Catherine Dollard

2.6k total citations · 1 hit paper
16 papers, 2.2k citations indexed

About

Catherine Dollard is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Catherine Dollard has authored 16 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 4 papers in Plant Science and 3 papers in Genetics. Recurrent topics in Catherine Dollard's work include Fungal and yeast genetics research (8 papers), Genomics and Chromatin Dynamics (5 papers) and RNA and protein synthesis mechanisms (4 papers). Catherine Dollard is often cited by papers focused on Fungal and yeast genetics research (8 papers), Genomics and Chromatin Dynamics (5 papers) and RNA and protein synthesis mechanisms (4 papers). Catherine Dollard collaborates with scholars based in United States, Canada and Germany. Catherine Dollard's co-authors include Fred Winston, Stephanie L. Ricupero‐Hovasse, David M. Eisenmann, Stephan Beck, Igor B. Dawid, Susan R. Haynes, John Trowsdale, Clyde L. Denis, Jeffrey R. Shuster and Joel R. Cherry and has published in prestigious journals such as Cell, Nucleic Acids Research and Molecular and Cellular Biology.

In The Last Decade

Catherine Dollard

16 papers receiving 2.2k citations

Hit Papers

Construction of a set of convenient saccharomyces cerevis... 1995 2026 2005 2015 1995 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catherine Dollard United States 13 1.9k 358 180 177 133 16 2.2k
Gemma Bellı́ Spain 23 1.9k 1.0× 345 1.0× 74 0.4× 289 1.6× 103 0.8× 35 2.4k
Koei Okazaki Japan 18 1.3k 0.7× 373 1.0× 100 0.6× 315 1.8× 62 0.5× 32 1.6k
Bertrand Daignan‐Fornier France 29 2.3k 1.2× 371 1.0× 120 0.7× 314 1.8× 206 1.5× 70 2.7k
Andreas Hartig Austria 29 2.8k 1.5× 308 0.9× 117 0.7× 276 1.6× 99 0.7× 65 3.1k
Andrew St. Jean Canada 6 2.6k 1.4× 685 1.9× 208 1.2× 432 2.4× 93 0.7× 7 3.1k
Alexander J. Kastaniotis Finland 29 1.8k 1.0× 403 1.1× 82 0.5× 177 1.0× 77 0.6× 50 2.5k
Joanna Rytka Poland 24 1.8k 0.9× 236 0.7× 85 0.5× 318 1.8× 117 0.9× 77 2.0k
Albert J. J. van Ooyen Netherlands 20 1.4k 0.7× 294 0.8× 252 1.4× 64 0.4× 88 0.7× 34 1.7k
Peter A. Meacock United Kingdom 22 1.6k 0.8× 434 1.2× 474 2.6× 224 1.3× 199 1.5× 40 2.0k
Joan E. McEwen United States 23 1.7k 0.9× 208 0.6× 242 1.3× 109 0.6× 51 0.4× 38 2.1k

Countries citing papers authored by Catherine Dollard

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Dollard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Dollard

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

All Works

16 of 16 papers shown
1.
Thompson, Chelsea R., et al.. (2018). Epigenetic Regulation via Altered Histone Acetylation Results in Suppression of Mast Cell Function and Mast Cell-Mediated Food Allergic Responses. Frontiers in Immunology. 9. 2414–2414. 38 indexed citations
2.
Pan, Liangwen, Shuya Zhang, Litao Yang, et al.. (2007). Interlaboratory Trial Validation of an Event-Specific Qualitative Polymerase Chain Reaction-Based Detection Method for Genetically Modified RT73 Rapeseed. Journal of AOAC International. 90(6). 1639–1646. 11 indexed citations
3.
Ikawa, Miyoshi, et al.. (2003). Utilization of Folin−Ciocalteu Phenol Reagent for the Detection of Certain Nitrogen Compounds. Journal of Agricultural and Food Chemistry. 51(7). 1811–1815. 130 indexed citations
4.
Farid, A., Emily L. O’Reilly, Catherine Dollard, & Chris R. Kelsey. (2000). Genetic analysis of ten sheep breeds using microsatellite markers. Canadian Journal of Animal Science. 80(1). 9–17. 31 indexed citations
5.
Almudevar, Anthony, et al.. (1998). Classification of crossbred animals using microsatellites.. 208–211. 1 indexed citations
6.
Gansheroff, Lisa J., Catherine Dollard, Philip K. Tan, & Fred Winston. (1995). The Saccharomyces cerevisiae SPT7 gene encodes a very acidic protein important for transcription in vivo.. Genetics. 139(2). 523–536. 84 indexed citations
7.
Winston, Fred, Catherine Dollard, & Stephanie L. Ricupero‐Hovasse. (1995). Construction of a set of convenient saccharomyces cerevisiae strains that are isogenic to S288C. Yeast. 11(1). 53–55. 816 indexed citations breakdown →
8.
Eisenmann, David M., C Chapon, Samuel Roberts, Catherine Dollard, & Fred Winston. (1994). The Saccharomyces cerevisiae SPT8 gene encodes a very acidic protein that is functionally related to SPT3 and TATA-binding protein.. Genetics. 137(3). 647–657. 78 indexed citations
9.
Dollard, Catherine, Stephanie L. Ricupero‐Hovasse, Georges Natsoulis, Jef D. Boeke, & Fred Winston. (1994). SPT10 and SPT21 are required for transcription of particular histone genes in Saccharomyces cerevisiae.. Molecular and Cellular Biology. 14(8). 5223–5228. 73 indexed citations
10.
Dollard, Catherine, Stephanie L. Ricupero‐Hovasse, Georges Natsoulis, Jef D. Boeke, & Fred Winston. (1994). SPT10 and SPT21 Are Required for Transcription of Particular Histone Genes in Saccharomyces cerevisiae. Molecular and Cellular Biology. 14(8). 5223–5228. 30 indexed citations
11.
Haynes, Susan R., Catherine Dollard, Fred Winston, et al.. (1992). The bromodomain: a conserved sequence found in human,Drosophilaand yeast proteins. Nucleic Acids Research. 20(10). 2603–2603. 318 indexed citations
12.
Natsoulis, Georges, Catherine Dollard, Fred Winston, & Jef D. Boeke. (1991). The products of the SPT10 and SPT21 genes of Saccharomyces cerevisiae increase the amplitude of transcriptional regulation at a large number of unlinked loci.. PubMed. 3(12). 1249–59. 49 indexed citations
13.
Eisenmann, David M., Catherine Dollard, & Fred Winston. (1989). SPT15, the gene encoding the yeast TATA binding factor TFIID, is required for normal transcription initiation in vivo. Cell. 58(6). 1183–1191. 223 indexed citations
14.
Cherry, Joel R., et al.. (1989). Cyclic AMP-dependent protein kinase phosphorylates and inactivates the yeast transcriptional activator ADR1. Cell. 56(3). 409–419. 213 indexed citations
15.
Ikawa, Miyoshi, et al.. (1988). Reaction of Folin-Ciocalteau phenol reagent with purines, pyrimidines, and pteridines and its relationship to structure. Journal of Agricultural and Food Chemistry. 36(2). 309–311. 5 indexed citations
16.
Winston, Fred, et al.. (1987). Three Genes Are Required for trans-Activation of Ty Transcription in Yeast. Genetics. 115(4). 649–656. 95 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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