David Ben-Menahem

906 total citations
37 papers, 759 citations indexed

About

David Ben-Menahem is a scholar working on Reproductive Medicine, Molecular Biology and Genetics. According to data from OpenAlex, David Ben-Menahem has authored 37 papers receiving a total of 759 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Reproductive Medicine, 16 papers in Molecular Biology and 13 papers in Genetics. Recurrent topics in David Ben-Menahem's work include Hypothalamic control of reproductive hormones (23 papers), Estrogen and related hormone effects (9 papers) and Reproductive Biology and Fertility (8 papers). David Ben-Menahem is often cited by papers focused on Hypothalamic control of reproductive hormones (23 papers), Estrogen and related hormone effects (9 papers) and Reproductive Biology and Fertility (8 papers). David Ben-Menahem collaborates with scholars based in Israel, United States and Austria. David Ben-Menahem's co-authors include Irving Boime, Zvi Naor, Mary R. Pixley, Aaron J.W. Hsueh, Asomi Sato, Emerald Perlas, Masataka Kudo, Sawako Minami, Rona Limor and Albina Jablonka‐Shariff and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

David Ben-Menahem

37 papers receiving 739 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 Ben-Menahem Israel 17 482 303 262 182 157 37 759
Mary R. Pixley United States 13 304 0.6× 242 0.8× 153 0.6× 102 0.6× 75 0.5× 14 489
Todd A. Farmerie United States 13 319 0.7× 309 1.0× 293 1.1× 205 1.1× 96 0.6× 18 748
J. L. TURGEON United States 15 552 1.1× 289 1.0× 373 1.4× 163 0.9× 276 1.8× 22 907
E. Buczko United States 7 258 0.5× 245 0.8× 172 0.7× 100 0.5× 99 0.6× 7 489
C. Finaz France 16 225 0.5× 361 1.2× 230 0.9× 131 0.7× 58 0.4× 50 724
Myoungkun Jeoung United States 17 148 0.3× 283 0.9× 85 0.3× 83 0.5× 26 0.2× 22 510
David Bonfil Israel 8 212 0.4× 153 0.5× 150 0.6× 71 0.4× 67 0.4× 8 372
Asami Oji Japan 14 310 0.6× 447 1.5× 233 0.9× 305 1.7× 17 0.1× 21 825
Gwen E. Dressing United States 10 138 0.3× 194 0.6× 426 1.6× 72 0.4× 63 0.4× 11 685
Henry N. Yu United States 10 192 0.4× 428 1.4× 100 0.4× 68 0.4× 87 0.6× 17 627

Countries citing papers authored by David Ben-Menahem

Since Specialization
Citations

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

Fields of papers citing papers by David Ben-Menahem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Ben-Menahem. 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 Ben-Menahem. The network helps show where David Ben-Menahem may publish in the future.

Co-authorship network of co-authors of David Ben-Menahem

This figure shows the co-authorship network connecting the top 25 collaborators of David Ben-Menahem. A scholar is included among the top collaborators of David Ben-Menahem 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 Ben-Menahem. David Ben-Menahem 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.
Ben-Menahem, David, et al.. (2019). Increasing telomerase enhanced steroidogenic genes expression and steroid hormones production in rat and human granulosa cells and in mouse ovary. The Journal of Steroid Biochemistry and Molecular Biology. 197. 105551–105551. 9 indexed citations
2.
Johnson, Ruth I., et al.. (2015). The LH/CG receptor activates canonical signaling pathway when expressed in Drosophila. Molecular and Cellular Endocrinology. 413. 145–156. 1 indexed citations
3.
Asraf, Hila, Abraham Amsterdam, & David Ben-Menahem. (2015). Modulation of the steroidogenic related activity according to the design of single-chain bovine FSH analogs. General and Comparative Endocrinology. 216. 171–181. 5 indexed citations
4.
Cohen, Limor, George R. Bousfield, & David Ben-Menahem. (2015). The recombinant equine LHβ subunit combines divergent intracellular traits of human LHβ and CGβ subunits. Theriogenology. 83(9). 1469–1476. 3 indexed citations
5.
Amor, Yehudit, Rakefet Rosenfeld, Förtüne Kohen, et al.. (2013). The role of the 3′ region of mammalian gonadotropin β subunit gene in the luteinizing hormone to chorionic gonadotropin evolution. Molecular and Cellular Endocrinology. 382(2). 781–790. 7 indexed citations
6.
Eisenstein, Miriam, Thomas L. Leto, Nurit Hadad, et al.. (2008). Cytosolic Phospholipase A2α Is Targeted to the p47 -PX Domain of the Assembled NADPH Oxidase via a Novel Binding Site in Its C2 Domain. Journal of Biological Chemistry. 283(46). 31898–31908. 22 indexed citations
7.
Dantes, Ada, et al.. (2007). The configuration of the alpha and beta subunit domains in single-chain bovine LH analogs influences the secretion and steroidogenic response. Molecular and Cellular Endocrinology. 283(1-2). 83–95. 6 indexed citations
8.
Dantes, Ada, Samsam C. Pen, R. Braw–Tal, et al.. (2006). Homologous and Heterologous Carboxyl Terminal Peptide (CTP) Linker Sequences Enhance the Secretion of Bioactive Single-Chain Bovine LH Analogs. Experimental and Clinical Endocrinology & Diabetes. 114(3). 95–104. 11 indexed citations
9.
Ben-Menahem, David & H. E. Grotjan. (2006). Strategies for construction of luteinizing hormone beta subunit analogs with carboxyl terminal extensions in non-primate, non-equid mammalian species. Molecular and Cellular Endocrinology. 260-262. 205–211. 4 indexed citations
10.
Braw–Tal, R., et al.. (2006). The steroidogenic effect of single-chain bovine LH analogs in cultured bovine follicular cells. Molecular and Cellular Endocrinology. 252(1-2). 136–141. 3 indexed citations
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Kanda, Masatoshi, Albina Jablonka‐Shariff, Asomi Sato, et al.. (1999). Genetic Fusion of an α-Subunit Gene to the Follicle-Stimulating Hormone and Chorionic Gonadotropin-β Subunit Genes: Production of a Bifunctional Protein. Molecular Endocrinology. 13(11). 1873–1881. 31 indexed citations
14.
Ben-Menahem, David, et al.. (1998). Conversion of Thyrotropin Heterodimer to a Biologically Active Single-Chain*. Endocrinology. 139(5). 2459–2464. 27 indexed citations
15.
Ben-Menahem, David, Masataka Kudo, Mary R. Pixley, et al.. (1997). The Biologic Action of Single-chain Choriogonadotropin Is Not Dependent on the Individual Disulfide Bonds of the β Subunit. Journal of Biological Chemistry. 272(11). 6827–6830. 31 indexed citations
16.
Sato, Asomi, Emerald Perlas, David Ben-Menahem, et al.. (1997). Cystine Knot of the Gonadotropin α Subunit Is Critical for Intracellular Behavior but Not for in Vitro Biological Activity. Journal of Biological Chemistry. 272(29). 18098–18103. 33 indexed citations
17.
Ben-Menahem, David & Irving Boime. (1996). Converting heterodimeric gonadotropins to genetically linked single chains. Trends in Endocrinology and Metabolism. 7(3). 100–105. 26 indexed citations
18.
García‐Navarro, Socorro, Yael Marantz, M. Kalina, et al.. (1994). Developmental expression of protein kinase C subspecies in rat brain-pituitary axis. Molecular and Cellular Endocrinology. 103(1-2). 133–138. 16 indexed citations
19.
20.
Ben-Menahem, David, et al.. (1990). The Gonadotropin-Releasing Hormone Receptor: Signals Involved in Gonadotropin Secretion and Biosynthesis. Hormone Research. 33(2-4). 76–86. 4 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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