Natalia R. Salvetti

2.2k total citations
93 papers, 1.7k citations indexed

About

Natalia R. Salvetti is a scholar working on Agronomy and Crop Science, Public Health, Environmental and Occupational Health and Reproductive Medicine. According to data from OpenAlex, Natalia R. Salvetti has authored 93 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Agronomy and Crop Science, 60 papers in Public Health, Environmental and Occupational Health and 29 papers in Reproductive Medicine. Recurrent topics in Natalia R. Salvetti's work include Reproductive Physiology in Livestock (62 papers), Reproductive Biology and Fertility (60 papers) and Ovarian function and disorders (18 papers). Natalia R. Salvetti is often cited by papers focused on Reproductive Physiology in Livestock (62 papers), Reproductive Biology and Fertility (60 papers) and Ovarian function and disorders (18 papers). Natalia R. Salvetti collaborates with scholars based in Argentina, United States and Chile. Natalia R. Salvetti's co-authors include Hugo H. Ortega, Florencia Rey, Vasantha Padmanabhan, Eduardo Juan Gimeno, Celina Baravalle, Pablo U. Díaz, M.M.L. Velázquez, F.M. Rodríguez, M.L. Stangaferro and N.C. Gareis and has published in prestigious journals such as Endocrinology, Life Sciences and British Journal Of Nutrition.

In The Last Decade

Natalia R. Salvetti

91 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Natalia R. Salvetti Argentina	25	948	932	623	383	269	93	1.7k
M. Khalid United Kingdom	25	1.1k 1.1×	745 0.8×	514 0.8×	552 1.4×	164 0.6×	76	1.8k
W. Kanitz Germany	25	860 0.9×	1.2k 1.3×	757 1.2×	537 1.4×	126 0.5×	89	2.1k
Izabela Wocławek-Potocka Poland	27	833 0.9×	531 0.6×	488 0.8×	358 0.9×	575 2.1×	87	1.8k
Tomás J. Acosta Japan	26	1.3k 1.4×	502 0.5×	315 0.5×	531 1.4×	516 1.9×	78	1.8k
M.O. Gastal United States	32	2.3k 2.4×	1.6k 1.7×	824 1.3×	817 2.1×	151 0.6×	111	2.9k
B.R. Downey Canada	25	821 0.9×	1.2k 1.3×	808 1.3×	697 1.8×	123 0.5×	70	2.2k
Tom Vanholder Belgium	12	1.3k 1.4×	775 0.8×	352 0.6×	741 1.9×	88 0.3×	28	1.7k
Mitsuhiro Takagi Japan	20	538 0.6×	632 0.7×	481 0.8×	278 0.7×	165 0.6×	137	1.8k
J.L.M.R. Leroy Belgium	16	1.0k 1.1×	730 0.8×	379 0.6×	553 1.4×	71 0.3×	27	1.5k
T. Wise United States	25	560 0.6×	504 0.5×	517 0.8×	932 2.4×	112 0.4×	84	1.9k

Countries citing papers authored by Natalia R. Salvetti

Since Specialization

Citations

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

Fields of papers citing papers by Natalia R. Salvetti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalia R. Salvetti. 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 Natalia R. Salvetti. The network helps show where Natalia R. Salvetti may publish in the future.

Co-authorship network of co-authors of Natalia R. Salvetti

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

All Works

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20 of 20 papers shown

Angeli, Emanuela, et al.. (2024). Association between endometrial protein expression of IFN-γ and delayed conception after parturition in dairy cows. Veterinary Research Communications. 48(5). 3187–3196. 1 indexed citations

Renna, María Sol, et al.. (2023). ACTH impairs the migratory and secretory profile of mononuclear cells during proestrus in cattle. Research in Veterinary Science. 164. 105031–105031. 1 indexed citations

Ortega, Hugo H., et al.. (2022). Association between heat stress during intrauterine development and the expression and regulation of ovarian steroid hormone receptors in adult Holstein cows. Reproduction Fertility and Development. 34(16). 1003–1022. 3 indexed citations

Rey, Florencia, et al.. (2022). Endometrial expression of members of the IL-1 family: their involvement in delayed conception of dairy cows. Theriogenology. 195. 168–175. 6 indexed citations

Gareis, N.C., F.M. Rodríguez, Natalia R. Salvetti, et al.. (2022). Contribution of key elements of nutritional metabolism to the development of cystic ovarian disease in dairy cattle. Theriogenology. 197. 209–223. 4 indexed citations

Renna, María Sol, Marcelo Signorini, N.C. Gareis, et al.. (2021). Association between phagocytic activity of monocytes and days to conception after parturition in dairy cows when considering the hormonal and metabolic milieu. Animal Reproduction Science. 232. 106818–106818. 5 indexed citations

Varela, María L., et al.. (2020). Effects of adrenocorticotrophic hormone on the expression of matrix metalloproteinases and their inhibitors in the bovine ovary. Reproduction Fertility and Development. 32(8). 748–762. 12 indexed citations

Hein, Gustavo Juan, et al.. (2018). Expression of TGFBR1, TGFBR2, TGFBR3, ACVR1B and ACVR2B is altered in ovaries of cows with cystic ovarian disease. Reproduction in Domestic Animals. 54(1). 46–54. 8 indexed citations

Angeli, Emanuela, et al.. (2018). Altered expression of IL-1β, IL-1RI, IL-1RII, IL-1RA and IL-4 could contribute to anovulation and follicular persistence in cattle. Theriogenology. 110. 61–73. 19 indexed citations

10.

Díaz, Pablo U., M.L. Stangaferro, N.C. Gareis, et al.. (2015). Characterization of persistent follicles induced by prolonged treatment with progesterone in dairy cows: An experimental model for the study of ovarian follicular cysts. Theriogenology. 84(7). 1149–1160. 45 indexed citations

11.

Velázquez, M.M.L., et al.. (2015). Altered Expression of Pro-inflammatory Cytokines in Ovarian Follicles of Cows with Cystic Ovarian Disease. Journal of Comparative Pathology. 153(2-3). 116–130. 25 indexed citations

12.

Velázquez, M.M.L., et al.. (2013). Changes in the expression of Heat Shock Proteins in ovaries from bovines with cystic ovarian disease induced by ACTH. Research in Veterinary Science. 95(3). 1059–1067. 10 indexed citations

13.

Salvetti, Natalia R., Hugo H. Ortega, Almudena Veiga-López, & Vasantha Padmanabhan. (2012). Developmental Programming: Impact of Prenatal Testosterone Excess on Ovarian Cell Proliferation and Apoptotic Factors in Sheep1. Biology of Reproduction. 87(1). 22, 1–10. 35 indexed citations

14.

Velázquez, M.M.L., et al.. (2009). Heat shock protein patterns in the bovine ovary and relation with cystic ovarian disease. Animal Reproduction Science. 118(2-4). 201–209. 32 indexed citations

15.

Rey, Florencia, et al.. (2009). Insulin-Like Growth Factor-II and Insulin-Like Growth Factor-Binding Proteins in Bovine Cystic Ovarian Disease. Journal of Comparative Pathology. 142(2-3). 193–204. 25 indexed citations

16.

Salvetti, Natalia R., et al.. (2008). Characterization of Pituitary Cell Populations in Rats with Induced Polycystic Ovaries. Cells Tissues Organs. 188(3). 310–319. 9 indexed citations

17.

Marini, Mirella, et al.. (2006). Análisis de técnicas de recuperación antigénica para la detección inmunohistoquímica del virus de la diarrea viral bovina. Redalyc (Universidad Autónoma del Estado de México). 8(1). 59–65. 1 indexed citations

18.

Ortega, Hugo H., et al.. (2006). Oestradiol Induced Inhibition of Neuroendocrine Marker Expression in Leydig Cells of Adult Rats. Reproduction in Domestic Animals. 41(3). 204–209. 6 indexed citations

19.

Salvetti, Natalia R., et al.. (2000). Lectinhistochemical and Cytometrical Evaluation of the Corpus Luteum of the Rat at the End of Pregnancy. Anatomia Histologia Embryologia. 29(3). 129–134. 3 indexed citations

20.

Ortega, Hugo H., et al.. (1999). Microwave-enhanced of a method of silver impregnation applied in dermatohistopathology.. PubMed. 23(2). 143–7. 2 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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