Chemistry. 271(43). 26971–26980. 57 indexed citations
15.
Bremner, Rod, Brenda Cohen, Mary Sopta, et al.. (1995). Direct Transcriptional Repression by pRB and Its Reversal by Specific Cyclins. Molecular and Cellular Biology. 15(6). 3256–3265. 161 indexed citations
16.
Zacksenhaus, Eldad, Rod Bremner, Zhe Jiang, et al.. (1993). Unraveling the Function of the Retinoblastoma Gene. Advances in cancer research. 61. 115–141. 41 indexed citations
17.
Phillips, Robert A., R. Gill, Eldad Zacksenhaus, et al.. (1992). Why Don’t Germline Mutations in RB1 Predispose to Leukemia?. Current topics in microbiology and immunology. 182. 485–491. 14 indexed citations
18.
Sopta, Mary, Zachary F. Burton, & Jack Greenblatt. (1989). Structure and associated DNA-helicase activity of a general transcription initiation factor that binds to RNA polymerase II. Nature. 341(6241). 410–414. 164 indexed citations
19.
Burton, Zachary F., et al.. (1988). RAP30/74: A General Initiation Factor That Binds to RNA Polymerase II. Molecular and Cellular Biology. 8(4). 1602–1613. 43 indexed citations
20.
Burton, Zachary F., et al.. (1988). RAP30/74: a general initiation factor that binds to RNA polymerase II.. Molecular and Cellular Biology. 8(4). 1602–1613. 106 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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