Robert L. Gladding

1.9k total citations
46 papers, 1.3k citations indexed

About

Robert L. Gladding is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Robert L. Gladding has authored 46 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Cellular and Molecular Neuroscience, 19 papers in Molecular Biology and 16 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Robert L. Gladding's work include Neuroscience and Neuropharmacology Research (17 papers), Receptor Mechanisms and Signaling (14 papers) and Drug Transport and Resistance Mechanisms (10 papers). Robert L. Gladding is often cited by papers focused on Neuroscience and Neuropharmacology Research (17 papers), Receptor Mechanisms and Signaling (14 papers) and Drug Transport and Resistance Mechanisms (10 papers). Robert L. Gladding collaborates with scholars based in United States, Sweden and Japan. Robert L. Gladding's co-authors include Victor W. Pike, Robert B. Innis, Sami S. Zoghbi, Jinsoo Hong, Jeih‐San Liow, Masahiro Fujita, Cheryl L. Morse, Kimberly J. Jenko, William Charles Kreisl and Nicholas Seneca and has published in prestigious journals such as NeuroImage, American Journal of Psychiatry and Biological Psychiatry.

In The Last Decade

Robert L. Gladding

46 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert L. Gladding United States	20	399	347	330	286	204	46	1.3k
Nicholas Seneca United States	22	436 1.1×	665 1.9×	280 0.8×	399 1.4×	218 1.1×	51	1.7k
Hisashi Doi Japan	26	634 1.6×	236 0.7×	220 0.7×	321 1.1×	99 0.5×	84	1.8k
Ryuji Nakao Japan	22	378 0.9×	371 1.1×	157 0.5×	424 1.5×	92 0.5×	73	1.3k
Jinsoo Hong United States	25	762 1.9×	706 2.0×	418 1.3×	566 2.0×	201 1.0×	58	2.2k
Kimberly J. Jenko United States	16	431 1.1×	299 0.9×	194 0.6×	221 0.8×	74 0.4×	26	1.4k
Jeih-San Liow United States	22	516 1.3×	433 1.2×	134 0.4×	673 2.4×	62 0.3×	43	1.8k
Qi-Huang Zheng United States	26	681 1.7×	327 0.9×	367 1.1×	484 1.7×	41 0.2×	93	1.9k
Marie‐Anne Peyronneau France	18	260 0.7×	159 0.5×	236 0.7×	166 0.6×	107 0.5×	34	848
William Trigg United Kingdom	19	406 1.0×	246 0.7×	156 0.5×	263 0.9×	45 0.2×	37	1.2k
Wadad Saba France	18	248 0.6×	318 0.9×	139 0.4×	203 0.7×	75 0.4×	45	905

Countries citing papers authored by Robert L. Gladding

Since Specialization

Citations

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

Fields of papers citing papers by Robert L. Gladding

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert L. Gladding. 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 Robert L. Gladding. The network helps show where Robert L. Gladding may publish in the future.

Co-authorship network of co-authors of Robert L. Gladding

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

All Works

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20 of 20 papers shown

Lee, Jae‐Hoon, Fabrice G. Siméon, Jeih‐San Liow, et al.. (2022). In Vivo Evaluation of 6 Analogs of ¹¹C-ER176 as Candidate ¹⁸F-Labeled Radioligands for 18-kDa Translocator Protein. Journal of Nuclear Medicine. 63(8). 1252–1258. 13 indexed citations

Siméon, Fabrice G., Jae‐Hoon Lee, Cheryl L. Morse, et al.. (2021). Synthesis and Screening in Mice of Fluorine-Containing PET Radioligands for TSPO: Discovery of a Promising ¹⁸F-Labeled Ligand. Journal of Medicinal Chemistry. 64(22). 16731–16745. 17 indexed citations

Paul, Soumen, Mohammad B. Haskali, Jeih-San Liow, et al.. (2018). Evaluation of a PET Radioligand to Image O-GlcNAcase in Brain and Periphery of Rhesus Monkey and Knock-Out Mouse. Journal of Nuclear Medicine. 60(1). 129–134. 27 indexed citations

Shrestha, Saurav, Prachi Singh, Cheryl L. Morse, et al.. (2018). Evaluation of Two Potent and Selective PET Radioligands to Image COX-1 and COX-2 in Rhesus Monkeys. Journal of Nuclear Medicine. 59(12). 1907–1912. 39 indexed citations

Zanotti‐Fregonara, Paolo, Rong Xu, Sami S. Zoghbi, et al.. (2015). The PET Radioligand ¹⁸F-FIMX Images and Quantifies Metabotropic Glutamate Receptor 1 in Proportion to the Regional Density of Its Gene Transcript in Human Brain. Journal of Nuclear Medicine. 57(2). 242–247. 26 indexed citations

Hong, Jinsoo, Shuiyu Lu, Rong Xu, et al.. (2015). [ carbonyl - 11 C]4-Fluoro- N -methyl- N -(4-(6-(methylamino)pyrimidin-4-yl)thiazol-2-yl)benzamide ([ 11 C]FIMX) is an effective radioligand for PET imaging of metabotropic glutamate receptor 1 (mGluR1) in monkey brain. Nuclear Medicine and Biology. 42(12). 967–974. 7 indexed citations

Shrestha, Saurav, Jeih‐San Liow, Shuiyu Lu, et al.. (2014). ¹¹C-CUMI-101, a PET Radioligand, Behaves as a Serotonin 1A Receptor Antagonist and Also Binds to α₁Adrenoceptors in Brain. Journal of Nuclear Medicine. 55(1). 141–146. 17 indexed citations

Tsujikawa, Tetsuya, Sami S. Zoghbi, Jinsoo Hong, et al.. (2013). In vitro and in vivo evaluation of 11C-SD5024, a novel PET radioligand for human brain imaging of cannabinoid CB1 receptors. NeuroImage. 84. 733–741. 25 indexed citations

Siméon, Fabrice G., Jeih‐San Liow, Yi Zhang, et al.. (2012). Synthesis and characterization in monkey of [11C]SP203 as a radioligand for imaging brain metabotropic glutamate 5 receptors. European Journal of Nuclear Medicine and Molecular Imaging. 39(12). 1949–1958. 11 indexed citations

10.

Kimura, Yasuyuki, Masahiro Fujita, Jinsoo Hong, et al.. (2011). Brain and Whole-Body Imaging in Rhesus Monkeys of ¹¹C-NOP-1A, a Promising PET Radioligand for Nociceptin/Orphanin FQ Peptide Receptors. Journal of Nuclear Medicine. 52(10). 1638–1645. 42 indexed citations

11.

Zanotti‐Fregonara, Paolo, Sami S. Zoghbi, Jeih-San Liow, et al.. (2010). Kinetic analysis in human brain of [11C](R)-rolipram, a positron emission tomographic radioligand to image phosphodiesterase 4: A retest study and use of an image-derived input function. NeuroImage. 54(3). 1903–1909. 28 indexed citations

12.

Terry, Garth E., Jussi Hirvonen, Jeih‐San Liow, et al.. (2009). Imaging and Quantitation of Cannabinoid CB₁ Receptors in Human and Monkey Brains Using ¹⁸F-Labeled Inverse Agonist Radioligands. Journal of Nuclear Medicine. 51(1). 112–120. 78 indexed citations

13.

Seneca, Nicholas, Sami S. Zoghbi, Jeih‐San Liow, et al.. (2009). Human Brain Imaging and Radiation Dosimetry of ¹¹C-N-Desmethyl-Loperamide, a PET Radiotracer to Measure the Function of P-Glycoprotein. Journal of Nuclear Medicine. 50(5). 807–813. 42 indexed citations

14.

Kreisl, William Charles, Masahiro Fujita, Yota Fujimura, et al.. (2009). Comparison of [11C]-(R)-PK 11195 and [11C]PBR28, two radioligands for translocator protein (18 kDa) in human and monkey: Implications for positron emission tomographic imaging of this inflammation biomarker. NeuroImage. 49(4). 2924–2932. 226 indexed citations

15.

Seneca, Nicholas, Lisheng Cai, Sami S. Zoghbi, et al.. (2009). Low Retention of [S-methyl-11C]MeS-IMPY to β-amyloid Plaques in Patients with Alzheimers Disease. Current Radiopharmaceuticals. 2(2). 129–136. 5 indexed citations

16.

Liow, Jeih‐San, William Charles Kreisl, Sami S. Zoghbi, et al.. (2008). P-Glycoprotein Function at the Blood–Brain Barrier Imaged Using ¹¹C-N-Desmethyl-Loperamide in Monkeys. Journal of Nuclear Medicine. 50(1). 108–115. 53 indexed citations

17.

Zoghbi, Sami S., Jeih‐San Liow, Fumihiko Yasuno, et al.. (2008). ¹¹C-Loperamide and ItsN-DesmethylRadiometabolite Are Avid Substrates for Brain Permeability-Glycoprotein Efflux. Journal of Nuclear Medicine. 49(4). 649–656. 73 indexed citations

18.

Yasuno, Fumihiko, Amira K. Brown, Sami S. Zoghbi, et al.. (2007). The PET Radioligand [11C]MePPEP Binds Reversibly and with High Specific Signal to Cannabinoid CB1 Receptors in Nonhuman Primate Brain. Neuropsychopharmacology. 33(2). 259–269. 63 indexed citations

19.

Imaizumi, Masao, Emmanuelle Briard, Sami S. Zoghbi, et al.. (2007). Kinetic evaluation in nonhuman primates of two new PET ligands for peripheral benzodiazepine receptors in brain. Synapse. 61(8). 595–605. 60 indexed citations

20.

Yasuno, Fumihiko, Sami S. Zoghbi, Julie A. McCarron, et al.. (2006). Quantification of serotonin 5-HT1A receptors in monkey brain with [11C](R)-(−)-RWAY. Synapse. 60(7). 510–520. 33 indexed citations

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