Luz Candenas

3.8k total citations
96 papers, 3.1k citations indexed

About

Luz Candenas is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Reproductive Medicine. According to data from OpenAlex, Luz Candenas has authored 96 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 37 papers in Cellular and Molecular Neuroscience and 34 papers in Reproductive Medicine. Recurrent topics in Luz Candenas's work include Neuropeptides and Animal Physiology (35 papers), Hypothalamic control of reproductive hormones (24 papers) and Receptor Mechanisms and Signaling (19 papers). Luz Candenas is often cited by papers focused on Neuropeptides and Animal Physiology (35 papers), Hypothalamic control of reproductive hormones (24 papers) and Receptor Mechanisms and Signaling (19 papers). Luz Candenas collaborates with scholars based in Spain, France and Australia. Luz Candenas's co-authors include Francisco M. Pinto, Julio D. Martı́n, Jocelyn N. Pennefather, Eva Patak, Mariano Hernández, Teresa Almeida, Carlo Alberto Maggi, Alessandro Lecci, Charles Advenier and Manuel Fernández Sánchez and has published in prestigious journals such as Chemical Reviews, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Luz Candenas

96 papers receiving 3.0k citations

Peers

Luz Candenas

CMN

PHYSI

GENET

Marco Cerbón Mexico

S. St‐Pierre Canada

Koji Koike Japan

M Schachter United Kingdom

Allan M. Judd United States

Tommie W. Redding United States

Jacqueline Van Sande Belgium

Gustavo Blanco United States

Ralf Middendorff Germany

A. Bèlanger Canada

Marco Cerbón Mexico

Luz Candenas

681 ×0.6

212 ×0.2

CMN

479 ×0.5

212 ×0.6

PHYSI

451 ×1.7

GENET

Citations per year, relative to Luz Candenas Luz Candenas (= 1×) peers Marco Cerbón

Countries citing papers authored by Luz Candenas

Since Specialization

Citations

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

Fields of papers citing papers by Luz Candenas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luz Candenas

This figure shows the co-authorship network connecting the top 25 collaborators of Luz Candenas. A scholar is included among the top collaborators of Luz Candenas 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 Luz Candenas. Luz Candenas 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

Moreno‐Navarrete, José María, Luz Candenas, Francisco M. Pinto, et al.. (2016). Ferroportin mRNA is down-regulated in granulosa and cervical cells from infertile women. Fertility and Sterility. 107(1). 236–242. 8 indexed citations

Pinto, Francisco M., et al.. (2015). Analysis of the Expression of Tachykinins and Tachykinin Receptors in the Rat Uterus During Early Pregnancy1. Biology of Reproduction. 93(2). 51–51. 3 indexed citations

Pinto, Francisco M., Manuel Fernández Sánchez, Teresa Almeida, et al.. (2014). Expression of neurokinin B/NK3 receptor and kisspeptin/KISS1 receptor in human granulosa cells. Human Reproduction. 29(12). 2736–2746. 53 indexed citations

Pinto, Francisco M., Nerea Subirán, Manuel Fernández Sánchez, et al.. (2013). The Voltage-Gated Sodium Channel Nav1.8 Is Expressed in Human Sperm. PLoS ONE. 8(9). e76084–e76084. 27 indexed citations

Subirán, Nerea, et al.. (2012). Autocrine regulation of human sperm motility by the met-enkephalin opioid peptide. Fertility and Sterility. 98(3). 617–625.e3. 16 indexed citations

Pinto, Francisco M., Teresa Almeida, Mariano Hernández, et al.. (2012). Analysis of the expression of neurokinin B, kisspeptin, and their cognate receptors NK3R and KISS1R in the human female genital tract. Fertility and Sterility. 97(5). 1213–1219. 95 indexed citations

Pennefather, Jocelyn N., Eva Patak, Sebastian Ziccone, et al.. (2006). Regulation of the Stimulant Actions of Neurokinin A and Human Hemokinin-1 on the Human Uterus: A Comparison with Histamine1. Biology of Reproduction. 75(3). 334–341. 15 indexed citations

Pennefather, Jocelyn N., Eva Patak, Francisco M. Pinto, & Luz Candenas. (2004). Mammalian tachykinins and uterine smooth muscle: the challenge escalates. European Journal of Pharmacology. 500(1-3). 15–26. 23 indexed citations

Bellucci, Francesca, Stefania Meini, Rose‐Marie Catalioto, et al.. (2004). Pharmacological evaluation of α and β human tachykinin NK2 receptor splice variants expressed in CHO cells. European Journal of Pharmacology. 499(3). 229–238. 13 indexed citations

10.

Pennefather, Jocelyn N., Alessandro Lecci, Luz Candenas, et al.. (2003). Tachykinins and tachykinin receptors: a growing family. Life Sciences. 74(12). 1445–1463. 380 indexed citations

11.

Pinto, Francisco M., et al.. (2001). Expression of preprotachykinin-B, the gene that encodes neurokinin B, in the rat uterus. European Journal of Pharmacology. 425(2). R1–R2. 17 indexed citations

12.

Pinto, Francisco M., et al.. (2000). Differential expression of amiloride-sensitive NA+ channel subunits messenger RNA in the rat uterus. Life Sciences. 66(22). PL313–PL317. 3 indexed citations

13.

Savineau, Jean‐Pierre, et al.. (2000). Cellular mechanisms involved in iso-osmotic high K+ solutions-induced contraction of the estrogen-primed rat myometrium. Life Sciences. 66(25). 2441–2453. 10 indexed citations

14.

Norte, Manuel, et al.. (1998). Complexation of okadaic acid : A preliminary study. Bioorganic & Medicinal Chemistry Letters. 8(9). 1007–1012. 4 indexed citations

15.

Pinto, Francisco M., Elsa Anselmi, Mariano Hernández, et al.. (1998). Characterization of tachykinin receptors in the uterus of the oestrogen‐primed rat. British Journal of Pharmacology. 123(2). 259–268. 29 indexed citations

16.

Loirand, Gervaise, Pierre Pacaud, Luz Candenas, et al.. (1997). An Analysis of the Mechanisms Involved in the Okadaic Acid-Induced Contraction of the Estrogen-Primed Rat Uterus. Journal of Pharmacology and Experimental Therapeutics. 282(1). 201–207. 29 indexed citations

17.

Advenier, Charles, et al.. (1992). Formoterol and salbutamol inhibit bradykinin‐ and histamine‐induced airway microvascular leakage in guinea‐pig. British Journal of Pharmacology. 105(4). 792–798. 57 indexed citations

18.

Candenas, Luz, Philippe Devillier, Emmanuel Naline, & Charles Advenier. (1992). Contractile effect ofα,β‐methylene ATP on the guinea‐pig isolated trachea. Fundamental and Clinical Pharmacology. 6(3). 135–144. 5 indexed citations

19.

Candenas, Luz, Emmanuel Naline, Louis Puybasset, P. Devillier, & Charles Advenier. (1991). Effect of atrial natriuretic peptide and on atriopeptins on the human isolated bronchus. Comparison with the reactivity of the guinea-pig isolated trachea. Pulmonary Pharmacology. 4(2). 120–125. 14 indexed citations

20.

Advenier, Charles, Luz Candenas, Emmanuel Naline, & Christine De Vos. (1991). The effect of cetirizine on the human isolated bronchus: Interaction with salbutamol. Journal of Allergy and Clinical Immunology. 88(1). 104–113. 19 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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