Fuji Yokoi

2.2k total citations
35 papers, 1.7k citations indexed

About

Fuji Yokoi is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Fuji Yokoi has authored 35 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 12 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Fuji Yokoi's work include Medical Imaging Techniques and Applications (10 papers), Neurotransmitter Receptor Influence on Behavior (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Fuji Yokoi is often cited by papers focused on Medical Imaging Techniques and Applications (10 papers), Neurotransmitter Receptor Influence on Behavior (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Fuji Yokoi collaborates with scholars based in United States, Japan and Denmark. Fuji Yokoi's co-authors include Dean F. Wong, Robert F. Dannals, Victor L. Villemagne, George A. Ricaurte, Una D. McCann, Hayden T. Ravert, John Hilton, Zsolt Szabó, S. Szymanski and Harvey S. Singer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and American Journal of Psychiatry.

In The Last Decade

Fuji Yokoi

34 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
Fuji Yokoi United States 15 862 520 308 263 240 35 1.7k
Joanna S. Fowler United States 15 1.2k 1.4× 499 1.0× 435 1.4× 564 2.1× 172 0.7× 19 1.9k
Linda Chang United States 16 1.1k 1.3× 401 0.8× 262 0.9× 329 1.3× 143 0.6× 27 2.0k
Payton King United States 23 885 1.0× 486 0.9× 283 0.9× 458 1.7× 150 0.6× 29 1.8k
Wynne K. Schiffer United States 27 1.1k 1.3× 498 1.0× 268 0.9× 423 1.6× 225 0.9× 50 1.9k
Weiguo Ye United States 15 622 0.7× 244 0.5× 548 1.8× 428 1.6× 167 0.7× 24 1.8k
Marc Laruelle United States 12 852 1.0× 357 0.7× 311 1.0× 276 1.0× 287 1.2× 15 1.4k
William B. Mathews United States 28 1.7k 1.9× 938 1.8× 185 0.6× 440 1.7× 253 1.1× 88 3.2k
David Alexoff United States 20 523 0.6× 303 0.6× 186 0.6× 348 1.3× 108 0.5× 41 1.5k
Anteneh M. Feyissa United States 19 794 0.9× 230 0.4× 445 1.4× 310 1.2× 292 1.2× 85 1.8k
Amira K. Brown United States 14 489 0.6× 229 0.4× 175 0.6× 320 1.2× 118 0.5× 20 1.1k

Countries citing papers authored by Fuji Yokoi

Since Specialization
Citations

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

Fields of papers citing papers by Fuji Yokoi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fuji Yokoi

This figure shows the co-authorship network connecting the top 25 collaborators of Fuji Yokoi. A scholar is included among the top collaborators of Fuji Yokoi 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 Fuji Yokoi. Fuji Yokoi 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.
Wilkes, Bradley J., et al.. (2023). Cell-specific Dyt1 ∆GAG knock-in to basal ganglia and cerebellum reveal differential effects on motor behavior and sensorimotor network function. Experimental Neurology. 367. 114471–114471. 4 indexed citations
2.
Yokoi, Fuji, et al.. (2011). Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models. Human Molecular Genetics. 21(4). 916–925. 27 indexed citations
3.
4.
Singer, Harvey S., S. Szymanski, Joseph Giuliano, et al.. (2002). Elevated Intrasynaptic Dopamine Release in Tourette’s Syndrome Measured by PET. American Journal of Psychiatry. 159(8). 1329–1336. 190 indexed citations
5.
Pomper, Martin G., Christakis Constantinides, Peter B. Barker, et al.. (2002). Quantitative MR Spectroscopic Imaging of Brain Lesions in Patients with AIDS. Academic Radiology. 9(4). 398–409. 25 indexed citations
6.
Shulman, S., et al.. (1999). A dual BGO HPLC detector for P.E.T. metabolite studies. Journal of Labelled Compounds and Radiopharmaceuticals. 42. 1 indexed citations
7.
Musachio, John L., Victor L. Villemagne, Ursula Scheffel, et al.. (1999). Synthesis of an I-123 analog of A-85380 and preliminary SPECT imaging of nicotinic receptors in baboon. Nuclear Medicine and Biology. 26(2). 201–207. 58 indexed citations
8.
Villemagne, Victor L., Dean F. Wong, Fuji Yokoi, et al.. (1999). GBR12909 attenuates amphetamine‐induced striatal dopamine release as measured by [11C]raclopride continuous infusion PET scans. Synapse. 33(4). 268–273.
9.
Cumming, Paul, Fuji Yokoi, Anjing Chen, et al.. (1999). Pharmacokinetics of radiotracers in human plasma during positron emission tomography. Synapse. 34(2). 124–134. 30 indexed citations
10.
McCann, Una D., Dean F. Wong, Fuji Yokoi, et al.. (1998). Reduced Striatal Dopamine Transporter Density in Abstinent Methamphetamine and Methcathinone Users: Evidence from Positron Emission Tomography Studies with [11C]WIN-35,428. Journal of Neuroscience. 18(20). 8417–8422. 487 indexed citations
11.
Wong, Dean F., G.A. Ricaurte, Gerhard Gründer, et al.. (1997). Dopamine Transporter Changes in Neuropsychiatric Disorders. Advances in pharmacology. 42. 219–223. 20 indexed citations
12.
Scheffel, Ursula, et al.. (1992). Dopamine transporter imaging with novel, selective cocaine analogs. Neuroreport. 3(11). 969–972. 25 indexed citations
13.
Ikeda, Ken, et al.. (1991). [Clinico-radiological correlation of Wilson's disease by magnetic resonance imaging, computed and positron emission tomography].. PubMed. 31(2). 147–53. 4 indexed citations
14.
Hara, Toshihiko, et al.. (1990). Quantitative measurement of regional myocardial blood flow in patients with coronary artery disease by intravenous injection of13N-ammonia in positron emission tomography. European Journal of Nuclear Medicine and Molecular Imaging. 16(4-6). 231–235. 14 indexed citations
15.
Yokoi, Fuji, et al.. (1990). 1-[11C]Pyruvate turnover in brain and muscle of patients with mitochondrial encephalomyopathy. Journal of the Neurological Sciences. 99(2-3). 339–348. 9 indexed citations
16.
Yasui, Masayuki, Masakuni Mukoyama, Fuji Yokoi, et al.. (1989). Metal metabolism in CNS tissues of amyotrophic lateral sclerosis with high aluminum deposition.. Nihon Naika Gakkai Zasshi. 78(1). 85–86. 1 indexed citations
17.
Yokoi, Fuji, et al.. (1989). [Positron emission tomography in two cases of transient global amnesia].. PubMed. 29(5). 599–605. 6 indexed citations
18.
Hara, Toshihiko, et al.. (1988). Measurement of human blood brain barrier integrity using 11C-inulin and positron emission tomography. European Journal of Nuclear Medicine and Molecular Imaging. 14(4). 173–6. 3 indexed citations
19.
Hara, Toshihiko, et al.. (1986). Brain ischemia and infarction positively visualized by pyruvate-1-11C using positron-emission tomography. European Journal of Nuclear Medicine and Molecular Imaging. 12(1). 21–26. 7 indexed citations
20.
Hara, Toshihiko, et al.. (1985). Synthesis of pyruvate-1-11C as a radiopharmaceutical for tumor imaging. European Journal of Nuclear Medicine and Molecular Imaging. 11-11(6-7). 275–278. 13 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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