David S. Gross

2.6k total citations
52 papers, 1.9k citations indexed

About

David S. Gross is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, David S. Gross has authored 52 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 6 papers in Cell Biology and 5 papers in Plant Science. Recurrent topics in David S. Gross's work include Heat shock proteins research (25 papers), Genomics and Chromatin Dynamics (24 papers) and RNA Research and Splicing (22 papers). David S. Gross is often cited by papers focused on Heat shock proteins research (25 papers), Genomics and Chromatin Dynamics (24 papers) and RNA Research and Splicing (22 papers). David S. Gross collaborates with scholars based in United States, United Kingdom and Japan. David S. Gross's co-authors include William T. Garrard, Alexander M. Erkine, Christopher C. Adams, Amoldeep S. Kainth, David Pincus, Jing Zhao, Henry Simpkins, Jayamani Anandhakumar, Sunyoung Kim and Lu Gao and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

David S. Gross

51 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David S. Gross United States 28 1.7k 238 231 152 97 52 1.9k
Daniel C. Masison United States 34 3.5k 2.1× 621 2.6× 190 0.8× 100 0.7× 129 1.3× 78 3.7k
Eman Basha United States 16 1.9k 1.1× 317 1.3× 282 1.2× 137 0.9× 77 0.8× 31 2.2k
Claes Andréasson Sweden 25 1.4k 0.8× 518 2.2× 101 0.4× 69 0.5× 112 1.2× 40 1.5k
С. Г. Инге-Вечтомов Russia 26 3.9k 2.3× 301 1.3× 147 0.6× 201 1.3× 47 0.5× 149 4.1k
Jens Tyedmers Germany 18 1.7k 1.0× 694 2.9× 75 0.3× 191 1.3× 156 1.6× 28 2.2k
Vitaly V. Kushnirov Russia 28 4.8k 2.8× 554 2.3× 171 0.7× 140 0.9× 57 0.6× 59 5.0k
David Balchin Germany 11 1.2k 0.7× 329 1.4× 46 0.2× 108 0.7× 53 0.5× 17 1.5k
Monika Ehrnsperger Germany 9 1.6k 1.0× 390 1.6× 36 0.2× 111 0.7× 80 0.8× 9 1.8k
Jens Demand Germany 7 1.1k 0.6× 380 1.6× 38 0.2× 54 0.4× 46 0.5× 9 1.2k
B. S. Cox United Kingdom 29 3.3k 2.0× 190 0.8× 590 2.6× 272 1.8× 30 0.3× 51 3.6k

Countries citing papers authored by David S. Gross

Since Specialization
Citations

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

Fields of papers citing papers by David S. Gross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David S. Gross. 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 David S. Gross. The network helps show where David S. Gross may publish in the future.

Co-authorship network of co-authors of David S. Gross

This figure shows the co-authorship network connecting the top 25 collaborators of David S. Gross. A scholar is included among the top collaborators of David S. Gross 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 David S. Gross. David S. Gross 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.
2.
Kainth, Amoldeep S., et al.. (2022). Inducible transcriptional condensates drive 3D genome reorganization in the heat shock response. Molecular Cell. 82(22). 4386–4399.e7. 42 indexed citations
3.
Mohajan, Suman, et al.. (2022). Phase-separation antagonists potently inhibit transcription and broadly increase nucleosome density. Journal of Biological Chemistry. 298(10). 102365–102365. 9 indexed citations
4.
Kainth, Amoldeep S., et al.. (2019). Chromosome conformation capture that detects novel cis- and trans-interactions in budding yeast. Methods. 170. 4–16. 8 indexed citations
5.
Kainth, Amoldeep S., et al.. (2019). Heat Shock Factor 1 Drives Intergenic Association of Its Target Gene Loci upon Heat Shock. Cell Reports. 26(1). 18–28.e5. 51 indexed citations
6.
Pincus, David, Jayamani Anandhakumar, Prathapan Thiru, et al.. (2018). Genetic and epigenetic determinants establish a continuum of Hsf1 occupancy and activity across the yeast genome. Molecular Biology of the Cell. 29(26). 3168–3182. 42 indexed citations
7.
Anandhakumar, Jayamani, et al.. (2016). Evidence for Multiple Mediator Complexes in Yeast Independently Recruited by Activated Heat Shock Factor. Molecular and Cellular Biology. 36(14). 1943–1960. 47 indexed citations
8.
Gross, David S., et al.. (2015). Chromatin. Current Biology. 25(24). R1158–R1163. 9 indexed citations
9.
Kim, Sunyoung & David S. Gross. (2013). Mediator Recruitment to Heat Shock Genes Requires Dual Hsf1 Activation Domains and Mediator Tail Subunits Med15 and Med16. Journal of Biological Chemistry. 288(17). 12197–12213. 58 indexed citations
10.
Kim, Sunyoung, et al.. (2012). Role of Mediator in Regulating Pol II Elongation and Nucleosome Displacement in Saccharomyces cerevisiae. Genetics. 191(1). 95–106. 33 indexed citations
11.
Kim, Sunyoung, et al.. (2011). p53 Interacts with RNA Polymerase II through Its Core Domain and Impairs Pol II Processivity In Vivo. PLoS ONE. 6(8). e22183–e22183. 9 indexed citations
12.
Gao, Lu & David S. Gross. (2008). Sir2 Silences Gene Transcription by Targeting the Transition between RNA Polymerase II Initiation and Elongation. Molecular and Cellular Biology. 28(12). 3979–3994. 41 indexed citations
13.
Zhao, Jing, et al.. (2005). Domain-Wide Displacement of Histones by Activated Heat Shock Factor Occurs Independently of Swi/Snf and Is Not Correlated with RNA Polymerase II Density. Molecular and Cellular Biology. 25(20). 8985–8999. 123 indexed citations
14.
Pirrotta, Vincenzo & David S. Gross. (2005). Epigenetic Silencing Mechanisms in Budding Yeast and Fruit Fly: Different Paths, Same Destinations. Molecular Cell. 18(4). 395–398. 49 indexed citations
15.
Erkine, Alexander M., et al.. (2000). Cell Cycle-Dependent Binding of Yeast Heat Shock Factor to Nucleosomes. Molecular and Cellular Biology. 20(17). 6435–6448. 22 indexed citations
16.
Raitt, Desmond C., Anthony L. Johnson, Alexander M. Erkine, et al.. (2000). The Skn7 Response Regulator ofSaccharomyces cerevisiaeInteracts with Hsf1 In Vivo and Is Required for the Induction of Heat Shock Genes by Oxidative Stress. Molecular Biology of the Cell. 11(7). 2335–2347. 144 indexed citations
17.
Gross, David S., et al.. (1997). A single-tube RNA prep for northern analysis from yeast and other cell types. 2(1). 4–5. 1 indexed citations
18.
Erkine, Alexandre M., Christopher C. Adams, Ming Gao, & David S. Gross. (1995). Multiple protein-DNA interactions over the yeast HSC82 heat shock gene promoter. Nucleic Acids Research. 23(10). 1822–1829. 26 indexed citations
19.
Lee, Seewoo & David S. Gross. (1993). Conditional Silencing: The HMRE Mating-Type Silencer Exerts a Rapidly Reversible Position Effect on the Yeast HSP82 Heat Shock Gene. Molecular and Cellular Biology. 13(2). 727–738. 10 indexed citations
20.
Caplan, Avrom J., Myeong‐Sok Lee, Christopher C. Adams, et al.. (1989). Basal-Level Expression of the Yeast HSP82 Gene Requires a Heat Shock Regulatory Element. Molecular and Cellular Biology. 9(11). 4789–4798. 21 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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