Debbie Yaver

4.5k total citations · 1 hit paper
24 papers, 2.9k citations indexed

About

Debbie Yaver is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Debbie Yaver has authored 24 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Cell Biology and 8 papers in Plant Science. Recurrent topics in Debbie Yaver's work include Fungal and yeast genetics research (8 papers), Enzyme-mediated dye degradation (6 papers) and Microbial Natural Products and Biosynthesis (5 papers). Debbie Yaver is often cited by papers focused on Fungal and yeast genetics research (8 papers), Enzyme-mediated dye degradation (6 papers) and Microbial Natural Products and Biosynthesis (5 papers). Debbie Yaver collaborates with scholars based in United States, Denmark and Austria. Debbie Yaver's co-authors include Daniel J. Klionsky, Stephen H.M. Brown, Rosario Cueva, Elizabeth J. Golightly, Randy M. Berka, Uvidelio Castillo, James B. Jensen, Gary A. Strobel, W. M. Hess and David B. Teplow 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

Debbie Yaver

24 papers receiving 2.7k citations

Hit Papers

Plectasin is a peptide antibiotic with therapeutic potent... 2005 2026 2012 2019 2005 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Debbie Yaver United States 19 1.3k 1.2k 692 547 537 24 2.9k
Antonio G. Pisabarro Spain 28 1.1k 0.8× 1.2k 1.0× 381 0.6× 825 1.5× 238 0.4× 73 2.4k
András Szekeres Hungary 26 781 0.6× 1.2k 1.0× 191 0.3× 453 0.8× 527 1.0× 134 2.4k
Stephanie Grond Germany 25 1.5k 1.1× 509 0.4× 313 0.5× 834 1.5× 152 0.3× 74 2.7k
Ionel Ciucanu Romania 13 1.6k 1.2× 1.8k 1.5× 280 0.4× 406 0.7× 213 0.4× 29 3.9k
Yuzhi Hong China 27 752 0.6× 647 0.5× 618 0.9× 199 0.4× 74 0.1× 61 1.9k
Hexiang Wang China 34 1.5k 1.1× 1.4k 1.2× 717 1.0× 1.6k 2.9× 169 0.3× 112 3.4k
Sergio Sánchez Mexico 30 2.2k 1.7× 805 0.7× 1.1k 1.6× 1.3k 2.4× 177 0.3× 114 4.1k
Tamás Emri Hungary 26 1.5k 1.1× 885 0.7× 259 0.4× 598 1.1× 193 0.4× 113 2.2k
Yair Aharonowitz Israel 36 2.4k 1.8× 296 0.2× 324 0.5× 947 1.7× 115 0.2× 73 3.5k
U. Ståhl Germany 24 1.4k 1.1× 501 0.4× 306 0.4× 179 0.3× 147 0.3× 41 2.1k

Countries citing papers authored by Debbie Yaver

Since Specialization
Citations

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

Fields of papers citing papers by Debbie Yaver

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Debbie Yaver

This figure shows the co-authorship network connecting the top 25 collaborators of Debbie Yaver. A scholar is included among the top collaborators of Debbie Yaver 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 Debbie Yaver. Debbie Yaver 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.
Yaver, Debbie, et al.. (2022). A bioinformatic-assisted workflow for genome-wide identification of ncRNAs. NAR Genomics and Bioinformatics. 4(3). lqac059–lqac059. 4 indexed citations
2.
Mello-de-Sousa, Thiago Machado, et al.. (2021). The phenomenon of degeneration of industrial Trichoderma reesei strains. Biotechnology for Biofuels. 14(1). 193–193. 7 indexed citations
3.
Derntl, Christian, et al.. (2019). Regulation of gene expression by the action of a fungal lncRNA on a transactivator. RNA Biology. 17(1). 47–61. 11 indexed citations
4.
Brown, Stephen H.M., Randy M. Berka, Michael McCulloch, et al.. (2013). Metabolic engineering of Aspergillus oryzae NRRL 3488 for increased production of l-malic acid. Applied Microbiology and Biotechnology. 97(20). 8903–8912. 163 indexed citations
5.
Mygind, Per, Kirk Schnorr, Mogens Trier Hansen, et al.. (2005). Plectasin is a peptide antibiotic with therapeutic potential from a saprophytic fungus. Nature. 437(7061). 975–980. 533 indexed citations breakdown →
6.
Lin, Janine, et al.. (2005). Global Transcriptional Response of Bacillus subtilis to Treatment with Subinhibitory Concentrations of Antibiotics That Inhibit Protein Synthesis. Antimicrobial Agents and Chemotherapy. 49(5). 1915–1926. 99 indexed citations
7.
Castillo, Uvidelio, James K. Harper, Gary A. Strobel, et al.. (2003). Kakadumycins, novel antibiotics fromStreptomycessp. NRRL 30566, an endophyte ofGrevillea pteridifolia. FEMS Microbiology Letters. 224(2). 183–190. 148 indexed citations
8.
Yaver, Debbie, et al.. (2000). Using DNA-Tagged Mutagenesis to Improve Heterologous Protein Production in Aspergillus oryzae. Fungal Genetics and Biology. 29(1). 28–37. 28 indexed citations
9.
Xu, Feng, Amy E. Palmer, Debbie Yaver, et al.. (1999). Targeted Mutations in a Trametes villosa Laccase. Journal of Biological Chemistry. 274(18). 12372–12375. 159 indexed citations
10.
Yaver, Debbie, Feng Xu, Beth A. Nelson, et al.. (1999). Molecular Characterization of Laccase Genes from the Basidiomycete Coprinus cinereus and Heterologous Expression of the Laccase Lcc1. Applied and Environmental Microbiology. 65(11). 4943–4948. 80 indexed citations
11.
Brzozowski, A.M., Keith S. Wilson, Stephen H.M. Brown, et al.. (1998). Crystal structure of the type-2 Cu depleted laccase from Coprinus dnereus at 2.2 Å resolution. Nature Structural Biology. 5(4). 310–316. 274 indexed citations
12.
Ducros, V.M.-A., G.J. Davies, David M. Lawson, et al.. (1997). Crystallization and preliminary X-ray analysis of the laccase fromCoprinus cinereus. Acta Crystallographica Section D Biological Crystallography. 53(5). 605–607. 15 indexed citations
13.
14.
Golightly, Elizabeth J., et al.. (1995). Nucleotide sequence of the Aspergillus niger srpA gene. Gene. 167(1-2). 337–338. 10 indexed citations
15.
Yaver, Debbie, Hannah Nelson, Nathan Nelson, & Daniel J. Klionsky. (1993). Vacuolar ATPase mutants accumulate precursor proteins in a pre-vacuolar compartment. Journal of Biological Chemistry. 268(14). 10564–10572. 19 indexed citations
16.
Fournier, Philippe, Abdelhamid Abbas, Marion Chasles, et al.. (1993). Colocalization of centromeric and replicative functions on autonomously replicating sequences isolated from the yeast Yarrowia lipolytica.. Proceedings of the National Academy of Sciences. 90(11). 4912–4916. 77 indexed citations
17.
Klionsky, Daniel J., Rosario Cueva, & Debbie Yaver. (1992). Aminopeptidase I of Saccharomyces cerevisiae is localized to the vacuole independent of the secretory pathway.. The Journal of Cell Biology. 119(2). 287–299. 306 indexed citations
18.
Klionsky, Daniel J., Hannah Nelson, Nathan Nelson, & Debbie Yaver. (1992). Mutations in the yeast vacuolar ATPase result in the mislocalization of vacuolar proteins. Journal of Experimental Biology. 172(1). 83–92. 19 indexed citations
20.
He, Feng, Debbie Yaver, Jean-Marie Beckerich, David M. Ogrydziak, & C. Gaillardin. (1990). The yeast Yarrowia lipolytica has two, functional, signal recognition particle 7S RNA genes. Current Genetics. 17(4). 289–292. 26 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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