Howard E. Smith

2.0k total citations
101 papers, 1.5k citations indexed

About

Howard E. Smith is a scholar working on Spectroscopy, Organic Chemistry and Physical and Theoretical Chemistry. According to data from OpenAlex, Howard E. Smith has authored 101 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Spectroscopy, 37 papers in Organic Chemistry and 31 papers in Physical and Theoretical Chemistry. Recurrent topics in Howard E. Smith's work include Molecular spectroscopy and chirality (33 papers), Various Chemistry Research Topics (26 papers) and Analytical Chemistry and Chromatography (15 papers). Howard E. Smith is often cited by papers focused on Molecular spectroscopy and chirality (33 papers), Various Chemistry Research Topics (26 papers) and Analytical Chemistry and Chromatography (15 papers). Howard E. Smith collaborates with scholars based in United States, France and Belarus. Howard E. Smith's co-authors include Jon R. Neergaard, Elizabeth P. Burrows, Antony F. McDonagh, Tomas de Paulis, Roy G. Smith, Fuming Chen, David O. Toft, Bert W. O’Malley, Fridolin Sulser and Philip L. Mobley and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and Physical Review Letters.

In The Last Decade

Howard E. Smith

101 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Howard E. Smith United States 22 626 423 383 230 136 101 1.5k
Eduard Schmid Germany 18 191 0.3× 519 1.2× 245 0.6× 135 0.6× 48 0.4× 68 1.3k
Hugo O. Villar United States 25 463 0.7× 1.1k 2.5× 280 0.7× 203 0.9× 56 0.4× 86 2.1k
Chin‐Hui Yu Taiwan 24 480 0.8× 513 1.2× 418 1.1× 295 1.3× 143 1.1× 106 1.8k
Ian L. Alberts United States 21 236 0.4× 661 1.6× 229 0.6× 236 1.0× 127 0.9× 60 1.8k
David A. Stauffer United States 8 408 0.7× 1.1k 2.6× 381 1.0× 143 0.6× 53 0.4× 9 1.7k
Satoshi Ono Japan 27 531 0.8× 986 2.3× 210 0.5× 370 1.6× 79 0.6× 107 2.4k
Masahiro Higashi Japan 19 409 0.7× 349 0.8× 226 0.6× 443 1.9× 109 0.8× 91 1.3k
Jörg Fleischhauer Germany 24 855 1.4× 715 1.7× 502 1.3× 552 2.4× 181 1.3× 112 2.1k
Masamichi Tsuboi Japan 21 138 0.2× 761 1.8× 238 0.6× 228 1.0× 66 0.5× 80 1.3k
Graziella Ranghino Italy 22 207 0.3× 363 0.9× 218 0.6× 411 1.8× 279 2.1× 41 1.2k

Countries citing papers authored by Howard E. Smith

Since Specialization
Citations

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

Fields of papers citing papers by Howard E. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard E. Smith. 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 Howard E. Smith. The network helps show where Howard E. Smith may publish in the future.

Co-authorship network of co-authors of Howard E. Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Howard E. Smith. A scholar is included among the top collaborators of Howard E. Smith 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 Howard E. Smith. Howard E. Smith 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.
Park, Jeong-Ho, W. C. Mitchel, Lawrence Grazulis, et al.. (2010). Epitaxial Graphene Growth by Carbon Molecular Beam Epitaxy (CMBE). Advanced Materials. 22(37). 4140–4145. 95 indexed citations
2.
Guo, Shiping, Xiang Gao, Han Wang, et al.. (2010). AlInN HEMT grown on SiC by metalorganic vapor phase epitaxy for millimeter‐wave applications. physica status solidi (a). 207(6). 1348–1352. 25 indexed citations
3.
Fazio, G. G., M. L. N. Ashby, P. Barmby, et al.. (2008). The Spitzer/IRAC Star Formation Reference Survey. 50128. 1 indexed citations
4.
Paulis, Tomas de, Jon R. Neergaard, Bruce M. Baron, et al.. (1995). Binding of 5H-Dibenzo[a,d]cycloheptene and Dibenz[b,f]oxepin Analogs of Clozapine to Dopamine and Serotonin Receptors. Journal of Medicinal Chemistry. 38(4). 708–714. 20 indexed citations
5.
6.
Polavarapu, Prasad L., et al.. (1993). Determination of absolute configurations from vibrational raman optical activity: Trans-2,3-dimethylthiirane. Talanta. 40(4). 545–549. 9 indexed citations
7.
8.
Davis, Daniel A., Tomas de Paulis, Aaron Janowsky, & Howard E. Smith. (1990). Chloro-substituted, sterically hindered 5,11-dicarbo analogs of clozapine as potential chiral antipsychotic agents. Journal of Medicinal Chemistry. 33(2). 809–814. 5 indexed citations
9.
Paulis, Tomas de, et al.. (1989). Sterically hindered 5,11-dicarbo analogs of clozapine as potential chiral antipsychotic agents. Journal of Medicinal Chemistry. 32(10). 2261–2268. 15 indexed citations
10.
Janowsky, Aaron, Tomas de Paulis, Jeffrey A. Clanton, et al.. (1988). [125I]iodopride: a specific high affinity radioligand for labelling striatal dopamine D-2 receptors. European Journal of Pharmacology. 150(1-2). 203–205. 7 indexed citations
11.
Paulis, Tomas de, Aaron Janowsky, Robert Kessler, Jeffrey A. Clanton, & Howard E. Smith. (1988). (S)-N-[(1-Ethyl-2-pyrrolidinyl)methyl]-5-[125I]iodo-2-methoxybenzamide hydrochloride, a new selective radioligand for dopamine D-2 receptors. Journal of Medicinal Chemistry. 31(10). 2027–2033. 31 indexed citations
12.
Polavarapu, Prasad L. & Howard E. Smith. (1988). Methine and methyl stretching vibrations in substituted phenylethanes. The Journal of Physical Chemistry. 92(7). 1774–1777. 2 indexed citations
13.
Smith, Howard E. & Fu-Ming Chen. (1979). Optically active amines. 27. CNDO/S calculations on the azomethine and conjugated azomethine chromophores. The Journal of Organic Chemistry. 44(15). 2775–2779. 8 indexed citations
14.
Smith, Howard E., Elizabeth P. Burrows, & Fuming Chen. (1976). Optically active amines. XXI. Application of the salicylidenimino chirality rule to cyclic steroidal amines. The Journal of Organic Chemistry. 41(4). 704–706. 1 indexed citations
15.
Smith, Howard E., Elizabeth P. Burrows, & Fuming Chen. (1975). Optically active amines. XIX. Circular dichroism of ortho-, meta-, and para-substituted .beta.-phenylalkylamine hydrochlorides. Further applications of the salicylidenimino chirality rule. The Journal of Organic Chemistry. 40(11). 1562–1567. 3 indexed citations
16.
Smith, Howard E., et al.. (1975). Optically active amines. XVIII. Spectral observations on optically active N-substituted pyrroles. Journal of the American Chemical Society. 97(11). 3126–3130. 20 indexed citations
17.
18.
Smith, Howard E., et al.. (1970). Pyrazines as optically active aromatic chromophores. Journal of the Chemical Society D Chemical Communications. 1112–1112. 2 indexed citations
19.
McDonagh, Antony F. & Howard E. Smith. (1966). Ring–chain tautomerism of derivatives of o-hydroxybenzylamine with aromatic aldehydes. Chemical Communications (London). 0(12). 374–374. 1 indexed citations
20.

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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