Edith Sánchez

994 total citations
19 papers, 814 citations indexed

About

Edith Sánchez is a scholar working on Endocrine and Autonomic Systems, Endocrinology, Diabetes and Metabolism and Behavioral Neuroscience. According to data from OpenAlex, Edith Sánchez has authored 19 papers receiving a total of 814 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Endocrine and Autonomic Systems, 8 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Behavioral Neuroscience. Recurrent topics in Edith Sánchez's work include Thyroid Disorders and Treatments (8 papers), Stress Responses and Cortisol (7 papers) and Regulation of Appetite and Obesity (7 papers). Edith Sánchez is often cited by papers focused on Thyroid Disorders and Treatments (8 papers), Stress Responses and Cortisol (7 papers) and Regulation of Appetite and Obesity (7 papers). Edith Sánchez collaborates with scholars based in United States, Hungary and Mexico. Edith Sánchez's co-authors include Ronald M. Lechan, Praful S. Singru, Csaba Fekete, Patricia Joseph‐Bravo, Antônio C. Bianco, Victor Ramı́rez-Amaya, Federico Bermúdez‐Rattoni, Patricia de Gortari, Argel Aguilar‐Valles and Jean‐Louis Charli and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Comparative Neurology and Brain Research.

In The Last Decade

Edith Sánchez

18 papers receiving 802 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edith Sánchez United States 16 356 331 179 162 139 19 814
I. Kakucska Hungary 16 225 0.6× 332 1.0× 273 1.5× 102 0.6× 186 1.3× 19 822
Francisca Díaz Spain 20 408 1.1× 128 0.4× 169 0.9× 297 1.8× 74 0.5× 46 929
Guibao Gu United States 13 260 0.7× 179 0.5× 68 0.4× 249 1.5× 365 2.6× 17 1.0k
Xue-Jun Yang United States 9 570 1.6× 191 0.6× 51 0.3× 362 2.2× 83 0.6× 10 1.1k
Naoto Minamitani Japan 17 290 0.8× 456 1.4× 114 0.6× 112 0.7× 301 2.2× 31 853
M A Borg United States 7 627 1.8× 423 1.3× 45 0.3× 274 1.7× 123 0.9× 8 1.1k
L K Malendowicz Italy 21 463 1.3× 321 1.0× 255 1.4× 166 1.0× 577 4.2× 80 1.3k
Bernard Gagné Canada 15 174 0.5× 298 0.9× 236 1.3× 92 0.6× 282 2.0× 22 1.2k
Vladimir Znamensky United States 11 94 0.3× 178 0.5× 179 1.0× 85 0.5× 290 2.1× 11 619
Bertalan Dudás United States 18 190 0.5× 104 0.3× 119 0.7× 110 0.7× 231 1.7× 47 774

Countries citing papers authored by Edith Sánchez

Since Specialization
Citations

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

Fields of papers citing papers by Edith Sánchez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edith Sánchez. 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 Edith Sánchez. The network helps show where Edith Sánchez may publish in the future.

Co-authorship network of co-authors of Edith Sánchez

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

All Works

19 of 19 papers shown
1.
Sánchez, Edith, et al.. (2012). The acute response of the amygdalar TRH system to psychogenic stressors varies dependent on the paradigm and circadian condition. Brain Research. 1452. 73–84. 8 indexed citations
3.
Marsili, Alessandro, Edith Sánchez, Praful S. Singru, et al.. (2011). Thyroxine-induced expression of pyroglutamyl peptidase II and inhibition of TSH release precedes suppression of TRH mRNA and requires type 2 deiodinase. Journal of Endocrinology. 211(1). 73–78. 22 indexed citations
4.
Freitas, Beatriz C.G., Balázs Gereben, Melany Castillo, et al.. (2010). Paracrine signaling by glial cell–derived triiodothyronine activates neuronal gene expression in the rodent brain and human cells. Journal of Clinical Investigation. 120(6). 2206–2217. 128 indexed citations
5.
Kádár, Andrea, Edith Sánchez, Gábor Wittmann, et al.. (2010). Distribution of hypophysiotropic thyrotropin‐releasing hormone (TRH)‐synthesizing neurons in the hypothalamic paraventricular nucleus of the mouse. The Journal of Comparative Neurology. 518(19). 3948–3961. 56 indexed citations
6.
Sánchez, Edith, Praful S. Singru, Gábor Wittmann, et al.. (2010). Contribution of TNF-α and Nuclear Factor-κB Signaling to Type 2 Iodothyronine Deiodinase Activation in the Mediobasal Hypothalamus after Lipopolysaccharide Administration. Endocrinology. 151(8). 3827–3835. 24 indexed citations
7.
Sánchez, Edith, Miguel Ángel Vargas, Praful S. Singru, et al.. (2009). Tanycyte Pyroglutamyl Peptidase II Contributes to Regulation of the Hypothalamic-Pituitary-Thyroid Axis through Glial-Axonal Associations in the Median Eminence. Endocrinology. 150(5). 2283–2291. 81 indexed citations
8.
Sánchez, Edith, Praful S. Singru, Monica Bodria, et al.. (2008). Differential Effects of Refeeding on Melanocortin-Responsive Neurons in the Hypothalamic Paraventricular Nucleus. Endocrinology. 149(9). 4329–4335. 23 indexed citations
9.
Sánchez, Edith, Praful S. Singru, Csaba Fekete, & Ronald M. Lechan. (2008). Induction of Type 2 Iodothyronine Deiodinase in the Mediobasal Hypothalamus by Bacterial Lipopolysaccharide: Role of Corticosterone. Endocrinology. 149(5). 2484–2493. 27 indexed citations
11.
Wajner, Simone Magagnin, Rossana C. N. Melo, Gleydes G. Parreira, et al.. (2007). Type 2 iodothyronine deiodinase is highly expressed in germ cells of adult rat testis. Journal of Endocrinology. 194(1). 47–54. 29 indexed citations
12.
Singru, Praful S., Edith Sánchez, Csaba Fekete, & Ronald M. Lechan. (2006). Importance of Melanocortin Signaling in Refeeding-Induced Neuronal Activation and Satiety. Endocrinology. 148(2). 638–646. 62 indexed citations
13.
Aguilar‐Valles, Argel, Edith Sánchez, Patricia de Gortari, et al.. (2006). The expression of TRH, its receptors and degrading enzyme is differentially modulated in the rat limbic system during training in the Morris water maze. Neurochemistry International. 50(2). 404–417. 35 indexed citations
14.
Sánchez, Edith, Csaba Fekete, Ronald M. Lechan, & Patricia Joseph‐Bravo. (2006). Cocaine- and amphetamine-regulated transcript (CART) expression is differentially regulated in the hypothalamic paraventricular nucleus of lactating rats exposed to suckling or cold stimulation. Brain Research. 1132(1). 120–128. 21 indexed citations
15.
16.
Fekete, Csaba, Praful S. Singru, Edith Sánchez, et al.. (2005). Differential Effects of Central Leptin, Insulin, or Glucose Administration during Fasting on the Hypothalamic-Pituitary-Thyroid Axis and Feeding-Related Neurons in the Arcuate Nucleus. Endocrinology. 147(1). 520–529. 77 indexed citations
18.
Sánchez, Edith, et al.. (1999). El primer año de vida del niño. Dialnet (Universidad de la Rioja).
19.
Sánchez, Edith, Jean‐Louis Charli, Gabriel Corkidi, et al.. (1997). Expression of the proprotein convertases PC1 and PC2 mRNAs in thyrotropin releasing hormone neurons of the rat paraventricular nucleus of hypothalamus. Brain Research. 761(1). 77–86. 21 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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