David J. Lapinsky

596 total citations
21 papers, 416 citations indexed

About

David J. Lapinsky is a scholar working on Molecular Biology, Organic Chemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, David J. Lapinsky has authored 21 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Organic Chemistry and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in David J. Lapinsky's work include Receptor Mechanisms and Signaling (9 papers), Chemical Synthesis and Analysis (6 papers) and Nicotinic Acetylcholine Receptors Study (6 papers). David J. Lapinsky is often cited by papers focused on Receptor Mechanisms and Signaling (9 papers), Chemical Synthesis and Analysis (6 papers) and Nicotinic Acetylcholine Receptors Study (6 papers). David J. Lapinsky collaborates with scholars based in United States, Australia and Switzerland. David J. Lapinsky's co-authors include Stephen C. Bergmeier, Douglas S. Johnson, R. Benjamin Free, Dennis B. McKay, Shaili Aggarwal, Christopher K. Surratt, John R. Lever, Karen J. Gregory, Sara M. Thomasy and Khadiga Ahmed Ismail and has published in prestigious journals such as Biochemistry, Annals of the New York Academy of Sciences and Journal of Medicinal Chemistry.

In The Last Decade

David J. Lapinsky

21 papers receiving 408 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David J. Lapinsky United States 11 279 199 59 55 47 21 416
Jo Alen Belgium 11 144 0.5× 118 0.6× 29 0.5× 40 0.7× 39 0.8× 17 395
Anne Stößel Germany 9 222 0.8× 120 0.6× 15 0.3× 65 1.2× 40 0.9× 10 352
Jesse A. May United States 14 340 1.2× 329 1.7× 18 0.3× 79 1.4× 66 1.4× 27 626
Patrice Désos France 10 210 0.8× 173 0.9× 14 0.2× 73 1.3× 29 0.6× 15 413
Linus S. Lin United States 13 157 0.6× 189 0.9× 33 0.6× 82 1.5× 68 1.4× 20 401
Marianna Mák Hungary 12 203 0.7× 87 0.4× 25 0.4× 32 0.6× 25 0.5× 49 386
Renée Zindell United States 9 119 0.4× 130 0.7× 17 0.3× 39 0.7× 93 2.0× 10 329
Douglas C. Beshore United States 16 391 1.4× 451 2.3× 24 0.4× 90 1.6× 114 2.4× 29 750
Yingzhi Bi United States 10 209 0.7× 245 1.2× 85 1.4× 15 0.3× 48 1.0× 15 423
Tom R. Dean United States 7 236 0.8× 142 0.7× 13 0.2× 18 0.3× 71 1.5× 7 409

Countries citing papers authored by David J. Lapinsky

Since Specialization
Citations

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

Fields of papers citing papers by David J. Lapinsky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David J. Lapinsky. 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 David J. Lapinsky. The network helps show where David J. Lapinsky may publish in the future.

Co-authorship network of co-authors of David J. Lapinsky

This figure shows the co-authorship network connecting the top 25 collaborators of David J. Lapinsky. A scholar is included among the top collaborators of David J. Lapinsky 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 David J. Lapinsky. David J. Lapinsky 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.
Christopoulos, Arthur, et al.. (2020). Differential contribution of metabotropic glutamate receptor 5 common allosteric binding site residues to biased allosteric agonism. Biochemical Pharmacology. 177. 114011–114011. 6 indexed citations
2.
Surratt, Christopher K., et al.. (2018). Clickable photoaffinity ligands for the human serotonin transporter based on the selective serotonin reuptake inhibitor (S)-citalopram. Bioorganic & Medicinal Chemistry Letters. 28(21). 3431–3435. 6 indexed citations
3.
Jackson, Paul & David J. Lapinsky. (2018). Appendage and Scaffold Diverse Fully Functionalized Small-Molecule Probes via a Minimalist Terminal Alkyne-Aliphatic Diazirine Isocyanide. The Journal of Organic Chemistry. 83(18). 11245–11253. 10 indexed citations
4.
Gregory, Karen J., et al.. (2016). Clickable Photoaffinity Ligands for Metabotropic Glutamate Receptor 5 Based on Select Acetylenic Negative Allosteric Modulators. ACS Chemical Biology. 11(7). 1870–1879. 27 indexed citations
5.
Kumar, Vivek, David J. Lapinsky, Michael J. Tomlinson, et al.. (2015). Novel Azido-Iodo Photoaffinity Ligands for the Human Serotonin Transporter Based on the Selective Serotonin Reuptake Inhibitor (S)-Citalopram. Journal of Medicinal Chemistry. 58(14). 5609–5619. 8 indexed citations
6.
Lapinsky, David J. & Douglas S. Johnson. (2015). Recent Developments and Applications of Clickable Photoprobes in Medicinal Chemistry and Chemical Biology. Future Medicinal Chemistry. 7(16). 2143–2171. 44 indexed citations
7.
Lapinsky, David J.. (2012). Tandem photoaffinity labeling–bioorthogonal conjugation in medicinal chemistry. Bioorganic & Medicinal Chemistry. 20(21). 6237–6247. 93 indexed citations
8.
Arias, Hugo R., Dominik Feuerbach, Katarzyna M. Targowska‐Duda, et al.. (2012). Structural and functional interaction of (±)-2-(N-tert-butylamino)-3′-iodo-4′-azidopropiophenone, a photoreactive bupropion derivative, with nicotinic acetylcholine receptors. Neurochemistry International. 61(8). 1433–1441. 14 indexed citations
9.
Lapinsky, David J., Christopher K. Surratt, John R. Lever, et al.. (2012). Evolution of a Compact Photoprobe for the Dopamine Transporter Based on (±)-threo-Methylphenidate. ACS Medicinal Chemistry Letters. 3(5). 378–382. 5 indexed citations
10.
Hamouda, Ayman K., Shaili Aggarwal, John R. Lever, et al.. (2012). Bupropion Binds to Two Sites in theTorpedoNicotinic Acetylcholine Receptor Transmembrane Domain: A Photoaffinity Labeling Study with the Bupropion Analogue [125I]-SADU-3-72. Biochemistry. 51(12). 2425–2435. 21 indexed citations
12.
13.
Lapinsky, David J., Yi Liu, Christopher K. Surratt, et al.. (2010). Azido-iodo-N-benzyl derivatives of threo-methylphenidate (Ritalin, Concerta): Rational design, synthesis, pharmacological evaluation, and dopamine transporter photoaffinity labeling. Bioorganic & Medicinal Chemistry. 19(1). 504–512. 12 indexed citations
14.
Lapinsky, David J., Shaili Aggarwal, Christopher K. Surratt, et al.. (2009). A novel photoaffinity ligand for the dopamine transporter based on pyrovalerone. Bioorganic & Medicinal Chemistry. 17(11). 3770–3774. 8 indexed citations
15.
Lapinsky, David J., et al.. (2008). Substitution effects in intramolecular aziridine–allylsilane cyclizations. Tetrahedron. 65(4). 741–747. 2 indexed citations
16.
Free, R. Benjamin, Sara M. Thomasy, David J. Lapinsky, et al.. (2002). Structure–activity studies with ring E analogues of methyllycaconitine on bovine adrenal α3β4* nicotinic receptors. Neuroscience Research. 42(1). 57–63. 40 indexed citations
17.
Free, R. Benjamin, Sara M. Thomasy, David J. Lapinsky, et al.. (2002). Effects of Methyllycaconitine and Related Analogues on Bovine Adrenal α3β4* Nicotinic Acetylcholine Receptors. Annals of the New York Academy of Sciences. 971(1). 139–141. 8 indexed citations
18.
Lapinsky, David J. & Stephen C. Bergmeier. (2002). Aziridine–allylsilane-mediated synthesis of exocyclic γ-amino olefins and azabicyclo[x.y.1]-systems. Tetrahedron. 58(35). 7109–7117. 23 indexed citations
19.
Lapinsky, David J. & Stephen C. Bergmeier. (2001). A Suzuki cross-coupling route to substituted aziridines. Tetrahedron Letters. 42(49). 8583–8586. 14 indexed citations
20.
Bergmeier, Stephen C., David J. Lapinsky, R. Benjamin Free, & Dennis B. McKay. (1999). Ring E analogs of methyllycaconitine (MLA) as novel nicotinic antagonists. Bioorganic & Medicinal Chemistry Letters. 9(15). 2263–2266. 42 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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