Deborah L. Segaloff

8.5k total citations · 2 hit papers
96 papers, 6.4k citations indexed

About

Deborah L. Segaloff is a scholar working on Molecular Biology, Reproductive Medicine and Genetics. According to data from OpenAlex, Deborah L. Segaloff has authored 96 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 48 papers in Reproductive Medicine and 23 papers in Genetics. Recurrent topics in Deborah L. Segaloff's work include Hypothalamic control of reproductive hormones (46 papers), Receptor Mechanisms and Signaling (43 papers) and Estrogen and related hormone effects (20 papers). Deborah L. Segaloff is often cited by papers focused on Hypothalamic control of reproductive hormones (46 papers), Receptor Mechanisms and Signaling (43 papers) and Estrogen and related hormone effects (20 papers). Deborah L. Segaloff collaborates with scholars based in United States, Brazil and Italy. Deborah L. Segaloff's co-authors include Mario Ascoli, Francesca Fanelli, Ya‐Xiong Tao, Rolf Sprengel, Károly Nikolics, Peter H. Seeburg, Nora Rosemblit, Keith McFarland, Martin Köhler and Heidi Phillips and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Deborah L. Segaloff

96 papers receiving 6.3k citations

Hit Papers

Lutropin-Choriogonadotrop... 1989 2026 2001 2013 1989 2002 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah L. Segaloff United States 43 3.2k 3.0k 1.6k 1.3k 1.2k 96 6.4k
Mario Ascoli United States 49 3.7k 1.1× 2.9k 1.0× 1.7k 1.1× 1.2k 1.0× 1.3k 1.1× 145 7.1k
Micheline Misrahi France 45 3.0k 0.9× 2.4k 0.8× 2.3k 1.4× 1.2k 1.0× 660 0.6× 110 6.7k
Kaoru Miyamoto Japan 44 3.0k 0.9× 1.5k 0.5× 1.4k 0.9× 1.3k 1.0× 344 0.3× 172 6.0k
Margaret A. Shupnik United States 49 2.2k 0.7× 2.3k 0.8× 3.4k 2.1× 905 0.7× 380 0.3× 109 7.1k
Mary Hunzicker-Dunn United States 41 2.7k 0.8× 1.5k 0.5× 1.2k 0.7× 1.9k 1.5× 512 0.4× 116 5.1k
John J. Peluso United States 45 1.8k 0.5× 1.6k 0.5× 2.0k 1.2× 1.8k 1.4× 384 0.3× 159 5.4k
John H. Nilson United States 42 2.4k 0.7× 1.7k 0.6× 2.4k 1.5× 1.3k 1.0× 239 0.2× 90 5.2k
Jean Djiane France 49 3.3k 1.0× 911 0.3× 2.5k 1.5× 348 0.3× 344 0.3× 231 9.1k
Chon‐Hwa Tsai‐Morris United States 34 2.4k 0.7× 1.0k 0.3× 1.4k 0.9× 505 0.4× 585 0.5× 80 4.4k
James A. Dias United States 34 1.8k 0.5× 1.9k 0.6× 914 0.6× 626 0.5× 384 0.3× 121 3.4k

Countries citing papers authored by Deborah L. Segaloff

Since Specialization
Citations

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

Fields of papers citing papers by Deborah L. Segaloff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah L. Segaloff. 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 Deborah L. Segaloff. The network helps show where Deborah L. Segaloff may publish in the future.

Co-authorship network of co-authors of Deborah L. Segaloff

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah L. Segaloff. A scholar is included among the top collaborators of Deborah L. Segaloff 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 Deborah L. Segaloff. Deborah L. Segaloff 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.
Costagliola, Sabine, James A. Dias, Marvin C. Gershengorn, et al.. (2020). Glycoprotein hormone receptors (version 2020.4) in the IUPHAR/BPS Guide to Pharmacology Database. IUPHAR/BPS Guide to Pharmacology CITE. 2020(4). 1 indexed citations
2.
Stilley, Julie A.W. & Deborah L. Segaloff. (2018). Deletion of fetoplacental Fshr inhibits fetal vessel angiogenesis in the mouse placenta. Molecular and Cellular Endocrinology. 476. 79–83. 13 indexed citations
3.
Peltoketo, Hellevi, Leena Strauss, Meilin Zhang, et al.. (2010). Female mice expressing constitutively active FSH receptor present with a phenotype of premature follicle depletion, premature aging and teratomas. 21. 1 indexed citations
4.
Segaloff, Deborah L.. (2010). Constitutive Activity of the Lutropin Receptor and Its Allosteric Modulation by Receptor Heterodimerization. Methods in enzymology on CD-ROM/Methods in enzymology. 484. 231–252. 1 indexed citations
5.
6.
Wu, Xueqing, et al.. (2009). Structural determinants underlying constitutive dimerization of unoccupied human follitropin receptors. Cellular Signalling. 22(2). 247–256. 45 indexed citations
7.
Mizrachi, Dario & Deborah L. Segaloff. (2004). Intracellularly Located Misfolded Glycoprotein Hormone Receptors Associate with Different Chaperone Proteins than Their Cognate Wild-Type Receptors. Molecular Endocrinology. 18(7). 1768–1777. 76 indexed citations
8.
Tao, Ya‐Xiong, et al.. (2004). Constitutive and Agonist-dependent Self-association of the Cell Surface Human Lutropin Receptor. Journal of Biological Chemistry. 279(7). 5904–5914. 81 indexed citations
9.
Shi, Haitao, et al.. (2001). Expression and localization of luteinizing hormone receptor in the female mouse reproductive tract (vol 64, pg 179, 2001). Biology of Reproduction. 64(3). 17 indexed citations
10.
Chen, Shi‐You, Hong Shi, Xuebo Liu, & Deborah L. Segaloff. (1999). Multiple Elements and Protein Factors Coordinate the Basal and Cyclic Adenosine 3′,5′-Monophosphate-Induced Transcription of the Lutropin Receptor Gene in Rat Granulosa Cells1. Endocrinology. 140(5). 2100–2109. 39 indexed citations
11.
Latronico, Ana Cláudia, Amy N. Abell, Vinícius Nahime Brito, et al.. (1998). A Unique Constitutively Activating Mutation in Third Transmembrane Helix of Luteinizing Hormone Receptor Causes Sporadic Male Gonadotropin-Independent Precocious Puberty1. The Journal of Clinical Endocrinology & Metabolism. 83(7). 2435–2440. 68 indexed citations
15.
Segaloff, Deborah L., et al.. (1990). The Orientation of the Lutropin/Choriogonadotropin Receptor in Rat Luteal Cells as Revealed by Site-Specific Antibodies*. Endocrinology. 127(2). 674–681. 32 indexed citations
16.
Segaloff, Deborah L., Haiyun Wang, & JoAnne S. Richards. (1990). Hormonal Regulation of Luteinizing Hormone/Chorionic Gonadotropin Receptor mRNA in Rat Ovarian Cells during Follicular Development and Luteinization. Molecular Endocrinology. 4(12). 1856–1865. 199 indexed citations
17.
Pereira, Maria Estér, Deborah L. Segaloff, & Mario Ascoli. (1988). Ca+2 Is an Inhibitor of Adenylate Cyclase in MA-10 Leydig Tumor Cells*. Endocrinology. 122(5). 2232–2239. 23 indexed citations
18.
Ascoli, Mario, et al.. (1987). Immunoprecipitation of the lutropin/choriogonadotropin receptor from biosynthetically labeled Leydig tumor cells. A 92-kDa Glycoprotein.. Journal of Biological Chemistry. 262(1). 470–477. 16 indexed citations
19.
Pereira, Maria Estér, Deborah L. Segaloff, Mario Ascoli, & F. Eckstein. (1987). Inhibition of choriogonadotropin-activated steroidogenesis in cultured Leydig tumor cells by the Rp diastereoisomer of adenosine 3′,5′-cyclic phosphorothioate.. Journal of Biological Chemistry. 262(13). 6093–6100. 77 indexed citations
20.
Ascoli, Mario & Deborah L. Segaloff. (1986). Effects of collagenase on the structure of the lutropin/choriogonadotropin receptor.. Journal of Biological Chemistry. 261(8). 3807–3815. 38 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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