Cyrielle Tréard

685 total citations
8 papers, 82 citations indexed

About

Cyrielle Tréard is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Cyrielle Tréard has authored 8 papers receiving a total of 82 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Pulmonary and Respiratory Medicine and 2 papers in Rheumatology. Recurrent topics in Cyrielle Tréard's work include Ion Transport and Channel Regulation (4 papers), Ion channel regulation and function (3 papers) and Magnesium in Health and Disease (2 papers). Cyrielle Tréard is often cited by papers focused on Ion Transport and Channel Regulation (4 papers), Ion channel regulation and function (3 papers) and Magnesium in Health and Disease (2 papers). Cyrielle Tréard collaborates with scholars based in France, Algeria and Greece. Cyrielle Tréard's co-authors include Nabila Bouatia‐Naji, Xavier Jeunemaı̂tre, Soto Romuald Kiando, Rosa Vargas‐Poussou, Anne Blanchard, Sjoerd Verkaart, Sabina Jeleń, Carolina Salvador, Ángel Valdez-Ortíz and Joost G.J. Hoenderop and has published in prestigious journals such as PLoS ONE, American Journal of Physiology-Renal Physiology and International Journal of Cardiology.

In The Last Decade

Cyrielle Tréard

8 papers receiving 80 citations

Peers

Cyrielle Tréard

MB

NEPHR

PRM

RHEUM

SURGE

Gaëtan Lebrun France

Maria Paola Carta Italy

Li Gong China

Shaukat Sadikot Belgium

Aaltje Y Adema Netherlands

Syuitsu Ueda Japan

Roman Cibulka Czechia

Gábor Zakar United States

Huacong Deng China

Elizabeth Swan United Kingdom

Gaëtan Lebrun France

Cyrielle Tréard

35 ×0.7

MB

23 ×1.1

NEPHR

12 ×0.8

PRM

3 ×0.2

RHEUM

28 ×2.0

SURGE

Citations per year, relative to Cyrielle Tréard Cyrielle Tréard (= 1×) peers Gaëtan Lebrun

Countries citing papers authored by Cyrielle Tréard

Since Specialization

Citations

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

Fields of papers citing papers by Cyrielle Tréard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cyrielle Tréard

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Kiando, Soto Romuald, et al.. (2019). Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city. Diabetes & Metabolic Syndrome Clinical Research & Reviews. 13(2). 1317–1320. 8 indexed citations

2.

Gil‐Peña, Helena, Eliécer Coto, Fernando Santos, et al.. (2017). A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry. Nefrología. 37(4). 423–428. 5 indexed citations

3.

Blanchard, Anne, Rosa Vargas‐Poussou, Adam Ogna, et al.. (2017). Signification of distal urinary acidification defects in hypocitraturic patients. PLoS ONE. 12(5). e0177329–e0177329. 6 indexed citations

4.

Gil‐Peña, Helena, Eliécer Coto, Fernando Santos, et al.. (2017). A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry. Nefrología (English Edition). 37(4). 423–428. 1 indexed citations

5.

Kiando, Soto Romuald, et al.. (2016). The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city. International Journal of Cardiology. 225. 408–411. 18 indexed citations

6.

Vargas‐Poussou, Rosa, Sjoerd Verkaart, Ángel Valdez-Ortíz, et al.. (2016). Functionomics of NCC mutations in Gitelman syndrome using a novel mammalian cell-based activity assay. American Journal of Physiology-Renal Physiology. 311(6). F1159–F1167. 23 indexed citations

7.

Escobar, Laura I., et al.. (2016). Mutations in ATP6V1B1 and ATP6V0A4 genes cause recessive distal renal tubular acidosis in Mexican families. Molecular Genetics & Genomic Medicine. 4(3). 303–311. 18 indexed citations

8.

Kiando, Soto Romuald, Nathan R. Tucker, Alexander Katz, et al.. (2015). CO-43: Genetic study identifies common variation in phactr1 to associate with fibromuscular dysplasia. Annales de Cardiologie et d Angéiologie. 64. S20–S20. 3 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.

Explore authors with similar magnitude of impact