Editte Gharakhanian

832 total citations
22 papers, 675 citations indexed

About

Editte Gharakhanian is a scholar working on Molecular Biology, Cell Biology and Ecology. According to data from OpenAlex, Editte Gharakhanian has authored 22 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Cell Biology and 7 papers in Ecology. Recurrent topics in Editte Gharakhanian's work include Cellular transport and secretion (11 papers), Bacteriophages and microbial interactions (7 papers) and Polyomavirus and related diseases (6 papers). Editte Gharakhanian is often cited by papers focused on Cellular transport and secretion (11 papers), Bacteriophages and microbial interactions (7 papers) and Polyomavirus and related diseases (6 papers). Editte Gharakhanian collaborates with scholars based in United States. Editte Gharakhanian's co-authors include Scott D. Emr, Joan Lin Cereghino, Eric G. Marcusson, Bruce Horazdovsky, Harumi Kasamatsu, Surya P. Manandhar, Jared L. Clever, Joseph S. Takahashi, Daniel K. Olson and Ana Rosa Pérez and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Editte Gharakhanian

22 papers receiving 654 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Editte Gharakhanian United States 10 416 362 116 112 82 22 675
Hugo Matern Germany 11 793 1.9× 715 2.0× 110 0.9× 48 0.4× 21 0.3× 12 1.1k
Yongwang Zhong United States 18 484 1.2× 237 0.7× 128 1.1× 29 0.3× 34 0.4× 32 808
Per Malkus United States 12 917 2.2× 776 2.1× 101 0.9× 23 0.2× 39 0.5× 13 1.3k
Xiayang Xie United States 14 353 0.8× 202 0.6× 30 0.3× 67 0.6× 27 0.3× 16 657
Suzanne Gokool United Kingdom 13 327 0.8× 266 0.7× 34 0.3× 22 0.2× 33 0.4× 19 741
Phi Luong United States 11 304 0.7× 96 0.3× 171 1.5× 43 0.4× 20 0.2× 17 676
Raul Salinas United States 13 528 1.3× 46 0.1× 261 2.3× 120 1.1× 42 0.5× 24 869
Karen McGee Sweden 10 402 1.0× 304 0.8× 32 0.3× 47 0.4× 31 0.4× 12 799
Robert Gauss Germany 12 790 1.9× 667 1.8× 73 0.6× 32 0.3× 14 0.2× 13 1.1k
Evelyn Sattlegger New Zealand 17 860 2.1× 256 0.7× 84 0.7× 38 0.3× 15 0.2× 39 1.1k

Countries citing papers authored by Editte Gharakhanian

Since Specialization
Citations

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

Fields of papers citing papers by Editte Gharakhanian

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Editte Gharakhanian

This figure shows the co-authorship network connecting the top 25 collaborators of Editte Gharakhanian. A scholar is included among the top collaborators of Editte Gharakhanian 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 Editte Gharakhanian. Editte Gharakhanian 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.
Manandhar, Surya P., et al.. (2020). A kinase cascade on the yeast lysosomal vacuole regulates its membrane dynamics: conserved kinase Env7 is phosphorylated by casein kinase Yck3. Journal of Biological Chemistry. 295(34). 12262–12278. 4 indexed citations
2.
Ricci, Anthony J., et al.. (2018). The Hydrophobic Domain of ENV9 is a Lipid Droplet Localization Signal in Saccharomyces cerevisiae. The FASEB Journal. 32(S1). 1 indexed citations
3.
Manandhar, Surya P., et al.. (2017). Yeast ENV9 encodes a conserved lipid droplet (LD) short-chain dehydrogenase involved in LD morphology. Current Genetics. 63(6). 1053–1072. 12 indexed citations
4.
5.
Manandhar, Surya P., et al.. (2015). Yeast Env9 is a Conserved Oxidoreductase Involved in Lipid Droplet Biogenesis. The FASEB Journal. 29(S1). 1 indexed citations
6.
Manandhar, Surya P., et al.. (2014). Distinct Palmitoylation Events at the Amino-terminal Conserved Cysteines of Env7 Direct Its Stability, Localization, and Vacuolar Fusion Regulation in S. cerevisiae. Journal of Biological Chemistry. 289(16). 11431–11442. 5 indexed citations
7.
Manandhar, Surya P., et al.. (2012). Saccharomyces cerevisiae Env7 Is a Novel Serine/Threonine Kinase 16-Related Protein Kinase and Negatively Regulates Organelle Fusion at the Lysosomal Vacuole. Molecular and Cellular Biology. 33(3). 526–542. 11 indexed citations
8.
Menjivar, Rosa E., et al.. (2011). A Genome-Wide Immunodetection Screen in S. cerevisiae Uncovers Novel Genes Involved in Lysosomal Vacuole Function and Morphology. PLoS ONE. 6(8). e23696–e23696. 20 indexed citations
9.
Gharakhanian, Editte, et al.. (2010). env1 Mutant of VPS35 gene exhibits unique protein localization and processing phenotype at Golgi and lysosomal vacuole in Saccharomyces cerevisiae. Molecular and Cellular Biochemistry. 346(1-2). 187–195. 2 indexed citations
10.
11.
Takahashi, Minoru, et al.. (2008). A novel immunodetection screen for vacuolar defects identifies a unique allele of VPS35 in S. cerevisiae. Molecular and Cellular Biochemistry. 311(1-2). 121–136. 5 indexed citations
12.
Gharakhanian, Editte, et al.. (2004). Cys254 and Cys49/Cys87of simian virus 40 Vp1 are essential in formation of infectious virions. Virus Research. 107(1). 21–25. 2 indexed citations
13.
Gharakhanian, Editte, et al.. (2003). The simian virus 40 minor structural protein Vp3, but not Vp2, is essential for infectious virion formation. Journal of General Virology. 84(8). 2111–2116. 9 indexed citations
14.
Orlando, Salvatore J., et al.. (2000). Rapid small-scale isolation of SV40 virions and SV40 DNA. Journal of Virological Methods. 90(2). 109–114. 8 indexed citations
15.
Jao, Christine C., et al.. (1999). Cys9, Cys104 and Cys207 of simian virus 40 Vp1 are essential for inter-pentamer disulfide-linkage and stabilization in cell-free lysates. Journal of General Virology. 80(9). 2481–2489. 16 indexed citations
16.
Gharakhanian, Editte, et al.. (1995). SV40 VP1 Assembles into Disulfide-Linked Postpentameric Complexes in Cell-Free Lysates. Virology. 207(1). 251–254. 8 indexed citations
17.
Marcusson, Eric G., Bruce Horazdovsky, Joan Lin Cereghino, Editte Gharakhanian, & Scott D. Emr. (1994). The sorting receptor for yeast vacuolar carboxypeptidase Y is encoded by the VPS10 gene. Cell. 77(4). 579–586. 421 indexed citations
18.
Gharakhanian, Editte & Harumi Kasamatsu. (1990). Two independent signals, a nuclear localization signal and a Vp1-interactive signal, reside within the carboxy-35 amino acids of SV40 Vp3. Virology. 178(1). 62–71. 24 indexed citations
19.
Gharakhanian, Editte, Joseph S. Takahashi, Jared L. Clever, & Harumi Kasamatsu. (1988). In vitro assay for protein-protein interaction: carboxyl-terminal 40 residues of simian virus 40 structural protein VP3 contain a determinant for interaction with VP1.. Proceedings of the National Academy of Sciences. 85(18). 6607–6611. 30 indexed citations
20.
Gharakhanian, Editte, et al.. (1987). The carboxyl 35 amino acids of SV40 Vp3 are essential for its nuclear accumulation. Virology. 157(2). 440–448. 50 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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