Harvey Yamane

1.9k total citations
24 papers, 1.6k citations indexed

About

Harvey Yamane is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, Harvey Yamane has authored 24 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 4 papers in Immunology and 3 papers in Surgery. Recurrent topics in Harvey Yamane's work include RNA and protein synthesis mechanisms (6 papers), Protein Structure and Dynamics (3 papers) and Retinal Development and Disorders (3 papers). Harvey Yamane is often cited by papers focused on RNA and protein synthesis mechanisms (6 papers), Protein Structure and Dynamics (3 papers) and Retinal Development and Disorders (3 papers). Harvey Yamane collaborates with scholars based in United States, Russia and Italy. Harvey Yamane's co-authors include B K Fung, Steven Clarke, Gary Elliott, Hongmei Xie, William N. Howald, John A. Glomset, Christopher C. Farnsworth, Michael H. Gelb, Irene Griswold‐Prenner and Andy Garcia 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

Harvey Yamane

24 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Harvey Yamane United States 19 1.1k 434 217 178 169 24 1.6k
Ronald J. Uhing United States 20 1.1k 1.0× 335 0.8× 207 1.0× 165 0.9× 283 1.7× 33 1.7k
Richard T. Pickard United States 14 536 0.5× 449 1.0× 83 0.4× 176 1.0× 189 1.1× 20 1.3k
Gérard Crémel France 21 950 0.8× 164 0.4× 348 1.6× 353 2.0× 184 1.1× 59 1.6k
R C Inhorn United States 16 828 0.7× 464 1.1× 99 0.5× 509 2.9× 193 1.1× 24 1.7k
Jiing-Dwan Lee United States 20 1.8k 1.5× 339 0.8× 149 0.7× 340 1.9× 324 1.9× 22 2.3k
Junji Kishino Japan 21 678 0.6× 589 1.4× 151 0.7× 85 0.5× 117 0.7× 36 1.6k
Emmanuel Normant United States 22 1.3k 1.1× 235 0.5× 131 0.6× 370 2.1× 417 2.5× 50 2.0k
Matthew N. Hodgkin United Kingdom 16 1.2k 1.0× 198 0.5× 87 0.4× 144 0.8× 419 2.5× 32 1.5k
Chi‐Kuang Huang United States 22 925 0.8× 588 1.4× 84 0.4× 244 1.4× 250 1.5× 36 1.7k
Elizabeth J. Ackermann United States 18 1.9k 1.7× 270 0.6× 128 0.6× 416 2.3× 410 2.4× 35 2.4k

Countries citing papers authored by Harvey Yamane

Since Specialization
Citations

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

Fields of papers citing papers by Harvey Yamane

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harvey Yamane

This figure shows the co-authorship network connecting the top 25 collaborators of Harvey Yamane. A scholar is included among the top collaborators of Harvey Yamane 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 Harvey Yamane. Harvey Yamane 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.
Vaish, Amit, et al.. (2018). Generation of membrane proteins in polymer-based lipoparticles as flow cytometry antigens. European Polymer Journal. 109. 483–488. 15 indexed citations
2.
Rulifson, Ingrid C., Ping Cao, David J. Kopecky, et al.. (2016). Identification of Human Islet Amyloid Polypeptide as a BACE2 Substrate. PLoS ONE. 11(2). e0147254–e0147254. 25 indexed citations
3.
Xu, Han, John J. Hill, Klaus Michelsen, et al.. (2015). Characterization of the direct interaction between KcsA-Kv1.3 and its inhibitors. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1848(10). 1974–1980. 19 indexed citations
4.
Liu, Gaohua, Leszek Poppe, Ken Aoki, et al.. (2014). High-Quality NMR Structure of Human Anti-Apoptotic Protein Domain Mcl-1(171-327) for Cancer Drug Design. PLoS ONE. 9(5). e96521–e96521. 25 indexed citations
5.
Zeng, Qingping, Matthew P. Bourbeau, Holger Monenschein, et al.. (2010). 2-Aminothiadiazole inhibitors of AKT1 as potential cancer therapeutics. Bioorganic & Medicinal Chemistry Letters. 20(5). 1652–1656. 15 indexed citations
6.
Lo, Mei-Chu, Minghan Wang, Ki Won Kim, et al.. (2008). A highly sensitive high-throughput luminescence assay for malonyl-CoA decarboxylase. Analytical Biochemistry. 376(1). 122–130. 2 indexed citations
7.
Kim, Ki Won, et al.. (2006). Expression, purification, and characterization of human acetyl-CoA carboxylase 2. Protein Expression and Purification. 53(1). 16–23. 17 indexed citations
8.
Zhang, Xiaoling, Shiwen Zhang, Harvey Yamane, et al.. (2006). Kinetic Mechanism of AKT/PKB Enzyme Family. Journal of Biological Chemistry. 281(20). 13949–13956. 35 indexed citations
9.
Li, Tiansheng, Harvey Yamane, Tsutomu Arakawa, Linda O. Narhi, & John S. Philo. (2002). Effect of the intermolecular disulfide bond on the conformation and stability of glial cell line-derived neurotrophic factor. Protein Engineering Design and Selection. 15(1). 59–64. 29 indexed citations
10.
Faggioni, Raffaella, Russell C. Cattley, Jane Guo, et al.. (2001). IL-18-Binding Protein Protects Against Lipopolysaccharide- Induced Lethality and Prevents the Development of Fas/Fas Ligand-Mediated Models of Liver Disease in Mice. The Journal of Immunology. 167(10). 5913–5920. 101 indexed citations
11.
Nakayama, Naoki, Sheila Scully, Ryuichi Nishinakamura, et al.. (2001). A Novel Chordin-like Protein Inhibitor for Bone Morphogenetic Proteins Expressed Preferentially in Mesenchymal Cell Lineages. Developmental Biology. 232(2). 372–387. 76 indexed citations
13.
Keesler, George A., Jeff Bray, John B. Hunt, et al.. (1998). Purification and Activation of Recombinant p38 Isoforms α, β, γ, and δ. Protein Expression and Purification. 14(2). 221–228. 60 indexed citations
14.
Goruppi, Sandro, Harvey Yamane, Andy Garcia, et al.. (1997). The product of a gas6 splice variant allows the release of the domain responsible for Axl tyrosine kinase receptor activation. FEBS Letters. 415(1). 59–63. 20 indexed citations
15.
Varnum, Brian, Gary Elliott, Andy Garcia, et al.. (1995). Axl receptor tyrosine kinase stimulated by the vitamin K-dependent protein encoded by growth-arrest-specific gene 6. Nature. 373(6515). 623–626. 407 indexed citations
16.
Fung, B K, Janmeet Anant, Wei Lin, O C Ong, & Harvey Yamane. (1994). [40] Isoprenylation of γ subunits and G-protein effectors. Methods in enzymology on CD-ROM/Methods in enzymology. 237. 509–519. 3 indexed citations
17.
Yamane, Harvey & B K Fung. (1993). Covalent Modifications of G-Proteins. The Annual Review of Pharmacology and Toxicology. 33(1). 201–241. 49 indexed citations
18.
Fung, B K, Harvey Yamane, Irene M. Ota, & Steven Clarke. (1990). The γ subunit of brain G‐proteins is methyl esterified at a C‐terminal cysteine. FEBS Letters. 260(2). 313–317. 52 indexed citations
19.
Fung, B K, et al.. (1990). Subunit stoichiometry of retinal rod cGMP phosphodiesterase. Biochemistry. 29(11). 2657–2664. 102 indexed citations
20.
Yamane, Harvey, Christopher C. Farnsworth, Hongmei Xie, et al.. (1990). Brain G protein gamma subunits contain an all-trans-geranylgeranylcysteine methyl ester at their carboxyl termini.. Proceedings of the National Academy of Sciences. 87(15). 5868–5872. 201 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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