Oscar González‐Flores

1.1k total citations
62 papers, 878 citations indexed

About

Oscar González‐Flores is a scholar working on Reproductive Medicine, Genetics and Social Psychology. According to data from OpenAlex, Oscar González‐Flores has authored 62 papers receiving a total of 878 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Reproductive Medicine, 25 papers in Genetics and 16 papers in Social Psychology. Recurrent topics in Oscar González‐Flores's work include Hypothalamic control of reproductive hormones (30 papers), Estrogen and related hormone effects (22 papers) and Ovarian function and disorders (16 papers). Oscar González‐Flores is often cited by papers focused on Hypothalamic control of reproductive hormones (30 papers), Estrogen and related hormone effects (22 papers) and Ovarian function and disorders (16 papers). Oscar González‐Flores collaborates with scholars based in Mexico, United States and Czechia. Oscar González‐Flores's co-authors include Carlos Beyer, Anne M. Etgen, Gabriela González‐Mariscal, Marcos García‐Juárez, Porfirio Gómora‐Arrati, Ignacio Camacho‐Arroyo, Aliesha González‐Arenas, Brigitte J. Todd, Kurt L. Hoffman and Jun Shu and has published in prestigious journals such as Brain Research, Endocrinology and Neuroscience & Biobehavioral Reviews.

In The Last Decade

Oscar González‐Flores

60 papers receiving 874 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oscar González‐Flores Mexico 18 496 340 231 145 117 62 878
Shailaja K. Mani United States 17 408 0.8× 357 1.1× 235 1.0× 160 1.1× 131 1.1× 21 948
Anne Duittoz France 18 364 0.7× 184 0.5× 220 1.0× 100 0.7× 72 0.6× 48 1.0k
Ede Marie Apostolakis United States 15 245 0.5× 263 0.8× 156 0.7× 150 1.0× 142 1.2× 19 633
Sabine Leonhardt Germany 17 504 1.0× 119 0.3× 295 1.3× 139 1.0× 178 1.5× 33 808
Katherine L. Rosewell United States 18 296 0.6× 318 0.9× 148 0.6× 252 1.7× 168 1.4× 27 1.0k
Vasilios T. Garyfallou United States 15 310 0.6× 196 0.6× 108 0.5× 167 1.2× 139 1.2× 21 632
Melinda A. Mittelman-Smith United States 12 469 0.9× 340 1.0× 108 0.5× 267 1.8× 70 0.6× 13 851
Richard H. Mills United States 12 266 0.5× 159 0.5× 146 0.6× 64 0.4× 122 1.0× 15 519
OK Rönnekleiv United States 10 246 0.5× 165 0.5× 117 0.5× 114 0.8× 105 0.9× 12 613
Junzo Kato Japan 16 465 0.9× 352 1.0× 144 0.6× 265 1.8× 172 1.5× 47 973

Countries citing papers authored by Oscar González‐Flores

Since Specialization
Citations

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

Fields of papers citing papers by Oscar González‐Flores

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Oscar González‐Flores. 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 Oscar González‐Flores. The network helps show where Oscar González‐Flores may publish in the future.

Co-authorship network of co-authors of Oscar González‐Flores

This figure shows the co-authorship network connecting the top 25 collaborators of Oscar González‐Flores. A scholar is included among the top collaborators of Oscar González‐Flores 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 Oscar González‐Flores. Oscar González‐Flores 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.
González‐Flores, Oscar, et al.. (2024). Participation of kisspeptin, progesterone, and GnRH receptors on lordosis behavior induced by kisspeptin. Physiology & Behavior. 283. 114609–114609. 2 indexed citations
2.
González‐Flores, Oscar, et al.. (2024). Hormonas y neurociencias. 15(39).
3.
Pfaus, James G., et al.. (2024). Cellular and molecular mechanisms of action of ovarian steroid hormones II: Regulation of sexual behavior in female rodents.. Neuroscience & Biobehavioral Reviews. 168. 105946–105946. 1 indexed citations
4.
García‐Juárez, Marcos, et al.. (2023). Participation of the nitric oxide pathway in lordosis induced by apelin-13 in female rats. Hormones and Behavior. 156. 105449–105449. 1 indexed citations
5.
Domı́nguez-Salazar, Emilio, et al.. (2021). Behavioral consequences of postnatal undernutrition and enriched environment during later life. Physiology & Behavior. 241. 113566–113566. 4 indexed citations
6.
García‐Juárez, Marcos, et al.. (2020). Tibolone facilitates lordosis behavior through estrogen, progestin, and GnRH-1 receptors in estrogen-primed rats. Neuroscience Letters. 736. 135299–135299. 2 indexed citations
7.
Fernández‐Martínez, Eduardo, Marcos García‐Juárez, Mario I. Ortíz, et al.. (2019). Two thalidomide analogs induce persistent estrous behavior and inhibit uterus contractility in rats: The central role of cAMP. Neuroscience Letters. 714. 134612–134612. 1 indexed citations
8.
Portillo, Wendy, Oscar González‐Flores, F. Camacho, Shaila K. Mani, & Raúl G. Paredes. (2016). Participation of progesterone receptors in facilitation and sequential inhibition of lordosis response induced by ring A-reduced progesterone metabolites in female mice.. Behavioral Neuroscience. 130(6). 624–634. 4 indexed citations
9.
García‐Juárez, Marcos, et al.. (2015). Sexual receptivity facilitated by unesterified estradiol: Dependence on estrogen and progestin receptors and priming dose of estradiol benzoate.. Behavioral Neuroscience. 129(6). 777–788. 14 indexed citations
10.
Eguibar, José R., et al.. (2015). Differential organization of male copulatory patterns in high- and low-yawning-frequency sublines versus outbred Sprague–Dawley rats. Physiology & Behavior. 153. 84–90. 5 indexed citations
11.
Gómora‐Arrati, Porfirio, Marcos García‐Juárez, Jeffrey D. Blaustein, et al.. (2014). Estrogen receptors regulate the estrous behavior induced by progestins, peptides, and prostaglandin E2. Hormones and Behavior. 66(2). 361–368. 7 indexed citations
12.
García‐Juárez, Marcos, Carlos Beyer, Porfirio Gómora‐Arrati, et al.. (2013). Lordosis facilitation by leptin in ovariectomized, estrogen-primed rats requires simultaneous or sequential activation of several protein kinase pathways. Pharmacology Biochemistry and Behavior. 110. 13–18. 7 indexed citations
13.
González‐Arenas, Aliesha, et al.. (2012). Expression pattern of Tau in the rat brain during pregnancy and the beginning of lactation. Brain Research Bulletin. 89(3-4). 108–114. 11 indexed citations
14.
Gómora‐Arrati, Porfirio, et al.. (2011). Effects of RU486 in the expression of progesterone receptor isoforms in the hypothalamus and the preoptic area of the rat during postpartum estrus. Neuroscience Letters. 504(2). 127–130. 7 indexed citations
15.
Gómora‐Arrati, Porfirio, et al.. (2010). Role of progesterone receptors during postpartum estrus in rats. Hormones and Behavior. 59(1). 37–43. 26 indexed citations
16.
17.
González‐Flores, Oscar, et al.. (2006). Facilitation of estrous behavior by vaginal cervical stimulation in female rats involves α1-adrenergic receptor activation of the nitric oxide pathway. Behavioural Brain Research. 176(2). 237–243. 26 indexed citations
18.
González‐Flores, Oscar, et al.. (2005). Differential effect of kinase A and C blockers on lordosis facilitation by progesterone and its metabolites in ovariectomized estrogen-primed rats. Hormones and Behavior. 49(3). 398–404. 31 indexed citations
19.
Beyer, Carlos, et al.. (1999). Indomethacin Inhibits Lordosis Induced by Ring A-Reduced Progestins: Possible Role of 3α-Oxoreduction in Progestin-Facilitated Lordosis. Hormones and Behavior. 35(1). 1–8. 33 indexed citations
20.
Beyer, Carlos, Oscar González‐Flores, & Gabriela González‐Mariscal. (1995). Ring a reduced progestins potently stimulate estrous behavior in rats: Paradoxical effect through the progesterone receptor. Physiology & Behavior. 58(5). 985–993. 49 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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