Andrew R. Vaino

616 total citations
21 papers, 481 citations indexed

About

Andrew R. Vaino is a scholar working on Molecular Biology, Organic Chemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Andrew R. Vaino has authored 21 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Organic Chemistry and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Andrew R. Vaino's work include Chemical Synthesis and Analysis (6 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Glycosylation and Glycoproteins Research (4 papers). Andrew R. Vaino is often cited by papers focused on Chemical Synthesis and Analysis (6 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Glycosylation and Glycoproteins Research (4 papers). Andrew R. Vaino collaborates with scholars based in United States, Canada and Italy. Andrew R. Vaino's co-authors include Kim D. Janda, Walter A. Szarek, David B. Goodin, Gregory R. J. Thatcher, Mark S. Hixon, R. L. Smith, Jianxin Chen, Thomas J. Lobl, Scott D. Collins and Edith Monteagudo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Chemical Communications.

In The Last Decade

Andrew R. Vaino

19 papers receiving 467 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew R. Vaino United States 13 283 245 68 60 45 21 481
David Alker United Kingdom 12 394 1.4× 254 1.0× 52 0.8× 54 0.9× 86 1.9× 26 599
Julia Subbotina Russia 13 201 0.7× 211 0.9× 35 0.5× 130 2.2× 26 0.6× 33 530
Wojciech Zawodny United Kingdom 10 320 1.1× 243 1.0× 34 0.5× 54 0.9× 42 0.9× 12 487
Airton G. Salles Brazil 12 360 1.3× 77 0.3× 45 0.7× 66 1.1× 54 1.2× 26 486
Swapan Majumdar India 14 331 1.2× 115 0.5× 26 0.4× 34 0.6× 26 0.6× 36 475
Jessica M. Grandner United States 12 200 0.7× 126 0.5× 31 0.5× 80 1.3× 36 0.8× 20 423
Mark Pickworth United Kingdom 11 575 2.0× 184 0.8× 197 2.9× 71 1.2× 86 1.9× 12 737
Vasily A. Migulin Russia 10 235 0.8× 116 0.5× 20 0.3× 89 1.5× 38 0.8× 25 359
Sorana Ionescu Romania 13 160 0.6× 235 1.0× 27 0.4× 125 2.1× 104 2.3× 48 489
A.‐B. Hörnfeldt Sweden 15 227 0.8× 101 0.4× 60 0.9× 33 0.6× 68 1.5× 21 451

Countries citing papers authored by Andrew R. Vaino

Since Specialization
Citations

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

Fields of papers citing papers by Andrew R. Vaino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew R. Vaino. 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 Andrew R. Vaino. The network helps show where Andrew R. Vaino may publish in the future.

Co-authorship network of co-authors of Andrew R. Vaino

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew R. Vaino. A scholar is included among the top collaborators of Andrew R. Vaino 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 Andrew R. Vaino. Andrew R. Vaino 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.
Wong, Dean F., Ganesh B. Chand, Anna Eramo, et al.. (2024). PET clinical study of novel antipsychotic LB-102 demonstrates unexpectedly prolonged dopamine receptor target engagement. Neuropsychopharmacology. 50(2). 372–377.
2.
3.
Vaino, Andrew R., Akiva Mintz, Anna Eramo, et al.. (2021). P.0830 LB-102 displays superior dopamine receptor occupancy compared to amisulpride in mouse and human PET studies. European Neuropsychopharmacology. 53. S606–S606. 1 indexed citations
4.
5.
Vaino, Andrew R., et al.. (2019). P.101 Building a translational bridge from animals to man for clinical candidate lb-102, a next-generation benzamide antipsychotic. European Neuropsychopharmacology. 29. S87–S88. 2 indexed citations
6.
Elbaum, Daniel, Maria Beconi, Edith Monteagudo, et al.. (2018). Fosmetpantotenate (RE-024), a phosphopantothenate replacement therapy for pantothenate kinase-associated neurodegeneration: Mechanism of action and efficacy in nonclinical models. PLoS ONE. 13(3). e0192028–e0192028. 21 indexed citations
7.
Neill, Joanna C., Ben Grayson, Giovanni Podda, et al.. (2017). Pre-clinical evaluation of two novel benzamides, LB-102 and 103, for the treatment of schizophrenia. European Neuropsychopharmacology. 27. S922–S923. 3 indexed citations
8.
Chen, Jianxin, Andrew R. Vaino, R. L. Smith, & Scott D. Collins. (2008). Photomediated crosslinking of cinnamated PDMS for in situ direct photopatterning. Journal of Polymer Science Part A Polymer Chemistry. 46(11). 3482–3487. 16 indexed citations
9.
Lobl, Thomas J., et al.. (2002). An Improved Procedure for the Synthesis of Nucleoside Phosphoramidates. Organic Process Research & Development. 6(6). 819–822. 14 indexed citations
10.
Vaino, Andrew R. & Walter A. Szarek. (2000). Iodine in carbohydrate chemistry. PubMed. 56. 9–63. 18 indexed citations
11.
Vaino, Andrew R., David B. Goodin, & Kim D. Janda. (2000). Investigating Resins for Solid Phase Organic Synthesis:  The Relationship between Swelling and Microenvironment As Probed by EPR and Fluorescence Spectroscopy. Journal of Combinatorial Chemistry. 2(4). 330–336. 37 indexed citations
12.
Vaino, Andrew R.. (2000). Sodium Percarbonate as an Oxygen Source for MTO Catalyzed Epoxidations. The Journal of Organic Chemistry. 65(13). 4210–4212. 16 indexed citations
13.
Vaino, Andrew R. & Kim D. Janda. (2000). Solid-Phase Organic Synthesis:  A Critical Understanding of the Resin. Journal of Combinatorial Chemistry. 2(6). 579–596. 130 indexed citations
14.
Vaino, Andrew R. & Kim D. Janda. (2000). Euclidean shape-encoded combinatorial chemical libraries. Proceedings of the National Academy of Sciences. 97(14). 7692–7696. 66 indexed citations
15.
16.
Vaino, Andrew R., William T. Depew, & Walter A. Szarek. (1997). Synthesis of 1,2,3-tri-O-β-lactosyl-d-threitol and 1-O-benzyl-2,3,4-tri-O-β-lactosyl-d-threitol. Carbohydrate Research. 305(1). 27–31. 1 indexed citations
17.
Vaino, Andrew R., Walter A. Szarek, Andrew R. Vaino, & William T. Depew. (1997). Synthesis of a D-lactosyl cluster–nucleoside conjugate†. Chemical Communications. 1871–1871. 3 indexed citations
18.
Vaino, Andrew R. & Walter A. Szarek. (1996). A mild and efficient method for the deprotection of tert-butyldimethylsilyl ethers using iodine in methanol. Chemical Communications. 2351–2351. 64 indexed citations
19.
Vaino, Andrew R., et al.. (1996). An Experimental Reexamination of the Reverse Anomeric Effect in N-Glycosylimidazoles. The Journal of Organic Chemistry. 61(14). 4514–4515. 20 indexed citations
20.
Vaino, Andrew R. & Walter A. Szarek. (1995). Iodine in Methanol: a Simple Selective Method for the Cleavage of p-Methoxybenzyl Ethers. Synlett. 1995(11). 1157–1158. 34 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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