Patrick J. Connors

441 total citations
15 papers, 369 citations indexed

About

Patrick J. Connors is a scholar working on Molecular Biology, Organic Chemistry and Reproductive Medicine. According to data from OpenAlex, Patrick J. Connors has authored 15 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Organic Chemistry and 4 papers in Reproductive Medicine. Recurrent topics in Patrick J. Connors's work include Chemical Synthesis and Analysis (5 papers), Synthesis and Biological Evaluation (5 papers) and Hypothalamic control of reproductive hormones (4 papers). Patrick J. Connors is often cited by papers focused on Chemical Synthesis and Analysis (5 papers), Synthesis and Biological Evaluation (5 papers) and Hypothalamic control of reproductive hormones (4 papers). Patrick J. Connors collaborates with scholars based in United States. Patrick J. Connors's co-authors include Timothy D. Gross, R. Scott Struthers, John Saunders, Greg J. Reinhart, Dimitrios Tzalis, Yitzhak Tor, Yunfei Zhu, Chen Chen, Yinghong Gao and Fábio C. Tucci and has published in prestigious journals such as Journal of Medicinal Chemistry, Inorganic Chemistry and Bioorganic & Medicinal Chemistry Letters.

In The Last Decade

Patrick J. Connors

15 papers receiving 363 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick J. Connors United States 13 186 139 120 62 47 15 369
V. N. Sorokoumov Russia 14 392 2.1× 90 0.6× 53 0.4× 21 0.3× 29 0.6× 56 612
Timothy D. Gross United States 17 261 1.4× 199 1.4× 184 1.5× 99 1.6× 5 0.1× 27 524
J.A. Crapster United States 8 228 1.2× 453 3.3× 28 0.2× 33 0.5× 16 0.3× 10 523
Thomas F. Brennan United States 11 187 1.0× 77 0.6× 8 0.1× 11 0.2× 67 1.4× 17 340
M. OHNO Japan 14 96 0.5× 443 3.2× 7 0.1× 41 0.7× 17 0.4× 32 602
Alexey B. Dyatkin United States 17 805 4.3× 171 1.2× 6 0.1× 4 0.1× 14 0.3× 31 956
G. Bischoff Germany 8 77 0.4× 162 1.2× 27 0.2× 12 0.2× 63 1.3× 26 308
Natalia de la Figuera Spain 12 237 1.3× 299 2.2× 2 0.0× 23 0.4× 22 0.5× 23 419
M. Vinković Croatia 8 111 0.6× 148 1.1× 4 0.0× 10 0.2× 15 0.3× 37 278

Countries citing papers authored by Patrick J. Connors

Since Specialization
Citations

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

Fields of papers citing papers by Patrick J. Connors

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick J. Connors

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

All Works

15 of 15 papers shown
1.
Rowbottom, Martin W., Fábio C. Tucci, Patrick J. Connors, et al.. (2004). Synthesis and structure–activity relationships of uracil derived human GnRH receptor antagonists: (R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5. Bioorganic & Medicinal Chemistry Letters. 14(19). 4967–4973. 13 indexed citations
2.
Guo, Zhiqiang, Yunfei Zhu, Timothy D. Gross, et al.. (2004). Synthesis and Structure−Activity Relationships of 1-Arylmethyl-5-aryl-6-methyluracils as Potent Gonadotropin-Releasing Hormone Receptor Antagonists. Journal of Medicinal Chemistry. 47(5). 1259–1271. 39 indexed citations
3.
Tucci, Fábio C., Yunfei Zhu, Zhiqiang Guo, et al.. (2004). 3-(2-Aminoalkyl)-1-(2,6-difluorobenzyl)-5- (2-fluoro-3-methoxyphenyl)-6-methyl- uracils as Orally Bioavailable Antagonists of the Human Gonadotropin Releasing Hormone Receptor. Journal of Medicinal Chemistry. 47(14). 3483–3486. 25 indexed citations
4.
Zhu, Yunfei, Xiaochuan Wang, Patrick J. Connors, et al.. (2003). Quinoline-Carboxylic acids are potent inhibitors that inhibit the binding of insulin-Like growth factor (IGF) to IGF-Binding proteins. Bioorganic & Medicinal Chemistry Letters. 13(11). 1931–1934. 23 indexed citations
5.
Tucci, Fábio C., Yunfei Zhu, Zhiqiang Guo, et al.. (2003). Synthesis and Structure–activity relationships of 1-arylmethyl-3-(1-methyl-2-amino)ethyl-5-aryl-6-methyluracils as antagonists of the human GnRH Receptor. Bioorganic & Medicinal Chemistry Letters. 13(19). 3317–3322. 24 indexed citations
6.
Zhu, Yunfei, Keith Wilcoxen, Timothy D. Gross, et al.. (2003). 6,7-Dihydroxyisoquinoline-3-carboxylic acids are potent inhibitors on the binding of insulin-Like growth factor (IGF) to IGF-binding proteins: optimization of the 1-position benzoyl side chain. Bioorganic & Medicinal Chemistry Letters. 13(11). 1927–1930. 9 indexed citations
7.
Zhu, Yunfei, Timothy D. Gross, Zhiqiang Guo, et al.. (2003). Identification of 1-Arylmethyl-3- (2-aminoethyl)-5-aryluracil as Novel Gonadotropin-Releasing Hormone Receptor Antagonists. Journal of Medicinal Chemistry. 46(11). 2023–2026. 23 indexed citations
8.
Zhu, Yunfei, Zhiqiang Guo, Timothy D. Gross, et al.. (2003). Design and Structure−Activity Relationships of 2-Alkyl-3-aminomethyl-6-(3-methoxyphenyl)-7-methyl-8-(2-fluorobenzyl)imidazolo[1,2-a]pyrimid-5-ones as Potent GnRH Receptor Antagonists. Journal of Medicinal Chemistry. 46(9). 1769–1772. 22 indexed citations
9.
Wilcoxen, Keith, Patrick J. Connors, John Saunders, et al.. (2002). Synthesis and initial structure–Activity relationships of a novel series of imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 12(16). 2179–2183. 25 indexed citations
10.
Gross, Timothy D., John Saunders, Keith Wilcoxen, et al.. (2002). Design, synthesis and structure–Activity relationships of novel imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 12(16). 2185–2187. 16 indexed citations
11.
Tucci, Fábio C., Yunfei Zhu, Zhiqiang Guo, et al.. (2002). A novel synthesis of 7-aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as potent, stable GnRH receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 12(23). 3491–3495. 24 indexed citations
12.
Zhu, Yunfei, Keith Wilcoxen, John Saunders, et al.. (2002). A Novel Synthesis of 2-Arylpyrrolo[1,2-a]pyrimid-7-ones and Their Structure–Activity Relationships as Potent GnRH Receptor Antagonists. Bioorganic & Medicinal Chemistry Letters. 12(3). 403–406. 17 indexed citations
13.
Zhu, Yunfei, R. Scott Struthers, Patrick J. Connors, et al.. (2002). Initial Structure–Activity Relationship Studies of a Novel Series of Pyrrolo[1,2-a]pyrimid-7-ones as GnRH Receptor Antagonists. Bioorganic & Medicinal Chemistry Letters. 12(3). 399–402. 23 indexed citations
14.
Connors, Patrick J., et al.. (1998). Coordination Compounds as Building Blocks:  Single-Step Synthesis of Heteronuclear Multimetallic Complexes Containing RuII and OsII. Inorganic Chemistry. 37(5). 1121–1123. 83 indexed citations
15.
Vij, Ashwani, et al.. (1995). Perfluorovinyl Morpholine and Perfluorovinyl Pyrrolidine with Nucleophiles and Electrophiles. Zeitschrift für anorganische und allgemeine Chemie. 621(11). 1865–1874. 3 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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